2191 result(s) have been found!
| Accession | Name | Sequence | Source/Organism | Mechanism | Assay Type | Cell Line | Cancer Type | Activity |
|---|---|---|---|---|---|---|---|---|
| dbacp00028 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 14.2% inhibition at 10-6 M |
| dbacp00029 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 19.7% inhibition at 10-5 M |
| dbacp00030 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 24.9% inhibition at 10-4 M |
| dbacp00031 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 30.4% inhibition at 10-3 M |
| dbacp00032 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 10% inhibition at 10-5 M |
| dbacp00033 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 8.2% inhibition at 10-4 M |
| dbacp00034 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 36.1% inhibition at 10-3 M |
| dbacp00035 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 6.5% inhibition at 10-6 M |
| dbacp00036 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 14% inhibition at 10-5 M |
| dbacp00037 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 7.5% inhibition at 10-4 M |
| dbacp00038 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 14% inhibition at 10-3 M |
| dbacp00039 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 9.8% inhibition at 10-6 M |
| dbacp00040 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 1.6% inhibition at 10-5 M |
| dbacp00041 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 5.4% inhibition at 10-4 M |
| dbacp00042 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 26.5% inhibition at 10-3 M |
| dbacp00043 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 12.9% inhibition at 10-6 M |
| dbacp00044 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 16.5% inhibition at 10-5 M |
| dbacp00045 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 28.1% inhibition at 10-4 M |
| dbacp00046 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 58.2% inhibition at 10-3 M |
| dbacp00047 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 3.5% inhibition at 10-6 M |
| dbacp00048 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 22.7% inhibition at 10-5 M |
| dbacp00049 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 18.9% inhibition at 10-4 M |
| dbacp00050 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 26.4% inhibition at 10-3 M |
| dbacp00051 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 2.4% inhibition at 10-5 M |
| dbacp00052 | Enkephalins7 analogue-8 | YA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 7.5% inhibition at 10-4 M |
| dbacp00053 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 6.2% inhibition at 10-6 M |
| dbacp00054 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 6.4% inhibition at 10-5 M |
| dbacp00055 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 8.2% inhibition at 10-4 M |
| dbacp00056 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 21.2% inhibition at 10-3 M |
| dbacp00057 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 7.5% inhibition at 10-6 M |
| dbacp00058 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 6.1% inhibition at 10-5 M |
| dbacp00059 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 3.1% inhibition at 10-4 M |
| dbacp00060 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 14.8% inhibition at 10-3 M |
| dbacp00061 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 3.9% inhibition at 10-5 M |
| dbacp00062 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 7.3% inhibition at 10-3 M |
| dbacp00063 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 4.9% inhibition at 10-6 M |
| dbacp00064 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 8.9% inhibition at 10-5 M |
| dbacp00065 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 3.4% inhibition at 10-4 M |
| dbacp00066 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 20.8% inhibition at 10-3 M |
| dbacp00067 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 10.5% inhibition at 10-6 M |
| dbacp00068 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 21.9% inhibition at 10-5 M |
| dbacp00069 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 11.8% inhibition at 10-4 M |
| dbacp00070 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 17.9% inhibition at 10-3 M |
| dbacp00071 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 3.7% inhibition at 10-6 M |
| dbacp00072 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 16.5% inhibition at 10-5 M |
| dbacp00073 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 8.4% inhibition at 10-4 M |
| dbacp00074 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 14.5% inhibition at 10-3 M |
| dbacp00075 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 1.1% inhibition at 10-5 M |
| dbacp00076 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 1.2% inhibition at 10-4 M |
| dbacp00077 | Enkephalins7 analogue-9 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 17.8% inhibition at 10-3 M |
| dbacp00078 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 8.5% inhibition at 10-6 M |
| dbacp00079 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 4.9% inhibition at 10-5 M |
| dbacp00080 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 1.9% inhibition at 10-4 M |
| dbacp00081 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 16.2% inhibition at 10-3 M |
| dbacp00082 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 7.2% inhibition at 10-6 M |
| dbacp00083 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 17.1% inhibition at 10-5 M |
| dbacp00084 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 11.0% inhibition at 10-4 M |
| dbacp00085 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 20.5% inhibition at 10-3 M |
| dbacp00086 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 3.0% inhibition at 10-6 M |
| dbacp00087 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 4.7% inhibition at 10-5 M |
| dbacp00088 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 2.7% inhibition at 10-4 M |
| dbacp00089 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 7.3% inhibition at 10-3 M |
| dbacp00090 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 0.7% inhibition at 10-6 M |
| dbacp00091 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 8.3% inhibition at 10-5 M |
| dbacp00092 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 10.5% inhibition at 10-4 M |
| dbacp00093 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 21.8% inhibition at 10-3 M |
| dbacp00094 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 10.7% inhibition at 10-6 M |
| dbacp00095 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 10.0% inhibition at 10-5 M |
| dbacp00096 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 7.7% inhibition at 10-4 M |
| dbacp00097 | Enkephalins7 analogue-10 | YSA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 18.7% inhibition at 10-3 M |
| dbacp00125 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 2.7% inhibition at 10-6 M |
| dbacp00126 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 2.0% inhibition at 10-5 M |
| dbacp00127 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 18.8% inhibition at 10-4 M |
| dbacp00128 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 26.7% inhibition at 10-3 M |
| dbacp00129 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 9.8% inhibition at 10-6 M |
| dbacp00130 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 7.3% inhibition at 10-5 M |
| dbacp00131 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 9.9% inhibition at 10-4 M |
| dbacp00132 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 28.2% inhibition at 10-3 M |
| dbacp00133 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 1.6% inhibition at 10-6 M |
| dbacp00134 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 2.9% inhibition at 10-5 M |
| dbacp00135 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 5.9% inhibition at 10-4 M |
| dbacp00136 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 17.9% inhibition at 10-3 M |
| dbacp00137 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 5.4% inhibition at 10-6 M |
| dbacp00138 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 7.4% inhibition at 10-5 M |
| dbacp00139 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 9.5% inhibition at 10-4 M |
| dbacp00140 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 15.7% inhibition at 10-3 M |
| dbacp00141 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 13.6% inhibition at 10-6 M |
| dbacp00142 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 20.4% inhibition at 10-5 M |
| dbacp00143 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 14.4% inhibition at 10-4 M |
| dbacp00144 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 23.4% inhibition at 10-3 M |
| dbacp00145 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 2.2% inhibition at 10-6 M |
| dbacp00146 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 4.2% inhibition at 10-5 M |
| dbacp00147 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 6.4% inhibition at 10-4 M |
| dbacp00148 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 6.2% inhibition at 10-3 M |
| dbacp00149 | Enkephalins7 analogue-15 | YSA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 21.2% inhibition at 10-3 M |
| dbacp00159 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 4.6% inhibition at 10-6 M |
| dbacp00160 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 4.9% inhibition at 10-5 M |
| dbacp00161 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 12.6% inhibition at 10-4 M |
| dbacp00162 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 26.4% inhibition at 10-3 M |
| dbacp00163 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 11.0% inhibition at 10-6 M |
| dbacp00164 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 11.7% inhibition at 10-5 M |
| dbacp00165 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 11.6% inhibition at 10-4 M |
| dbacp00166 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 28.2% inhibition at 10-3 M |
| dbacp00167 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 1.2% inhibition at 10-5 M |
| dbacp00168 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 3.3% inhibition at 10-4 M |
| dbacp00169 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 19.4% inhibition at 10-3 M |
| dbacp00170 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 7.6% inhibition at 10-6 M |
| dbacp00171 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 3.8% inhibition at 10-5 M |
| dbacp00172 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 12.4% inhibition at 10-4 M |
| dbacp00173 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 22.4% inhibition at 10-3 M |
| dbacp00174 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 17.0% inhibition at 10-6 M |
| dbacp00175 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 13.5% inhibition at 10-5 M |
| dbacp00176 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 13.5% inhibition at 10-4 M |
| dbacp00177 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 25.3% inhibition at 10-3 M |
| dbacp00178 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 8.1% inhibition at 10-6 M |
| dbacp00179 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 6.9% inhibition at 10-5 M |
| dbacp00180 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 8.1% inhibition at 10-4 M |
| dbacp00181 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 8.6% inhibition at 10-3 M |
| dbacp00182 | Enkephalins7 analogue-16 | YRA*G | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 15.6% inhibition at 10-3 M |
| dbacp00192 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 1.0% inhibition at 10-6 M |
| dbacp00193 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 10.1% inhibition at 10-5 M |
| dbacp00194 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 16.8% inhibition at 10-4 M |
| dbacp00195 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 36.1% inhibition at 10-3 M |
| dbacp00196 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 4.9% inhibition at 10-6 M |
| dbacp00197 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 10.2% inhibition at 10-5 M |
| dbacp00198 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 13.3% inhibition at 10-4 M |
| dbacp00199 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 28.0% inhibition at 10-3 M |
| dbacp00200 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 0.8% inhibition at 10-6 M |
| dbacp00201 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 1.4% inhibition at 10-5 M |
| dbacp00202 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 2.4% inhibition at 10-4 M |
| dbacp00203 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 18.3% inhibition at 10-3 M |
| dbacp00204 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 3.3% inhibition at 10-6 M |
| dbacp00205 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 11.0% inhibition at 10-5M |
| dbacp00206 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 7.9% inhibition at 10-4 M |
| dbacp00207 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 23.7% inhibition at 10-3 M |
| dbacp00208 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 12.2% inhibition at 10-6 M |
| dbacp00209 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 15.5% inhibition at 10-5 M |
| dbacp00210 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 24.7% inhibition at 10-4 M |
| dbacp00211 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 29.0% inhibition at 10-3 M |
| dbacp00212 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 3.0% inhibition at 10-6 M |
| dbacp00213 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 8.4% inhibition at 10-5 M |
| dbacp00214 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 18.5% inhibition at 10-4 M |
| dbacp00215 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 10.6% inhibition at 10-3 M |
| dbacp00216 | Enkephalins7 analogue-17 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 22.8% inhibition at 10-3 M |
| dbacp00226 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 13.7% inhibition at 10-6 M |
| dbacp00227 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 25.8% inhibition at 10-5 M |
| dbacp00228 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 34.7% inhibition at 10-4 M |
| dbacp00229 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 44.5% inhibition at 10-3 M |
| dbacp00230 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 8.5% inhibition at 10-6 M |
| dbacp00231 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 9.5% inhibition at 10-5 M |
| dbacp00232 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 15.4% inhibition at 10-4 M |
| dbacp00233 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 24.1% inhibition at 10-3 M |
| dbacp00234 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 2.4% inhibition at 10-6 M |
| dbacp00235 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 4.5% inhibition at 10-5 M |
| dbacp00236 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 11.4% inhibition at 10-4 M |
| dbacp00237 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 23.2% inhibition at 10-3 M |
| dbacp00238 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 16.2% inhibition at 10-6 M |
| dbacp00239 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 6.6% inhibition at 10-5 M |
| dbacp00240 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 5.1% inhibition at 10-4 M |
| dbacp00241 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 14.5% inhibition at 10-3 M |
| dbacp00242 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 26.4% inhibition at 10-6 M |
| dbacp00243 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 13.1% inhibition at 10-5 M |
| dbacp00244 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 14.6% inhibition at 10-4 M |
| dbacp00245 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | SW-620 | Colon cancer | 38.4% inhibition at 10-3 M |
| dbacp00246 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 17.7% inhibition at 10-6 M |
| dbacp00247 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 10.9% inhibition at 10-5 M |
| dbacp00248 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 12.1% inhibition at 10-4 M |
| dbacp00249 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 8.1% inhibition at 10-3 M |
| dbacp00250 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 9.6% inhibition at 10-4 M |
| dbacp00251 | Enkephalins7 analogue-18 | YA*GFM | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 29.9% inhibition at 10-3 M |
| dbacp00279 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 3.9% inhibition at 10-5 M |
| dbacp00280 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HEp-2 | Larynx cancer | 45% inhibition at 10-3 M |
| dbacp00281 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HeLa | Cervical cancer | 9.3% inhibition at 10-3 M |
| dbacp00282 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 4.1% inhibition at 10-6 M |
| dbacp00283 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 70.7% inhibition at 10-5 M |
| dbacp00284 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HBL | Skin cancer | 34.4% inhibition at 10-3 M |
| dbacp00285 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | HT-29 | Colon cancer | 9.2% inhibition at 10-3 M |
| dbacp00286 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 11.08% inhibition at 10-5 M |
| dbacp00287 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | CaCo-2 | Colon cancer | 47.0% inhibition at 10-3 M |
| dbacp00288 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 2.2% inhibition at 10-6 M |
| dbacp00289 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 7.1% inhibition at 10-5 M |
| dbacp00290 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 6.9% inhibition at 10-4 M |
| dbacp00291 | Enkephalins7 analogue-23 | YGGFMA* | Synthetic Peptide | Apoptosis inducing | MTT/MTS assay | MCF-7 | Breast cancer | 25.9% inhibition at 10-3 M |
| dbacp00312 | (HHPHG)2 | HHPHGHHPHG | Synthetic Peptide | Antiangiogenesis | Tropomyosin binding assay | Not found | Tumor | IC50 : 11.6 µM |
| dbacp00313 | (HHPHG)2 | HHPHGHHPHG | Synthetic Peptide | Antiangiogenesis | Tropomyosin binding assay | Not found | Tumor | IC50 : 26.9 µM |
| dbacp00314 | (HHPHG)3 | HHPHGHHPHGHHPHG | Synthetic Peptide | Antiangiogenesis | Tropomyosin binding assay | Not found | Tumor | IC50 : 1.25 µM |
| dbacp00315 | (HHPHG)3 | HHPHGHHPHGHHPHG | Synthetic Peptide | Antiangiogenesis | Tropomyosin binding assay | Not found | Tumor | IC50 : 1.56 µM |
| dbacp00316 | (HHPHG)4 | HHPHGHHPHGHHPHGHHPHG | Synthetic Peptide | Antiangiogenesis | Tropomyosin binding assay | Not found | Tumor | IC50 : 0.256 µM |
| dbacp00317 | (HHPHG)4 | HHPHGHHPHGHHPHGHHPHG | Synthetic Peptide | Antiangiogenesis | Tropomyosin binding assay | Not found | Tumor | IC50 : 0.245 µM |
| dbacp00318 | (RGD-4C)-GG-D(KLAKLAK)2 | ACDCRGDCFCGGKLAKLAKKLAKLAK | Synthetic Peptide | Apoptosis inducing | Internalization assay,Mitochondrial swelling assay,Cell-free apoptosis assay,Caspase activation assay | KS1767 | Not specified | LC50 : 10 μM |
| dbacp00322 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Epithelial cancer | CC50 : 46.2 ± 7.6 μM |
| dbacp00323 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Chronic myeloid Leukemia | CC50 : 46.2 ± 7.6 μM |
| dbacp00324 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Gastric cancer | CC50 : 46.2 ± 7.6 μM |
| dbacp00325 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Breast cancer | CC50 : 46.2 ± 7.6 μM |
| dbacp00326 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Cervical cancer | CC50 : 46.2 ± 7.6 μM |
| dbacp00327 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Epithelial cancer | CC50 : 2.3 ± 0.2 μM |
| dbacp00328 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Chronic myeloid Leukemia | CC50 : 2.3 ± 0.2 μM |
| dbacp00329 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Gastric cancer | CC50 : 2.3 ± 0.2 μM |
| dbacp00330 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Breast cancer | CC50 : 2.3 ± 0.2 μM |
| dbacp00331 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Cervical cancer | CC50 : 2.3 ± 0.2 μM |
| dbacp00332 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Epithelial cancer | CC50 : 30.8 ± 2.0 μM |
| dbacp00333 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Chronic myeloid Leukemia | CC50 : 30.8 ± 2.0 μM |
| dbacp00334 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Gastric cancer | CC50 : 30.8 ± 2.0 μM |
| dbacp00335 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Breast cancer | CC50 : 30.8 ± 2.0 μM |
| dbacp00336 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Cervical cancer | CC50 : 30.8 ± 2.0 μM |
| dbacp00337 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Epithelial cancer | CC50 : 36.2 ± 2.8 μM |
| dbacp00338 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Chronic myeloid Leukemia | CC50 : 36.2 ± 2.8 μM |
| dbacp00339 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Gastric cancer | CC50 : 36.2 ± 2.8 μM |
| dbacp00340 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Breast cancer | CC50 : 36.2 ± 2.8 μM |
| dbacp00341 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Cervical cancer | CC50 : 36.2 ± 2.8 μM |
| dbacp00342 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Epithelial cancer | CC50 : 29.0 ± 3.7 μM |
| dbacp00343 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Chronic myeloid Leukemia | CC50 : 29.0 ± 3.7 μM |
| dbacp00344 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Gastric cancer | CC50 : 29.0 ± 3.7 μM |
| dbacp00345 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Breast cancer | CC50 : 29.0 ± 3.7 μM |
| dbacp00346 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Cervical cancer | CC50 : 29.0 ± 3.7 μM |
| dbacp00347 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Epithelial cancer | CC50 : 6.4 ± 0.6 μM |
| dbacp00348 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Chronic myeloid Leukemia | CC50 : 6.4 ± 0.6 μM |
| dbacp00349 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Gastric cancer | CC50 : 6.4 ± 0.6 μM |
| dbacp00350 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Breast cancer | CC50 : 6.4 ± 0.6 μM |
| dbacp00351 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Cervical cancer | CC50 : 6.4 ± 0.6 μM |
| dbacp00352 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Epithelial cancer | CC50 : 33.3 ±7.4 μM |
| dbacp00353 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Chronic myeloid Leukemia | CC50 : 33.3 ±7.4 μM |
| dbacp00354 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Gastric cancer | CC50 : 33.3 ±7.4 μM |
| dbacp00355 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Breast cancer | CC50 : 33.3 ±7.4 μM |
| dbacp00356 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Cervical cancer | CC50 : 33.3 ±7.4 μM |
| dbacp00357 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Epithelial cancer | CC50 : 9.5 ± 0.5 μM |
| dbacp00358 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Chronic myeloid Leukemia | CC50 : 9.5 ± 0.5 μM |
| dbacp00359 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Gastric cancer | CC50 : 9.5 ± 0.5 μM |
| dbacp00360 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Breast cancer | CC50 : 9.5 ± 0.5 μM |
| dbacp00361 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Cervical cancer | CC50 : 9.5 ± 0.5 μM |
| dbacp00362 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Epithelial cancer | CC50 : 51.0 ± 4.6 μM |
| dbacp00363 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Chronic myeloid Leukemia | CC50 : 51.0 ± 4.6 μM |
| dbacp00364 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Gastric cancer | CC50 : 51.0 ± 4.6 μM |
| dbacp00365 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Breast cancer | CC50 : 51.0 ± 4.6 μM |
| dbacp00366 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Cervical cancer | CC50 : 51.0 ± 4.6 μM |
| dbacp00367 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Epithelial cancer | CC50 : 4.6 ± 0.2 μM |
| dbacp00368 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Chronic myeloid Leukemia | CC50 : 4.6 ± 0.2 μM |
| dbacp00369 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Gastric cancer | CC50 : 4.6 ± 0.2 μM |
| dbacp00370 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Breast cancer | CC50 : 4.6 ± 0.2 μM |
| dbacp00371 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Cervical cancer | CC50 : 4.6 ± 0.2 μM |
| dbacp00372 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Epithelial cancer | CC50 : 15.6 ± 3.6 μM |
| dbacp00373 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Chronic myeloid Leukemia | CC50 : 15.6 ± 3.6 μM |
| dbacp00374 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Gastric cancer | CC50 : 15.6 ± 3.6 μM |
| dbacp00375 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Breast cancer | CC50 : 15.6 ± 3.6 μM |
| dbacp00376 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Cervical cancer | CC50 : 15.6 ± 3.6 μM |
| dbacp00377 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Epithelial cancer | CC50 : > 64 μM |
| dbacp00378 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Chronic myeloid Leukemia | CC50 : > 64 μM |
| dbacp00379 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Gastric cancer | CC50 : > 64 μM |
| dbacp00380 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Breast cancer | CC50 : > 64 μM |
| dbacp00381 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Cervical cancer | CC50 : > 64 μM |
| dbacp00382 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Epithelial cancer | CC50 : 37.5 ± 3.3 μM |
| dbacp00383 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Chronic myeloid Leukemia | CC50 : 37.5 ± 3.3 μM |
| dbacp00384 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Gastric cancer | CC50 : 37.5 ± 3.3 μM |
| dbacp00385 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Breast cancer | CC50 : 37.5 ± 3.3 μM |
| dbacp00386 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Cervical cancer | CC50 : 37.5 ± 3.3 μM |
| dbacp00387 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Epithelial cancer | CC50 : 1.4 ± 0.2 μM |
| dbacp00388 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Chronic myeloid Leukemia | CC50 : 1.4 ± 0.2 μM |
| dbacp00389 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Gastric cancer | CC50 : 1.4 ± 0.2 μM |
| dbacp00390 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Breast cancer | CC50 : 1.4 ± 0.2 μM |
| dbacp00391 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Cervical cancer | CC50 : 1.4 ± 0.2 μM |
| dbacp00392 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Epithelial cancer | CC50 : 38.5 ± 4.8 μM |
| dbacp00393 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Chronic myeloid Leukemia | CC50 : 38.5 ± 4.8 μM |
| dbacp00394 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Gastric cancer | CC50 : 38.5 ± 4.8 μM |
| dbacp00395 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Breast cancer | CC50 : 38.5 ± 4.8 μM |
| dbacp00396 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Cervical cancer | CC50 : 38.5 ± 4.8 μM |
| dbacp00397 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Epithelial cancer | CC50 : 15.5 ± 0.8 μM |
| dbacp00398 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Chronic myeloid Leukemia | CC50 : 15.5 ± 0.8 μM |
| dbacp00399 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Gastric cancer | CC50 : 15.5 ± 0.8 μM |
| dbacp00400 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Breast cancer | CC50 : 15.5 ± 0.8 μM |
| dbacp00401 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Cervical cancer | CC50 : 15.5 ± 0.8 μM |
| dbacp00403 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Epithelial cancer | CC50 : 22.5 ± 3.3 μM |
| dbacp00404 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Chronic myeloid Leukemia | CC50 : 22.5 ± 3.3 μM |
| dbacp00405 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Gastric cancer | CC50 : 22.5 ± 3.3 μM |
| dbacp00406 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Breast cancer | CC50 : 22.5 ± 3.3 μM |
| dbacp00407 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Cervical cancer | CC50 : 22.5 ± 3.3 μM |
| dbacp00408 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Epithelial cancer | CC50 : 3.0 ± 0.1 μM |
| dbacp00409 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Chronic myeloid Leukemia | CC50 : 3.0 ± 0.1 μM |
| dbacp00410 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Gastric cancer | CC50 : 3.0 ± 0.1 μM |
| dbacp00411 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Breast cancer | CC50 : 3.0 ± 0.1 μM |
| dbacp00412 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Cervical cancer | CC50 : 3.0 ± 0.1 μM |
| dbacp00413 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Epithelial cancer | CC50 : 14.9 ± 0.8 μM |
| dbacp00414 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Chronic myeloid Leukemia | CC50 : 14.9 ± 0.8 μM |
| dbacp00415 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Gastric cancer | CC50 : 14.9 ± 0.8 μM |
| dbacp00416 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Breast cancer | CC50 : 14.9 ± 0.8 μM |
| dbacp00417 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Cervical cancer | CC50 : 14.9 ± 0.8 μM |
| dbacp00418 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Epithelial cancer | CC50 : 51.5 ± 3.9 μM |
| dbacp00419 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Chronic myeloid Leukemia | CC50 : 51.5 ± 3.9 μM |
| dbacp00420 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Gastric cancer | CC50 : 51.5 ± 3.9 μM |
| dbacp00421 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Breast cancer | CC50 : 51.5 ± 3.9 μM |
| dbacp00422 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Cervical cancer | CC50 : 51.5 ± 3.9 μM |
| dbacp00423 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Epithelial cancer | CC50 : 3.9 ± 0.2 μM |
| dbacp00424 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Chronic myeloid Leukemia | CC50 : 3.9 ± 0.2 μM |
| dbacp00425 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Gastric cancer | CC50 : 3.9 ± 0.2 μM |
| dbacp00426 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Breast cancer | CC50 : 3.9 ± 0.2 μM |
| dbacp00427 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Cervical cancer | CC50 : 3.9 ± 0.2 μM |
| dbacp00428 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Epithelial cancer | CC50 : 14.1 ± 0.9 μM |
| dbacp00429 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Chronic myeloid Leukemia | CC50 : 14.1 ± 0.9 μM |
| dbacp00430 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Gastric cancer | CC50 : 14.1 ± 0.9 μM |
| dbacp00431 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Breast cancer | CC50 : 14.1 ± 0.9 μM |
| dbacp00432 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Cervical cancer | CC50 : 14.1 ± 0.9 μM |
| dbacp00440 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Epithelial cancer | CC50 : 19.5 ± 0.5 μM |
| dbacp00441 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Chronic myeloid Leukemia | CC50 : 19.5 ± 0.5 μM |
| dbacp00442 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Gastric cancer | CC50 : 19.5 ± 0.5 μM |
| dbacp00443 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Breast cancer | CC50 : 19.5 ± 0.5 μM |
| dbacp00444 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Cervical cancer | CC50 : 19.5 ± 0.5 μM |
| dbacp00445 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Epithelial cancer | CC50 : 1.7 ± 0.1 μM |
| dbacp00446 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Chronic myeloid Leukemia | CC50 : 1.7 ± 0.1 μM |
| dbacp00447 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Gastric cancer | CC50 : 1.7 ± 0.1 μM |
| dbacp00448 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Breast cancer | CC50 : 1.7 ± 0.1 μM |
| dbacp00449 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Cervical cancer | CC50 : 1.7 ± 0.1 μM |
| dbacp00450 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Epithelial cancer | CC50 : 9.0 ± 0.5 μM |
| dbacp00451 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Chronic myeloid Leukemia | CC50 : 9.0 ± 0.5 μM |
| dbacp00452 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Gastric cancer | CC50 : 9.0 ± 0.5 μM |
| dbacp00453 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Breast cancer | CC50 : 9.0 ± 0.5 μM |
| dbacp00454 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Cervical cancer | CC50 : 9.0 ± 0.5 μM |
| dbacp00455 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Epithelial cancer | CC50 : 44.2 ± 2.2 μM |
| dbacp00456 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Chronic myeloid Leukemia | CC50 : 44.2 ± 2.2 μM |
| dbacp00457 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Gastric cancer | CC50 : 44.2 ± 2.2 μM |
| dbacp00458 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Breast cancer | CC50 : 44.2 ± 2.2 μM |
| dbacp00459 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Cervical cancer | CC50 : 44.2 ± 2.2 μM |
| dbacp00460 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Epithelial cancer | CC50 : 6.7 ± 0.7 μM |
| dbacp00461 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Chronic myeloid Leukemia | CC50 : 6.7 ± 0.7 μM |
| dbacp00462 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Gastric cancer | CC50 : 6.7 ± 0.7 μM |
| dbacp00463 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Breast cancer | CC50 : 6.7 ± 0.7 μM |
| dbacp00464 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Cervical cancer | CC50 : 6.7 ± 0.7 μM |
| dbacp00465 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Epithelial cancer | CC50 : 2.1 ± 0.2 μM |
| dbacp00466 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Chronic myeloid Leukemia | CC50 : 2.1 ± 0.2 μM |
| dbacp00467 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Gastric cancer | CC50 : 2.1 ± 0.2 μM |
| dbacp00468 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Breast cancer | CC50 : 2.1 ± 0.2 μM |
| dbacp00469 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Cervical cancer | CC50 : 2.1 ± 0.2 μM |
| dbacp00470 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Epithelial cancer | CC50 : 9.0 ± 1.1μM |
| dbacp00471 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Chronic myeloid Leukemia | CC50 : 9.0 ± 1.1μM |
| dbacp00472 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Gastric cancer | CC50 : 9.0 ± 1.1μM |
| dbacp00473 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Breast cancer | CC50 : 9.0 ± 1.1μM |
| dbacp00474 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Cervical cancer | CC50 : 9.0 ± 1.1μM |
| dbacp00475 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Epithelial cancer | CC50 : 5.1 ± 0.3 μM |
| dbacp00476 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Chronic myeloid Leukemia | CC50 : 5.1 ± 0.3 μM |
| dbacp00477 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Gastric cancer | CC50 : 5.1 ± 0.3 μM |
| dbacp00478 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Breast cancer | CC50 : 5.1 ± 0.3 μM |
| dbacp00479 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Cervical cancer | CC50 : 5.1 ± 0.3 μM |
| dbacp00480 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Epithelial cancer | CC50 : 26.5 ± 2.4 μM |
| dbacp00481 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Chronic myeloid Leukemia | CC50 : 26.5 ± 2.4 μM |
| dbacp00482 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Gastric cancer | CC50 : 26.5 ± 2.4 μM |
| dbacp00483 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Breast cancer | CC50 : 26.5 ± 2.4 μM |
| dbacp00484 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Cervical cancer | CC50 : 26.5 ± 2.4 μM |
| dbacp00485 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Epithelial cancer | CC50 : 2.0 ± 0.1 μM |
| dbacp00486 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Chronic myeloid Leukemia | CC50 : 2.0 ± 0.1 μM |
| dbacp00487 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Gastric cancer | CC50 : 2.0 ± 0.1 μM |
| dbacp00488 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Breast cancer | CC50 : 2.0 ± 0.1 μM |
| dbacp00489 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Cervical cancer | CC50 : 2.0 ± 0.1 μM |
| dbacp00490 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Epithelial cancer | CC50 : 14.7 ± 1.5 μM |
| dbacp00491 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Chronic myeloid Leukemia | CC50 : 14.7 ± 1.5 μM |
| dbacp00492 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Gastric cancer | CC50 : 14.7 ± 1.5 μM |
| dbacp00493 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Breast cancer | CC50 : 14.7 ± 1.5 μM |
| dbacp00494 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Cervical cancer | CC50 : 14.7 ± 1.5 μM |
| dbacp00495 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Epithelial cancer | CC50 : 20.9 ± 1.4 μM |
| dbacp00496 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Chronic myeloid Leukemia | CC50 : 20.9 ± 1.4 μM |
| dbacp00497 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Gastric cancer | CC50 : 20.9 ± 1.4 μM |
| dbacp00498 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Breast cancer | CC50 : 20.9 ± 1.4 μM |
| dbacp00499 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Cervical cancer | CC50 : 20.9 ± 1.4 μM |
| dbacp00500 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Epithelial cancer | CC50 : 15.2 ± 1.9 μM |
| dbacp00501 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Chronic myeloid Leukemia | CC50 : 15.2 ± 1.9 μM |
| dbacp00502 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Gastric cancer | CC50 : 15.2 ± 1.9 μM |
| dbacp00503 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Breast cancer | CC50 : 15.2 ± 1.9 μM |
| dbacp00504 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Cervical cancer | CC50 : 15.2 ± 1.9 μM |
| dbacp00505 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Epithelial cancer | CC50 : 1.3 ± 0.1 μM |
| dbacp00506 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Chronic myeloid Leukemia | CC50 : 1.3 ± 0.1 μM |
| dbacp00507 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Gastric cancer | CC50 : 1.3 ± 0.1 μM |
| dbacp00508 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Breast cancer | CC50 : 1.3 ± 0.1 μM |
| dbacp00509 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Cervical cancer | CC50 : 1.3 ± 0.1 μM |
| dbacp00510 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Epithelial cancer | CC50 : 15.7 ±1.1μM |
| dbacp00511 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Chronic myeloid Leukemia | CC50 : 15.7 ±1.1μM |
| dbacp00512 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Gastric cancer | CC50 : 15.7 ±1.1μM |
| dbacp00513 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Breast cancer | CC50 : 15.7 ±1.1μM |
| dbacp00514 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Cervical cancer | CC50 : 15.7 ±1.1μM |
| dbacp00515 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Epithelial cancer | CC50 : 10.4 ± 1.0 μM |
| dbacp00516 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Chronic myeloid Leukemia | CC50 : 10.4 ± 1.0 μM |
| dbacp00517 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Gastric cancer | CC50 : 10.4 ± 1.0 μM |
| dbacp00518 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Breast cancer | CC50 : 10.4 ± 1.0 μM |
| dbacp00519 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Cervical cancer | CC50 : 10.4 ± 1.0 μM |
| dbacp00520 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Epithelial cancer | CC50 : 29.4 ± 1.1 μM |
| dbacp00521 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Chronic myeloid Leukemia | CC50 : 29.4 ± 1.1 μM |
| dbacp00522 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Gastric cancer | CC50 : 29.4 ± 1.1 μM |
| dbacp00523 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Breast cancer | CC50 : 29.4 ± 1.1 μM |
| dbacp00524 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Cervical cancer | CC50 : 29.4 ± 1.1 μM |
| dbacp00525 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Epithelial cancer | CC50 : 5.0 ± 0.3 μM |
| dbacp00526 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Chronic myeloid Leukemia | CC50 : 5.0 ± 0.3 μM |
| dbacp00527 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Gastric cancer | CC50 : 5.0 ± 0.3 μM |
| dbacp00528 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Breast cancer | CC50 : 5.0 ± 0.3 μM |
| dbacp00529 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Cervical cancer | CC50 : 5.0 ± 0.3 μM |
| dbacp00530 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Epithelial cancer | CC50 : 34.5 ± 3.6 μM |
| dbacp00531 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Chronic myeloid Leukemia | CC50 : 34.5 ± 3.6 μM |
| dbacp00532 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Gastric cancer | CC50 : 34.5 ± 3.6 μM |
| dbacp00533 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Breast cancer | CC50 : 34.5 ± 3.6 μM |
| dbacp00534 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Cervical cancer | CC50 : 34.5 ± 3.6 μM |
| dbacp00535 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Epithelial cancer | CC50 : 39.4 ± 2.6 μM |
| dbacp00536 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Chronic myeloid Leukemia | CC50 : 39.4 ± 2.6 μM |
| dbacp00537 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Gastric cancer | CC50 : 39.4 ± 2.6 μM |
| dbacp00538 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Breast cancer | CC50 : 39.4 ± 2.6 μM |
| dbacp00539 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Cervical cancer | CC50 : 39.4 ± 2.6 μM |
| dbacp00540 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Epithelial cancer | CC50 : 3.1 ± 0.1 μM |
| dbacp00541 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Chronic myeloid Leukemia | CC50 : 3.1 ± 0.1 μM |
| dbacp00542 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Gastric cancer | CC50 : 3.1 ± 0.1 μM |
| dbacp00543 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Breast cancer | CC50 : 3.1 ± 0.1 μM |
| dbacp00544 | [K8R]cGm | GCRRLCYRQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Cervical cancer | CC50 : 3.1 ± 0.1 μM |
| dbacp00545 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Epithelial cancer | CC50 : 18.3 ± 1.4 μM |
| dbacp00546 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Chronic myeloid Leukemia | CC50 : 18.3 ± 1.4 μM |
| dbacp00547 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Gastric cancer | CC50 : 18.3 ± 1.4 μM |
| dbacp00548 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Breast cancer | CC50 : 18.3 ± 1.4 μM |
| dbacp00549 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Cervical cancer | CC50 : 18.3 ± 1.4 μM |
| dbacp00550 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Epithelial cancer | CC50 : 4.0 ± 0.1 μM |
| dbacp00551 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Chronic myeloid Leukemia | CC50 : 4.0 ± 0.1 μM |
| dbacp00552 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Gastric cancer | CC50 : 4.0 ± 0.1 μM |
| dbacp00553 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Breast cancer | CC50 : 4.0 ± 0.1 μM |
| dbacp00554 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Cervical cancer | CC50 : 4.0 ± 0.1 μM |
| dbacp00555 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Epithelial cancer | CC50 : 25.0 ± 2.9 μM |
| dbacp00556 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Chronic myeloid Leukemia | CC50 : 25.0 ± 2.9 μM |
| dbacp00557 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Gastric cancer | CC50 : 25.0 ± 2.9 μM |
| dbacp00558 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Breast cancer | CC50 : 25.0 ± 2.9 μM |
| dbacp00559 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Cervical cancer | CC50 : 25.0 ± 2.9 μM |
| dbacp00560 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Epithelial cancer | CC50 : 17.1 ± 0.7 μM |
| dbacp00561 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Chronic myeloid Leukemia | CC50 : 17.1 ± 0.7 μM |
| dbacp00562 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Gastric cancer | CC50 : 17.1 ± 0.7 μM |
| dbacp00563 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Breast cancer | CC50 : 17.1 ± 0.7 μM |
| dbacp00564 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Cervical cancer | CC50 : 17.1 ± 0.7 μM |
| dbacp00565 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Epithelial cancer | CC50 : 1.0 ± 0.1 μM |
| dbacp00566 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Chronic myeloid Leukemia | CC50 : 1.0 ± 0.1 μM |
| dbacp00567 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Gastric cancer | CC50 : 1.0 ± 0.1 μM |
| dbacp00568 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Breast cancer | CC50 : 1.0 ± 0.1 μM |
| dbacp00569 | [L5W]cGm | GCRRWCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Cervical cancer | CC50 : 1.0 ± 0.1 μM |
| dbacp00573 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Epithelial cancer | CC50 : > 64 μM |
| dbacp00574 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Chronic myeloid Leukemia | CC50 : > 64 μM |
| dbacp00575 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Gastric cancer | CC50 : > 64 μM |
| dbacp00576 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Breast cancer | CC50 : > 64 μM |
| dbacp00577 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Cervical cancer | CC50 : > 64 μM |
| dbacp00578 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Epithelial cancer | CC50 : 10.3 ± 1.1 μM |
| dbacp00579 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Chronic myeloid Leukemia | CC50 : 10.3 ± 1.1 μM |
| dbacp00580 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Gastric cancer | CC50 : 10.3 ± 1.1 μM |
| dbacp00581 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Breast cancer | CC50 : 10.3 ± 1.1 μM |
| dbacp00582 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Cervical cancer | CC50 : 10.3 ± 1.1 μM |
| dbacp00583 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Epithelial cancer | CC50 : 51.2 ± 4.0 μM |
| dbacp00584 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Chronic myeloid Leukemia | CC50 : 51.2 ± 4.0 μM |
| dbacp00585 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Gastric cancer | CC50 : 51.2 ± 4.0 μM |
| dbacp00586 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Breast cancer | CC50 : 51.2 ± 4.0 μM |
| dbacp00587 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Cervical cancer | CC50 : 51.2 ± 4.0 μM |
| dbacp00588 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Epithelial cancer | CC50 : > 64 μM |
| dbacp00589 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Chronic myeloid Leukemia | CC50 : > 64 μM |
| dbacp00590 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Gastric cancer | CC50 : > 64 μM |
| dbacp00591 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Breast cancer | CC50 : > 64 μM |
| dbacp00592 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Cervical cancer | CC50 : > 64 μM |
| dbacp00593 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Epithelial cancer | CC50 : 48.4 ± 0.7 μM |
| dbacp00594 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Chronic myeloid Leukemia | CC50 : 48.4 ± 0.7 μM |
| dbacp00595 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Gastric cancer | CC50 : 48.4 ± 0.7 μM |
| dbacp00596 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Breast cancer | CC50 : 48.4 ± 0.7 μM |
| dbacp00597 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Cervical cancer | CC50 : 48.4 ± 0.7 μM |
| dbacp00598 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Epithelial cancer | CC50 : 11.5 ± 0.6 μM |
| dbacp00599 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Chronic myeloid Leukemia | CC50 : 11.5 ± 0.6 μM |
| dbacp00600 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Gastric cancer | CC50 : 11.5 ± 0.6 μM |
| dbacp00601 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Breast cancer | CC50 : 11.5 ± 0.6 μM |
| dbacp00602 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Cervical cancer | CC50 : 11.5 ± 0.6 μM |
| dbacp00603 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Epithelial cancer | CC50 : 34.1 ± 3.9 μM |
| dbacp00604 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Chronic myeloid Leukemia | CC50 : 34.1 ± 3.9 μM |
| dbacp00605 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Gastric cancer | CC50 : 34.1 ± 3.9 μM |
| dbacp00606 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Breast cancer | CC50 : 34.1 ± 3.9 μM |
| dbacp00607 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HL-60 | Cervical cancer | CC50 : 34.1 ± 3.9 μM |
| dbacp00608 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Epithelial cancer | CC50 : 30.8 ± 2.5 μM |
| dbacp00609 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Chronic myeloid Leukemia | CC50 : 30.8 ± 2.5 μM |
| dbacp00610 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Gastric cancer | CC50 : 30.8 ± 2.5 μM |
| dbacp00611 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Breast cancer | CC50 : 30.8 ± 2.5 μM |
| dbacp00612 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Cervical cancer | CC50 : 30.8 ± 2.5 μM |
| dbacp00621 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Epithelial cancer | CC50 : 30.3 ± 1.1 μM |
| dbacp00622 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Chronic myeloid Leukemia | CC50 : 30.3 ± 1.1 μM |
| dbacp00623 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Gastric cancer | CC50 : 30.3 ± 1.1 μM |
| dbacp00624 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Breast cancer | CC50 : 30.3 ± 1.1 μM |
| dbacp00625 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Cervical cancer | CC50 : 30.3 ± 1.1 μM |
| dbacp00626 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Epithelial cancer | CC50 : 4.0 ± 0.1 μM |
| dbacp00627 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Chronic myeloid Leukemia | CC50 : 4.0 ± 0.1 μM |
| dbacp00628 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Gastric cancer | CC50 : 4.0 ± 0.1 μM |
| dbacp00629 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Breast cancer | CC50 : 4.0 ± 0.1 μM |
| dbacp00630 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Cervical cancer | CC50 : 4.0 ± 0.1 μM |
| dbacp00631 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Epithelial cancer | CC50 : 68.4 ± 9.6 μM |
| dbacp00632 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Chronic myeloid Leukemia | CC50 : 68.4 ± 9.6 μM |
| dbacp00633 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Gastric cancer | CC50 : 68.4 ± 9.6 μM |
| dbacp00634 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Breast cancer | CC50 : 68.4 ± 9.6 μM |
| dbacp00635 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Cervical cancer | CC50 : 68.4 ± 9.6 μM |
| dbacp00636 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Epithelial cancer | CC50 : 50.4 ± 2.4 μM |
| dbacp00637 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Chronic myeloid Leukemia | CC50 : 50.4 ± 2.4 μM |
| dbacp00638 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Gastric cancer | CC50 : 50.4 ± 2.4 μM |
| dbacp00639 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Breast cancer | CC50 : 50.4 ± 2.4 μM |
| dbacp00640 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Cervical cancer | CC50 : 50.4 ± 2.4 μM |
| dbacp00641 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Epithelial cancer | CC50 : 2.7 ± 0.1 μM |
| dbacp00642 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Chronic myeloid Leukemia | CC50 : 2.7 ± 0.1 μM |
| dbacp00643 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Gastric cancer | CC50 : 2.7 ± 0.1 μM |
| dbacp00644 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Breast cancer | CC50 : 2.7 ± 0.1 μM |
| dbacp00645 | [Y14W]cGm | GCRRLCYKQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Cervical cancer | CC50 : 2.7 ± 0.1 μM |
| dbacp00646 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Epithelial cancer | CC50 : 31.6 ± 1.3 μM |
| dbacp00647 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Chronic myeloid Leukemia | CC50 : 31.6 ± 1.3 μM |
| dbacp00648 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Gastric cancer | CC50 : 31.6 ± 1.3 μM |
| dbacp00649 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Breast cancer | CC50 : 31.6 ± 1.3 μM |
| dbacp00650 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Cervical cancer | CC50 : 31.6 ± 1.3 μM |
| dbacp00651 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Epithelial cancer | CC50 : 5.4 ± 0.3 μM |
| dbacp00652 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Chronic myeloid Leukemia | CC50 : 5.4 ± 0.3 μM |
| dbacp00653 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Gastric cancer | CC50 : 5.4 ± 0.3 μM |
| dbacp00654 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Breast cancer | CC50 : 5.4 ± 0.3 μM |
| dbacp00655 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Cervical cancer | CC50 : 5.4 ± 0.3 μM |
| dbacp00656 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Epithelial cancer | CC50 : 31.3 ± 2.6 μM |
| dbacp00657 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Chronic myeloid Leukemia | CC50 : 31.3 ± 2.6 μM |
| dbacp00658 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Gastric cancer | CC50 : 31.3 ± 2.6 μM |
| dbacp00659 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Breast cancer | CC50 : 31.3 ± 2.6 μM |
| dbacp00660 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Cervical cancer | CC50 : 31.3 ± 2.6 μM |
| dbacp00661 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Epithelial cancer | CC50 : 41.0 ± 4.2 μM |
| dbacp00662 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Chronic myeloid Leukemia | CC50 : 41.0 ± 4.2 μM |
| dbacp00663 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Gastric cancer | CC50 : 41.0 ± 4.2 μM |
| dbacp00664 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Breast cancer | CC50 : 41.0 ± 4.2 μM |
| dbacp00665 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Cervical cancer | CC50 : 41.0 ± 4.2 μM |
| dbacp00666 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Epithelial cancer | CC50 : 15.1 ± 1.4 μM |
| dbacp00667 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Chronic myeloid Leukemia | CC50 : 15.1 ± 1.4 μM |
| dbacp00668 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Gastric cancer | CC50 : 15.1 ± 1.4 μM |
| dbacp00669 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Breast cancer | CC50 : 15.1 ± 1.4 μM |
| dbacp00670 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Cervical cancer | CC50 : 15.1 ± 1.4 μM |
| dbacp00671 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Epithelial cancer | CC50 : 3.9 ± 0.1 μM |
| dbacp00672 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Chronic myeloid Leukemia | CC50 : 3.9 ± 0.1 μM |
| dbacp00673 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Gastric cancer | CC50 : 3.9 ± 0.1 μM |
| dbacp00674 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Breast cancer | CC50 : 3.9 ± 0.1 μM |
| dbacp00675 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Cervical cancer | CC50 : 3.9 ± 0.1 μM |
| dbacp00676 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Epithelial cancer | CC50 : 23.3 ± 0.4 μM |
| dbacp00677 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Chronic myeloid Leukemia | CC50 : 23.3 ± 0.4 μM |
| dbacp00678 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Gastric cancer | CC50 : 23.3 ± 0.4 μM |
| dbacp00679 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Breast cancer | CC50 : 23.3 ± 0.4 μM |
| dbacp00680 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Cervical cancer | CC50 : 23.3 ± 0.4 μM |
| dbacp00681 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Epithelial cancer | CC50 : 5.1 ± 0.3 μM |
| dbacp00682 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Chronic myeloid Leukemia | CC50 : 5.1 ± 0.3 μM |
| dbacp00683 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Gastric cancer | CC50 : 5.1 ± 0.3 μM |
| dbacp00684 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Breast cancer | CC50 : 5.1 ± 0.3 μM |
| dbacp00685 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Cervical cancer | CC50 : 5.1 ± 0.3 μM |
| dbacp00686 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Epithelial cancer | CC50 : 39.7 ± 3.8 μM |
| dbacp00687 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Chronic myeloid Leukemia | CC50 : 39.7 ± 3.8 μM |
| dbacp00688 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Gastric cancer | CC50 : 39.7 ± 3.8 μM |
| dbacp00689 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Breast cancer | CC50 : 39.7 ± 3.8 μM |
| dbacp00690 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Cervical cancer | CC50 : 39.7 ± 3.8 μM |
| dbacp00691 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Epithelial cancer | CC50 : > 64 μM |
| dbacp00692 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Chronic myeloid Leukemia | CC50 : > 64 μM |
| dbacp00693 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Gastric cancer | CC50 : > 64 μM |
| dbacp00694 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Breast cancer | CC50 : > 64 μM |
| dbacp00695 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Cervical cancer | CC50 : > 64 μM |
| dbacp00696 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Epithelial cancer | CC50 : 3.9 ± 0.2 μM |
| dbacp00697 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Chronic myeloid Leukemia | CC50 : 3.9 ± 0.2 μM |
| dbacp00698 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Gastric cancer | CC50 : 3.9 ± 0.2 μM |
| dbacp00699 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Breast cancer | CC50 : 3.9 ± 0.2 μM |
| dbacp00700 | [Y7W]cGm | GCRRLCWKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Cervical cancer | CC50 : 3.9 ± 0.2 μM |
| dbacp00704 | 10a | NA | Synthetic b2,2-amino acid derivatives | Induction of apoptosis; Disruption of cell membrane | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 28 µM |
| dbacp00705 | 10b | NA | Synthetic b2,2-amino acid derivatives | Induction of apoptosis; Disruption of cell membrane | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 11.4 µM |
| dbacp00706 | 10c | NA | Synthetic b2,2-amino acid derivatives | Induction of apoptosis; Disruption of cell membrane | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 6.6 µM |
| dbacp00707 | 11a | NA | Synthetic b2,2-amino acid derivatives | Induction of apoptosis; Disruption of cell membrane | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 5.2 µM |
| dbacp00708 | 11b | NA | Synthetic b2,2-amino acid derivatives | Induction of apoptosis; Disruption of cell membrane | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 19 µM |
| dbacp00709 | 11c | NA | Synthetic b2,2-amino acid derivatives | Induction of apoptosis; Disruption of cell membrane | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 7.2 µM |
| dbacp00710 | 12a | NA | Synthetic b2,2-amino acid derivatives | Induction of apoptosis; Disruption of cell membrane | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 6.1 µM |
| dbacp00711 | 12b | NA | Synthetic b2,2-amino acid derivatives | Induction of apoptosis; Disruption of cell membrane | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 27 µM |
| dbacp00712 | 12c | NA | Synthetic b2,2-amino acid derivatives | Induction of apoptosis; Disruption of cell membrane | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 14 µM |
| dbacp00805 | A4K14-citropin1.1 | GLFAVIKKVASVIKGL | Synthetic construct | Cell membrane disintegration | CCK-8 test | C4-2B | Prostate cancer | IC50 : 29.05 μM |
| dbacp00806 | A4K14-citropin1.1 | GLFAVIKKVASVIKGL | Synthetic construct | Cell membrane disintegration | CCK-8 test | C4-2B | Lung cancer | IC50 : 29.05 μM |
| dbacp00807 | A4K14-citropin1.1 | GLFAVIKKVASVIKGL | Synthetic construct | Cell membrane disintegration | CCK-8 test | A549 | Prostate cancer | IC50 : 14.97 μM |
| dbacp00808 | A4K14-citropin1.1 | GLFAVIKKVASVIKGL | Synthetic construct | Cell membrane disintegration | CCK-8 test | A549 | Lung cancer | IC50 : 14.97 μM |
| dbacp00809 | A4K14-citropin1.1 | GLFAVIKKVASVIKGL | Synthetic construct | Cell membrane disintegration | CCK-8 test | U87 | Prostate cancer | IC50 : 14.8 μM |
| dbacp00810 | A4K14-citropin1.1 | GLFAVIKKVASVIKGL | Synthetic construct | Cell membrane disintegration | CCK-8 test | U87 | Lung cancer | IC50 : 14.8 μM |
| dbacp00811 | A4K14-citropin1.1 | GLFAVIKKVASVIKGL | Synthetic construct | Cell membrane disintegration | CCK-8 test | MCF-7 | Prostate cancer | IC50 : 14.16 μM |
| dbacp00812 | A4K14-citropin1.1 | GLFAVIKKVASVIKGL | Synthetic construct | Cell membrane disintegration | CCK-8 test | MCF-7 | Lung cancer | IC50 : 14.16 μM |
| dbacp00951 | ABP-dHC-Cecropin A | RWKIFKKIERVGQNVRDGIIKAGPAIQVLGTAKALGK | Synthetic construct | Apoptosis inducing | MTT assay | K562 cells | Leukemia | IC50 : 349.5 μM |
| dbacp00952 | ABP-dHC-Cecropin A | RWKIFKKIERVGQNVRDGIIKAGPAIQVLGTAKALGK | Synthetic construct | Apoptosis inducing | MTT assay | U937 cells | Leukemia | IC50 : 303.2 μM |
| dbacp00953 | ABP-dHC-Cecropin A | RWKIFKKIERVGQNVRDGIIKAGPAIQVLGTAKALGK | Synthetic construct | Apoptosis inducing | MTT assay | THP-1 cells | Leukemia | IC50 : 228.5 μM |
| dbacp00954 | ABP-dHC-Cecropin A-K | RWKIFKKIERVGQNVRDGIIKAGKAIQVLGTAKALGK | Synthetic construct | Apoptosis inducing | MTT assay | K562 cells | Leukemia | IC50 : 349.5 μM |
| dbacp00955 | ABP-dHC-Cecropin A-K | RWKIFKKIERVGQNVRDGIIKAGKAIQVLGTAKALGK | Synthetic construct | Apoptosis inducing | MTT assay | U937 cells | Leukemia | IC50 : 303.2 μM |
| dbacp00956 | ABP-dHC-Cecropin A-K | RWKIFKKIERVGQNVRDGIIKAGKAIQVLGTAKALGK | Synthetic construct | Apoptosis inducing | MTT assay | THP-1 cells | Leukemia | IC50 : 228.5 μM |
| dbacp01174 | AP | ACDCRGDCFCGGGGIVRRADRAAVP | Endostatin derived synthetic peptide | Necrosis; Antiangiogenesis | MTT/MTS assay | BAE | Tumor | 50% inhibition at 2.5 µg/ml |
| dbacp01175 | AP | ACDCRGDCFCGGGGIVRRADRAAVP | Endostatin derived synthetic peptide | Necrosis; Antiangiogenesis | MTT/MTS assay | BAE | Tumor | 40% inhibition at 5 µg/ml |
| dbacp01176 | AP | ACDCRGDCFCGGGGIVRRADRAAVP | Endostatin derived synthetic peptide | Necrosis; Antiangiogenesis | MTT/MTS assay | BAE | Tumor | 75% inhibition at 10 µg/ml |
| dbacp01177 | AP(O) | ACDCRGDCFCGGGGIVRRADRAAVP | Endostatin derived synthetic peptide | Necrosis; Antiangiogenesis | MTT/MTS assay | BAE | Tumor | 40% inhibition at 2.5 µg/ml |
| dbacp01178 | AP(O) | ACDCRGDCFCGGGGIVRRADRAAVP | Endostatin derived synthetic peptide | Necrosis; Antiangiogenesis | MTT/MTS assay | BAE | Tumor | 42% inhibition at 5 µg/ml |
| dbacp01179 | AP(O) | ACDCRGDCFCGGGGIVRRADRAAVP | Endostatin derived synthetic peptide | Necrosis; Antiangiogenesis | MTT/MTS assay | BAE | Tumor | 52% inhibition at 10 µg/ml |
| dbacp01186 | APQQ | NA | Synthetic construct | Cell metatstasis inhibition | Transwell assay | MDA-MB-231 | Breast cancer | Not found |
| dbacp01187 | APQQ | NA | Synthetic construct | Cell metatstasis inhibition | Transwell assay | MCF-7 | Breast cancer | Not found |
| dbacp01188 | APQQ | NA | Synthetic construct | Cell metatstasis inhibition | Transwell assay | U251 | Brain cancer | Not found |
| dbacp01192 | Ascaphin-8 [T16A] | GFKDLLKGAAKALVKAVLF | Synthetic construct | Not specified | Not specified | Not found | Liver cancer | Not found |
| dbacp01442 | Baceridin | cyclo(L-Trp-D-Ala-D-allo-Ile-L-Val-D-Leu-L-Leu-) | Synthetic construct | Apoptosis inducing | MTT assay | HCT116 | Not specified | Not found |
| dbacp01443 | Baceridin | cyclo(L-Trp-D-Ala-D-allo-Ile-L-Val-D-Leu-L-Leu-) | Synthetic construct | Apoptosis inducing | MTT assay | RKO | Not specified | Not found |
| dbacp01444 | Baceridin | cyclo(L-Trp-D-Ala-D-allo-Ile-L-Val-D-Leu-L-Leu-) | Synthetic construct | Apoptosis inducing | MTT assay | HeLa | Not specified | Not found |
| dbacp01598 | BF2d | TRSSRAGLQWPVGRVHRLLRKGGC | Synthetic | Cell membrane disintegration | MTT/MTS assay | HeLa | Cervical cancer | At 1 µM 90-100% viablity |
| dbacp01599 | BF2d | TRSSRAGLQWPVGRVHRLLRKGGC | Synthetic | Cell membrane disintegration | MTT/MTS assay | HeLa | Cervical cancer | At 10 µM 90-95% viablity |
| dbacp01600 | BF2d | TRSSRAGLQWPVGRVHRLLRKGGC | Synthetic | Cell membrane disintegration | MTT/MTS assay | HeLa | Cervical cancer | At 100 µM 90-100% viablity |
| dbacp01892 | BPC194 | KKLKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | MDA-MB-231 | Cervical cancer | IC50 : 32.5 ± 0.5 μM |
| dbacp01893 | BPC194 | KKLKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | HeLa | Cervical cancer | IC50 : 29.5 ± 2 μM |
| dbacp01894 | BPC194 | KKLKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | HepG2 | Cervical cancer | IC50 : 46.0 ± 3 μM |
| dbacp01895 | BPC194 | KKLKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | A431 | Cervical cancer | IC50 : 50.0 ± 10 μM |
| dbacp01896 | BPC194 | KKLKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | Panc-1 | Cervical cancer | IC50 : 40.0 ± 3 Μm |
| dbacp01897 | BPC88 | KKLLKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | MDA-MB-231 | Cervical cancer | IC50 : 31.2 ± 5 μM |
| dbacp01898 | BPC88 | KKLLKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | HeLa | Cervical cancer | IC50 : 22.5 ± 0 μM |
| dbacp01899 | BPC88 | KKLLKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | HepG2 | Cervical cancer | IC50 : 32.5 ± 4 μM |
| dbacp01900 | BPC88 | KKLLKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | A431 | Cervical cancer | IC50 : 28.0 ± 3 μM |
| dbacp01901 | BPC88 | KKLLKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | Panc-1 | Cervical cancer | IC50 : 32.5 ± 11 μM |
| dbacp01902 | BPC96 | LKLKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | MDA-MB-231 | Cervical cancer | IC50 : 40.0 ± 7 μM |
| dbacp01903 | BPC96 | LKLKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | HeLa | Cervical cancer | IC50 : 24.5 ± 0.7 μM |
| dbacp01904 | BPC96 | LKLKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | HepG2 | Cervical cancer | IC50 : 34.5 ± 2 μM |
| dbacp01905 | BPC96 | LKLKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | A431 | Cervical cancer | IC50 : 35.0 ± 7 μM |
| dbacp01906 | BPC96 | LKLKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | Panc-1 | Cervical cancer | IC50 : 51.0 ± 6 Μm |
| dbacp01907 | BPC98 | LLKKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | MDA-MB-231 | Cervical cancer | IC50 : 40.7 ± 3 μM |
| dbacp01908 | BPC98 | LLKKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | HeLa | Cervical cancer | IC50 : 38.5 ± 4 μM |
| dbacp01909 | BPC98 | LLKKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | HepG2 | Cervical cancer | IC50 : 44.0 ± 3 μM |
| dbacp01910 | BPC98 | LLKKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | A431 | Cervical cancer | IC50 : 47.5 ± 4 μM |
| dbacp01911 | BPC98 | LLKKKFKKLQ | Synthetic Peptide | Inducing apoptosis | MTT assay | Panc-1 | Cervical cancer | IC50 : 44.5 ± 0.7 Μm |
| dbacp02108 | cMastoparan-C(cMP-C) | CLNLKALLAVAKKILC | Synthetic construct | Apoptosis | MTT assay | H157 | Non-small cell Lung cancer | IC50 : 7.02 μM |
| dbacp02109 | cMastoparan-C(cMP-C) | CLNLKALLAVAKKILC | Synthetic construct | Apoptosis | MTT assay | MBD-MB-435S | Melanocyte | IC50 : 13.87 μM |
| dbacp02110 | cMastoparan-C(cMP-C) | CLNLKALLAVAKKILC | Synthetic construct | Apoptosis | MTT assay | PC-3 | Human prostate carcinoma | IC50 : 13.87 μM |
| dbacp02111 | cMastoparan-C(cMP-C) | CLNLKALLAVAKKILC | Synthetic construct | Apoptosis | MTT assay | U251-MG | Human glioblastoma astrocytoma | IC50 : 8.56 μM |
| dbacp02112 | cMastoparan-C(cMP-C) | CLNLKALLAVAKKILC | Synthetic construct | Apoptosis | MTT assay | MCF-7 | Human breast cancer | IC50 : 13.66 μM |
| dbacp02145 | C1 | KKWβ2,2WKK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 10 ±2 µMol/L |
| dbacp02146 | C1 | KKWβ2,2WKK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 22 ±5 µMol/L |
| dbacp02148 | C2 | KWβ2,2WKK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 7.9 ± 0.3 µMol/L |
| dbacp02149 | C2 | KWβ2,2WKK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 1.71 ± 0.6 µMol/L |
| dbacp02150 | C3 | KKβ2,2WKK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 15 ± 2 µMol/L |
| dbacp02151 | C3 | KKβ2,2WKK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 92 ± 2 µMol/L |
| dbacp02152 | C4 | KWβ2,2KK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 12.6 ± 0.6 µMol/L |
| dbacp02153 | C4 | KWβ2,2KK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 99 ± 15 µMol/L |
| dbacp02154 | C5 | KKWβ2,2WKK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 11 ± 2 µMol/L |
| dbacp02155 | C5 | KKWβ2,2WKK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 23 ± 3 µMol/L |
| dbacp02156 | C6 | KWβ2,2WKK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 8 ± 1 µMol/L |
| dbacp02157 | C6 | KWβ2,2WKK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 26 ± 2 µMol/L |
| dbacp02158 | C7 | KKβ2,2WKK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 16 ± 5 µMol/L |
| dbacp02159 | C7 | KKβ2,2WKK | Synthetic construct | Membrane disruptive mode of action | MTT/MTS assay | Ramos | Lymphoma cancer | IC50 : 157 ± 30 µMol/L |
| dbacp02160 | C7A | KILRGVAKKIMRTFLRRISKDILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 :10.6 ± 0.4 µM |
| dbacp02161 | C7A | KILRGVAKKIMRTFLRRISKDILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 :13.0 ± 1.0 µM |
| dbacp02162 | C7A | KILRGVAKKIMRTFLRRISKDILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 :12.1 ± 1.6 µM |
| dbacp02163 | C7A | KILRGVAKKIMRTFLRRISKDILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 :37 ± 4.3 µM |
| dbacp02181 | C7A-D21K | KILRGVAKKIMRTFLRRISKKILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : 8.4 ± 0.2 µM |
| dbacp02182 | C7A-D21K | KILRGVAKKIMRTFLRRISKKILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : 12.3 ± 2.0 µM |
| dbacp02183 | C7A-D21K | KILRGVAKKIMRTFLRRISKKILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : 8.3 ± 0.5 µM |
| dbacp02184 | C7A-D21K | KILRGVAKKIMRTFLRRISKKILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : 12.3 ± 1.0 µM |
| dbacp02206 | C7A-Δ | KILRGVAKKIMRTFLRRILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : 13.8 ± 2.0 µM |
| dbacp02207 | C7A-Δ | KILRGVAKKIMRTFLRRILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : 9.3 ± 1.5 µM |
| dbacp02208 | C7A-Δ | KILRGVAKKIMRTFLRRILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : 13.1 ± 0.9 µM |
| dbacp02222 | C7A-Δ | KILRGVAKKIMRTFLRRILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : 7.5 ± 0.4 µM |
| dbacp02274 | CAMP1 | HVLFFFFNH2 | Synthetic | Cell membrane penetrating | MTT assay | UM-UC-5 | Not specified | IC50 : >100 μM |
| dbacp02275 | CAMP1 | HVLFFFFNH2 | Synthetic | Cell membrane penetrating | MTT assay | A549 | Not specified | IC50 : 12.39 μM |
| dbacp02276 | CAMP2 | HVLLFFFFNH2 | Synthetic | Cell membrane penetrating | MTT assay | UM-UC-5 | Not specified | IC50 : 21.61 μM |
| dbacp02277 | CAMP2 | HVLLFFFFNH2 | Synthetic | Cell membrane penetrating | MTT assay | A549 | Not specified | IC50 : 5.77μM |
| dbacp02278 | CAMP3 | HVLFFFFLFFNH2 | Synthetic | Cell membrane penetrating | MTT assay | UM-UC-5 | Not specified | IC50 : >100 μM |
| dbacp02279 | CAMP3 | HVLFFFFLFFNH2 | Synthetic | Cell membrane penetrating | MTT assay | A549 | Not specified | IC50 : 17.63μM |
| dbacp02280 | CAMP5 | HVLLLLLLLFNH2 | Synthetic | Cell membrane penetrating | MTT assay | UM-UC-5 | Not specified | IC50 : >100 μM |
| dbacp02281 | CAMP5 | HVLLLLLLLFNH2 | Synthetic | Cell membrane penetrating | MTT assay | A549 | Not specified | IC50 : 19.65 μM |
| dbacp02282 | CAMP7 | HVLLLLFFFFNH2 | Synthetic | Cell membrane penetrating | MTT assay | UM-UC-5 | Not specified | IC50 : >100 μM |
| dbacp02283 | CAMP7 | HVLLLLFFFFNH2 | Synthetic | Cell membrane penetrating | MTT assay | A549 | Not specified | IC50 : >100 μM |
| dbacp02321 | CB | KWKVFKKIEKMGRNIRNGIVKAGPAIAVLGEAKAL | Synthetic | Cell membrane disintegration | Not specified | Ags | Gastric cancer | Not found |
| dbacp02395 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Epithelial cancer | CC50 : 39.8 ± 1.0 μM |
| dbacp02396 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Chronic myeloid leukemia | CC50 : 39.8 ± 1.0 μM |
| dbacp02397 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Gastric cancer | CC50 : 39.8 ± 1.0 μM |
| dbacp02398 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Breast cancer | CC50 : 39.8 ± 1.0 μM |
| dbacp02399 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | CRL-1739 | Cervical cancer | CC50 : 39.8 ± 1.0 μM |
| dbacp02400 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Epithelial cancer | CC50 : 2.9 ± 0.1 μM |
| dbacp02401 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Chronic myeloid leukemia | CC50 : 2.9 ± 0.1 μM |
| dbacp02402 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Gastric cancer | CC50 : 2.9 ± 0.1 μM |
| dbacp02403 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Breast cancer | CC50 : 2.9 ± 0.1 μM |
| dbacp02404 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MM96L | Cervical cancer | CC50 : 2.9 ± 0.1 μM |
| dbacp02405 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Epithelial cancer | CC50 : 71.7 ± 9.2 μM |
| dbacp02406 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Chronic myeloid leukemia | CC50 : 71.7 ± 9.2 μM |
| dbacp02407 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Gastric cancer | CC50 : 71.7 ± 9.2 μM |
| dbacp02408 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Breast cancer | CC50 : 71.7 ± 9.2 μM |
| dbacp02409 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HFF-1 | Cervical cancer | CC50 : 71.7 ± 9.2 μM |
| dbacp02410 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Epithelial cancer | CC50 : > 64 μM |
| dbacp02411 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Chronic myeloid leukemia | CC50 : > 64 μM |
| dbacp02412 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Gastric cancer | CC50 : > 64 μM |
| dbacp02413 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Breast cancer | CC50 : > 64 μM |
| dbacp02414 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | HeLa | Cervical cancer | CC50 : > 64 μM |
| dbacp02415 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Epithelial cancer | CC50 : 15.3 ± 1.4 μM |
| dbacp02416 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Chronic myeloid leukemia | CC50 : 15.3 ± 1.4 μM |
| dbacp02417 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Gastric cancer | CC50 : 15.3 ± 1.4 μM |
| dbacp02418 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Breast cancer | CC50 : 15.3 ± 1.4 μM |
| dbacp02419 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | MCF-7 | Cervical cancer | CC50 : 15.3 ± 1.4 μM |
| dbacp02420 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Epithelial cancer | CC50 : 2.7 ± 0.1 μM |
| dbacp02421 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Chronic myeloid leukemia | CC50 : 2.7 ± 0.1 μM |
| dbacp02422 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Gastric cancer | CC50 : 2.7 ± 0.1 μM |
| dbacp02423 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Breast cancer | CC50 : 2.7 ± 0.1 μM |
| dbacp02424 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | K-562 | Cervical cancer | CC50 : 2.7 ± 0.1 μM |
| dbacp02425 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Epithelial cancer | CC50 : 12.7 ± 1.1 μM |
| dbacp02426 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Chronic myeloid leukemia | CC50 : 12.7 ± 1.1 μM |
| dbacp02427 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Gastric cancer | CC50 : 12.7 ± 1.1 μM |
| dbacp02428 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Breast cancer | CC50 : 12.7 ± 1.1 μM |
| dbacp02429 | cGm (Derived from Gm) | GCRRLCYKQRCVTYCRGR | Synthetic construct | Target and destroy tumor cell membranes | Cell viability assay | PBMCs | Cervical cancer | CC50 : 12.7 ± 1.1 μM |
| dbacp02556 | CPP2 | HVRRRRRRRNH2 | Synthetic | Cell membrane penetrating | MTT assay | UM-UC-A | Not specified | IC50 : 5.47 μM |
| dbacp02557 | CPP2 | HVRRRRRRRNH2 | Synthetic | Cell membrane penetrating | MTT assay | A549 | Not specified | IC50 : >100 μM |
| dbacp02558 | CPP4 | HVRRRRRRRRNH2 | Synthetic | Cell membrane penetrating | MTT assay | UM-UC-5 | Not specified | IC50 : >100 μM |
| dbacp02559 | CPP4 | HVRRRRRRRRNH2 | Synthetic | Cell membrane penetrating | MTT assay | A549 | Not specified | IC50 : >100 μM |
| dbacp02564 | CRAMP-18 E2K | GKKLKKIGQKIKNFFQKL | Synthetic | Disrupt cell membrane structure | MTT assay | K-562 | Chronic myelogenous Leukemia | IC50 : 20–34 uM |
| dbacp02565 | CRAMP-18 E2K | GKKLKKIGQKIKNFFQKL | Synthetic | Disrupt cell membrane structure | MTT assay | Jurkat | Acute T cell Leukemia | IC50 : 20–34 uM |
| dbacp02566 | CRAMP-18 E2K | GKKLKKIGQKIKNFFQKL | Synthetic | Disrupt cell membrane structure | MTT assay | K-549 | Acute T cell Leukemia | IC50 : 20–34 uM |
| dbacp02627 | D-SVS-1 | kvkvkvkvPptkvkvkvk | Synthetic peptide | Disruption of cell membranes | MTT/MTS assay | A-549 | Lung cancer | IC50 : 3.2 ± 0.6 µM |
| dbacp02628 | D-SVS-1 | kvkvkvkvPptkvkvkvk | Synthetic peptide | Disruption of cell membranes | MTT/MTS assay | KB | Oral cancer | IC50 : 4.5 ± 0.5 µM |
| dbacp02629 | D-SVS-1 | kvkvkvkvPptkvkvkvk | Synthetic peptide | Disruption of cell membranes | MTT/MTS assay | MCF-7 | Breast cancer | IC50 : 4.7 ± 0.4 µM |
| dbacp02630 | D-SVS-1 | kvkvkvkvPptkvkvkvk | Synthetic peptide | Disruption of cell membranes | MTT/MTS assay | MDA-MB-436 | Breast cancer | IC50 : 3.2 ± 0.4 µM |
| dbacp02744 | Dex-(KW)3 | KWKWKW | Synthetic | Cell membrane disruption | MTT/MTS assay | PC-3 | Prostate cancer | At 10 µM 60% viablity |
| dbacp02745 | Dex-(KW)3 | KWKWKW | Synthetic | Cell membrane disruption | MTT/MTS assay | MCF-7 | Breast cancer | At 10 µM 35-40% viablity |
| dbacp02757 | Dimer of peptide-paclitaxel conjugate | (K-Aib-C(CH2CO-2'-Pac))2 | Synthetic peptide paclitaxel conjugate | Not specified | MTT/MTS assay | HeLa | Cervical cancer | IC50 : 1.31 nM |
| dbacp02758 | Dimer of peptide-paclitaxel conjugate | (K-Aib-C(CH2CO-2'-Pac))2 | Synthetic peptide paclitaxel conjugate | Not specified | MTT/MTS assay | DU | Prostate cancer | IC50 : 2.85 nM |
| dbacp02759 | Dimer of peptide-paclitaxel conjugate | (K-Aib-C(CH2CO-2'-Pac))2 | Synthetic peptide paclitaxel conjugate | Not specified | MTT/MTS assay | MCF-7 | Breast cancer | IC50 : 0.62 nM |
| dbacp02826 | EGFR-lytic | YHWYGYTPQNVIGGGKLlLKlLkkLLKlLKKK | Synthetic Peptide | Cell membrane lysis | ELISA | MDA-MB-231 | Breast cancer | IC50 : 0.12 µM |
| dbacp02827 | EGFR-lytic | YHWYGYTPQNVIGGGKLlLKlLkkLLKlLKKK | Synthetic Peptide | Cell membrane lysis | ELISA | MDA-MB-231 | Breast cancer | IC50 : 0.46 µM |
| dbacp02914 | ES-2 | IVRRADRAAVP | Endostatin derived synthetic peptide | Necrosis; Anti-angiogenesis | MTT/MTS assay | BAE | Tumor | 60% inhibition at 2.5µg/ml |
| dbacp02915 | ES-2 | IVRRADRAAVP | Endostatin derived synthetic peptide | Necrosis; Anti-angiogenesis | MTT/MTS assay | BAE | Tumor | 60% inhibition at 5µg/ml |
| dbacp02916 | ES-2 | IVRRADRAAVP | Endostatin derived synthetic peptide | Necrosis; Anti-angiogenesis | MTT/MTS assay | BAE | Tumor | 60% inhibition at 10µg/ml |
| dbacp03067 | GLK-19 | GLKKLLGKLLKKLGKLLLK | Synthetic construct | Not specified | Not specified | Not found | Not found | Not found |
| dbacp03177 | H-11 | IKLSPETKKNLKKVLKGAIKGAIAVAKMV | Synthetic construct | Inducing apoptosis | MTT assay | A549 | Not found | IC50 : 1.82 ± 0.23 μM |
| dbacp03178 | H-11 | IKLSPETKKNLKKVLKGAIKGAIAVAKMV | Synthetic construct | Inducing apoptosis | MTT assay | HCT116 | Not found | IC50 : 6.50 ± 0.32 μM |
| dbacp03179 | H-11 | IKLSPETKKNLKKVLKGAIKGAIAVAKMV | Synthetic construct | Inducing apoptosis | MTT assay | HepG2 | Not found | IC50 : 4.96 ± 0.43 μM |
| dbacp03180 | H-12 | IKLSKETKDNLKKVLKGAIKGAIAVAKMV | Synthetic construct | Inducing apoptosis | MTT assay | A549 | Not found | IC50 : 2.35 ± 0.31 μM |
| dbacp03181 | H-12 | IKLSKETKDNLKKVLKGAIKGAIAVAKMV | Synthetic construct | Inducing apoptosis | MTT assay | HCT116 | Not found | IC50 : 8.09 ± 0.40 μM |
| dbacp03182 | H-12 | IKLSKETKDNLKKVLKGAIKGAIAVAKMV | Synthetic construct | Inducing apoptosis | MTT assay | HepG2 | Not found | IC50 : 4.28 ± 0.38 μM |
| dbacp03183 | H-13 | IKLSKETKKNLKKVLKGAIKGAIAVAKMV | Synthetic construct | Inducing apoptosis | MTT assay | A549 | Not found | IC50 : 1.17 ± 0.23 μM |
| dbacp03184 | H-13 | IKLSKETKKNLKKVLKGAIKGAIAVAKMV | Synthetic construct | Inducing apoptosis | MTT assay | HCT116 | Not found | IC50 : 4.93 ± 0.51 μM |
| dbacp03185 | H-13 | IKLSKETKKNLKKVLKGAIKGAIAVAKMV | Synthetic construct | Inducing apoptosis | MTT assay | HepG2 | Not found | IC50 : 2.46 ± 0.32 μM |
| dbacp03186 | H-14 | IKLSKKTKKNLKKVLKGAIKGAIAVAKMV | Synthetic construct | Inducing apoptosis | MTT assay | A549 | Not found | IC50 : 0.98 ± 0.11 μM |
| dbacp03187 | H-14 | IKLSKKTKKNLKKVLKGAIKGAIAVAKMV | Synthetic construct | Inducing apoptosis | MTT assay | HCT116 | Not found | IC50 : 1.841 ± 0.34 μM |
| dbacp03188 | H-14 | IKLSKKTKKNLKKVLKGAIKGAIAVAKMV | Synthetic construct | Inducing apoptosis | MTT assay | HepG2 | Not found | IC50 : 4.54 ± 0.25 μM |
| dbacp03289 | HCAP18(109-135) | FRKSKEKIGKEFKRIVQRIKDFLRNLV | HCAP18 synthetic peptide | Apoptosis inducing | Not specified | SAS-H1 | Oral cancer | Not found |
| dbacp03297 | HHPHG | HHPHG | Synthetic Peptide | Anti-angiogenesis | Tropomyosin binding assay | Not found | Tumor | IC50 : 92 µM |
| dbacp03530 | KW5 | KAAKKAAKAAKKAAKAAKKAA | Synthetic peptide | Through interactions with the plasma membrane | MTT/MTS assay | HT-29 | Colon cancer | IC50 : 55 ± 14 µM |
| dbacp04130 | LK1 (Temporin-1CEa Analog peptide) | FVDLKKIANIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | MCF-7 | Breast cancer | IC50 : 20.97 µM |
| dbacp04131 | LK1 (Temporin-1CEa Analog peptide) | FVDLKKIANIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | Bcap-37 | Breast cancer | IC50 : 18.7 µM |
| dbacp04132 | LK1 (Temporin-1CEa Analog peptide) | FVDLKKIANIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | MDA-MB-231 | Breast cancer | IC50 : 66.4µM |
| dbacp04133 | LK2(5) (Temporin-1CEa Analog peptide) | FKDLKKIANIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | MCF-7 | Breast cancer | IC50 : 44.7 µM |
| dbacp04134 | LK2(5) (Temporin-1CEa Analog peptide) | FKDLKKIANIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | Bcap-37 | Breast cancer | IC50 : 83.49 µM |
| dbacp04135 | LK2(5) (Temporin-1CEa Analog peptide) | FKDLKKIANIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | MDA-MB-231 | Breast cancer | IC50 : 894.7 µM |
| dbacp04136 | LK2(6) (Temporin-1CEa Analog peptide) | FVKLKKIANIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | MCF-7 | Breast cancer | IC50 : 15.54 µM |
| dbacp04137 | LK2(6) (Temporin-1CEa Analog peptide) | FVKLKKIANIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | Bcap-37 | Breast cancer | IC50 : 18.9 µM |
| dbacp04138 | LK2(6) (Temporin-1CEa Analog peptide) | FVKLKKIANIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | MDA-MB-231 | Breast cancer | IC50 : 85.41 µM |
| dbacp04139 | LK2(6)A(L) (Temporin-1CEa Analog peptide) | FVKLKKILNIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | MCF-7 | Breast cancer | IC50 : 9.01 µM |
| dbacp04140 | LK2(6)A(L) (Temporin-1CEa Analog peptide) | FVKLKKILNIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | Bcap-37 | Breast cancer | IC50 : 10.52 µM |
| dbacp04141 | LK2(6)A(L) (Temporin-1CEa Analog peptide) | FVKLKKILNIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | MDA-MB-231 | Breast cancer | IC50 : 34.74 µM |
| dbacp04142 | LK2(6)AN(2L) (Temporin-1CEa Analog peptide) | FVKLKKILNIILSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | MCF-7 | Breast cancer | IC50 : 11 µM |
| dbacp04143 | LK2(6)AN(2L) (Temporin-1CEa Analog peptide) | FVKLKKILNIILSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | Bcap-37 | Breast cancer | IC50 : 9.39 µM |
| dbacp04144 | LK2(6)AN(2L) (Temporin-1CEa Analog peptide) | FVKLKKILNIILSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | MDA-MB-231 | Breast cancer | IC50 : 41.55 µM |
| dbacp04145 | LK3 (Temporin-1CEa Analog peptide) | FKKLKKIANIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | MCF-7 | Breast cancer | IC50 : 27.72 µM |
| dbacp04146 | LK3 (Temporin-1CEa Analog peptide) | FKKLKKIANIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | Bcap-37 | Breast cancer | IC50 : 25.04 µM |
| dbacp04147 | LK3 (Temporin-1CEa Analog peptide) | FKKLKKIANIINSIFKK | Synthetic construct | Cell membrane disintegration | MTT-assay | MDA-MB-231 | Breast cancer | IC50 : 224.8 µM |
| dbacp04296 | LTX-302 | WKKW-Dip-KKWK | Synthetic peptide | Cell membrane disintegration | MTT/MTS assay | HT-29 | Colon cancer | IC50 : 75 ± 5 µM |
| dbacp04297 | LTX-302 | WKKW-Dip-KKWK | Synthetic peptide | Cell membrane disintegration | MTT/MTS assay | MT-1 | Breast cancer | IC50 : 73 ± 2 µM |
| dbacp04298 | LTX-302 | WKKW-Dip-KKWK | Synthetic peptide | Cell membrane disintegration | MTT/MTS assay | Kelly | Brain tumor | IC50 : 28 ± 0 µM |
| dbacp04299 | LTX-315 | KKWWKKW-Dip-K | Synthetic peptide | Cell membrane disintegration | MTT/MTS assay | HT-29 | Colon cancer | IC50 : 38 ± 3 µM |
| dbacp04300 | LTX-315 | KKWWKKW-Dip-K | Synthetic peptide | Cell membrane disintegration | MTT/MTS assay | MT-1 | Breast cancer | IC50 : 31 ± 3 µM |
| dbacp04301 | LTX-315 | KKWWKKW-Dip-K | Synthetic peptide | Cell membrane disintegration | MTT/MTS assay | Kelly | Brain tumor | IC50 : 14 ± 1 µM |
| dbacp04302 | LTX-315 | KKWWKKW-Dip-K | Synthetic peptide | Necrosis | MTT/MTS assay | B16F1 | Skin cancer | IC50 : 13.3 µM |
| dbacp04303 | LTX-315 | KKWWKKW-Dip-K | Synthetic peptide | Necrosis | MTT/MTS assay | A375 | Skin cancer | IC50 : 12.7 µM |
| dbacp04304 | LTX-315 | KKWWKKW-Dip-K | Synthetic peptide | Necrosis | MTT/MTS assay | Fem-X | Skin cancer | IC50 : 15.3 µM |
| dbacp04305 | LTX-318 | OOW-Dip-OOWWO | Synthetic peptide | Cell membrane disintegration | MTT/MTS assay | HT-29 | Colon cancer | IC50 : 248 ± 5 µM |
| dbacp04306 | LTX-318 | OOW-Dip-OOWWO | Synthetic peptide | Cell membrane disintegration | MTT/MTS assay | MT-1 | Breast cancer | IC50 : 216 ± 36 µM |
| dbacp04307 | LTX-318 | OOW-Dip-OOWWO | Synthetic peptide | Cell membrane disintegration | MTT/MTS assay | Kelly | Brain tumor | IC50 : 78 ± 7 µM |
| dbacp04308 | LTX-328 | KAQ-Dip-QKQAW | Synthetic peptide | Necrosis | MTT/MTS assay | Fem-X | Skin cancer | IC50 : >350 µM |
| dbacp04643 | Melittin | GIGAVLKVLTTGLPALISWIKRKRQQ | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 :3.2 ± 0.1 µM |
| dbacp04644 | Melittin | GIGAVLKVLTTGLPALISWIKRKRQQ | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 :2.1 ± 0.1 µM |
| dbacp04645 | Melittin | GIGAVLKVLTTGLPALISWIKRKRQQ | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 :1.8 ± 0.1 µM |
| dbacp04646 | Melittin | GIGAVLKVLTTGLPALISWIKRKRQQ | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 :1.4 ± 0.1 µM |
| dbacp04677 | MG2d | GIGKFLHSAKKWGKAFVGQIMNC | Synthetic | Cell membrane disintegration | MTT/MTS assay | HeLa | Cervical cancer | At 1 µM 90-100% viablity |
| dbacp04794 | N29D | PDEDAINDALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SW-480 | Colon cancer | > 100% cell viability at 5 µM |
| dbacp04795 | N29D | PDEDAINDALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SW-480 | Colon cancer | 60% cell viability at 50 µM |
| dbacp04796 | N29D | PDEDAINDALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | U-937 | Lymphoma cancer | 100% cell viability at 5 µM |
| dbacp04797 | N29D | PDEDAINDALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | U-937 | Lymphoma cancer | < 60% cell viability at 50 µM |
| dbacp04798 | N29D | PDEDAINDALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SNU-1 | Gastric cancer | < 100% cell viability at 5 µM |
| dbacp04799 | N29D | PDEDAINDALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SNU-1 | Gastric cancer | < 40% cell viability at 50 µM |
| dbacp04800 | N29D | PDEDAINDALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SW-480 | Colon cancer | > 100% cell viability at 5 µM |
| dbacp04801 | N29D | PDEDAINDALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SW-480 | Colon cancer | 60% cell viability at 50 µM |
| dbacp04802 | N29D | PDEDAINDALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | U-937 | Lymphoma cancer | 100% cell viability at 5 µM |
| dbacp04803 | N29D | PDEDAINDALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | U-937 | Lymphoma cancer | < 60% cell viability at 50 µM |
| dbacp04804 | N29D | PDEDAINDALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SNU-1 | Gastric cancer | 100% cell viability at 5 µM |
| dbacp04805 | N29D | PDEDAINDALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SNU-1 | Gastric cancer | < 40% cell viability at 50 µM |
| dbacp04806 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SW-480 | Colon cancer | 100% cell viability at 5 µM |
| dbacp04807 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SW-480 | Colon cancer | 40% cell viability at 50 µM |
| dbacp04808 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | U-937 | Lymphoma cancer | 100% cell viability at 5 µM |
| dbacp04809 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | U-937 | Lymphoma cancer | < 40% cell viability at 50 µM |
| dbacp04810 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SNU-1 | Gastric cancer | < 100% cell viability at 5 µM |
| dbacp04811 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SNU-1 | Gastric cancer | < 20% cell viability at 50 µM |
| dbacp04812 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SW-480 | Colon cancer | 100% cell viability at 5 µM |
| dbacp04813 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SW-480 | Colon cancer | 40% cell viability at 50 µM |
| dbacp04814 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | U-937 | Lymphoma cancer | 100% cell viability at 5 µM |
| dbacp04815 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | U-937 | Lymphoma cancer | < 40% cell viability at 50 µM |
| dbacp04816 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SNU-1 | Gastric cancer | < 100% cell viability at 5 µM |
| dbacp04817 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SNU-1 | Gastric cancer | < 20% cell viability at 50 µM |
| dbacp04818 | N29N | PDEDAINNALNKVCSTGRRQRSICKQLLKK | Synthetic peptide | Apoptotic inducing | Cell viability assay | SW-480 | Colon cancer | MIC : 5 µM |
| dbacp04855 | NK-2 | KILRGVCKKIMRTFLRRISKDILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : 70 µM |
| dbacp04856 | NK-2 | KILRGVCKKIMRTFLRRISKDILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : 50 µM |
| dbacp04857 | NK-2 | KILRGVCKKIMRTFLRRISKDILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : 50 µM |
| dbacp04858 | NK-2 | KILRGVCKKIMRTFLRRISKDILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : 40 µM |
| dbacp04872 | NK-dpro (Derived from NK-2) | KILPGVCKKIMRPFLRRISKDILTGKK | Synthetic construct | Not specified | MTT assay | EJ | Not found | IC50 : 28.7 μM |
| dbacp04873 | NK-dpro (Derived from NK-2) | KILPGVCKKIMRPFLRRISKDILTGKK | Synthetic construct | Not specified | MTT assay | PC-3 | Not found | IC50 : 9.6 μM |
| dbacp04874 | NK-dpro (Derived from NK-2) | KILPGVCKKIMRPFLRRISKDILTGKK | Synthetic construct | Not specified | MTT assay | T24 | Not found | IC50 : 39.6 μM |
| dbacp04875 | NK-dpro (Derived from NK-2) | KILPGVCKKIMRPFLRRISKDILTGKK | Synthetic construct | Not specified | MTT assay | HL-60 | Not found | IC50 : 48.4 μM |
| dbacp04876 | NK-pro (Derived from NK-2) | KILRGVCKKIMRPFLRRISKDILTGKK | Synthetic construct | Not specified | MTT assay | EJ | Not found | IC50 : 23.3 μM |
| dbacp04877 | NK-pro (Derived from NK-2) | KILRGVCKKIMRPFLRRISKDILTGKK | Synthetic construct | Not specified | MTT assay | PC-3 | Not found | IC50 : 9.3 μM |
| dbacp04878 | NK-pro (Derived from NK-2) | KILRGVCKKIMRPFLRRISKDILTGKK | Synthetic construct | Not specified | MTT assay | T24 | Not found | IC50 : 33.0 μM |
| dbacp04879 | NK-pro (Derived from NK-2) | KILRGVCKKIMRPFLRRISKDILTGKK | Synthetic construct | Not specified | MTT assay | HL-60 | Not found | IC50 : 26.1 μM |
| dbacp04880 | NK11 | KISKRILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : >100 µM |
| dbacp04881 | NK11 | KISKRILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : >100 µM |
| dbacp04882 | NK11 | KISKRILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : >100 µM |
| dbacp04883 | NK11 | KISKRILTGKK | Synthetic peptide | Physical membrane disruption | MTT/MTS assay | E42/02 | Skin cancer | IC50 : >100 µM |
| dbacp05039 | P18 | KWKLFKKIPKFLHLAKKF | Synthetic peptide | Necrosis; Cell membrane rupture | MTT/MTS assay | M14 | Skin cancer | 71.1 ± 2.84% cell viability at 20 µM |
| dbacp05040 | P18 | KWKLFKKIPKFLHLAKKF | Synthetic peptide | Necrosis; Cell membrane rupture | MTT/MTS assay | M14 | Skin cancer | 50 ± 3.09% cell viability at 40 µM |
| dbacp05041 | P18 | KWKLFKKIPKFLHLAKKF | Synthetic peptide | Necrosis; Cell membrane rupture | MTT/MTS assay | M14 | Skin cancer | 31.5 ± 1.49% cell viability at 60 µM |
| dbacp05042 | P18 | KWKLFKKIPKFLHLAKKF | Synthetic peptide | Necrosis; Cell membrane rupture | MTT/MTS assay | M14 | Skin cancer | 13.8 ± 1.44% cell viability at 80 µM |
| dbacp05043 | P18 | KWKLFKKIPKFLHLAKKF | Synthetic peptide | Necrosis; Cell membrane rupture | MTT/MTS assay | A-375 | Skin cancer | 86 ± 0.57% cell viability at 10 µM |
| dbacp05044 | P18 | KWKLFKKIPKFLHLAKKF | Synthetic peptide | Necrosis; Cell membrane rupture | MTT/MTS assay | A-375 | Skin cancer | 63.8 ± 0.8% cell viability at 20 µM |
| dbacp05045 | P18 | KWKLFKKIPKFLHLAKKF | Synthetic peptide | Necrosis; Cell membrane rupture | MTT/MTS assay | A-375 | Skin cancer | 47.5 ± 1.66% cell viability at 40 µM |
| dbacp05046 | P18 | KWKLFKKIPKFLHLAKKF | Synthetic peptide | Necrosis; Cell membrane rupture | MTT/MTS assay | A-375 | Skin cancer | 26.9 ± 0.5% cell viability at 60 µM |
| dbacp05047 | P18 | KWKLFKKIPKFLHLAKKF | Synthetic peptide | Necrosis; Cell membrane rupture | MTT/MTS assay | A-375 | Skin cancer | 6.5 ± 1.07% cell viability at 80 µM |
| dbacp05051 | P18 (Cecropin A(1-8)-Magainin 2(112) hybrid peptide Analogue) | KWKLFKKIPKFLHLAKKF | Synthetic construct | Not specified | Not specified | Not found | Not found | Not found |
| dbacp05061 | P369-CTL-A2xFVB | KIFGSLAFL | Synthetic Peptide | Antiangiogenis; Immune regulation | Peptide dose curve assay | N202.A2 | Tumor | 8% Inhibition at 10-10 M |
| dbacp05062 | P369-CTL-A2xFVB | KIFGSLAFL | Synthetic Peptide | Antiangiogenis; Immune regulation | Peptide dose curve assay | N202.A2 | Tumor | 25% Inhibition at 10-9 M |
| dbacp05063 | P369-CTL-A2xFVB | KIFGSLAFL | Synthetic Peptide | Antiangiogenis; Immune regulation | Peptide dose curve assay | N202.A2 | Tumor | 80% Inhibition at 10-8 M |
| dbacp05064 | P369-CTL-A2xFVB | KIFGSLAFL | Synthetic Peptide | Antiangiogenis; Immune regulation | Peptide dose curve assay | N202.A2 | Tumor | 85% Inhibition at 10-7 M |
| dbacp05065 | P369-CTL-A2xFVB | KIFGSLAFL | Synthetic Peptide | Antiangiogenis; Immune regulation | Peptide dose curve assay | N202.A2 | Tumor | 92% Inhibition at 10-6 M |
| dbacp05066 | P369-CTL-A2xneu | KIFGSLAFL | Synthetic Peptide | Antiangiogenis; Immune regulation | Peptide dose curve assay | N202.A2 | Tumor | 0.1% Inhibition at 10-10 M |
| dbacp05067 | P369-CTL-A2xneu | KIFGSLAFL | Synthetic Peptide | Antiangiogenis; Immune regulation | Peptide dose curve assay | N202.A2 | Tumor | 1% Inhibition at 10-9 M |
| dbacp05068 | P369-CTL-A2xneu | KIFGSLAFL | Synthetic Peptide | Antiangiogenis; Immune regulation | Peptide dose curve assay | N202.A2 | Tumor | 5% Inhibition at 10-8 M |
| dbacp05069 | P369-CTL-A2xneu | KIFGSLAFL | Synthetic Peptide | Antiangiogenis; Immune regulation | Peptide dose curve assay | N202.A2 | Tumor | 10% Inhibition at 10-7 M |
| dbacp05070 | P369-CTL-A2xneu | KIFGSLAFL | Synthetic Peptide | Antiangiogenis; Immune regulation | Peptide dose curve assay | N202.A2 | Tumor | 20% Inhibition at 10-6 M |
| dbacp05098 | p776 | GVGSPYVSRLLGICL | Synthetic Peptide | Inducing apoptosis | ELISPOT assay | Not found | Tumor | Not found |
| dbacp05102 | p85 | LIAHNQVRQV | Synthetic Peptide | Inducing apoptosis | ELISPOT assay | Not found | Tumor | Not found |
| dbacp05103 | PA10 | RQIKIWFQNRRMKWKKGGGGNNETTSIQIAGSLHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | MDA-MB231 | Breast cancer | MIC : 10 μM |
| dbacp05104 | PA10 | RQIKIWFQNRRMKWKKGGGGNNETTSIQIAGSLHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | HCC1806 | Breast cancer | MIC : 10 μM |
| dbacp05105 | PA10 | RQIKIWFQNRRMKWKKGGGGNNETTSIQIAGSLHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | 184B5 | Breast cancer | MIC : 10 μM |
| dbacp05106 | PA10 | RQIKIWFQNRRMKWKKGGGGNNETTSIQIAGSLHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | MCF10A | Breast cancer | MIC : 10 μM |
| dbacp05107 | PA15 | RQIKIWFQNRRMKWKKGGSLSAACHEQWSLGAQHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | MDA-MB231 | Breast cancer | MIC : 10 μM |
| dbacp05108 | PA15 | RQIKIWFQNRRMKWKKGGSLSAACHEQWSLGAQHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | HCC1806 | Breast cancer | MIC : 10 μM |
| dbacp05109 | PA15 | RQIKIWFQNRRMKWKKGGSLSAACHEQWSLGAQHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | 184B5 | Breast cancer | MIC : 10 μM |
| dbacp05110 | PA15 | RQIKIWFQNRRMKWKKGGSLSAACHEQWSLGAQHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | MCF10A | Breast cancer | MIC : 10 μM |
| dbacp05111 | PA2 | RQIKIWFQNRRMKWKKGGATRPRVDTQPELCGMHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | MDA-MB231 | Breast cancer | MIC : 10 μM |
| dbacp05112 | PA2 | RQIKIWFQNRRMKWKKGGATRPRVDTQPELCGMHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | HCC1806 | Breast cancer | MIC : 10 μM |
| dbacp05113 | PA2 | RQIKIWFQNRRMKWKKGGATRPRVDTQPELCGMHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | 184B5 | Breast cancer | MIC : 10 μM |
| dbacp05114 | PA2 | RQIKIWFQNRRMKWKKGGATRPRVDTQPELCGMHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | MCF10A | Breast cancer | MIC : 10 μM |
| dbacp05115 | PA3 | RQIKIWFQNRRMKWKKGGDCLCISRRARLLRATHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | MDA-MB231 | Breast cancer | MIC : 10 μM |
| dbacp05116 | PA3 | RQIKIWFQNRRMKWKKGGDCLCISRRARLLRATHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | HCC1806 | Breast cancer | MIC : 10 μM |
| dbacp05117 | PA3 | RQIKIWFQNRRMKWKKGGDCLCISRRARLLRATHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | 184B5 | Breast cancer | MIC : 10 μM |
| dbacp05118 | PA3 | RQIKIWFQNRRMKWKKGGDCLCISRRARLLRATHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | MCF10A | Breast cancer | MIC : 10 μM |
| dbacp05119 | PA38 | RQIKIWFQNRRMKWKKGGKYNGRFTTHHLLHLLNHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | MDA-MB231 | Breast cancer | MIC : 10 μM |
| dbacp05120 | PA38 | RQIKIWFQNRRMKWKKGGKYNGRFTTHHLLHLLNHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | HCC1806 | Breast cancer | MIC : 10 μM |
| dbacp05121 | PA38 | RQIKIWFQNRRMKWKKGGKYNGRFTTHHLLHLLNHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | 184B5 | Breast cancer | MIC : 10 μM |
| dbacp05122 | PA38 | RQIKIWFQNRRMKWKKGGKYNGRFTTHHLLHLLNHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | MCF10A | Breast cancer | MIC : 10 μM |
| dbacp05123 | PA49 | RQIKIWFQNRRMKWKKGGAGVYTFLVGADNRGWEHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | MDA-MB231 | Breast cancer | MIC : 10 μM |
| dbacp05124 | PA49 | RQIKIWFQNRRMKWKKGGAGVYTFLVGADNRGWEHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | HCC1806 | Breast cancer | MIC : 10 μM |
| dbacp05125 | PA49 | RQIKIWFQNRRMKWKKGGAGVYTFLVGADNRGWEHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | 184B5 | Breast cancer | MIC : 10 μM |
| dbacp05126 | PA49 | RQIKIWFQNRRMKWKKGGAGVYTFLVGADNRGWEHHHHHH | Synthetic construct | Cell proliferation inhibition; Cell penetration; Apoptosis | Cell viability assay | MCF10A | Breast cancer | MIC : 10 μM |
| dbacp05307 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | KB | Oral cancer | 10.6 % inhibition of cell proliferation at 1 nM |
| dbacp05308 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | KB | Oral cancer | 18.2 % inhibition of cell proliferation at 10 nM |
| dbacp05309 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | KB | Oral cancer | 30.7 % inhibition of cell proliferation at 100 nM |
| dbacp05310 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | KB | Oral cancer | 43.1 % inhibition of cell proliferation at 1 µM |
| dbacp05311 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | KB | Oral cancer | 98.3 % inhibition of cell proliferation at 10 µM |
| dbacp05312 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | MiaPaCa.2 | Pancreatic cancer | 24.2 % inhibition of cell proliferation at 1 nM |
| dbacp05313 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | MiaPaCa.2 | Pancreatic cancer | 37.8 % inhibition of cell proliferation at 10 nM |
| dbacp05314 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | MiaPaCa.2 | Pancreatic cancer | 48.2 % inhibition of cell proliferation at 100 nM |
| dbacp05315 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | MiaPaCa.2 | Pancreatic cancer | 59.6 % inhibition of cell proliferation at 1 µM |
| dbacp05316 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | MiaPaCa.2 | Pancreatic cancer | 84.5 % inhibition of cell proliferation at 10 µM |
| dbacp05317 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | PTC | Colon cancer | 16.5 % inhibition of cell proliferation at 1 nM |
| dbacp05318 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | PTC | Colon cancer | 14.2 % inhibition of cell proliferation at 10 nM |
| dbacp05319 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | PTC | Colon cancer | 16.8 % inhibition of cell proliferation at 100 nM |
| dbacp05320 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | PTC | Colon cancer | 21.7 % inhibition of cell proliferation at 1 µM |
| dbacp05321 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | PTC | Colon cancer | 27.9 % inhibition of cell proliferation at 10 µM |
| dbacp05322 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | MOLT-4 | Leukemia cancer | 10.4 % inhibition of cell proliferation at 1 nM |
| dbacp05323 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | MOLT-4 | Leukemia cancer | 18.7 % inhibition of cell proliferation at 10 nM |
| dbacp05324 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | MOLT-4 | Leukemia cancer | 34.7 % inhibition of cell proliferation at 100 nM |
| dbacp05325 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | MOLT-4 | Leukemia cancer | 54.3 % inhibition of cell proliferation at 1 µM |
| dbacp05326 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | MOLT-4 | Leukemia cancer | 94.5 % inhibition of cell proliferation at 10 µM |
| dbacp05327 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | KB | Oral cancer | ED50 : 2.1 µM |
| dbacp05328 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | MiaPaCa.2 | Pancreatic cancer | ED50 : 0.210 µM |
| dbacp05329 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | PTC | Colon cancer | ED50 : >10 µM |
| dbacp05330 | Peptide 5 | fCYwO-CyLeu-Pen-TKKrPKPfQwFwL-CyLeu-KKLMYPTYLKKfQWAV-Aib-HL | Synthetic peptide of four designed analogs of vasoactive intestinal peptide, bombesin | Not specified | MTT/MTS assay | MOLT-4 | Leukemia cancer | ED50 : 0.29 µM |
| dbacp05434 | Peptide-1 | IELLQARGGC-Pem | Synthetic construct | Cell membrane disintegration | MTT/MTS assay | HL-60 | Leukemia cancer | IC50 : 2.17 µM |
| dbacp05435 | Peptide-1 | IELLQARGGC-Pem | Synthetic construct | Cell membrane disintegration | MTT/MTS assay | NCI-H358 | Lung cancer | IC50 : 4.63 mM |
| dbacp05436 | Peptide-2 | IELLQARGGC-Pem-GGRRRRRRRR | Synthetic construct | Cell membrane disintegration | MTT/MTS assay | HL-60 | Leukemia cancer | IC50 : 2.64 µM |
| dbacp05437 | Peptide-2 | IELLQARGGC-Pem-GGRRRRRRRR | Synthetic construct | Cell membrane disintegration | MTT/MTS assay | NCI-H358 | Lung cancer | IC50 : 2.19 µM |
| dbacp05438 | Peptide-20 | CSSRTMHHC | Synthetic Peptide | Inducing apoptosis | MTT/MTS assay | HL-60 | Leukemia cancer | At 100 µM 90% viablity |
| dbacp05439 | Peptide-20 | CSSRTMHHC | Synthetic Peptide | Inducing apoptosis | MTT/MTS assay | MDA-MB-231 | Breast cancer | At 100 µM 55% viablity |
| dbacp05440 | Peptide-20 | CSSRTMHHC | Synthetic Peptide | Inducing apoptosis | MTT/MTS assay | HeLa | Cervical cancer | At 100 µM 50% viablity |
| dbacp05441 | Peptide-20 | CSSRTMHHC | Synthetic Peptide | Inducing apoptosis | MTT/MTS assay | B16F10-Nex 2 | Skin cancer | At 100 µM 50% viablity |
| dbacp05442 | Peptide-20 | CSSRTMHHC | Synthetic Peptide | Inducing apoptosis | MTT/MTS assay | A-2058 | Skin cancer | At100 µM 30% viablity |
| dbacp05443 | Peptide-20 | CSSRTMHHC | Synthetic Peptide | Inducing apoptosis | MTT/MTS assay | Skmel-25 | Skin cancer | At 100 µM 55 - 60% viablity |
| dbacp05444 | Peptide-20 | CSSRTMHHC | Synthetic Peptide | Inducing apoptosis | MTT/MTS assay | Skmel-28 | Skin cancer | At 100 µM 35 - 40% viablity |
| dbacp05445 | Peptide-3 | RRRRRRRRGGC-Pem | Synthetic construct | Cell membrane disintegration | MTT/MTS assay | HL-60 | Leukemia cancer | IC50 : 6.24 µM |
| dbacp05446 | Peptide-3 | RRRRRRRRGGC-Pem | Synthetic construct | Cell membrane disintegration | MTT/MTS assay | NCI-H358 | Lung cancer | IC50 : 8.41 µM |
| dbacp05706 | PTP-7a | FLGALFHALSKLL | Synthetic peptide | Inducing cell membrane damage | MTT/MTS assay | A-549 | Lung cancer | IC50 : 28 µM |
| dbacp05707 | PTP-7b | FLGALFKALSHLL | Synthetic peptide | Inducing cell membrane damage | MTT/MTS assay | A-549 | Lung cancer | IC50 : 32 µM |
| dbacp05825 | R8-BadBH3 | rrrrrrrrGNLWAAQRYGRELRRMSDEFVDSFKK | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | SK-N-AS | Brain tumor | 0% apoptosis at 10 µM |
| dbacp05826 | R8-BadBH3 | rrrrrrrrGNLWAAQRYGRELRRMSDEFVDSFKK | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | SK-N-AS | Brain tumor | 10% apoptosis at 20 µM |
| dbacp05827 | R8-BadBH3 | rrrrrrrrGNLWAAQRYGRELRRMSDEFVDSFKK | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | SK-N-AS | Brain tumor | 30% apoptosis at 50 µM |
| dbacp05828 | R8-BadBH3 | rrrrrrrrGNLWAAQRYGRELRRMSDEFVDSFKK | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NB69 | Brain tumor | 30% apoptosis at 10 µM |
| dbacp05829 | R8-BadBH3 | rrrrrrrrGNLWAAQRYGRELRRMSDEFVDSFKK | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NB69 | Brain tumor | 80% apoptosis at 20 µM |
| dbacp05830 | R8-BadBH3 | rrrrrrrrGNLWAAQRYGRELRRMSDEFVDSFKK | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NB69 | Brain tumor | 80% apoptosis at 50 µM |
| dbacp05831 | R8-BadBH3 | rrrrrrrrGNLWAAQRYGRELRRMSDEFVDSFKK | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NGP | Tumor | 20% apoptosis at 10 µM |
| dbacp05832 | R8-BadBH3 | rrrrrrrrGNLWAAQRYGRELRRMSDEFVDSFKK | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NGP | Tumor | > 50% apoptosis at 20 µM |
| dbacp05833 | R8-BadBH3 | rrrrrrrrGNLWAAQRYGRELRRMSDEFVDSFKK | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NGP | Tumor | 30% apoptosis at 50 µM |
| dbacp05834 | R8-BadBH3 | rrrrrrrrGNLWAAQRYGRELRRMSDEFVDSFKK | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | IMR5 | Tumor | 15% apoptosis at 10 µM |
| dbacp05835 | R8-BadBH3 | rrrrrrrrGNLWAAQRYGRELRRMSDEFVDSFKK | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | IMR5 | Tumor | 20% apoptosis at 20 µM |
| dbacp05836 | R8-BadBH3 | rrrrrrrrGNLWAAQRYGRELRRMSDEFVDSFKK | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | IMR5 | Tumor | 50% apoptosis at 50 µM |
| dbacp05839 | R8-BidBH3 | rrrrrrrrGEDIIRNIARHLAQVGDSMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | SK-N-AS | Brain tumor | 8% apoptosis at 10 µM |
| dbacp05840 | R8-BidBH3 | rrrrrrrrGEDIIRNIARHLAQVGDSMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | SK-N-AS | Brain tumor | 45% apoptosis at 20 µM |
| dbacp05841 | R8-BidBH3 | rrrrrrrrGEDIIRNIARHLAQVGDSMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | SK-N-AS | Brain tumor | 65% apoptosis at 50 µM |
| dbacp05842 | R8-BidBH3 | rrrrrrrrGEDIIRNIARHLAQVGDSMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NB69 | Brain tumor | 25% apoptosis at 10 µM |
| dbacp05843 | R8-BidBH3 | rrrrrrrrGEDIIRNIARHLAQVGDSMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NB69 | Brain tumor | 66% apoptosis at 20 µM |
| dbacp05844 | R8-BidBH3 | rrrrrrrrGEDIIRNIARHLAQVGDSMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NB69 | Brain tumor | 68% apoptosis at 50 µM |
| dbacp05845 | R8-BidBH3 | rrrrrrrrGEDIIRNIARHLAQVGDSMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NGP | Tumor | 43% apoptosis at 10 µM |
| dbacp05846 | R8-BidBH3 | rrrrrrrrGEDIIRNIARHLAQVGDSMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NGP | Tumor | 46% apoptosis at 20 µM |
| dbacp05847 | R8-BidBH3 | rrrrrrrrGEDIIRNIARHLAQVGDSMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NGP | Tumor | 79% apoptosis at 50 µM |
| dbacp05848 | R8-BidBH3 | rrrrrrrrGEDIIRNIARHLAQVGDSMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | IMR5 | Tumor | 23% apoptosis at 10 µM |
| dbacp05849 | R8-BidBH3 | rrrrrrrrGEDIIRNIARHLAQVGDSMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | IMR5 | Tumor | 35% apoptosis at 20 µM |
| dbacp05850 | R8-BidBH3 | rrrrrrrrGEDIIRNIARHLAQVGDSMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | IMR5 | Tumor | 55% apoptosis at 50 µM |
| dbacp05851 | R8-BidBH3Alt | rrrrrrrrGEDIIRNIARHAAQVGASMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | SK-N-AS | Brain tumor | 1% apoptosis at 10 µM |
| dbacp05852 | R8-BidBH3Alt | rrrrrrrrGEDIIRNIARHAAQVGASMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | SK-N-AS | Brain tumor | 2% apoptosis at 20 µM |
| dbacp05853 | R8-BidBH3Alt | rrrrrrrrGEDIIRNIARHAAQVGASMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | SK-N-AS | Brain tumor | 3% apoptosis at 50 µM |
| dbacp05854 | R8-BidBH3Alt | rrrrrrrrGEDIIRNIARHAAQVGASMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NB69 | Brain tumor | 2% apoptosis at 10 µM |
| dbacp05855 | R8-BidBH3Alt | rrrrrrrrGEDIIRNIARHAAQVGASMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NB69 | Brain tumor | 1% apoptosis at 20 µM |
| dbacp05856 | R8-BidBH3Alt | rrrrrrrrGEDIIRNIARHAAQVGASMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NB69 | Brain tumor | 5% apoptosis at 50 µM |
| dbacp05857 | R8-BidBH3Alt | rrrrrrrrGEDIIRNIARHAAQVGASMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NGP | Tumor | 1% apoptosis at 10 µM |
| dbacp05858 | R8-BidBH3Alt | rrrrrrrrGEDIIRNIARHAAQVGASMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NGP | Tumor | 2% apoptosis at 20 µM |
| dbacp05859 | R8-BidBH3Alt | rrrrrrrrGEDIIRNIARHAAQVGASMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | NGP | Tumor | 3% apoptosis at 50 µM |
| dbacp05860 | R8-BidBH3Alt | rrrrrrrrGEDIIRNIARHAAQVGASMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | IMR5 | Tumor | 0% apoptosis at 10 µM |
| dbacp05861 | R8-BidBH3Alt | rrrrrrrrGEDIIRNIARHAAQVGASMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | IMR5 | Tumor | 1% apoptosis at 20 µM |
| dbacp05862 | R8-BidBH3Alt | rrrrrrrrGEDIIRNIARHAAQVGASMDR | Synthetic Peptide | Inducing mitochondrial apoptosis | MTT/MTS assay | IMR5 | Tumor | 2% apoptosis at 50 µM |
| dbacp06023 | Sansalv amide A | NA | Synthetic Peptide | Apoptosis | Cell viability assay | S2-13 | Pancreatic cancer | EC50 : 7.5 µM |
| dbacp06169 | SVS-1 | KVKVKVKVpPTKVKVKVK | Synthetic peptide | Disruption of cell membranes | MTT/MTS assay | A-549 | Lung cancer | Not found |
| dbacp06171 | SVS-1 | KVKVKVKVpPTKVKVKVK | Synthetic peptide | Disruption of cell membranes | MTT/MTS assay | MCF-7 | Breast cancer | IC50 : 8.1 ± 0.8 µM |
| dbacp06172 | SVS-1 | KVKVKVKVpPTKVKVKVK | Synthetic peptide | Disruption of cell membranes | MTT/MTS assay | MDA-MB-436 | Breast cancer | IC50 : 5.6 ± 0.5 µM |
| dbacp06173 | SVS-2 | KVKVKVKVPPTKVKVKVK | Synthetic peptide | Disruption of cell membranes | MTT/MTS assay | A-549 | Lung cancer | IC50 : >100 µM |
| dbacp06174 | SVS-2 | KVKVKVKVPPTKVKVKVK | Synthetic peptide | Disruption of cell membranes | MTT/MTS assay | KB | Oral cancer | IC50 : >100 µM |
| dbacp06175 | SVS-2 | KVKVKVKVPPTKVKVKVK | Synthetic peptide | Disruption of cell membranes | MTT/MTS assay | MCF-7 | Breast cancer | IC50 : >100 µM |
| dbacp06176 | SVS-2 | KVKVKVKVPPTKVKVKVK | Synthetic peptide | Disruption of cell membranes | MTT/MTS assay | MDA-MB-436 | Breast cancer | IC50 : >100 µM |
| dbacp06177 | Synthetic peptide | KWKKLLKKPPPLLKKLLKKL | Synthetic peptide | Not specified | MTT/MTS assay | Calu-6 | Lung cancer | 35% survival rate at 10 µM |
| dbacp06178 | Synthetic peptide | KWKKLLKKPPPLLKKLLKKL | Synthetic peptide | Not specified | MTT/MTS assay | Calu-6 | Lung cancer | 0% survival rate at 100 µM |
| dbacp06179 | Synthetic peptide | KWKKLLKKPPPLLKKLLKKL | Synthetic peptide | Not specified | MTT/MTS assay | Jurkat | Blood cancer | ~60% survival rate at 10 µM |
| dbacp06180 | Synthetic peptide | KWKKLLKKPPPLLKKLLKKL | Synthetic peptide | Not specified | MTT/MTS assay | Jurkat | Blood cancer | 0% survival rate at 100 µM |
| dbacp06181 | Synthetic peptide | KWKKLLKKPPPLLKKLLKKL | Synthetic peptide | Not specified | MTT/MTS assay | SNU-601 | Gastric cancer | ~20% survival rate at 10 µM |
| dbacp06182 | Synthetic peptide | KWKKLLKKPPPLLKKLLKKL | Synthetic peptide | Not specified | MTT/MTS assay | SNU-601 | Gastric cancer | 0% survival rate at 100 µM |
| dbacp06183 | t Mastoparan-C(tMP-C, Tat (49-57)-Mastoparan-C) | RKKRRQRRRLNLKALLAVAKKIL | Synthetic construct | Apoptosis inducing | MTT assay | H157 | Non-small cell Lung cancer | IC50 : 2.79 μM |
| dbacp06184 | t Mastoparan-C(tMP-C, Tat (49-57)-Mastoparan-C) | RKKRRQRRRLNLKALLAVAKKIL | Synthetic construct | Apoptosis inducing | MTT assay | MBD-MB-435S | Melanocyte | IC50 : 3.86 μM |
| dbacp06185 | t Mastoparan-C(tMP-C, Tat (49-57)-Mastoparan-C) | RKKRRQRRRLNLKALLAVAKKIL | Synthetic construct | Apoptosis inducing | MTT assay | PC-3 | Human prostate carcinoma | IC50 : 3.86 μM |
| dbacp06186 | t Mastoparan-C(tMP-C, Tat (49-57)-Mastoparan-C) | RKKRRQRRRLNLKALLAVAKKIL | Synthetic construct | Apoptosis inducing | MTT assay | U251-MG | Human glioblastoma astrocytoma | IC50 : 3.36 μM |
| dbacp06187 | t Mastoparan-C(tMP-C, Tat (49-57)-Mastoparan-C) | RKKRRQRRRLNLKALLAVAKKIL | Synthetic construct | Apoptosis inducing | MTT assay | MCF-7 | Human breast cancer | IC50 : 3.70 μM |
| dbacp06196 | Tat (47-57) | YGRKKRRQRRR | Synthetic construct | Cell membrane disintegration | MTT/MTS assay | HeLa | Cervical cancer | At 1 µM 90 - 100% viablity |
| dbacp06197 | Tat (47-57) | YGRKKRRQRRR | Synthetic construct | Cell membrane disintegration | MTT/MTS assay | HeLa | Cervical cancer | At 10 µM 80% viablity |
| dbacp06198 | Tat (47-57) | YGRKKRRQRRR | Synthetic construct | Cell membrane disintegration | MTT/MTS assay | HeLa | Cervical cancer | At 100 µM 60% viablity |
| dbacp06293 | Tetramer of peptide-paclitaxel conjugate | (K-Aib-C(CH2CO-2'-Pac))4 | Synthetic peptide paclitaxel conjugate | Not specified | MTT/MTS assay | HeLa | Cervical cancer | IC50 : 0.96 nM |
| dbacp06294 | Tetramer of peptide-paclitaxel conjugate | (K-Aib-C(CH2CO-2'-Pac))4 | Synthetic peptide paclitaxel conjugate | Not specified | MTT/MTS assay | DU | Prostate cancer | IC50 : 1.30 nM |
| dbacp06295 | Tetramer of peptide-paclitaxel conjugate | (K-Aib-C(CH2CO-2'-Pac))4 | Synthetic peptide paclitaxel conjugate | Not specified | MTT/MTS assay | MCF-7 | Breast cancer | IC50 : 0.64 nM |
| dbacp06346 | Trimer of peptide-paclitaxel conjugate | (K-Aib-C(CH2CO-2'-Pac))3 | Synthetic peptide paclitaxel conjugate | Not specified | MTT/MTS assay | HeLa | Cervical cancer | IC50 : 1.70 nM |
| dbacp06347 | Trimer of peptide-paclitaxel conjugate | (K-Aib-C(CH2CO-2'-Pac))3 | Synthetic peptide paclitaxel conjugate | Not specified | MTT/MTS assay | DU | Prostate cancer | IC50 : 3.88 nM |
| dbacp06348 | Trimer of peptide-paclitaxel conjugate | (K-Aib-C(CH2CO-2'-Pac))3 | Synthetic peptide paclitaxel conjugate | Not specified | MTT/MTS assay | MCF-7 | Breast cancer | IC50 : 3.00 nM |
| dbacp06404 | Tyroserleutide | YSL | Synthetic Peptide | Necrosis; Immune regulation | MTT/MTS assay | B16-F10 | Skin cancer | 49.4% Cytotoxic at 0.1 µg/ml |
| dbacp06405 | Tyroserleutide | YSL | Synthetic Peptide | Necrosis; Immune regulation | MTT/MTS assay | B16-F10 | Skin cancer | 51.2% Cytotoxic at 1 µg/ml |
| dbacp06406 | Tyroserleutide | YSL | Synthetic Peptide | Necrosis; Immune regulation | MTT/MTS assay | B16-F10 | Skin cancer | 53.0% Cytotoxic at 10 µg/ml |
| dbacp06407 | Tyroserleutide | YSL | Synthetic Peptide | Necrosis; Immune regulation | MTT/MTS assay | B16-F10 | Skin cancer | 61.2% Cytotoxic at 100 µg/ml |
| dbacp06408 | Tyroserleutide | YSL | Synthetic Peptide | Necrosis; Immune regulation | MTT/MTS assay | BEL-7402 | Liver cancer | 39.0% Cytotoxic at 0.1 µg/ml |
| dbacp06409 | Tyroserleutide | YSL | Synthetic Peptide | Necrosis; Immune regulation | MTT/MTS assay | BEL-7402 | Liver cancer | 20.8% Cytotoxic at 1 µg/ml |
| dbacp06410 | Tyroserleutide | YSL | Synthetic Peptide | Necrosis; Immune regulation | MTT/MTS assay | BEL-7402 | Liver cancer | 33.8% Cytotoxic at 10 µg/ml |
| dbacp06411 | Tyroserleutide | YSL | Synthetic Peptide | Necrosis; Immune regulation | MTT/MTS assay | BEL-7402 | Liver cancer | 35.6% Cytotoxic at 100 µg/ml |
| dbacp06548 | Z1 | KAAKKWAKAAKKAAKAWKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | Meth A | Skin cancer | EC50 : > 211 µM |
| dbacp06549 | Z1 | KAAKKWAKAAKKWAKAWKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | MT-1 | Breast cancer | EC50 : 186 µM |
| dbacp06550 | Z1 | KAAKKWAKAAKKWAKAWKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | HT-29 | Colon cancer | EC50 : > 211 µM |
| dbacp06551 | Z10 | AAKKWAKAKWAKAKKWAKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | Meth A | Skin cancer | EC50 : > 211 µM |
| dbacp06552 | Z10 | AAKKWAKAKWAKAKKWAKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | MT-1 | Breast cancer | EC50 : > 211 µM |
| dbacp06553 | Z10 | AAKKWAKAKWAKAKKWAKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | HT-29 | Colon cancer | EC50 : > 211 µM |
| dbacp06554 | Z2 | KAAKKWAKAWKKAAKAWKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | Meth A | Skin cancer | EC50 : > 211 µM |
| dbacp06555 | Z2 | KAAKKWAKAWKKAAKAWKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | MT-1 | Breast cancer | EC50 : 173 µM |
| dbacp06556 | Z2 | KAAKKWAKAWKKAAKAWKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | HT-29 | Colon cancer | EC50 : > 211 µM |
| dbacp06567 | Z3 | KAAKKAWKAWKKAAKAAWKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | Meth A | Skin cancer | EC50 : >211 µM |
| dbacp06568 | Z3 | KAAKKAWKAWKKAAKAAWKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | MT-1 | Breast cancer | EC50 : 128 µM |
| dbacp06569 | Z3 | KAAKKAWKAWKKAAKAAWKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | HT-29 | Colon cancer | EC50 : >211 µM |
| dbacp06570 | Z4 | KAAKKAWKAAKKAAKWWKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | Meth A | Skin cancer | EC50 : 155 µM |
| dbacp06571 | Z4 | KAAKKAWKAAKKAAKWWKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | MT-1 | Breast cancer | EC50 : 68 µM |
| dbacp06572 | Z4 | KAAKKAWKAAKKAAKWWKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | HT-29 | Colon cancer | EC50 : 173 µM |
| dbacp06583 | Z5 | KAAKKAWKWAKKAAKWAKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | Meth A | Skin cancer | EC50 : 42 µM |
| dbacp06584 | Z5 | KAAKKAWKWAKKAAKWAKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | MT-1 | Breast cancer | EC50 : 28 µM |
| dbacp06585 | Z5 | KAAKKAWKWAKKAAKWAKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | HT-29 | Colon cancer | EC50 : 67 µM |
| dbacp06586 | Z6 | KWWKKAAKAAKKAAKAAKKWA | Synthetic | Disruption of cell membrane | MTT/MTS assay | Meth A | Skin cancer | EC50 : 17 µM |
| dbacp06587 | Z6 | KWWKKAAKAAKKAAKAAKKWA | Synthetic | Disruption of cell membrane | MTT/MTS assay | MT-1 | Breast cancer | EC50 : 16 µM |
| dbacp06588 | Z6 | KWWKKAAKAAKKAAKAAKKWA | Synthetic | Disruption of cell membrane | MTT/MTS assay | HT-29 | Colon cancer | EC50 : 31 µM |
| dbacp06589 | Z7 | KAAKKAWKAAKKAWKAAKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | Meth A | Skin cancer | EC50 : 15 µM |
| dbacp06590 | Z7 | KAAKKAWKAAKKAWKAAKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | MT-1 | Breast cancer | EC50 : 15 µM |
| dbacp06591 | Z7 | KAAKKAWKAAKKAWKAAKKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | HT-29 | Colon cancer | EC50 : 21 µM |
| dbacp06592 | Z8 | AWKKWAKAWKWAKAKWWAKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | Meth A | Skin cancer | EC50 : 19 µM |
| dbacp06593 | Z8 | AWKKWAKAWKWAKAKWWAKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | MT-1 | Breast cancer | EC50 : 14 µM |
| dbacp06594 | Z8 | AWKKWAKAWKWAKAKWWAKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | HT-29 | Colon cancer | EC50 : 23 µM |
| dbacp06595 | Z9 | AAWKWAWAKKWAKAKKWAKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | Meth A | Skin cancer | EC50 : 9 µM |
| dbacp06596 | Z9 | AAWKWAWAKKWAKAKKWAKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | MT-1 | Breast cancer | EC50 : 16 µM |
| dbacp06597 | Z9 | AAWKWAWAKKWAKAKKWAKAA | Synthetic | Disruption of cell membrane | MTT/MTS assay | HT-29 | Colon cancer | EC50 : 13 µM |
| dbacp06639 | C-Mel | CGIGAVLKVLTTGLPALISWIKRKRQQ | Synthetic analogue | Plasma memberane pore formation | MTT assay | HeLa | Cervical Cancer | IC50 = 64.15 µg/mL |
| dbacp06640 | C-Mel | CGIGAVLKVLTTGLPALISWIKRKRQQ | Synthetic analogue | Plasma memberane pore formation | MTT assay | C-33A | Cervical Cancer | IC50 = 44.76 µg/mL |
| dbacp06641 | C-Mel | CGIGAVLKVLTTGLPALISWIKRKRQQ | Synthetic analogue | Plasma memberane pore formation | MTT assay | MCF-7 | Breast Cancer | IC50 = 110.59 µg/mL |
| dbacp06642 | CM–FA | CGIGAVLKVLTTGLPALISWIKRKRQQ | Synthetic analogue | Plasma memberane pore formation | MTT assay | HeLa | Cervical Cancer | IC50 = 67.34 µg/mL |
| dbacp06643 | CM–FA | CGIGAVLKVLTTGLPALISWIKRKRQQ | Synthetic analogue | Plasma memberane pore formation | MTT assay | C-33A | Cervical Cancer | IC50 = 35.75 µg/mL |
| dbacp06644 | CM–FA | CGIGAVLKVLTTGLPALISWIKRKRQQ | Synthetic analogue | Plasma memberane pore formation | MTT assay | MCF-7 | Breast Cancer | IC50 = 10.38 µg/mL |
| dbacp06645 | Mel-C | GIGAVLKVLTTGLPALISWIKRKRQQC | Synthetic analogue | Plasma memberane pore formation | MTT assay | HeLa | Cervical Cancer | IC50 = 50.72 µg/mL |
| dbacp06646 | Mel-C | GIGAVLKVLTTGLPALISWIKRKRQQC | Synthetic analogue | Plasma memberane pore formation | MTT assay | C-33A | Cervical Cancer | IC50 = 58.63 µg/mL |
| dbacp06647 | Mel-C | GIGAVLKVLTTGLPALISWIKRKRQQC | Synthetic analogue | Plasma memberane pore formation | MTT assay | MCF-7 | Breast Cancer | IC50 = 160.62 µg/mL |
| dbacp06648 | MC–FA | GIGAVLKVLTTGLPALISWIKRKRQQC | Synthetic analogue | Plasma memberane pore formation | MTT assay | HeLa | Cervical Cancer | IC50 = 66.43 µg/mL |
| dbacp06649 | MC–FA | GIGAVLKVLTTGLPALISWIKRKRQQC | Synthetic analogue | Plasma memberane pore formation | MTT assay | C-33A | Cervical Cancer | IC50 = 35.22 µg/ mL |
| dbacp06650 | MC–FA | GIGAVLKVLTTGLPALISWIKRKRQQC | Synthetic analogue | Plasma memberane pore formation | MTT assay | MCF-7 | Breast Cancer | IC50 = 12.63 µg/mL |
| dbacp06651 | LUNA18 | Not Available | Synthetic | Not available | CellTiter-Glo Cell Viability assay | NCI-H2122 | NSCLC | IC50 = 1.4 ± 0.3 nmol/L |
| dbacp06652 | LUNA18 | Not Available | Synthetic | Not available | CellTiter-Glo Cell Viability assay | MiaPaCa.2 | Pancreatic Cancer | IC50 = 1.4 ± 0.2 nmol/L |
| dbacp06653 | LUNA18 | Not Available | Synthetic | Not available | CellTiter-Glo Cell Viability assay | NCI-H441 | NSCLC | IC50 = 2.9 ± 0.7 nmol/L |
| dbacp06654 | LUNA18 | Not Available | Synthetic | Not available | CellTiter-Glo Cell Viability assay | LS 180 | Colon Cancer | IC50 = 2.7 ± 0.4 nmol/L |
| dbacp06655 | LUNA18 | Not Available | Synthetic | Not available | CellTiter-Glo Cell Viability assay | GSU | Stomach Cancer | IC50 = 0.17 ± 0.02 nmol/L |
| dbacp06659 | Ahx-[Pal] | Ahx-RWQWRWQWR | Synthetic | Apoptosis inducing | MTT assay | HT-29 | Colon Cancer | IC50 = 119 μM |
| dbacp06660 | Ahx-[Pal] | Ahx-RWQWRWQWR | Synthetic | Apoptosis inducing | MTT assay | CaCo-2 | Colorectal Cancer | IC50 = 40 μM |
| dbacp06661 | 9[Orn] [Pal] | RWQWRWQWO | Synthetic | Apoptosis inducing | MTT assay | HT-29 | Colon Cancer | IC50 = 109 μM |
| dbacp06662 | 9[Orn] [Pal] | RWQWRWQWO | Synthetic | Apoptosis inducing | MTT assay | CaCo-2 | Colorectal Cancer | IC50 = 40 μM |
| dbacp06663 | 9[Orn] [Pal] | RWQWRWQWO | Synthetic | Apoptosis inducing | MTT assay | DU-145 | Prostrate Cancer | IC50 = 62 μM |
| dbacp06664 | CH3CO-Ahx-[Pal] | CH3-CO-Ahx-RWQWRWQWR | Synthetic | Apoptosis inducing | MTT assay | CaCo-2 | Colorectal Cancer | IC50 = 31 μM |
| dbacp06665 | 1[dR][Pal] | rWQWRWQWR | Synthetic | Apoptosis inducing | MTT assay | CaCo-2 | Colorectal Cancer | IC50 = 105 μM |
| dbacp06666 | 1[Orn] [Pal] | OWQWRWQWR | Synthetic | Apoptosis inducing | MTT assay | CaCo-2 | Colorectal Cancer | IC50 = 91 μM |
| dbacp06667 | 5[Orn] [Pal] | RWQWOWQWR | Synthetic | Apoptosis inducing | MTT assay | CaCo-2 | Colorectal Cancer | IC50 = 64 μM |
| dbacp06668 | 1[dR] 5[Orn] [Pal] | rWQWOWQWR | Synthetic | Apoptosis inducing | MTT assay | CaCo-2 | Colorectal Cancer | IC50 = 109 μM |
| dbacp06674 | Crabrolin-4R | FLPRILRKIVTAL | Synthetic Analog of Crabrolin | Not available | MTT assay | H-838 | Lung Cancer | IC50 = 11.40 μM |
| dbacp06675 | Crabrolin-4R | FLPRILRKIVTAL | Synthetic Analog of Crabrolin | Not available | MTT assay | PC-3 | Prostate Cancer | IC50 = 17.98 μM |
| dbacp06676 | Crabrolin-4R | FLPRILRKIVTAL | Synthetic Analog of Crabrolin | Not available | MTT assay | U-251-MG | Brain Tumor | IC50 = 25.09 μM |
| dbacp06677 | Crabrolin-4R | FLPRILRKIVTAL | Synthetic Analog of Crabrolin | Not available | MTT assay | HCT-116 | Colon Cancer | IC50 = 47.02 μM |
| dbacp06678 | Crabrolin-4R | FLPRILRKIVTAL | Synthetic Analog of Crabrolin | Not available | MTT assay | MCF-7 | Breast Cancer | IC50 = 20.26 μM |
| dbacp06679 | Crabrolin-4K | FLPKILRKIVTAL | Synthetic Analog of Crabrolin | Not available | MTT assay | H-838 | Lung Cancer | IC50 = 22.55 μM |
| dbacp06680 | Crabrolin-4K | FLPKILRKIVTAL | Synthetic Analog of Crabrolin | Not available | MTT assay | PC-3 | Prostate Cancer | IC50 = 20.58 μM |
| dbacp06681 | Crabrolin-4K | FLPKILRKIVTAL | Synthetic Analog of Crabrolin | Not available | MTT assay | U-251-MG | Brain Tumor | IC50 = 23.51 μM |
| dbacp06682 | Crabrolin-4K | FLPKILRKIVTAL | Synthetic Analog of Crabrolin | Not available | MTT assay | HCT-116 | Colon Cancer | IC50 = 42.88 μM |
| dbacp06683 | Crabrolin-4K | FLPKILRKIVTAL | Synthetic Analog of Crabrolin | Not available | MTT assay | MCF-7 | Breast Cancer | IC50 = 23.18 μM |
| dbacp06684 | Crabrolin-TR | FLPRILRKIVRAL | Synthetic Analog of Crabrolin | Not available | MTT assay | H-838 | Lung Cancer | IC50 = 4.637 μM |
| dbacp06685 | Crabrolin-TR | FLPRILRKIVRAL | Synthetic Analog of Crabrolin | Not available | MTT assay | PC-3 | Prostate Cancer | IC50 = 3.944 μM |
| dbacp06686 | Crabrolin-TR | FLPRILRKIVRAL | Synthetic Analog of Crabrolin | Not available | MTT assay | U-251-MG | Brain Tumor | IC50 = 12.40 μM |
| dbacp06687 | Crabrolin-TR | FLPRILRKIVRAL | Synthetic Analog of Crabrolin | Not available | MTT assay | HCT-116 | Colon Cancer | IC50 = 2.810 μM |
| dbacp06688 | Crabrolin-TR | FLPRILRKIVRAL | Synthetic Analog of Crabrolin | Not available | MTT assay | MCF-7 | Breast Cancer | IC50 = 3.459 μM |
| dbacp06689 | Crabrolin-FR | RLPRILRKIVRAL | Synthetic Analog of Crabrolin | Not available | MTT assay | H-838 | Lung Cancer | IC50 = 31.51 μM |
| dbacp06690 | Crabrolin-FR | RLPRILRKIVRAL | Synthetic Analog of Crabrolin | Not available | MTT assay | PC-3 | Prostate Cancer | IC50 = 15.87 μM |
| dbacp06691 | Crabrolin-FR | RLPRILRKIVRAL | Synthetic Analog of Crabrolin | Not available | MTT assay | U-251-MG | Brain Tumor | IC50 = 62.17 μM |
| dbacp06692 | Crabrolin-FR | RLPRILRKIVRAL | Synthetic Analog of Crabrolin | Not available | MTT assay | HCT-116 | Colon Cancer | IC50 = 30.29 μM |
| dbacp06693 | Crabrolin-FR | RLPRILRKIVRAL | Synthetic Analog of Crabrolin | Not available | MTT assay | MCF-7 | Breast Cancer | IC50 = 33.85 μM |
| dbacp06694 | Crabrolin-AR | RLPRILRKIVRRL | Synthetic Analog of Crabrolin | Not available | MTT assay | H-838 | Lung Cancer | IC50 = 41.31 μM |
| dbacp06695 | Crabrolin-AR | RLPRILRKIVRRL | Synthetic Analog of Crabrolin | Not available | MTT assay | PC-3 | Prostate Cancer | IC50 = 28.78 μM |
| dbacp06696 | Crabrolin-AR | RLPRILRKIVRRL | Synthetic Analog of Crabrolin | Not available | MTT assay | U-251-MG | Brain Tumor | IC50 = 52.01 μM |
| dbacp06697 | Crabrolin-AR | RLPRILRKIVRRL | Synthetic Analog of Crabrolin | Not available | MTT assay | HCT-116 | Colon Cancer | IC50 = 29.90 μM |
| dbacp06698 | Crabrolin-AR | RLPRILRKIVRRL | Synthetic Analog of Crabrolin | Not available | MTT assay | MCF-7 | Breast Cancer | IC50 = 32.51 μM |
| dbacp06699 | Crabrolin-PR | RLRRILRKIVRRL | Synthetic Analog of Crabrolin | Not available | MTT assay | H-838 | Lung Cancer | IC50 = 32.32 μM |
| dbacp06700 | Crabrolin-PR | RLRRILRKIVRRL | Synthetic Analog of Crabrolin | Not available | MTT assay | PC-3 | Prostate Cancer | IC50 = 22.37 μM |
| dbacp06701 | Crabrolin-PR | RLRRILRKIVRRL | Synthetic Analog of Crabrolin | Not available | MTT assay | U-251-MG | Brain Tumor | IC50 = 17.70 μM |
| dbacp06702 | Crabrolin-PR | RLRRILRKIVRRL | Synthetic Analog of Crabrolin | Not available | MTT assay | HCT-116 | Colon Cancer | IC50 = 16.29 μM |
| dbacp06703 | Crabrolin-PR | RLRRILRKIVRRL | Synthetic Analog of Crabrolin | Not available | MTT assay | MCF-7 | Breast Cancer | IC50 = 12.29 μM |
| dbacp06737 | Aurein 1.2_mutant (Aurm) | GLFDIIKKIIKSF | Synthetic | Necrotic activity via cell membrane lysis and apoptotic activity through disrupting mitochondrial membrane | MTT assay | SW-480 | Colon Cancer | 51.63% cell viability |
| dbacp06738 | Aurein 1.2_mutant (Aurm) | GLFDIIKKIIKSF | Synthetic | Necrotic activity via cell membrane lysis and apoptotic activity through disrupting mitochondrial membrane | MTT assay | HT-29 | Colon Cancer | 66.10% cell viability |
| dbacp06739 | Aurein 1.2_R5 (R5-Aur) | RRRRRGLFDIIKKIAESF | Synthetic | Necrotic activity via cell membrane lysis and apoptotic activity through disrupting mitochondrial membrane | MTT assay | SW-480 | Colon Cancer | 43.89% cell viability |
| dbacp06740 | Aurein 1.2_R5 (R5-Aur) | RRRRRGLFDIIKKIAESF | Synthetic | Necrotic activity via cell membrane lysis and apoptotic activity through disrupting mitochondrial membrane | MTT assay | HT-29 | Colon Cancer | 61.56% cell viability |
| dbacp06741 | Aurein 1.2_mutant_R5 (R5-Aurm) | RRRRRGLFDIIKKIIKSF | Synthetic | Necrotic activity via cell membrane lysis and apoptotic activity through disrupting mitochondrial membrane | MTT assay | SW-480 | Colon Cancer | 40.62% cell viability |
| dbacp06742 | Aurein 1.2_mutant_R5 (R5-Aurm) | RRRRRGLFDIIKKIIKSF | Synthetic | Necrotic activity via cell membrane lysis and apoptotic activity through disrupting mitochondrial membrane | MTT assay | HT-29 | Colon Cancer | 54.22% cell viability |
| dbacp06743 | M1-20 | grrrqrrkkrlgpfsidllikslsdnmtdl | Synthetic | Inhibits FOXM1 transcriptional activities | CCK-8 assay | MDA-MB-231 | Breast Cancer | IC50 = 18.15 µM |
| dbacp06744 | M1-20 | grrrqrrkkrlgpfsidllikslsdnmtdl | Synthetic | Inhibits FOXM1 transcriptional activities | CCK-8 assay | MCF-7 | Breast Cancer | IC50 = 31.05 µM |
| dbacp06745 | M1-20 | grrrqrrkkrlgpfsidllikslsdnmtdl | Synthetic | Inhibits FOXM1 transcriptional activities | CCK-8 assay | ZR-75-30 | Breast Cancer | IC50 = 23.57 µM |
| dbacp06746 | M1-20 | grrrqrrkkrlgpfsidllikslsdnmtdl | Synthetic | Inhibits FOXM1 transcriptional activities | CCK-8 assay | HeLa | Cervical Cancer | IC50 = 42.95 µM |
| dbacp06747 | M1-20 | grrrqrrkkrlgpfsidllikslsdnmtdl | Synthetic | Inhibits FOXM1 transcriptional activities | CCK-8 assay | U-2 OS | Bone Cancer | IC50 = 25.65 µM |
| dbacp06748 | M1-20 | grrrqrrkkrlgpfsidllikslsdnmtdl | Synthetic | Inhibits FOXM1 transcriptional activities | CCK-8 assay | A-549 | Lung Cancer | IC50 = 32.47 µM |
| dbacp06749 | mPNC-NLS | QETFSDLWKLLVQRKRQKLMP | Synthetic | p53-mediated apoptosis | MTT assay | A-549 | Lung Cancer | IC50 = 44.9 μM |
| dbacp06750 | mPNC-NLS | QETFSDLWKLLVQRKRQKLMP | Synthetic | p53-mediated apoptosis | MTT assay | U-87 | Brain Tumor | IC50 = 56.9 μM |
| dbacp06751 | mPNC-NLS | QETFSDLWKLLVQRKRQKLMP | Synthetic | p53-mediated apoptosis | Cytotoxicity assay | A-549 | Lung Cancer | IC50 = 45 μM |
| dbacp06754 | 37-mer peptide | TKEQKEQIAKATGLTTKQVRNWYVQLNASIKVCMCSC | Synthetic | Apoptosis inducing | MTT assay | SNU-449 | Liver Cancer | IC50 = 76.4 ± 0.6015 μM |
| dbacp06755 | 37-mer peptide | TKEQKEQIAKATGLTTKQVRNWYVQLNASIKVCMCSC | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 = 33.65 ± 1.09 μM |
| dbacp06756 | 37-mer peptide | TKEQKEQIAKATGLTTKQVRNWYVQLNASIKVCMCSC | Synthetic | Apoptosis inducing | MTT assay | SK-OV-3 | Ovarian cancer | IC50 = 27.45 ± 1.5085 μM |
| dbacp06757 | ATMP5 | THPPTTTTTTTTTTTYTAAPATTT | Synthetic Analog of ATMP1 | Apoptosis inducing | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 64.04 ± 0.021 μg /ml |
| dbacp06763 | M1-21 | rrrqrrkkrg-QTQPRLGPPQTPAGGCSILIF | Synthetic | FOXM1 inhibitor | Cell Viability assay | MDA-MB-231 | Breast Cancer | IC50 = 24.25 µM |
| dbacp06764 | M1-21 | rrrqrrkkrg-QTQPRLGPPQTPAGGCSILIF | Synthetic | FOXM1 inhibitor | Cell Viability assay | 5637 | Bladder cancer | IC50 = 9.33 µM |
| dbacp06765 | M1-21 | rrrqrrkkrg-QTQPRLGPPQTPAGGCSILIF | Synthetic | FOXM1 inhibitor | Cell Viability assay | HeLa | Cervical Cancer | IC50 = 31.83 µM |
| dbacp06766 | M1-21 | rrrqrrkkrg-QTQPRLGPPQTPAGGCSILIF | Synthetic | FOXM1 inhibitor | Cell Viability assay | 786-0 | Renal Cancer | IC50 = 13.5 µM |
| dbacp06767 | M1-21 | rrrqrrkkrg-QTQPRLGPPQTPAGGCSILIF | Synthetic | FOXM1 inhibitor | Cell Viability assay | HCT-116 | Colon Cancer | IC50 = 9.08 µM |
| dbacp06768 | M1-21 | rrrqrrkkrg-QTQPRLGPPQTPAGGCSILIF | Synthetic | FOXM1 inhibitor | Cell Viability assay | A-549 | Lung Cancer | IC50 = 22.00 µM |
| dbacp06769 | M1-21 | rrrqrrkkrg-QTQPRLGPPQTPAGGCSILIF | Synthetic | FOXM1 inhibitor | Cell Viability assay | U-251 | BrainTumor | IC50 = 18.17 µM |
| dbacp06770 | M1-21 | rrrqrrkkrg-QTQPRLGPPQTPAGGCSILIF | Synthetic | FOXM1 inhibitor | Cell Viability assay | ZR-75-30 | Breast Cancer | IC50 = 12.92 µM |
| dbacp06774 | PMAP-NC | RIIDRLWLVRRPQKPKFVLVWVL | Synthetic Analgog of PMAP-23 | Membrane permeabilization | MTT assay | MDA-MB-361 | Breast Cancer | IC50 = 6.4 μM |
| dbacp06775 | PMAP-NC | RIIDRLWLVRRPQKPKFVLVWVL | Synthetic Analgog of PMAP-24 | Membrane permeabilization | MTT assay | A-549 | Lung Cancer | IC50 = 7.1 μM |
| dbacp06777 | BK-1 | rRP-Hyp-G-Thi-S-Apc-Thi-R | Synthetic analogue of Bradykinin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06778 | BK-2 | rRP-Hyp-G-Thi-S-f-Apc-R | Synthetic analogue of Bradykinin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06779 | BK-3 | Aaa-rRP-Hyp-G-Thi-S-Acc-Thi-R | Synthetic analogue of Bradykinin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06780 | BK-4 | Aaa-rRP-Hyp-G-Thi-S-f-Acc-R | Synthetic analogue of Bradykinin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06781 | BK-5 | rRP-Hyp-G-Thi-S-f-(L)Pip-R | Synthetic analogue of Bradykinin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06782 | BK-6 | Aaa-rRP-Hyp-G-Thi-S-(D)Pip-(L)Pip-R | Synthetic analogue of Bradykinin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06783 | BK-7 | rRP-Hyp-G-Thi-S-(D)Pip-Thi-R | Synthetic analogue of Bradykinin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06784 | BK-8 | Aaa-rRP-Hyp-G-Thi-S-(D)Pip-Thi-R | Synthetic analogue of Bradykinin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06785 | NT-9 | RRPYIL | Synthetic analogue of Neurotensin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06786 | NT-10 | RRPAIL | Synthetic analogue of Neurotensin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06787 | NT-11 | RRPYAL | Synthetic analogue of Neurotensin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06788 | NT-12 | PEGRKPY-Tle-L | Synthetic analogue of Neurotensin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06789 | NT-12 | PEGKRPY-Tle-L | Synthetic analogue of Neurotensin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06790 | NT-12 | PEGKKPY-Tle-L | Synthetic analogue of Neurotensin | Not available | MTS assay | HCT-116 | Colorectal Cancer | Not Available |
| dbacp06796 | LHRH-BinBC | QHWSYGLRPGGRGPKDAVRAVKGSALLPCIIVHDPNLNNSDKMKFNTYYLLEYKEYWHQLWSQIIPAHQTVKIQERTGISEVVQNSMIEDLNMYIGADFGMYFYLRSSGFKEQITRGLNRPLSQTTTQLGERVEEMEYYNSNDLDVRYVKYALAREFTLKRVNGEIVKNWVAVDYRMAGIQSYPNAPITNPLTLT | Synthetic | Apoptosis inducing | MTT assay | MCF-7 | Breast Cancer | IC50 = 10.96 μM |
| dbacp06797 | LHRH-BinBC | QHWSYGLRPGGRGPKDAVRAVKGSALLPCIIVHDPNLNNSDKMKFNTYYLLEYKEYWHQLWSQIIPAHQTVKIQERTGISEVVQNSMIEDLNMYIGADFGMYFYLRSSGFKEQITRGLNRPLSQTTTQLGERVEEMEYYNSNDLDVRYVKYALAREFTLKRVNGEIVKNWVAVDYRMAGIQSYPNAPITNPLTLT | Synthetic | Apoptosis inducing | LDH leakage assay | MCF-7 | Breast Cancer | 40% LDH efflux at 16 µM |
| dbacp06803 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | CRL-1739 | Gastric Cancer | CC50 = 46.2 ± 7.6 μM |
| dbacp06804 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 2.3 ± 0.2 μM |
| dbacp06805 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | HeLa | Cervical Cancer | CC50 = 36.2 ± 2.8 μM |
| dbacp06806 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MCF-7 | Breast Cancer | CC50 = 29.0 ± 3.7 μM |
| dbacp06807 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 6.4 ± 0.6 μM |
| dbacp06808 | [C/U, G1K, L5Y, K8R]cGm | KURRYUYRQRUVTYURGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | HL-60 | Leukemia Cancer | CC50 = 33.3 ±7.4μM |
| dbacp06809 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | CRL-1739 | Gastric Cancer | CC50 = 26.5 ± 2.4 μM |
| dbacp06810 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 2.0 ± 0.1 μM |
| dbacp06811 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | HeLa | Cervical Cancer | CC50 = 20.9 ± 1.4 μM |
| dbacp06812 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MCF-7 | Breast Cancer | CC50 = 15.2 ± 1.9 μM |
| dbacp06813 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 1.3 ± 0.1 μM |
| dbacp06814 | [G1K, L5Y, K8R]cGm | KCRRYCYRQRCVTYCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | HL-60 | Leukemia Cancer | CC50 = 15.7 ±1.1μM |
| dbacp06815 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | CRL-1739 | Gastric Cancer | CC50 = 22.5 ± 3.3 μM |
| dbacp06816 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 3.0 ± 0.1 μM |
| dbacp06817 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | HeLa | Cervical Cancer | CC50 = 51.5 ± 3.9 μM |
| dbacp06818 | [D-P L-P]cGm | GCRRLCYKQRCVTYCRGpPR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 3.9 ± 0.2 μM |
| dbacp06819 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | CRL-1739 | Gastric Cancer | CC50 = 51.0 ± 4.6 μM |
| dbacp06820 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 4.6 ± 0.2 μM |
| dbacp06821 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | HeLa | Cervical Cancer | CC50 > 64 μM |
| dbacp06822 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MCF-7 | Breast Cancer | CC50 = 37.5 ± 3.3 μM |
| dbacp06823 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 1.4 ± 0.2 μM |
| dbacp06824 | [C/U]cGm | GURRLUYKQRUVTYURGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | HL-60 | Leukemia Cancer | CC50 = 38.5 ± 4.8 μM |
| dbacp06825 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | CRL-1739 | Gastric Cancer | CC50 = 19.5 ± 0.5 μM |
| dbacp06826 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 1.7 ± 0.1 μM |
| dbacp06827 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | HeLa | Cervical Cancer | CC50 = 44.2 ± 2.2μM |
| dbacp06828 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MCF-7 | Breast Cancer | CC50 = 6.7 ± 0.7 μM |
| dbacp06829 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 2.1 ± 0.2 μM |
| dbacp06830 | [G1K, K8R]cGm | KCRRLCYRQRCVTYCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | HL-60 | Leukemia Cancer | CC50 = 9.0 ± 1.1μM |
| dbacp06831 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | CRL-1739 | Gastric Cancer | CC50 > 64 μM |
| dbacp06832 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 10.3 ± 1.1 μM |
| dbacp06833 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | HeLa | Cervical Cancer | CC50 > 64 μM |
| dbacp06834 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MCF-7 | Breast Cancer | CC50 = 48.4 ± 0.7 μM |
| dbacp06835 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 11.5 ± 0.6 μM |
| dbacp06836 | [R4A, R18A]cGm | GCRALCYKQRCVTYCRGA | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | HL-60 | Leukemia Cancer | CC50 = 34.1 ± 3.9 μM |
| dbacp06837 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | CRL-1739 | Gastric Cancer | CC50 = 31.6 ± 1.3 μM |
| dbacp06838 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 5.4 ± 0.3 μM |
| dbacp06839 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | HeLa | Cervical Cancer | CC50 = 41.0 ± 4.2 μM |
| dbacp06840 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | MCF-7 | Breast Cancer | CC50 = 15.1 ± 1.4 μM |
| dbacp06841 | [Y7W, K8R, Y14W]cGm | GCRRLCWRQRCVTWCRGR | Synthetic Analogue of Gomesin | Cell membrane penetration | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 3.9 ± 0.1 μM |
| dbacp06861 | LK-LE1 | CLKKLLKLLKKLLKLCLHELLEHLHELLEH | Synthetic | Membrane disruption | MTT assay | HeLa | Cervical Cancer | IC50 = 11.3 µM at pH 6 |
| dbacp06862 | LK-LE2 | CLKKLLKLLKKLLKLCLEHLLEHLEHLLEH | Synthetic | Membrane disruption | MTT assay | HeLa | Cervical Cancer | IC50 = 12.9 µM at pH 6 |
| dbacp06863 | LK-LE3 | CLKKLLKLLKKLLKLCLEELLHHLEELLHH | Synthetic | Membrane disruption | MTT assay | HeLa | Cervical Cancer | IC50 = 10.2 µM at pH 6 |
| dbacp06871 | RR-1-RR | RRWQWRWQWRR | Synthetic analogue of LfcinB(21-25)Pal | Apoptosis inducing | MTT assay | MCF-7 | Breast Cancer | IC50 = 58 µM |
| dbacp06872 | RR-1-RR | RRWQWRWQWRR | Synthetic analogue of LfcinB(21-25)Pal | Apoptosis inducing | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 67 µM |
| dbacp06873 | R-1-RR | RWQWRWQWRR | Synthetic analogue of LfcinB(21-25)Pal | Apoptosis inducing | MTT assay | MCF-7 | Breast Cancer | IC50 = 122 µM |
| dbacp06874 | R-1-RR | RWQWRWQWRR | Synthetic analogue of LfcinB(21-25)Pal | Apoptosis inducing | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 95 µM |
| dbacp06875 | RR-1-R | RRWQWRWQWR | Synthetic analogue of LfcinB(21-25)Pal | Apoptosis inducing | MTT assay | MCF-7 | Breast Cancer | IC50 = 68 µM |
| dbacp06876 | RR-1-R | RRWQWRWQWR | Synthetic analogue of LfcinB(21-25)Pal | Apoptosis inducing | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 73 µM |
| dbacp06877 | 1 | WQWRWQW | Synthetic analogue of LfcinB(21-25)Pal | Apoptosis inducing | MTT assay | MCF-7 | Breast Cancer | IC50 = 105 µM |
| dbacp06878 | 1 | WQWRWQW | Synthetic analogue of LfcinB(21-25)Pal | Apoptosis inducing | MTT assay | MDA-MB-231 | Breast Cancer | IC50 > 170 µM |
| dbacp06879 | R-1 | RWQWRWQW | Synthetic analogue of LfcinB(21-25)Pal | Apoptosis inducing | MTT assay | MCF-7 | Breast Cancer | IC50 = 58 µM |
| dbacp06880 | R-1 | RWQWRWQW | Synthetic analogue of LfcinB(21-25)Pal | Apoptosis inducing | MTT assay | MDA-MB-231 | Breast Cancer | IC50 > 150 µM |
| dbacp06881 | 1-R | WQWRWQWR | Synthetic analogue of LfcinB(21-25)Pal | Apoptosis inducing | MTT assay | MCF-7 | Breast Cancer | IC50 = 130 µM |
| dbacp06882 | 1-R | WQWRWQWR | Synthetic analogue of LfcinB(21-25)Pal | Apoptosis inducing | MTT assay | MDA-MB-231 | Breast Cancer | IC50 > 150 µM |
| dbacp06903 | CIGB-300 | GRKKRRQRRRPPQ-X-CWMSPRHLGTC | Synthetic | Cell Penetration | Crystal Violet assay | NCI-H-460 | Lung Cancer | IC50 = 30 ± 5.3 µM |
| dbacp06908 | LFchimera | FKCRRWQWRMKKLG-K-RSKNKGFKEQAKSLLKWILD | Synthetic - Lectoferrin chimera | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | cell viability ~ 44% at 10 µM |
| dbacp06909 | LFchimera | FKCRRWQWRMKKLG-K-RSKNKGFKEQAKSLLKWILD | Synthetic - Lectoferrin chimera | Apoptosis inducing | MTT assay | Jurkat | Blood Cancer | cell viability ~ 8% at 20 µM |
| dbacp06910 | mtp1 | DGDWDAWTRETS | Synthetic | Disrupts transcription | MTS assay | MDA-MB-231 | Breast Cancer | 33.6% decrease in cell viability at 10 μM |
| dbacp06911 | mtp1 | DGDWDAWTRETS | Synthetic | Disrupts transcription | MTS assay | HeLa | Cervical Cancer | 30.2 % decrease in cell viability at 10 μM |
| dbacp06912 | mtp1 | DGDWDAWTRETS | Synthetic | Disrupts transcription | MTS assay | A-549 | Lung Cancer | 17.4% decrease in cell viability at 10 μM |
| dbacp06913 | AC-P19M | FAKKLAKLKKKLAKLAKKR | Synthetic analogue of AC-P19 | Inhibition of cell signalling | WST-8 assay | A-549 | Lung Cancer | IC50 = 9.84 µM |
| dbacp06914 | AC-P19M | FAKKLAKLKKKLAKLAKKR | Synthetic analogue of AC-P19 | Inhibition of cell signalling | WST-8 assay | H-460 | Lung Cancer | IC50 = 6.29 µM |
| dbacp06915 | AC-P19 | FAKKLAKLKKKLAKLALAL | Synthetic | Inhibition of cell signalling | WST-8 assay | A-549 | Lung Cancer | IC50 = 52.14 µM |
| dbacp06916 | AC-P19 | FAKKLAKLKKKLAKLALAL | Synthetic | Inhibition of cell signalling | WST-8 assay | H-460 | Lung Cancer | IC50 = 49.08 µM |
| dbacp06917 | KM8 | KLLKINLKALAALAKKIL | Synthetic derivative of Mastoparan | Apoptosis inducing | Not Available | Not Available | Not Available | Not Available |
| dbacp06918 | KM8-Aib | KLLKINLK(Aib)LAALAKKIL | Synthetic derivative of KM8 | Apoptosis inducing | Not Available | Not Available | Not Available | Not Available |
| dbacp06920 | HAZ | GVKFAKRFWRFAKKAFKRFEK | Synthetic | Cell membrane destabilization | MTT assay | A-549 | Lung Cancer | IC50 = 5.44 μM |
| dbacp06975 | C16-E4Y | EEEEY | Synthetic | Inhibition of cell signalling | WST-8 assay | A-431 | Skin Cancer | 10 % cell viability at 0.05 wt % |
| dbacp06976 | C16-E4Y | EEEEY | Synthetic | Inhibition of cell signalling | WST-8 assay | HeLa | Cervical Cancer | 60% cell viability at 0.05 wt % |
| dbacp06977 | C16-E4Y | EEEEY | Synthetic | Inhibition of cell signalling | WST-8 assay | HepG-2 | Liver Cancer | 50 % cell viability at 0.05 wt % |
| dbacp06978 | C16-E4Y | EEEEY | Synthetic | Inhibition of cell signalling | WST-8 assay | MCF-7 | Breast Cancer | 50 % cell viability at 0.05 wt % |
| dbacp06980 | Ponericin-W1 (11-25), At1 | KLLPSVVGLFKKKKQ | Synthetic | Apoptosis inducing | MTT assay | A-549 | Lung Cancer | IC50 > 100 µM |
| dbacp06981 | Ponericin-W1 (11-25), At1 | KLLPSVVGLFKKKKQ | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 >100 µM |
| dbacp06982 | Ponericin-W1 (11-25) [P4K | KLLKKVVKLFKKKKK | Synthetic | Apoptosis inducing | MTT assay | A-549 | Lung Cancer | IC50 >100 µM |
| dbacp06983 | Ponericin-W1 (11-25) [P4K | KLLKKVVKLFKKKKK | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 >100 µM |
| dbacp06984 | Ponericin-W1 (11-25) [P4K | KLLKKVVKLFKKLLK | Synthetic | Apoptosis inducing | MTT assay | A-549 | Lung Cancer | IC50 = 4.3 µM |
| dbacp06985 | Ponericin-W1 (11-25) [P4K | KLLKKVVKLFKKLLK | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 = 2.2 µM |
| dbacp06986 | At4 | KLLKKLLKLLKKLLK | Synthetic | Apoptosis inducing | MTT assay | A-549 | Lung Cancer | IC50 = 7.2 µM |
| dbacp06987 | At4 | KLLKKLLKLLKKLLK | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 = 2.5 µM |
| dbacp06988 | At5 | KIIKKIIKIIKKIIK | Synthetic | Apoptosis inducing | MTT assay | A-549 | Lung Cancer | IC50 = 3.6 µM |
| dbacp06989 | At5 | KIIKKIIKIIKKIIK | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 = 1.5 µM |
| dbacp06990 | At6 | KVVKKVVKVVKKVVK | Synthetic | Apoptosis inducing | MTT assay | A-549 | Lung Cancer | IC50 > 100 µM |
| dbacp06991 | At6 | KVVKKVVKVVKKVVK | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 = 70.8 µM |
| dbacp06992 | At7 | KIIKKIKKKIKKIIK | Synthetic | Apoptosis inducing | MTT assay | A-549 | Lung Cancer | IC50 = 10.3 µM |
| dbacp06993 | At7 | KIIKKIKKKIKKIIK | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 = 8.8 µM |
| dbacp06994 | At8 | KLLKKLKKKLKKLLK | Synthetic | Apoptosis inducing | MTT assay | A-549 | Lung Cancer | IC50 = 13.4 µM |
| dbacp06995 | At8 | KLLKKLKKKLKKLLK | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 = 8.9 µM |
| dbacp06996 | At9 | KVVKKVKKKVKKVVK | Synthetic | Apoptosis inducing | MTT assay | A-549 | Lung Cancer | IC50 = 100 µM |
| dbacp06997 | At9 | KVVKKVKKKVKKVVK | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 = 51.7 µM |
| dbacp06998 | At10 | IKKIIKIIKKIIKKI | Synthetic | Apoptosis inducing | MTT assay | A-549 | Lung Cancer | IC50 = 4.4 µM |
| dbacp06999 | At10 | IKKIIKIIKKIIKKI | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 = 3.2 µM |
| dbacp07000 | At11 | IIIKKIKKKIKKIII | Synthetic | Apoptosis inducing | MTT assay | A-549 | Lung Cancer | IC50 = 7.9 µM |
| dbacp07001 | At11 | IIIKKIKKKIKKIII | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 = 7.6 µM |
| dbacp07002 | At12 | KIIIKIKKKIKIIIK | Synthetic | Apoptosis inducing | MTT assay | A-549 | Lung Cancer | IC50 = 14.0 µM |
| dbacp07003 | At12 | KIIIKIKKKIKIIIK | Synthetic | Apoptosis inducing | MTT assay | HepG-2 | Liver Cancer | IC50 = 13.4 µM |
| dbacp07006 | ST101 | vaeareelerlearlgqargelkkwkmrrnqfwlklqr | Synthetic | Prevents C/EBPβ dimerization, induces degradation | Annexin V/ PI staining assay | U-251 | Brain Tumor | mean EC50 value of 2.1 ± 0.4 μmol/L |
| dbacp07007 | ST101 | vaeareelerlearlgqargelkkwkmrrnqfwlklqr | Synthetic | Prevents C/EBPβ dimerization, induces degradation | Annexin V/ PI staining assay | MCF-7 | Breast Cancer | mean EC50 value of 2.1 ± 0.4 μmol/L |
| dbacp07008 | ST101 | vaeareelerlearlgqargelkkwkmrrnqfwlklqr | Synthetic | Prevents C/EBPβ dimerization, induces degradation | Annexin V/ PI staining assay | A-375 | Skin Cancer | mean EC50 value of 2.1 ± 0.4 μmol/L |
| dbacp07009 | ST101 | vaeareelerlearlgqargelkkwkmrrnqfwlklqr | Synthetic | Prevents C/EBPβ dimerization, induces degradation | Annexin V/ PI staining assay | DU-145 | Prostate Cancer | mean EC50 value of 2.1 ± 0.4 μmol/L |
| dbacp07010 | ST101 | vaeareelerlearlgqargelkkwkmrrnqfwlklqr | Synthetic | Prevents C/EBPβ dimerization, induces degradation | Annexin V/ PI staining assay | A-549 | Lung Cancer | mean EC50 value of 2.1 ± 0.4 μmol/L |
| dbacp07011 | ST101 | vaeareelerlearlgqargelkkwkmrrnqfwlklqr | Synthetic | Prevents C/EBPβ dimerization, induces degradation | Annexin V/ PI staining assay | T98G | Brain Tumor | mean EC50 value of 2.1 ± 0.4 μmol/L |
| dbacp07017 | D-LAK-120-A | kklalalakkwlalakklalalakk | Synthetic | ROS induction, mitochondria-mediated apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 5.55 ± 0.13 μM |
| dbacp07018 | D-LAK-120-A | kklalalakkwlalakklalalakk | Synthetic | ROS induction, mitochondria-mediated apoptosis. | MTT assay | H-358 | Non Small Cell Lung Cancer (NSCLC) | IC50 = 4.00 ± 0.20 μM |
| dbacp07019 | D-LAK-120-A | kklalalakkwlalakklalalakk | Synthetic | ROS induction, mitochondria-mediated apoptosis. | MTT assay | H-1975 | Non Small Cell Lung Cancer (NSCLC) | IC50 between 4.0 and 5.5 μM |
| dbacp07020 | D-LAK-120-A | kklalalakkwlalakklalalakk | Synthetic | ROS induction, mitochondria-mediated apoptosis. | MTT assay | HCC-827 | Lung Adenocarcinoma | IC50 between 4.0 and 5.5 μM |
| dbacp07055 | Temporin-PKE-2K | FLPLIIGKLSSLLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | U251-MG | Brain Tumor | IC50 = 2.49 μM |
| dbacp07056 | Temporin-PKE-2K | FLPLIIGKLSSLLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | PC-3 | Prostate Cancer | IC50 = 2.64 μM |
| dbacp07057 | Temporin-PKE-2K | FLPLIIGKLSSLLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | H-838 | Lung Cancer | IC50 = 3.07 μM |
| dbacp07058 | Temporin-PKE-2K | FLPLIIGKLSSLLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | HCT-116 | Colorectal Cancer | IC50 = 2.84 μM |
| dbacp07059 | Temporin-PKE-2K | FLPLIIGKLSSLLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | H-157 | Lung Cancer | IC50 = 2.78 μM |
| dbacp07060 | Temporin-PKE-K12 | FLPLIIGALSSKLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | U251-MG | Brain Tumor | IC50 = 25.75 μM |
| dbacp07061 | Temporin-PKE-K12 | FLPLIIGALSSKLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | PC-3 | Prostate Cancer | IC50 = 27.32 μM |
| dbacp07062 | Temporin-PKE-K12 | FLPLIIGALSSKLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | H-838 | Lung Cancer | IC50 = 22.67 μM |
| dbacp07063 | Temporin-PKE-K12 | FLPLIIGALSSKLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | HCT-116 | Colorectal Cancer | IC50 = 22.09 μM |
| dbacp07064 | Temporin-PKE-K12 | FLPLIIGALSSKLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | H-157 | Lung Cancer | IC50 = 24.03 μM |
| dbacp07065 | Temporin-PKE-3K | FLPKIIGKLSSLLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | U251-MG | Brain Tumor | IC50 = 2.83 μM |
| dbacp07066 | Temporin-PKE-3K | FLPKIIGKLSSLLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | PC-3 | Prostate Cancer | IC50 = 3.01 μM |
| dbacp07067 | Temporin-PKE-3K | FLPKIIGKLSSLLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | H-838 | Lung Cancer | IC50 = 0.51 μM |
| dbacp07068 | Temporin-PKE-3K | FLPKIIGKLSSLLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | HCT-116 | Colorectal Cancer | IC50 = 0.38 μM |
| dbacp07069 | Temporin-PKE-3K | FLPKIIGKLSSLLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | H-157 | Lung Cancer | IC50 = 3.29 μM |
| dbacp07070 | Temporin-PKE-4K | FLPKIIGKLSSKLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | U251-MG | Brain Tumor | IC50 = 85.52 μM |
| dbacp07071 | Temporin-PKE-4K | FLPKIIGKLSSKLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | PC-3 | Prostate Cancer | IC50 = 49.50 μM |
| dbacp07072 | Temporin-PKE-4K | FLPKIIGKLSSKLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | H-838 | Lung Cancer | IC50 = 35.28 μM |
| dbacp07073 | Temporin-PKE-4K | FLPKIIGKLSSKLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | HCT-116 | Colorectal Cancer | IC50 = 99.36 μM |
| dbacp07074 | Temporin-PKE-4K | FLPKIIGKLSSKLPKIF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | H-157 | Lung Cancer | IC50 = 27.76 μM |
| dbacp07075 | Temporin-PKE-i | FLPLIIGALSSLLPKiF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | U251-MG | Brain Tumor | IC50 = 4.46 μM |
| dbacp07076 | Temporin-PKE-i | FLPLIIGALSSLLPKiF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | PC-3 | Prostate Cancer | IC50 = 3.35 μM |
| dbacp07077 | Temporin-PKE-i | FLPLIIGALSSLLPKiF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | H-838 | Lung Cancer | IC50 = 5.28 μM |
| dbacp07078 | Temporin-PKE-i | FLPLIIGALSSLLPKiF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | HCT-116 | Colorectal Cancer | IC50 = 3.07 μM |
| dbacp07079 | Temporin-PKE-i | FLPLIIGALSSLLPKiF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | H-157 | Lung Cancer | IC50 = 2.94 μM |
| dbacp07080 | Temporin-PKE-3i | FLPLiiGALSSLLPKiF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | U251-MG | Brain Tumor | IC50 = 120.6 μM |
| dbacp07081 | Temporin-PKE-3i | FLPLiiGALSSLLPKiF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | PC-3 | Prostate Cancer | IC50 = 167 μM |
| dbacp07082 | Temporin-PKE-3i | FLPLiiGALSSLLPKiF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | H-838 | Lung Cancer | IC50 = 193.4 μM |
| dbacp07083 | Temporin-PKE-3i | FLPLiiGALSSLLPKiF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | HCT-116 | Colorectal Cancer | IC50 = 72.06 μM |
| dbacp07084 | Temporin-PKE-3i | FLPLiiGALSSLLPKiF | Synthetic | Charge-optimized membranolysis induces apoptosis. | MTT assay | H-157 | Lung Cancer | IC50 = 71.18 μM |
| dbacp07085 | HB43 | FAKLLAKLAKKLL | Synthetic | Motif-driven membrane insertion triggers cytotoxicity | AlamarBlue assay | SW-480 | Colon Cancer | IC50 = 12 ± 4 μM |
| dbacp07086 | HB43 | FAKLLAKLAKKLL | Synthetic | Motif-driven membrane insertion triggers cytotoxicity | AlamarBlue assay | SW-620 | Colon Cancer | IC50 = 10 ± 1 μM |
| dbacp07087 | HB43 | FAKLLAKLAKKLL | Synthetic | Motif-driven membrane insertion triggers cytotoxicity | AlamarBlue assay | HT-29 | Colon Cancer | IC50 = 11 ± 1 μM |
| dbacp07088 | HB43 | FAKLLAKLAKKLL | Synthetic | Motif-driven membrane insertion triggers cytotoxicity | AlamarBlue assay | MDA-MB-231 | Breast Cancer | 50% cell viability at 20 μM |
| dbacp07089 | HB43-mut2 | FAKLLAKLAKLLK | Synthetic | Motif-driven membrane insertion triggers cytotoxicity | AlamarBlue assay | SW-480 | Colon Cancer | IC50 = 34 ± 2 μM |
| dbacp07090 | HB43-mut2 | FAKLLAKLAKLLK | Synthetic | Motif-driven membrane insertion triggers cytotoxicity | AlamarBlue assay | SW-620 | Colon Cancer | IC50 = 40 ± 3 μM |
| dbacp07091 | HB43-mut2 | FAKLLAKLAKLLK | Synthetic | Motif-driven membrane insertion triggers cytotoxicity | AlamarBlue assay | HT-29 | Colon Cancer | IC50 = 50 ± 3 μM |
| dbacp07092 | HB43-mut2 | FAKLLAKLAKLLK | Synthetic | Motif-driven membrane insertion triggers cytotoxicity | AlamarBlue assay | MDA-MB-231 | Breast Cancer | 80% cell viability at 20 μM |
| dbacp07093 | HB43-mut3 | FAKLLAKLARRLL | Synthetic | Motif-driven membrane insertion triggers cytotoxicity | AlamarBlue assay | SW-480 | Colon Cancer | IC50 = 8 ± 1 μM |
| dbacp07094 | HB43-mut3 | FAKLLAKLARRLL | Synthetic | Motif-driven membrane insertion triggers cytotoxicity | AlamarBlue assay | SW-620 | Colon Cancer | IC50 = 9 ± 1 μM |
| dbacp07095 | HB43-mut3 | FAKLLAKLARRLL | Synthetic | Motif-driven membrane insertion triggers cytotoxicity | AlamarBlue assay | HT-29 | Colon Cancer | IC50 = 9 ± 1 μM |
| dbacp07096 | HB43-mut3 | FAKLLAKLARRLL | Synthetic | Motif-driven membrane insertion triggers cytotoxicity | AlamarBlue assay | MDA-MB-231 | Breast Cancer | 75% cell viability at 20 μM |
| dbacp07097 | K2F6K2 | KKFFFFFFKK | Synthetic | Positive charge–driven membrane disruption apoptosis | CCK-8 assay | A-549 | Lung Cancer | IC50 = 1146.23 ± 346.83 μg/mL |
| dbacp07098 | K3F6K3 | KKKFFFFFFKKK | Synthetic | Positive charge–driven membrane disruption apoptosis | CCK-8 assay | A-549 | Lung Cancer | IC50 = 123.10 ± 35.19 μg/mL |
| dbacp07099 | K4F6K4 | KKKKFFFFFFKKKK | Synthetic | Positive charge–driven membrane disruption apoptosis | CCK-8 assay | A-549 | Lung Cancer | IC50 = 62.64 ± 9.55 μg/mL |
| dbacp07100 | K4F6K4 | KKKKFFFFFFKKKK | Synthetic | Positive charge–driven membrane disruption apoptosis | AnnexinV-FITC/PI double staining assay | A-549 | Lung Cancer | apoptotic cells (early and late) increased from 9.59 ± 1.00% to 43.03 ± 2.13% |
| dbacp07101 | K4F8K4 | KKKKFFFFFFFFKKKK | Synthetic | Positive charge–driven membrane disruption apoptosis | CCK-8 assay | A-549 | Lung Cancer | IC50 = 571.87 ± 66.23 μg/mL |
| dbacp07107 | Nigrocin-M1 | GLLGKILGAGKKVLLGVSGLL | Synthetic | Membrane disruption mediates selective cytotoxicity. | MTT assay | H-157 | Non-small cell lung cancer | IC50 = 24 μM |
| dbacp07108 | Nigrocin-M1 | GLLGKILGAGKKVLLGVSGLL | Synthetic | Membrane disruption mediates selective cytotoxicity. | MTT assay | PC-3 | Prostate cancer | IC50 = 31.27 μM |
| dbacp07109 | Nigrocin-M1 | GLLGKILGAGKKVLLGVSGLL | Synthetic | Membrane disruption mediates selective cytotoxicity. | MTT assay | U-251-MG | Brain Tumor | IC50 = 25.06 μM |
| dbacp07110 | Nigrocin-M1 | GLLGKILGAGKKVLLGVSGLL | Synthetic | Membrane disruption mediates selective cytotoxicity. | MTT assay | MCF-7 | Breast Cancer | IC50 = 24.60 μM |
| dbacp07111 | LyeTx-I-b | IWLTALKFLGKNLGKLAKQQLAKL | Synthetic | Synergistic autophagic death via AKT inhibition. | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 2.47 µM |
| dbacp07117 | Z-1 | L(N-Me-L)LPL | Synthetic | Cell-cycle arrest induces apoptosis | MTT assay | MCF-7 | Breast Cancer | IC50 = 5.85 ± 1.28 µg/ml |
| dbacp07118 | Z-1 | L(N-Me-L)LPL | Synthetic | Cell-cycle arrest induces apoptosis | MTT assay | HepG-2 | Liver Cancer | IC50 = 7.57 ± 0.17 µg/ml |
| dbacp07119 | Z-1 | L(N-Me-L)LPL | Synthetic | Cell-cycle arrest induces apoptosis | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 17.81 ± 0.6 µg/ml |
| dbacp07120 | Z-1 | L(N-Me-L)LPL | Synthetic | Cell-cycle arrest induces apoptosis | MTT assay | HeLa | Cervical Cancer | IC50 = 11.56 ± 0.65 µg/ml |
| dbacp07121 | Z-1 | L(N-Me-L)LPL | Synthetic | Cell-cycle arrest induces apoptosis | MTT assay | A-549 | Lung Cancer | IC50 = 4.92 ± 0.84 µg/ml |
| dbacp07122 | DEE | GLLDLLELLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 5.55 ± 0.35 µM |
| dbacp07123 | DEE | GLLDLLELLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 6.05 ± 2.76 µM |
| dbacp07124 | DEE | GLLDLLELLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 61.00 ± 1.41 µM |
| dbacp07125 | EEE | GLLELLELLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 6.25 ± 1.77 µM |
| dbacp07126 | EEE | GLLELLELLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 10.55 ± 3.46 µM |
| dbacp07127 | EEE | GLLELLELLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 78.75 ± 5.30 µM |
| dbacp07128 | HEE | GLLHLLELLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 6.50 ± 0.71 µM |
| dbacp07129 | HEE | GLLHLLELLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 4.95 ± 0.49 µM |
| dbacp07130 | HEE | GLLHLLELLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 47.50 ± 11 µM |
| dbacp07131 | KEE | GLLKLLELLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 3.75 ± 0.78 µM |
| dbacp07132 | KEE | GLLKLLELLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 2.05 ± 0.21 µM |
| dbacp07133 | KEE | GLLKLLELLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 49.38 ± 13.26 µM |
| dbacp07134 | DHE | GLLDLLHLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 3.75 ± 0.92 µM |
| dbacp07135 | DHE | GLLDLLHLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 2.80 ± 0.14 µM |
| dbacp07136 | DHE | GLLDLLHLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 17.25 ± 1.06 µM |
| dbacp07137 | EHE | GLLELLHLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 3.90 ± 0.28 µM |
| dbacp07138 | EHE | GLLELLHLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 2.55 ± 0.07 µM |
| dbacp07139 | EHE | GLLELLHLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 18.25 ± 1.06 µM |
| dbacp07140 | HHE | GLLHLLHLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 16.70 ± 2.26 µM |
| dbacp07141 | HHE | GLLHLLHLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 10.75 ± 0.78 µM |
| dbacp07142 | HHE | GLLHLLHLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 53.25 ± 5.30 µM |
| dbacp07143 | KHE | GLLKLLHLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 3.70 ± 0.14 µM |
| dbacp07144 | KHE | GLLKLLHLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 2.92 ± 0.17 µM |
| dbacp07145 | KHE | GLLKLLHLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 53 ± 2.83 µM |
| dbacp07146 | DKE | GLLDLLKLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 2.10 ± 0 µM |
| dbacp07147 | DKE | GLLDLLKLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 1.57 ± 0.33 µM |
| dbacp07148 | DKE | GLLDLLKLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 9.93 ± 0.25 µM |
| dbacp07149 | EKE | GLLELLKLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 1.80 ± 0.28 µM |
| dbacp07150 | EKE | GLLELLKLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 1.30 ± 0.14 µM |
| dbacp07151 | EKE | GLLELLKLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 8.00 ± 0.71 µM |
| dbacp07152 | HKE | GLLHLLKLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 2.70 ± 0.28 µM |
| dbacp07153 | HKE | GLLHLLKLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 1.90 ± 0.42 µM |
| dbacp07154 | HKE | GLLHLLKLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 15.95 ± 0.78 µM |
| dbacp07155 | KKE | GLLKLLKLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 2.05 ± 0.64 µM |
| dbacp07156 | KKE | GLLKLLKLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 1.70 ± 0 µM |
| dbacp07157 | KKE | GLLKLLKLLLEAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 12.75 ± 1.20 µM |
| dbacp07158 | DEH | GLLDLLELLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 5.35 ± 1.91 µM |
| dbacp07159 | DEH | GLLDLLELLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 3.60 ± 0.42 µM |
| dbacp07160 | DEH | GLLDLLELLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 36.48 ± 3.92 µM |
| dbacp07161 | EEH | GLLELLELLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 3.30 ± 0.14 µM |
| dbacp07162 | EEH | GLLELLELLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 3.60 ± 0.85 µM |
| dbacp07163 | EEH | GLLELLELLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 19.60 ± 3.96 µM |
| dbacp07164 | HEH | GLLHLLELLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 28.60 ± 10.75 µM |
| dbacp07165 | HEH | GLLHLLELLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 10.95 ± 1.06 µM |
| dbacp07166 | HEH | GLLHLLELLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 106 ± 14 µM |
| dbacp07167 | KEH | GLLKLLELLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 3.30 ± 0.42 µM |
| dbacp07168 | KEH | GLLKLLELLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 2.35 ± 0.07 µM |
| dbacp07169 | KEH | GLLKLLELLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 49.25 ± 5.30 µM |
| dbacp07170 | DHH | GLLDLLHLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 21.45 ± 2.47 µM |
| dbacp07171 | DHH | GLLDLLHLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 11.90 ± 0.14 µM |
| dbacp07172 | DHH | GLLDLLHLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 55.85 ± 18.88 µM |
| dbacp07173 | EHH | GLLELLHLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 25.35 ± 2.76 µM |
| dbacp07174 | EHH | GLLELLHLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 16.05 ± 3.18 µM |
| dbacp07175 | EHH | GLLELLHLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 117 ± 7 µM |
| dbacp07176 | HHH | GLLHLLHLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 21.10 ± 6.93 µM |
| dbacp07177 | HHH | GLLHLLHLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 9.50 ± 0.99 µM |
| dbacp07178 | HHH | GLLHLLHLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 185 ± 7 µM |
| dbacp07179 | KHH | GLLKLLHLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 5.20 ± 0.71 µM |
| dbacp07180 | KHH | GLLKLLHLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 4.45 ± 0.49 µM |
| dbacp07181 | KHH | GLLKLLHLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 39.75 ± 5.30 µM |
| dbacp07182 | DKH | GLLDLLKLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 3.45 ± 0.07 µM |
| dbacp07183 | DKH | GLLDLLKLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 2.80 ± 0.28 µM |
| dbacp07184 | DKH | GLLDLLKLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 21.13 ± 3.01 µM |
| dbacp07185 | EKH | GLLELLKLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 2.75 ± 0.07 µM |
| dbacp07186 | EKH | GLLELLKLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 2.18 ± 0.31 µM |
| dbacp07187 | EKH | GLLELLKLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 23.83 ± 0.81 µM |
| dbacp07188 | HKH | GLLHLLKLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 3.45 ± 0.21 µM |
| dbacp07189 | HKH | GLLHLLKLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 3.10 ± 0.57 µM |
| dbacp07190 | HKH | GLLHLLKLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 18.88 ± 1.24 µM |
| dbacp07191 | KKH | GLLKLLKLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 2.40 ± 0.85 µM |
| dbacp07192 | KKH | GLLKLLKLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 2.20 ± 0.42 µM |
| dbacp07193 | KKH | GLLKLLKLLLHAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 13.30 ± 0.99 µM |
| dbacp07194 | DEK | GLLDLLELLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 1.14 ± 0.52 µM |
| dbacp07195 | DEK | GLLDLLELLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 0.70 ± 0.07 µM |
| dbacp07196 | DEK | GLLDLLELLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 19.88 ± 2.65 µM |
| dbacp07197 | EEK | GLLELLELLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 1.10 ± 0.14 µM |
| dbacp07198 | EEK | GLLELLELLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 1.08 ± 0.18 µM |
| dbacp07199 | EEK | GLLELLELLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 32.88 ± 4.07 µM |
| dbacp07200 | HEK | GLLHLLELLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 2.35 ± 1.06 µM |
| dbacp07201 | HEK | GLLHLLELLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 3.45 ± 2.19 µM |
| dbacp07202 | HEK | GLLHLLELLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 143.20 ± 80.33 µM |
| dbacp07203 | KEK | GLLKLLELLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 1.60 ± 0.14 µM |
| dbacp07204 | KEK | GLLKLLELLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 1.35 ± 0.07 µM |
| dbacp07205 | KEK | GLLKLLELLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 8.15 ± 0.49 µM |
| dbacp07206 | DHK | GLLDLLHLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 1.75 ±0.49 µM |
| dbacp07207 | DHK | GLLDLLHLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 1.02 ± 0.12 µM |
| dbacp07208 | DHK | GLLDLLHLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 20.45 ± 2.05 µM |
| dbacp07209 | EHK | GLLELLHLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 1.35 ± 0.35 µM |
| dbacp07210 | EHK | GLLELLHLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 0.71 ± 0.13 µM |
| dbacp07211 | EHK | GLLELLHLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 25.00 ± 0 µM |
| dbacp07212 | HHK | GLLHLLHLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 3.15 ± 0.07 µM |
| dbacp07213 | HHK | GLLHLLHLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 1.75 ± 0.21 µM |
| dbacp07214 | HHK | GLLHLLHLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 12.65 ± 1.91 µM |
| dbacp07215 | KHK | GLLKLLHLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 2.59 ± 0.92 µM |
| dbacp07216 | KHK | GLLKLLHLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 1.40 ± 0.14 µM |
| dbacp07217 | KHK | GLLKLLHLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 12.88 ± 1.24 µM |
| dbacp07218 | DKK | GLLDLLKLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 1.95 ± 0.35 µM |
| dbacp07219 | DKK | GLLDLLKLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 1.20 ± 0.14 µM |
| dbacp07220 | DKK | GLLDLLKLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 10.40 ± 1.70 µM |
| dbacp07221 | EKK | GLLELLKLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 1.72 ± 0.21 µM |
| dbacp07222 | EKK | GLLELLKLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 1.19 ± 0.40 µM |
| dbacp07223 | EKK | GLLELLKLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 12.20 ± 1.84 µM |
| dbacp07224 | HKK | GLLHLLKLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 3.40 ± 0.71 µM |
| dbacp07225 | HKK | GLLHLLKLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 2.60 ± 0.42 µM |
| dbacp07226 | HKK | GLLHLLKLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 12.23 ± 0.11 µM |
| dbacp07227 | KKK | GLLKLLKLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 1.57 ± 0.24 µM |
| dbacp07228 | KKK | GLLKLLKLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 1.35 ± 0.40 µM |
| dbacp07229 | KKK | GLLKLLKLLLKAAGW | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 9.65 ± 1.20 µM |
| dbacp07230 | d-DHK | GlldllhlllkaaGw | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 0.32 ± 0.07 µM |
| dbacp07231 | d-DHK | GlldllhlllkaaGw | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 0.23 ± 0.04 µM |
| dbacp07232 | d-DHK | GlldllhlllkaaGw | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 1.24 ± 0.03 µM |
| dbacp07233 | d-DEK | GlldllelllkaaGw | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 0.44 ± 0.10 µM |
| dbacp07234 | d-DEK | GlldllelllkaaGw | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 0.36 ± 0 µM |
| dbacp07235 | d-DEK | GlldllelllkaaGw | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 5.84 ± 0.04 µM |
| dbacp07236 | d-EEK | GllellelllkaaGw | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER | Breast Cancer | IC50 = 0.29 ± 0.01 µM |
| dbacp07237 | d-EEK | GllellelllkaaGw | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | HMLER-shEcad | Breast Cancer | IC50 = 0.29 ± 0.01 µM |
| dbacp07238 | d-EEK | GllellelllkaaGw | Synthetic | Selective membrane perforation prevents resistance. | MTT assay | U-2 OS | Bone Cancer | IC50 = 4.78 ± 0.02 µM |
| dbacp07244 | CIGB-552 | HARIKpTFRRlKWKYKGKFW | Synthetic | NF-κB inhibition enhances cisplatin synergy | Sulforhodamine B assay | NCI-H-460 | Lung Cancer | IC50 = 287.9 μM |
| dbacp07245 | CIGB-552 | HARIKpTFRRlKWKYKGKFW | Synthetic | NF-κB inhibition enhances cisplatin synergy | Sulforhodamine B assay | A-549 | Lung Cancer | IC50 = 44.6 μM |
| dbacp07246 | ATX-101 | MDRWLVKWKKKRKIRRRRRRRRRRR | Synthetic | PCNA interference disrupts DNA repair. | CCK-8 assay | U87-MG | Brain Tumor | IC50 = 4.3 ± 0.3 μM |
| dbacp07247 | ATX-101 | MDRWLVKWKKKRKIRRRRRRRRRRR | Synthetic | PCNA interference disrupts DNA repair. | CCK-8 assay | U-251 | Brain Tumor | IC50 = 4.9 ± 0.3 μM |
| dbacp07248 | ATX-101 | MDRWLVKWKKKRKIRRRRRRRRRRR | Synthetic | PCNA interference disrupts DNA repair. | CCK-8 assay | A-172 | Brain Tumor | IC50 = 6.4 ± 0.4 μM |
| dbacp07249 | ATX-101 | MDRWLVKWKKKRKIRRRRRRRRRRR | Synthetic | PCNA interference disrupts DNA repair. | CCK-8 assay | T98G | Brain Tumor | IC50 = 7.1 ± 0.2 μM |
| dbacp07250 | ATX-101 | MDRWLVKWKKKRKIRRRRRRRRRRR | Synthetic | PCNA interference disrupts DNA repair. | CCK-8 assay | U-373 | Brain Tumor | IC50 = 5.0 ± 0.2 μM |
| dbacp07251 | ATX-101 | MDRWLVKWKKKRKIRRRRRRRRRRR | Synthetic | PCNA interference disrupts DNA repair. | CCK-8 assay | U-118 | Brain Tumor | IC50 = 6.8 ± 0.2 μM |
| dbacp07252 | ATX-101 | MDRWLVKWKKKRKIRRRRRRRRRRR | Synthetic | PCNA interference disrupts DNA repair. | CCK-8 assay | D54 | Brain Tumor | IC50 = 8.4 ± 0.1 μM |
| dbacp07253 | ATX-101 | MDRWLVKWKKKRKIRRRRRRRRRRR | Synthetic | PCNA interference disrupts DNA repair. | CCK-8 assay | SW-1783 | Brain Tumor | IC50 = 4.8 ± 0.2 μM |
| dbacp07254 | ATX-101 | MDRWLVKWKKKRKIRRRRRRRRRRR | Synthetic | PCNA interference disrupts DNA repair. | CCK-8 assay | LN229 | Brain Tumor | IC50 = 4.7 ± 0.2 μM |
| dbacp07255 | ATX-101 | MDRWLVKWKKKRKIRRRRRRRRRRR | Synthetic | PCNA interference disrupts DNA repair. | CCK-8 assay | U-138 | Brain Tumor | IC50 = 7.5 ± 0.3 μM |
| dbacp07256 | ATX-101 | MDRWLVKWKKKRKIRRRRRRRRRRR | Synthetic | PCNA interference disrupts DNA repair. | CCK-8 assay | SF-268 | Brain Tumor | IC50 = 4.8 ± 0.1 μM |
| dbacp07257 | ATX-101 | MDRWLVKWKKKRKIRRRRRRRRRRR | Synthetic | PCNA interference disrupts DNA repair. | CCK-8 assay | SNB-19 | Brain Tumor | IC50 = 12.0 ± 0.6 μM |
| dbacp07258 | trans-Phakellistatin 18 | trans(P)PIPYPIF | Synthetic | Not Available | MTT assay | HepG-2 | Liver Cancer | IC50 = 67.5 ± 2.938 µM |
| dbacp07309 | LyeTxI-b | IWLTALKFLGKNLGKLAKQQLAKL | Synthetic | Apoptosis induction and immune modulation. | MTT assay | 4T1 | Breast Cancer | IC50 = 6.5 ± 5.30 µM |
| dbacp07310 | LyeTxI-b | IWLTALKFLGKNLGKLAKQQLAKL | Synthetic | Apoptosis induction and immune modulation. | MTT assay | MCF-7 | Breast Cancer | IC50 = 7.34 ± 3.09 µM |
| dbacp07311 | LyeTxI-b | IWLTALKFLGKNLGKLAKQQLAKL | Synthetic | Apoptosis induction and immune modulation. | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 5.77 ± 0.83 µM |
| dbacp07324 | IK13 | CIIKKIIKKIIKK | Synthetic | Mitochondrial mediated apoptosis | MTT assay | HCT-116 | Colorectal Cancer | IC50 = 29 ± 6 µM |
| dbacp07325 | IK13 | CIIKKIIKKIIKK | Synthetic | Mitochondrial mediated apoptosis | MTT assay | HeLa | Cervical Cancer | IC50 = 47±5 µM |
| dbacp07326 | LK13 | CLLKKLLKKLLKK | Synthetic | Mitochondrial mediated apoptosis | MTT assay | HCT-116 | Colorectal Cancer | IC50 = 23 ± 2 µM |
| dbacp07327 | LK13 | CLLKKLLKKLLKK | Synthetic | Mitochondrial mediated apoptosis | MTT assay | HeLa | Cervical Cancer | IC50 = 83 ± 9 µM |
| dbacp07328 | IR13 | CIIRRIIRRIIRR | Synthetic | Mitochondrial mediated apoptosis | MTT assay | HCT-116 | Colorectal Cancer | IC50 > 100 µM |
| dbacp07329 | IR13 | CIIRRIIRRIIRR | Synthetic | Mitochondrial mediated apoptosis | MTT assay | HeLa | Cervical Cancer | IC50 > 100 µM |
| dbacp07330 | LR13 | CLLRRLLRRLLRR | Synthetic | Mitochondrial mediated apoptosis | MTT assay | HCT-116 | Colorectal Cancer | IC50 = 15.6 ± 1.0 µM |
| dbacp07331 | LR13 | CLLRRLLRRLLRR | Synthetic | Mitochondrial mediated apoptosis | MTT assay | HeLa | Cervical Cancer | IC50 = 26.7 ± 1.3 µM |
| dbacp07332 | CI-15 | CIIKKIIKKIIKKII | Synthetic | Mitochondrial mediated apoptosis | MTT assay | HCT-116 | Colorectal Cancer | IC50 = 7.7 ± 0.2 µM |
| dbacp07333 | CI-15 | CIIKKIIKKIIKKII | Synthetic | Mitochondrial mediated apoptosis | MTT assay | HeLa | Cervical Cancer | IC50 = 2.7 ± 0.5 µM |
| dbacp07334 | GI-15 | LC-Propargyl-GIIKKIIKKIIKKII | Synthetic | Mitochondrial mediated apoptosis | MTT assay | HCT-116 | Colorectal Cancer | IC50 = 13.6 ± 0.2 µM |
| dbacp07335 | GI-15 | LC-Propargyl-GIIKKIIKKIIKKII | Synthetic | Mitochondrial mediated apoptosis | MTT assay | HeLa | Cervical Cancer | IC50 = 16.6 ± 0.8 µM |
| dbacp07339 | D-melittin | gigavlkvlttglpaliswikrkrqqc | Synthetic | pH-triggered release, membrane lysis, immunogenic death | MTS assay | A-549 | Lung Cancer | IC50 = 4.5 µM |
| dbacp07340 | D-melittin | gigavlkvlttglpaliswikrkrqqc | Synthetic | pH-triggered release, membrane lysis, immunogenic death | MTS assay | CT-26 | Colorectal Cancer | IC50 = 2.2 µM |
| dbacp07341 | D-melittin | gigavlkvlttglpaliswikrkrqqc | Synthetic | pH-triggered release, membrane lysis, immunogenic death | MTS assay | MDA-MB-435 WT | Breast Cancer | IC50 = 3.5 µM |
| dbacp07342 | D-melittin | gigavlkvlttglpaliswikrkrqqc | Synthetic | pH-triggered release, membrane lysis, immunogenic death | MTS assay | MDA-MB-435 DOX-R | Breast Cancer | IC50 = 3.4 µM |
| dbacp07347 | GA - 2 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | MCF-7 | Breast Cancer | IC50 = 7.70 ± 1.3 µg/mL |
| dbacp07348 | GA - 2 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | HCT-116 | Colon Cancer | IC50 = 70.30 ± 0.9 µg/mL |
| dbacp07349 | GA - 3 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | MCF-7 | Breast Cancer | IC50 = 5.1 ± 0.7 µg/mL |
| dbacp07350 | GA - 3 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | HCT-116 | Colon Cancer | IC50 = 7.40 ± 0.4 µg/mL |
| dbacp07351 | GA - 4 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | MCF-7 | Breast Cancer | IC50 = 6.10 ± 0.4 µg/mL |
| dbacp07352 | GA - 4 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | HCT-116 | Colon Cancer | IC50 = 73.0 ± 1.4 µg/mL |
| dbacp07353 | GA - 5 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | MCF-7 | Breast Cancer | IC50 = 5.0 ± 0.3 µg/mL |
| dbacp07354 | GA - 5 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | HCT-116 | Colon Cancer | IC50 = 5.2 ± 0.8 µg/mL |
| dbacp07355 | GA - 7 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | MCF-7 | Breast Cancer | IC50 = 3.70 ± 0.2 µg/mL |
| dbacp07356 | GA - 7 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | HCT-116 | Colon Cancer | IC50 = 3.0 ± 1.1 µg/mL |
| dbacp07357 | GA - 7 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | HepG-2 | Liver Cancer | IC50 = 3.30 ± 0.1 µg/mL |
| dbacp07358 | GA - 8 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | MCF-7 | Breast Cancer | IC50 = 6.90 ± 1.1 µg/mL |
| dbacp07359 | GA - 8 | Structure given in figure | Synthetic (glycyrrhetinic acid (GA)-based peptides) | Apoptosis induction, Bax/p53/caspase activation | MTT assay | HCT-116 | Colon Cancer | IC50 = 60.70 ± 0.6 µg/mL |
| dbacp07360 | N-Ter-TAT | RDVFTKGYGFGL-GRK(Dansylglycine)KRRQRRRPQ | Synthetic | Mitochondrial targeting, VDAC1-HKII dissociation | MTT assay | A-375 | Skin Cancer | IC50 > 50.0 μM |
| dbacp07397 | Pugnin A | RLMRIFRILKLAR | Synthetic | Membrane disruption induces necrotic death | MTT assay | MCF-7 | Breast Cancer | 12% Cytotoxicity at 100 µM |
| dbacp07398 | Pugnin A | RLMRIFRILKLAR | Synthetic | Membrane disruption induces necrotic death | MTT assay | PC-3 | Prostate Cancer | 74% Cytotoxicity at 100 µM |
| dbacp07399 | Pugnin B | RMMRIFWVIKLAR | Synthetic | Membrane disruption induces necrotic death | MTT assay | MCF-7 | Breast Cancer | 5% Cytotoxicity at 100 µM |
| dbacp07400 | Pugnin B | RMMRIFWVIKLAR | Synthetic | Membrane disruption induces necrotic death | MTT assay | PC-3 | Prostate Cancer | 90% Cytotoxicity at 100 µM |
| dbacp07402 | Pep | GKLRLIKKLWVKKWKKKGWKA | Synthetic | Membrane disruption induces necrotic death | MTT assay | A-549 | Lung Cancer | IC50 = 4 µM |
| dbacp07403 | Pep | GKLRLIKKLWVKKWKKKGWKA | Synthetic | Membrane disruption induces necrotic death | MTT assay | MCF-7 | Breast Cancer | IC50 = 2 µM |
| dbacp07411 | Si1 | (KLAKLAK)2 | Synthetic | Membrane disruption induces cancer apoptosis | MTT assay | MCF-7 | Breast Cancer | IC50 = 124.1 ± 8.12 µM |
| dbacp07412 | Si1 | (KLAKLAK)2 | Synthetic | Membrane disruption induces cancer apoptosis | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 746.5 ± 7.6 µM |
| dbacp07413 | Si3 | KL(Beta-A)KL(Beta-A)AK | Synthetic | Membrane disruption induces cancer apoptosis | MTT assay | MCF-7 | Breast Cancer | IC50 = 176.3 ± 4.66 µM |
| dbacp07414 | Si2 | KL(Beta-A)KL(Beta-A)K | Synthetic | Membrane disruption induces cancer apoptosis | MTT assay | MCF-7 | Breast Cancer | IC50 = 662.9 ± 20.02 µM |
| dbacp07415 | Si2 | KL(Beta-A)KL(Beta-A)K | Synthetic | Membrane disruption induces cancer apoptosis | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 840 ± 21.18 µM |
| dbacp07416 | Si11 | KL(Beta-A)KL(Beta-A)K | Synthetic | Membrane disruption induces cancer apoptosis | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 1087 ± 70.71 µM |
| dbacp07417 | Si11 | KL(Beta-A)KLAK | Synthetic | Membrane disruption induces cancer apoptosis | MTT assay | MCF-7 | Breast Cancer | IC50 = 228.8 ± 7.18 µM |
| dbacp07418 | Si13 | KnLAKnLAK | Synthetic | Membrane disruption induces cancer apoptosis | MTT assay | MCF-7 | Breast Cancer | IC50 = 1704 ± 112 µM |
| dbacp07419 | Si14 | KnLAKnLAK | Synthetic | Membrane disruption induces cancer apoptosis | MTT assay | MCF-7 | Breast Cancer | IC50 = 593.3 ± 60.3 µM |
| dbacp07420 | Si14 | KnLAKnLAK | Synthetic | Membrane disruption induces cancer apoptosis | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 1049 ± 49.77 µM |
| dbacp07421 | Si15 | KnLAKnLAK | Synthetic | Membrane disruption induces cancer apoptosis | MTT assay | MCF-7 | Breast Cancer | IC50 = 140.3 ± 7.12 µM |
| dbacp07422 | Si15 | KnLAKnLAK | Synthetic | Membrane disruption induces cancer apoptosis | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 346.3 ± 7.91 µM |
| dbacp07432 | [Arg]3-VmCT1 | FLRALWNVAKSVF | Synthetic | Membrane disruption via cationic interaction | MTT assay | MCF-7 | Breast Cancer | IC50 = 20.6 ± 3.1 μmol/L |
| dbacp07433 | [Arg]7-VmCT1 | FLGALWRVAKSVF | Synthetic | Membrane disruption via cationic interaction | MTT assay | MCF-7 | Breast Cancer | IC50 = 18.0 ± 2.7 μmol/L |
| dbacp07434 | [Arg]11-VmCT1 | FLGALWNVAKRVF | Synthetic | Membrane disruption via cationic interaction | MTT assay | MCF-7 | Breast Cancer | IC50 = 25.8 ± 5.2 μmol/L |
| dbacp07435 | L9H5-1 | LHLLLHLLHHLLHL | Synthetic | Acid-triggered membrane disruption apoptosis | MTT assay | HeLa | Cervical Cancer | IC50 = 5.4 µM |
| dbacp07436 | L8H6 | LHHLLHLLHHLLHL | Synthetic | Acid-triggered membrane disruption apoptosis | MTT assay | HeLa | Cervical Cancer | IC50 = 16.4 µM |
| dbacp07437 | A4K14 - Citropin 1.1 - Sp 7 | GLFAVR8KKVASVS5KGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | C4-2B | Prostate Cancer | IC50 = 10.23 µM |
| dbacp07438 | A4K14 - Citropin 1.1 - Sp 7 | GLFAVR8KKVASVS5KGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | A-549 | Lung Cancer | IC50 = 16.37 µM |
| dbacp07439 | A4K14 - Citropin 1.1 - Sp 7 | GLFAVR8KKVASVS5KGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | U-87 | Brain Tumor | IC50 = 14.72 µM |
| dbacp07440 | A4K14 - Citropin 1.1 - Sp 7 | GLFAVR8KKVASVS5KGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | MCF-7 | Breast Cancer | IC50 = 12.1 µM |
| dbacp07441 | A4K14 - Citropin 1.1 - Sp 6 | GR8FAVIKKS5ASVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | C4-2B | Prostate Cancer | IC50 = 35.84 µM |
| dbacp07442 | A4K14 - Citropin 1.1 - Sp 6 | GR8FAVIKKS5ASVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | A-549 | Lung Cancer | IC50 = 30.19 µM |
| dbacp07443 | A4K14 - Citropin 1.1 - Sp 6 | GR8FAVIKKS5ASVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | U-87 | Brain Tumor | IC50 = 34.49 µM |
| dbacp07444 | A4K14 - Citropin 1.1 - Sp 6 | GR8FAVIKKS5ASVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | MCF-7 | Breast Cancer | IC50 = 23.78 µM |
| dbacp07445 | A4K14 - Citropin 1.1 - Sp 5 | GLFAVIKKVAS5VIKS5L | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | C4-2B | Prostate Cancer | IC50 = 11.9 µM |
| dbacp07446 | A4K14 - Citropin 1.1 - Sp 5 | GLFAVIKKVAS5VIKS5L | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | A-549 | Lung Cancer | IC50 = 9.899 µM |
| dbacp07447 | A4K14 - Citropin 1.1 - Sp 5 | GLFAVIKKVAS5VIKS5L | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | U-87 | Brain Tumor | IC50 = 8.229 µM |
| dbacp07448 | A4K14 - Citropin 1.1 - Sp 5 | GLFAVIKKVAS5VIKS5L | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | MCF-7 | Breast Cancer | IC50 = 12.42 µM |
| dbacp07449 | A4K14 - Citropin 1.1 - Sp 4 | GLFAVIKKS5ASVS5KGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | C4-2B | Prostate Cancer | IC50 = 8.9 µM |
| dbacp07450 | A4K14 - Citropin 1.1 - Sp 4 | GLFAVIKKS5ASVS5KGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | A-549 | Lung Cancer | IC50 = 10.51 µM |
| dbacp07451 | A4K14 - Citropin 1.1 - Sp 4 | GLFAVIKKS5ASVS5KGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | U-87 | Brain Tumor | IC50 = 7.277 µM |
| dbacp07452 | A4K14 - Citropin 1.1 - Sp 4 | GLFAVIKKS5ASVS5KGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | MCF-7 | Breast Cancer | IC50 = 10.49 µM |
| dbacp07453 | A4K14 - Citropin 1.1 - Sp 3 | GLFAVS5KKVS5SVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | C4-2B | Prostate Cancer | IC50 = 17.89 µM |
| dbacp07454 | A4K14 - Citropin 1.1 - Sp 3 | GLFAVS5KKVS5SVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | A-549 | Lung Cancer | IC50 = 12.11 µM |
| dbacp07455 | A4K14 - Citropin 1.1 - Sp 3 | GLFAVS5KKVS5SVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | U-87 | Brain Tumor | IC50 = 11.93 µM |
| dbacp07456 | A4K14 - Citropin 1.1 - Sp 3 | GLFAVS5KKVS5SVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | MCF-7 | Breast Cancer | IC50 = 11.92 µM |
| dbacp07457 | A4K14 - Citropin 1.1 - Sp 2 | GLFAS5IKKS5ASVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | C4-2B | Prostate Cancer | IC50 = 10.14 µM |
| dbacp07458 | A4K14 - Citropin 1.1 - Sp 2 | GLFAS5IKKS5ASVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | A-549 | Lung Cancer | IC50 = 12.55 µM |
| dbacp07459 | A4K14 - Citropin 1.1 - Sp 2 | GLFAS5IKKS5ASVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | U-87 | Brain Tumor | IC50 = 14.76 µM |
| dbacp07460 | A4K14 - Citropin 1.1 - Sp 2 | GLFAS5IKKS5ASVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | MCF-7 | Breast Cancer | IC50 = 12.65 µM |
| dbacp07461 | A4K14 - Citropin 1.1 - Sp 1 | GS5FAVS5KKVASVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | C4-2B | Prostate Cancer | IC50 = 8.94 µM |
| dbacp07462 | A4K14 - Citropin 1.1 - Sp 1 | GS5FAVS5KKVASVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | A-549 | Lung Cancer | IC50 = 12.48 µM |
| dbacp07463 | A4K14 - Citropin 1.1 - Sp 1 | GS5FAVS5KKVASVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | U-87 | Brain Tumor | IC50 = 11.88 µM |
| dbacp07464 | A4K14 - Citropin 1.1 - Sp 1 | GS5FAVS5KKVASVIKGL | Synthetic | Stapled peptide enhances helical apoptosis | CCK-8 assay | MCF-7 | Breast Cancer | IC50 = 11.26 µM |
| dbacp07465 | ΔM4 | NFFKRIRRAWKRIWKWIYSA | Synthetic | Membrane disruption triggers mitochondrial apoptosis | Not Available | A-375 | Skin Cancer | IC50 = 9.31 μM |
| dbacp07477 | (LLKK)4 linear peptide | LLKKLLKKLLKKLLKK | Synthetic | Apoptosis, drug-resistance reversal, tumor suppression | MTT assay | SK-HEP-1 | Liver Cancer | Cell Viability (%) ~ 14.1 ± 0.8 at 30 µg/mL |
| dbacp07478 | (LLKK)4 linear peptide | LLKKLLKKLLKKLLKK | Synthetic | Apoptosis, drug-resistance reversal, tumor suppression | MTT assay | HCT-116 | Colon Cancer | Cell Viability (%) ~ 10.73 ± 2.4 at 30 µg/mL |
| dbacp07479 | (LLKK)4 linear peptide | LLKKLLKKLLKKLLKK | Synthetic | Apoptosis, drug-resistance reversal, tumor suppression | MTT assay | Bcap-37 | Breast Cancer | Cell Viability (%) ~ 15.07 ± 0.5 at 30 µg/mL |
| dbacp07480 | (LLKK)4 linear peptide | LLKKLLKKLLKKLLKK | Synthetic | Apoptosis, drug-resistance reversal, tumor suppression | MTT assay | PC-3 | Prostate Cancer | Cell Viability (%) ~ 17.1 ± 5.0 at 30 µg/mL |
| dbacp07481 | 2-arm branched peptide | [LLKKLLKK]2kC | Synthetic | Apoptosis, drug-resistance reversal, tumor suppression | MTT assay | SK-HEP-1 | Liver Cancer | Cell Viability (%) ~ 85.7 ± 4.3 at 30 µg/mL |
| dbacp07482 | 2-arm branched peptide | [LLKKLLKK]2kC | Synthetic | Apoptosis, drug-resistance reversal, tumor suppression | MTT assay | HCT-116 | Colon Cancer | Cell Viability (%) ~ 78.6 ± 10.5 at 30 µg/mL |
| dbacp07483 | 2-arm branched peptide | [LLKKLLKK]2kC | Synthetic | Apoptosis, drug-resistance reversal, tumor suppression | MTT assay | Bcap-37 | Breast Cancer | Cell Viability (%) ~ 81.8 ± 8.8 at 30 µg/mL |
| dbacp07484 | 2-arm branched peptide | [LLKKLLKK]2kC | Synthetic | Apoptosis, drug-resistance reversal, tumor suppression | MTT assay | PC-3 | Prostate Cancer | Cell Viability (%) ~ 73.5 ± 2.2 at 30 µg/mL |
| dbacp07485 | 4-arm branched peptide | {[LLKKLLKK]2kC}2 | Synthetic | Apoptosis, drug-resistance reversal, tumor suppression | MTT assay | SK-HEP-1 | Liver Cancer | Cell Viability (%) ~ 31.7 ± 5.1 at 30 µg/mL |
| dbacp07486 | 4-arm branched peptide | {[LLKKLLKK]2kC}2 | Synthetic | Apoptosis, drug-resistance reversal, tumor suppression | MTT assay | HCT-116 | Colon Cancer | Cell Viability (%) ~ 67.6 ± 5.8 at 30 µg/mL |
| dbacp07487 | 4-arm branched peptide | {[LLKKLLKK]2kC}2 | Synthetic | Apoptosis, drug-resistance reversal, tumor suppression | MTT assay | Bcap-37 | Breast Cancer | Cell Viability (%) ~ 51.4 ± 4.2 at 30 µg/mL |
| dbacp07488 | 4-arm branched peptide | {[LLKKLLKK]2kC}2 | Synthetic | Apoptosis, drug-resistance reversal, tumor suppression | MTT assay | PC-3 | Prostate Cancer | Cell Viability (%) ~ 49.0 ± 0.8 at 30 µg/mL |
| dbacp07489 | LRH7-G5 | Not Available | Synthetic | GPR1 antagonism, PI3K/AKT inhibition | MTT assay | MDA-MB-231 | Breast Cancer | 60% cell viability at 0.01 μM |
| dbacp07490 | LRH7-G5 | Not Available | Synthetic | GPR1 antagonism, PI3K/AKT inhibition | MTT assay | HCC-1937 | Breast Cancer | 60% cell viability at 0.1 μM |
| dbacp07494 | RA-3 | RWrGGGGGLFDIIKKIAESF | Synthetic | Integrin-targeting, α-helix mediated lysis | MTT assay | U87-MG | Brain Tumor | IC50 = 32.27 μM |
| dbacp07495 | RA-3 | RWrGGGGGLFDIIKKIAESF | Synthetic | Integrin-targeting, α-helix mediated lysis | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 28.4 μM |
| dbacp07496 | RA-3 | RWrGGGGGLFDIIKKIAESF | Synthetic | Integrin-targeting, α-helix mediated lysis | MTT assay | MCF-7 | Breast Cancer | IC50 = 44.14 μM |
| dbacp07497 | HX-12A | FFRKVLKLIRKI | Synthetic derivative of Temporin-Pta | ABCB1 inhibition, MDR reversal, sensitization | MTT assay | KB-C2 | Cervical Cancer | IC50 = 6.45 μM |
| dbacp07498 | HX-12B | FFRKVLKLIRKIF | Synthetic derivative of Temporin-Pta | ABCB1 inhibition, MDR reversal, sensitization | MTT assay | KB-C2 | Cervical Cancer | IC50 = 7.61 μM |
| dbacp07499 | HX-12C | FFRKVLKLIRKIWR | Synthetic derivative of Temporin-Pta | ABCB1 inhibition, MDR reversal, sensitization | MTT assay | KB-C2 | Cervical Cancer | IC50 = 6.06 μM |
| dbacp07509 | cyclic dipeptide - 2b | WA | Synthetic | Not Available | MTT assay | HeLa | Cervical Cancer | IC50 = 93.1 µM |
| dbacp07510 | cyclic dipeptide - 2b | WA | Synthetic | Not Available | MTT assay | MCF-7 | Breast Cancer | IC50 = 45.6 µM |
| dbacp07517 | LL-37 Analogue 2 | LKRIVQRIKDFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 33.7 µg/mL |
| dbacp07518 | LL-37 Analogue 3 | AKRIVQRIKDFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 29.8 µg/mL |
| dbacp07519 | LL-37 Analogue 4 | FΚRIVQRILDFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 3.9 µg/mL |
| dbacp07520 | LL-37 Analogue 5 | FKSARIVQRILDFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 10.7 µg/mL |
| dbacp07521 | LL-37 Analogue 6 | FKRIVQRIRDFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 56 µg/mL |
| dbacp07522 | LL-37 Analogue 7 | FKRIVQRIRDFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 12.5 µg/mL |
| dbacp07523 | LL-37 Analogue 8 | FKRIVQKIKDFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 145 µg/mL |
| dbacp07524 | LL-37 Analogue 9 | FKRIVQLIKDFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 18.9 µg/mL |
| dbacp07525 | LL-37 Analogue 10 | FKRIVQLIKDFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 13.9 µg/mL |
| dbacp07526 | LL-37 Analogue 11 | FKRIVQRIKDLLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 75 µg/mL |
| dbacp07527 | LL-37 Analogue 12 | FKRIVQRIKDLLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 45.5 µg/mL |
| dbacp07528 | LL-37 Analogue 13 | FKRIVQIIKKFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 20.0 µg/mL |
| dbacp07529 | LL-37 Analogue 14 | FKRIVQIIKKFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 12.9 µg/mL |
| dbacp07530 | LL-37 Analogue 15 | FKRIVQLLKKLLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 12.8 µg/mL |
| dbacp07531 | LL-37 Analogue 16 | FKRIVQLLKKLLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 9.8 µg/mL |
| dbacp07532 | LL-37 Analogue 17 | FKRILQRIKDFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 19.2 µg/mL |
| dbacp07533 | LL-37 Analogue 18 | FKRILQRIKDFLR | Synthetic Analog of LL-37 | Helical peptides disrupt cancer membranes | MTT assay | A-549 | Lung Cancer | IC50 = 29.2 µg/mL |
| dbacp07535 | AEM-28 | LRKLRKRLLRDWLKAFYDKVAEKLKEAF | Synthetic | LPA reduction suppresses tumor growth | MTS assay | CT-26 | Colorectal Cancer | ~20% cell viability at 10 μg/mL |
| dbacp07536 | AEM-28 | LRKLRKRLLRDWLKAFYDKVAEKLKEAF | Synthetic | LPA reduction suppresses tumor growth | MTS assay | ID8 | Colon Cancer | ~60% cell viability at 10 μg/mL |
| dbacp07537 | AEM-28 | LRKLRKRLLRDWLKAFYDKVAEKLKEAF | Synthetic | LPA reduction suppresses tumor growth | MTS assay | OV-2008 | Ovarian Cancer | ~60% cell viability at 10 μg/mL |
| dbacp07538 | AEM-28 | LRKLRKRLLRDWLKAFYDKVAEKLKEAF | Synthetic | LPA reduction suppresses tumor growth | MTS assay | SK-OV-3 | Ovarian Cancer | ~50% cell viability at 10 μg/mL |
| dbacp07539 | AEM-28 | LRKLRKRLLRDWLKAFYDKVAEKLKEAF | Synthetic | LPA reduction suppresses tumor growth | MTS assay | CaCo-2 | Colon Cancer | ~70% cell viability at 10 μg/mL |
| dbacp07540 | HM-10/10 | LRKLRKRLLRLVGRQLEEFL | Synthetic | LPA reduction suppresses tumor growth | MTS assay | CT-26 | Colorectal Cancer | ~60% cell viability at 10 μg/mL |
| dbacp07541 | AEM-28–2 | Aha-LRRLRRRLLRDWLKAFYDKVAEKLKEAF | Synthetic | LPA reduction suppresses tumor growth | MTS assay | CT-26 | Colorectal Cancer | ~30% cell viability at 10 μg/mL |
| dbacp07542 | AEM-28–2 | Aha-LRRLRRRLLRDWLKAFYDKVAEKLKEAF | Synthetic | LPA reduction suppresses tumor growth | MTS assay | ID8 | Colon Cancer | ~20% cell viability at 10 μg/mL |
| dbacp07543 | AEM-28–2 | Aha-LRRLRRRLLRDWLKAFYDKVAEKLKEAF | Synthetic | LPA reduction suppresses tumor growth | MTS assay | OV-2008 | Ovarian Cancer | ~40% cell viability at 10 μg/mL |
| dbacp07544 | AEM-28–2 | Aha-LRRLRRRLLRDWLKAFYDKVAEKLKEAF | Synthetic | LPA reduction suppresses tumor growth | MTS assay | SK-OV-3 | Ovarian Cancer | ~30% cell viability at 10 μg/mL |
| dbacp07545 | AEM-28–2 | Aha-LRRLRRRLLRDWLKAFYDKVAEKLKEAF | Synthetic | LPA reduction suppresses tumor growth | MTS assay | CaCo-2 | Colon Cancer | ~60% cell viability at 10 μg/mL |
| dbacp07546 | Sur-X | YGRKKRRQRRRKDHRISTFKNWPFLEGCACTPERM | Synthetic | Disrupts XIAP-survivin, induces apoptosis/necroptosis | MTT assay | HCT-116 | Colon Cancer | 20% cell viability at at 20 μM |
| dbacp07547 | Sur-X | YGRKKRRQRRRKDHRISTFKNWPFLEGCACTPERM | Synthetic | Disrupts XIAP-survivin, induces apoptosis/necroptosis | MTT assay | HCT-15 | Colon Cancer | Not Available |
| dbacp07548 | Sur-X | YGRKKRRQRRRKDHRISTFKNWPFLEGCACTPERM | Synthetic | Disrupts XIAP-survivin, induces apoptosis/necroptosis | MTT assay | RKO | Colon Cancer | 25% cell viability at at 20 μM |
| dbacp07549 | Sur-X | YGRKKRRQRRRKDHRISTFKNWPFLEGCACTPERM | Synthetic | Disrupts XIAP-survivin, induces apoptosis/necroptosis | MTT assay | HT-29 | Colon Cancer | Not Available |
| dbacp07552 | macrocyclic pyridoheptapeptide derivative 1a | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | MCF-7 | Breast Cancer | IC50 = 15.329 ± 0.672 μM |
| dbacp07553 | macrocyclic pyridoheptapeptide derivative 1a | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 6.615 ± 0.353 μM |
| dbacp07554 | macrocyclic pyridoheptapeptide derivative 1b | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | MCF-7 | Breast Cancer | IC50 = 10.904 ± 0.534 μM |
| dbacp07555 | macrocyclic pyridoheptapeptide derivative 1b | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 8.724 ± 0.474 μM |
| dbacp07556 | macrocyclic pyridoheptapeptide derivative 1c | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | MCF-7 | Breast Cancer | IC50 = 34.894 ± 1.273 μM |
| dbacp07557 | macrocyclic pyridoheptapeptide derivative 1c | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 17.011 ± 0.965 μM |
| dbacp07558 | macrocyclic pyridoheptapeptide derivative 2a | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 17.513 ± 0.876 μM |
| dbacp07559 | macrocyclic pyridoheptapeptide derivative 2b | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | MCF-7 | Breast Cancer | IC50 = 20.697 ± 0.974 μM |
| dbacp07560 | macrocyclic pyridoheptapeptide derivative 2b | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 18.681 ± 0.988 μM |
| dbacp07561 | macrocyclic pyridoheptapeptide derivative 2c | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | MCF-7 | Breast Cancer | IC50 = 24.943 ± 1.082 μM |
| dbacp07562 | macrocyclic pyridoheptapeptide derivative 2c | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 19.318 ± 1.057 μM |
| dbacp07563 | macrocyclic pyridoheptapeptide derivative 3a | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | MCF-7 | Breast Cancer | IC50 = 10.316 ± 0.546 μM |
| dbacp07564 | macrocyclic pyridoheptapeptide derivative 3a | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 8.063 ± 0.863 μM |
| dbacp07565 | macrocyclic pyridoheptapeptide derivative 3b | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | MCF-7 | Breast Cancer | IC50 = 9.911 ± 0.491 μM |
| dbacp07566 | macrocyclic pyridoheptapeptide derivative 3b | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.66 ± 0.792 μM |
| dbacp07567 | macrocyclic pyridoheptapeptide derivative 3c | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | MCF-7 | Breast Cancer | IC50 = 22.864 ± 0.992 μM |
| dbacp07568 | macrocyclic pyridoheptapeptide derivative 3c | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 16.957 ± 1.161 μM |
| dbacp07569 | macrocyclic pyridoheptapeptide derivative 4a | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | MCF-7 | Breast Cancer | IC50 = 9.304 ± 0.536 μM |
| dbacp07570 | macrocyclic pyridoheptapeptide derivative 4a | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 7.31 ± 0.595 μM |
| dbacp07571 | macrocyclic pyridoheptapeptide derivative 4b | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | MCF-7 | Breast Cancer | IC50 = 9.188 ± 0.545 μM |
| dbacp07572 | macrocyclic pyridoheptapeptide derivative 4b | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 7.166 ± 0.892 μM |
| dbacp07573 | macrocyclic pyridoheptapeptide derivative 4c | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | MCF-7 | Breast Cancer | IC50 = 19.552 ± 1.032 μM |
| dbacp07574 | macrocyclic pyridoheptapeptide derivative 4c | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.631 ± 0.932 μM |
| dbacp07575 | macrocyclic pyridoheptapeptide derivative 5a | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 7.117 ± 0.790 μM |
| dbacp07576 | macrocyclic pyridoheptapeptide derivative 5b | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 7.088 ± 0.784 μM |
| dbacp07577 | macrocyclic pyridoheptapeptide derivative 5c | Structure given in Scheme 1 | Synthetic | Macrocyclic peptides disrupt cancer growth | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.568 ± 1.139 μM |
| dbacp07578 | R-DIM-P-LF11 | FQWQRNIRKVRPRVKRINRQWQF | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | A-375 | Skin Cancer | LC50 = 125.0 ± 16.8 μM |
| dbacp07579 | R-DIM-P-LF11 | FQWQRNIRKVRPRVKRINRQWQF | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | SBcl2 | Skin Cancer | LC50 = 10.7 ± 0.2 μM |
| dbacp07580 | R-DIM-P-LF11 | FQWQRNIRKVRPRVKRINRQWQF | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | WM164 | Skin Cancer | LC50 = 20.9 ± 3.9 μM |
| dbacp07581 | R-DIM-P-LF11-322 | PFWRIRIRRPRRIRIRWFP | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | A-375 | Skin Cancer | LC50 = 4.2 ± 0.2 μM |
| dbacp07582 | R-DIM-P-LF11-322 | PFWRIRIRRPRRIRIRWFP | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | SBcl2 | Skin Cancer | LC50 = 2.5 ± 0.1 μM |
| dbacp07583 | R-DIM-P-LF11-322 | PFWRIRIRRPRRIRIRWFP | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | WM164 | Skin Cancer | LC50 = 4.7 ± 0.2 μM |
| dbacp07584 | DIM-LF11-322 | PFWRIRIRRPFWRIRIRR | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | A-375 | Skin Cancer | LC50 = 6.3 ± 0.3 μM |
| dbacp07585 | DIM-LF11-322 | PFWRIRIRRPFWRIRIRR | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | SBcl2 | Skin Cancer | LC50 < 1 ± 0.0 μM |
| dbacp07586 | DIM-LF11-322 | PFWRIRIRRPFWRIRIRR | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | WM164 | Skin Cancer | LC50 = 4.6 ± 0.1 μM |
| dbacp07587 | R-DIM-P-LF11-215 | FWRIRIRRPRRIRIRWF | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | A-375 | Skin Cancer | LC50 = 2.7 ± 0.9 μM |
| dbacp07588 | R-DIM-P-LF11-215 | FWRIRIRRPRRIRIRWF | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | SBcl2 | Skin Cancer | LC50 < 1 ± 0.0 μM |
| dbacp07589 | R-DIM-P-LF11-215 | FWRIRIRRPRRIRIRWF | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | WM164 | Skin Cancer | LC50 = 4.6 ± 0.1 μM |
| dbacp07590 | R-DIM-P-LF11-334 | PWRIRIRRPRRIRIWP | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | A-375 | Skin Cancer | LC50 = 6.6 ± 0.3 μM |
| dbacp07591 | R-DIM-P-LF11-334 | PWRIRIRRPRRIRIWP | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | SBcl2 | Skin Cancer | LC50 = 3.4 ± 0.4 μM |
| dbacp07592 | R-DIM-P-LF11-334 | PWRIRIRRPRRIRIWP | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | WM164 | Skin Cancer | LC50 = 5.0 ± 0.1 μM |
| dbacp07593 | R-DIM-LF11-334-LF11-334 | PWRIRIRRRRIRIRWPPWRIRIRR | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | A-375 | Skin Cancer | LC50 < 1 ± 0.1 μM |
| dbacp07594 | R-DIM-LF11-334-LF11-334 | PWRIRIRRRRIRIRWPPWRIRIRR | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | SBcl2 | Skin Cancer | LC50 < 1 ± 0.1 μM |
| dbacp07595 | R-DIM-LF11-334-LF11-334 | PWRIRIRRRRIRIRWPPWRIRIRR | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | WM164 | Skin Cancer | LC50 = 3.6 ± 0.7 μM |
| dbacp07596 | DIM-LF11-339 | RRWFWRRRRWFWRR | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | A-375 | Skin Cancer | LC50 = 4.8 ± 0.4 μM |
| dbacp07597 | DIM-LF11-339 | RRWFWRRRRWFWRR | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | SBcl2 | Skin Cancer | LC50 = 4.7 ± 0.3 μM |
| dbacp07598 | DIM-LF11-339 | RRWFWRRRRWFWRR | Synthetic | Peptides target phosphatidylserine, trigger apoptosis | MTS assay | WM164 | Skin Cancer | LC50 = 3.8 ± 0.3 μM |
| dbacp07599 | Tritrp-Agb | V(Agb)(Agb)FPWWWPFL(Agb)(Agb) | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 9.6 μM |
| dbacp07600 | Tritrp-hArg | V(hArg)(hArg)FPWWWPFL(hArg)(hArg) | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 13.3 μM |
| dbacp07601 | Tritrp-Lys | VKKFPWWWPFLKK | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 11.5 μM |
| dbacp07602 | Tritrp-Dap | V(Dap)(Dap)FPWWWPFL(Dap)(Dap) | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 ≥ 65 μM |
| dbacp07603 | Tritrp-Dab | V(Dab)(Dab)FPWWWPFL(Dab)(Dab) | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 ≤ 6.5 μM |
| dbacp07604 | Tritrp-Orn | V(Orn)(Orn)FPWWWPFL(Orn)(Orn) | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 ≤ 6.5 μM |
| dbacp07605 | Tritrp-P59A | VRRFAWWWAFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 12.5 μM |
| dbacp07606 | Tritrp-P59A-Lys | VKKFAWWWAFLKK | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 27.6 μM |
| dbacp07607 | Tritrp-P5A | VRRFAWWWPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 16.2 μM |
| dbacp07608 | Tritrp-P5A-Lys | VKKFAWWWPFLKK | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 27.6 μM |
| dbacp07609 | Tritrp-P9A | VRRFPWWWAFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 6.8 μM |
| dbacp07610 | Tritrp-P9A-Lys | VKKFPWWWAFLKK | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 15.1 μM |
| dbacp07611 | Tritrp-W678F | VRRFPFFFPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 24.6 μM |
| dbacp07612 | Tritrp-W678bTA | VRRFP(bTA)(bTA)(bTA)PFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 9.6 μM |
| dbacp07613 | Tritrp-W6hW | VRRFP(hW)WWPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 16.1 μM |
| dbacp07614 | Tritrp-W7hW | VRRFPW(hW)WPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 15.1 μM |
| dbacp07615 | Tritrp-W8hW | VRRFPWW(hW)PFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 10.7 μM |
| dbacp07616 | Tritrp-W789hW | VRRFP(hW)(hW)(hW)PFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 44.8 μM |
| dbacp07617 | Tritrp-W6A | VRRFPAWWPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 36.5 μM |
| dbacp07618 | Tritrp-W7A | VRRFPWAWPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 48.2 μM |
| dbacp07619 | Tritrp-W8A | VRRFPWWAPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 22.8 μM |
| dbacp07620 | Tritrp-W67A | VRRFPAAWPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 ≥ 65 μM |
| dbacp07621 | Tritrp-W68A | VRRFPAWAPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 ≥ 65 μM |
| dbacp07622 | Tritrp-W78A | VRRFPWAAPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 ≥ 65 μM |
| dbacp07623 | Tritrp-W678A | VRRFPAAAPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 ≥ 65 μM |
| dbacp07624 | Tritrp-W6Y | VRRFPYWWPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 19.3 μM |
| dbacp07625 | Tritrp-W7Y | VRRFPWYWPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 11.4 μM |
| dbacp07626 | Tritrp-W8Y | VRRFPWWYPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 12.0 μM |
| dbacp07627 | Tritrp-W67Y | VRRFPYYWPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 32.2 μM |
| dbacp07628 | Tritrp-W68Y | VRRFPYWYPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 35.4 μM |
| dbacp07629 | Tritrp-W78Y | VRRFPWYYPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 25.6 μM |
| dbacp07630 | Tritrp-W678Y | VRRFPYYYPFLRR | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 ≥ 65 μM |
| dbacp07631 | Tritrp DiSu | CVRRFPWWYPFLRRC | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 12.3 μM |
| dbacp07632 | MagaininF5W-Lys | GIGKWLHSAKKFGKAFVGEIMNS | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 16.8 μM |
| dbacp07633 | MagaininF5W-Arg | GIGRWLHSARRFGRAFVGEIMNS | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 16.8 μM |
| dbacp07634 | PuroA-Arg | FPVTWKWWKWWKG | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 10.0 μM |
| dbacp07635 | PuroA-Lys | FPVTWRWWRWWRG | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 12.0 μM |
| dbacp07636 | Indolicidin-Lys | ILPWKWPWWPWKK | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 9.5 μM |
| dbacp07637 | MPG | GALFLGFLGAAGSTMGAWSQPKKKRKV | Synthetic | Membrane permeabilization via lysine substitution | MTT assay | Jurkat | Blood Cancer | IC50 = 15.8 μM |
| dbacp07638 | branched tetrapeptide Schiff bases derivative 4a | Figure given in Scheme 1 | Synthetic | p53 stabilization and LDHA inhibition | MTT assay | MCF-7 | Breast Cancer | IC50 between 8.12 ± 0.14 to 17.55 ± 0.27 μM |
| dbacp07639 | branched tetrapeptide Schiff bases derivative 4b | Figure given in Scheme 1 | Synthetic | p53 stabilization and LDHA inhibition | MTT assay | MCF-7 | Breast Cancer | IC50 between 8.12 ± 0.14 to 17.55 ± 0.27 μM |
| dbacp07640 | branched tetrapeptide Schiff bases derivative 4c | Figure given in Scheme 1 | Synthetic | p53 stabilization and LDHA inhibition | MTT assay | MCF-7 | Breast Cancer | IC50 between 8.12 ± 0.14 to 17.55 ± 0.27 μM |
| dbacp07641 | branched tetrapeptide Schiff bases derivative 5c | Figure given in Scheme 1 | Synthetic | p53 stabilization and LDHA inhibition | MTT assay | MCF-7 | Breast Cancer | IC50 between 8.12 ± 0.14 to 17.55 ± 0.27 μM |
| dbacp07642 | branched tetrapeptide Schiff bases derivative 5d | Figure given in Scheme 1 | Synthetic | p53 stabilization and LDHA inhibition | MTT assay | MCF-7 | Breast Cancer | IC50 between 8.12 ± 0.14 to 17.55 ± 0.27 μM |
| dbacp07643 | branched tetrapeptide Schiff bases derivative 5e | Figure given in Scheme 1 | Synthetic | p53 stabilization and LDHA inhibition | MTT assay | MCF-7 | Breast Cancer | IC50 between 8.12 ± 0.14 to 17.55 ± 0.27 μM |
| dbacp07668 | Longicalycinin A linear analogue 1 | GYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.66 ± 0.0007 µg/ml |
| dbacp07669 | Longicalycinin A linear analogue 1 | GYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 10.45 ± 0.0042 µg/ml |
| dbacp07670 | Longicalycinin A linear analogue 1 | GYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 13.29% Cell death at 100 µg/ml |
| dbacp07671 | Longicalycinin A linear analogue 1 | GYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 83.02% Cell death at 100 µg/ml |
| dbacp07672 | Longicalycinin A Cyclic analogue 1 | GYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 10.2 ± 0.007 µg/ml |
| dbacp07673 | Longicalycinin A Cyclic analogue 1 | GYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 11.4 ± 0.0028 µg/ml |
| dbacp07674 | Longicalycinin A Cyclic analogue 1 | GYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 69.73% Cell death at 100 µg/ml |
| dbacp07675 | Longicalycinin A Cyclic analogue 1 | GYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 71.5% Cell death at 100 µg/ml |
| dbacp07676 | Longicalycinin A linear analogue 2 | LYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 8.76 ± 0.0035 µg/ml |
| dbacp07677 | Longicalycinin A linear analogue 2 | LYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 12.33 ± 0 µg/ml |
| dbacp07678 | Longicalycinin A linear analogue 2 | LYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 71.37% Cell death at 100 µg/ml |
| dbacp07679 | Longicalycinin A linear analogue 2 | LYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 88.47% Cell death at 100 µg/ml |
| dbacp07683 | Longicalycinin A | FYPFG | Synthetic | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 10.45 ± 0.0042 µg/ml |
| dbacp07684 | Longicalycinin A | FYPFG | Synthetic | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 11.87 ± 0.0021 µg/ml |
| dbacp07685 | Longicalycinin A (Linear) | FYPFG | Synthetic | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.18 ± 0.0014 µg/ml |
| dbacp07686 | Longicalycinin A (Linear) | FYPFG | Synthetic | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 9.61 ± 0.0007 µg/ml |
| dbacp07687 | Longicalycinin A linear analogue 14 | PYFFL | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.67 ± 0.0007 µg/ml |
| dbacp07688 | Longicalycinin A linear analogue 14 | PYFFL | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 9.12 ± 0.0042 µg/ml |
| dbacp07689 | Longicalycinin A linear analogue 14 | PYFFL | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 13.02% Cell death at 100 µg/ml |
| dbacp07690 | Longicalycinin A linear analogue 14 | PYFFL | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 82.36% Cell death at 100 µg/ml |
| dbacp07691 | Longicalycinin A cyclic analogue 14 | PYFFL | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 10.46 ± 0.0028 µg/ml |
| dbacp07692 | Longicalycinin A cyclic analogue 14 | PYFFL | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 10.92 ± 0.0021 µg/ml |
| dbacp07693 | Longicalycinin A cyclic analogue 14 | PYFFL | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 70.69% Cell death at 100 µg/ml |
| dbacp07694 | Longicalycinin A cyclic analogue 14 | PYFFL | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 52.38% Cell death at 100 µg/ml |
| dbacp07695 | Longicalycinin A linear analogue 3 | GYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.77 ± 0.0007 µg/ml |
| dbacp07696 | Longicalycinin A linear analogue 3 | GYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 11.4 ± 0 µg/ml |
| dbacp07697 | Longicalycinin A linear analogue 3 | GYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 82.33% Cell death at 100 µg/ml |
| dbacp07698 | Longicalycinin A linear analogue 3 | GYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 87.56% Cell death at 100 µg/ml |
| dbacp07699 | Longicalycinin A cyclic analogue 3 | GYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.5 ± 0.0056 µg/ml |
| dbacp07700 | Longicalycinin A cyclic analogue 3 | GYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 11.28 ± 0.0063 µg/ml |
| dbacp07701 | Longicalycinin A cyclic analogue 3 | GYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 56.72% Cell death at 100 µg/ml |
| dbacp07702 | Longicalycinin A cyclic analogue 3 | GYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 28.51% Cell death at 100 µg/ml |
| dbacp07703 | Longicalycinin A linear analogue 4 | AYPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.53 ± 0.0014 µg/ml |
| dbacp07704 | Longicalycinin A linear analogue 4 | AYPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 10.78 ± 0.0021 µg/ml |
| dbacp07705 | Longicalycinin A linear analogue 4 | AYPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 27.13% Cell death at 100 µg/ml |
| dbacp07706 | Longicalycinin A linear analogue 4 | AYPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 75.91% Cell death at 100 µg/ml |
| dbacp07707 | Longicalycinin A cyclic analogue 4 | AYPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.77 ± 0.007 µg/ml |
| dbacp07708 | Longicalycinin A cyclic analogue 4 | AYPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 11.33 ± 0.0035 µg/ml |
| dbacp07709 | Longicalycinin A cyclic analogue 4 | AYPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 71.1% Cell death at 100 µg/ml |
| dbacp07710 | Longicalycinin A cyclic analogue 4 | AYPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 52.49% Cell death at 100 µg/ml |
| dbacp07711 | Longicalycinin A linear analogue 5 | FSPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 8.99 ± 0.0014 µg/ml |
| dbacp07712 | Longicalycinin A linear analogue 5 | FSPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 10.97 ± 0.0049 µg/ml |
| dbacp07713 | Longicalycinin A linear analogue 5 | FSPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 76.72% Cell death at 100 µg/ml |
| dbacp07714 | Longicalycinin A linear analogue 5 | FSPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 91.52% Cell death at 100 µg/ml |
| dbacp07715 | Longicalycinin A cyclic analogue 5 | FSPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.45 ± 0.0056 µg/ml |
| dbacp07716 | Longicalycinin A cyclic analogue 5 | FSPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 9.98 ± 0.4256 µg/ml |
| dbacp07717 | Longicalycinin A cyclic analogue 5 | FSPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 41.37% Cell death at 100 µg/ml |
| dbacp07718 | Longicalycinin A cyclic analogue 5 | FSPFG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 97.74% Cell death at 100 µg/ml |
| dbacp07719 | Longicalycinin A linear analogue 6 | VYPIA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 10.98 ± 0.0014 µg/ml |
| dbacp07720 | Longicalycinin A linear analogue 6 | VYPIA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 12.31 ± 0.0063 µg/ml |
| dbacp07721 | Longicalycinin A linear analogue 6 | VYPIA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 38.64% Cell death at 100 µg/ml |
| dbacp07722 | Longicalycinin A linear analogue 6 | VYPIA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 49.33% Cell death at 100 µg/ml |
| dbacp07723 | Longicalycinin A cyclic analogue 6 | VYPIA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 17.34 ± 0.0014 µg/ml |
| dbacp07724 | Longicalycinin A cyclic analogue 6 | VYPIA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 10.2 ± 0.0021 µg/ml |
| dbacp07725 | Longicalycinin A cyclic analogue 6 | VYPIA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 51.79% Cell death at 100 µg/ml |
| dbacp07726 | Longicalycinin A cyclic analogue 6 | VYPIA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 27.61% Cell death at 100 µg/ml |
| dbacp07727 | Longicalycinin A linear analogue 7 | PYVFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.6 ± 0.0007 µg/ml |
| dbacp07728 | Longicalycinin A linear analogue 7 | PYVFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 9.78 ± 0.0212 µg/ml |
| dbacp07729 | Longicalycinin A linear analogue 7 | PYVFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 82.33% Cell death at 100 µg/ml |
| dbacp07730 | Longicalycinin A linear analogue 7 | PYVFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 84.17% Cell death at 100 µg/ml |
| dbacp07731 | Longicalycinin A cyclic analogue 7 | PYVFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.21 ± 0.0056 µg/ml |
| dbacp07732 | Longicalycinin A cyclic analogue 7 | PYVFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 12.11 ± 0.0035 µg/ml |
| dbacp07733 | Longicalycinin A cyclic analogue 7 | PYVFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 47.68% Cell death at 100 µg/ml |
| dbacp07734 | Longicalycinin A cyclic analogue 7 | PYVFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 22.86% Cell death at 100 µg/ml |
| dbacp07735 | Longicalycinin A linear analogue 8 | FYPVG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 10.35 ± 0.0014 µg/ml |
| dbacp07736 | Longicalycinin A linear analogue 8 | FYPVG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 12.88 ± 0.0014 µg/ml |
| dbacp07737 | Longicalycinin A linear analogue 8 | FYPVG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 15.35% Cell death at 100 µg/ml |
| dbacp07738 | Longicalycinin A linear analogue 8 | FYPVG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 88.01% Cell death at 100 µg/ml |
| dbacp07739 | Longicalycinin A cyclic analogue 8 | FYPVG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.12 ± 0.0007 µg/ml |
| dbacp07740 | Longicalycinin A cyclic analogue 8 | FYPVG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 12.67 ± 0.0028 µg/ml |
| dbacp07741 | Longicalycinin A cyclic analogue 8 | FYPVG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 36.85% Cell death at 100 µg/ml |
| dbacp07742 | Longicalycinin A cyclic analogue 8 | FYPVG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 29.87% Cell death at 100 µg/ml |
| dbacp07743 | Longicalycinin A linear analogue 9 | FYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.33 ± 0.0007 µg/ml |
| dbacp07744 | Longicalycinin A linear analogue 9 | FYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 10.44 ± 0.5536 µg/ml |
| dbacp07745 | Longicalycinin A linear analogue 9 | FYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 72.74% Cell death at 100 µg/ml |
| dbacp07746 | Longicalycinin A linear analogue 9 | FYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 1.59% Cell death at 100 µg/ml |
| dbacp07747 | Longicalycinin A cyclic analogue 9 | FYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 10.67 ± 0 µg/ml |
| dbacp07748 | Longicalycinin A cyclic analogue 9 | FYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 10.7 ± 0.0056 µg/ml |
| dbacp07749 | Longicalycinin A cyclic analogue 9 | FYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 73.98% Cell death at 100 µg/ml |
| dbacp07750 | Longicalycinin A cyclic analogue 9 | FYPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 76.25% Cell death at 100 µg/ml |
| dbacp07751 | Longicalycinin A linear analogue 10 | FYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 10.5 ± 0.0014 µg/ml |
| dbacp07752 | Longicalycinin A linear analogue 10 | FYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 10.5 ± 0.0007 µg/ml |
| dbacp07753 | Longicalycinin A linear analogue 10 | FYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 76.72% Cell death at 100 µg/ml |
| dbacp07754 | Longicalycinin A linear analogue 10 | FYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 92.09% Cell death at 100 µg/ml |
| dbacp07755 | Longicalycinin A cyclic analogue 10 | FYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 10.28 ± 0 µg/ml |
| dbacp07756 | Longicalycinin A cyclic analogue 10 | FYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 11.56 ± 0.0028 µg/ml |
| dbacp07757 | Longicalycinin A cyclic analogue 10 | FYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 72.06% Cell death at 100 µg/ml |
| dbacp07758 | Longicalycinin A cyclic analogue 10 | FYPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 71.27% Cell death at 100 µg/ml |
| dbacp07759 | Longicalycinin A linear analogue 11 | TVPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.56 ± 0.0021 µg/ml |
| dbacp07760 | Longicalycinin A linear analogue 11 | TVPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 11.67 ± 0.0014 µg/ml |
| dbacp07761 | Longicalycinin A linear analogue 11 | TVPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 70.28% Cell death at 100 µg/ml |
| dbacp07762 | Longicalycinin A linear analogue 11 | TVPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 88.47% Cell death at 100 µg/ml |
| dbacp07763 | Longicalycinin A cyclic analogue 11 | TVPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 10.36 ± 0 µg/ml |
| dbacp07764 | Longicalycinin A cyclic analogue 11 | TVPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 10.61 ± 0.0007 µg/ml |
| dbacp07765 | Longicalycinin A cyclic analogue 11 | TVPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 72.06% Cell death at 100 µg/ml |
| dbacp07766 | Longicalycinin A cyclic analogue 11 | TVPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 74.89% Cell death at 100 µg/ml |
| dbacp07767 | Longicalycinin A linear analogue 12 | FYPFI | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 11.32 ± 0.0014 µg/ml |
| dbacp07768 | Longicalycinin A linear analogue 12 | FYPFI | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 14.2 ± 0.0014 µg/ml |
| dbacp07769 | Longicalycinin A linear analogue 12 | FYPFI | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 12.06% Cell death at 100 µg/ml |
| dbacp07770 | Longicalycinin A linear analogue 12 | FYPFI | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 81.34% Cell death at 100 µg/ml |
| dbacp07771 | Longicalycinin A cyclic analogue 12 | FYPFI | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 12.37 ± 0.0014 µg/ml |
| dbacp07772 | Longicalycinin A cyclic analogue 12 | FYPFI | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 13.2 ± 0 µg/ml |
| dbacp07773 | Longicalycinin A cyclic analogue 12 | FYPFI | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 63.84% Cell death at 100 µg/ml |
| dbacp07774 | Longicalycinin A cyclic analogue 12 | FYPFI | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 52.72% Cell death at 100 µg/ml |
| dbacp07775 | Longicalycinin A cyclic analogue 15 | PYGFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 10.33 ± 0 µg/ml |
| dbacp07776 | Longicalycinin A cyclic analogue 15 | PYGFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 11.23 ± 0.0007 µg/ml |
| dbacp07777 | Longicalycinin A cyclic analogue 15 | PYGFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 52.33% Cell death at 100 µg/ml |
| dbacp07778 | Longicalycinin A cyclic analogue 15 | PYGFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 27.43% Cell death at 100 µg/ml |
| dbacp07779 | Longicalycinin A linear analogue 16 | FTPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 11.1 ± 0.0007 µg/ml |
| dbacp07780 | Longicalycinin A linear analogue 16 | FTPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 12.11 ± 0.0056 µg/ml |
| dbacp07781 | Longicalycinin A linear analogue 16 | FTPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 15.76% Cell death at 100 µg/ml |
| dbacp07782 | Longicalycinin A linear analogue 16 | FTPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 88.24% Cell death at 100 µg/ml |
| dbacp07783 | Longicalycinin A cyclic analogue 16 | FTPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 12.1 ± 0.0007 µg/ml |
| dbacp07784 | Longicalycinin A cyclic analogue 16 | FTPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 10.4 ± 0.0028 µg/ml |
| dbacp07785 | Longicalycinin A cyclic analogue 16 | FTPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 42.33% Cell death at 100 µg/ml |
| dbacp07786 | Longicalycinin A cyclic analogue 16 | FTPFV | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 29.87% Cell death at 100 µg/ml |
| dbacp07787 | Longicalycinin A linear analogue 17 | FSPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.33 ± 0.0007 µg/ml |
| dbacp07788 | Longicalycinin A linear analogue 17 | FSPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 11.33 ± 0.0035 µg/ml |
| dbacp07789 | Longicalycinin A linear analogue 17 | FSPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 27.54% Cell death at 100 µg/ml |
| dbacp07790 | Longicalycinin A linear analogue 17 | FSPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 75.68% Cell death at 100 µg/ml |
| dbacp07791 | Longicalycinin A cyclic analogue 17 | FSPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.4 ± 0.0014 µg/ml |
| dbacp07792 | Longicalycinin A cyclic analogue 17 | FSPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 11.2 ± 0.0007 µg/ml |
| dbacp07793 | Longicalycinin A cyclic analogue 17 | FSPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 74.53% Cell death at 100 µg/ml |
| dbacp07794 | Longicalycinin A cyclic analogue 17 | FSPFA | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 76.14% Cell death at 100 µg/ml |
| dbacp07795 | Longicalycinin A linear analogue 18 | FSPAG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 10.33 ± 0.0007 µg/ml |
| dbacp07796 | Longicalycinin A linear analogue 18 | FSPAG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 10.2 ± 0.0014 µg/ml |
| dbacp07797 | Longicalycinin A linear analogue 18 | FSPAG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 15.55% Cell death at 100 µg/ml |
| dbacp07798 | Longicalycinin A linear analogue 18 | FSPAG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | 56.51% Cell death at 100 µg/ml |
| dbacp07799 | Longicalycinin A cyclic analogue 18 | FSPAG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | IC50 = 9.68 ± 0.0014 µg/ml |
| dbacp07800 | Longicalycinin A cyclic analogue 18 | FSPAG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colorectal Cancer | IC50 = 9.06 ± 0.0014 µg/ml |
| dbacp07801 | Longicalycinin A cyclic analogue 18 | FSPAG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HepG-2 | Liver Cancer | 46.58% Cell death at 100 µg/ml |
| dbacp07802 | Longicalycinin A cyclic analogue 18 | FSPAG | Synthetic Analogue of Longicalycinin A | Cyclization enhances apoptosis via lysosomes | MTT assay | HT-29 | Colon Cancer | 22.8% Cell death at 100 µg/ml |
| dbacp07803 | cT1 | KWCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 1.3 ± 0.1 µM |
| dbacp07804 | cT1 | KWCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | HT-144 | Skin Cancer | CC50 = 1.4 ± 0.1 µM |
| dbacp07805 | cT1 | KWCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | WM164 | Skin Cancer | CC50 = 2.7 ± 0.1 µM |
| dbacp07806 | cT1 | KWCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | MDA-MB-435S | Skin Cancer | CC50 = 2.7 ± 0.3 µM |
| dbacp07807 | cT1 | KWCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 2.0 ± 0.1 µM |
| dbacp07808 | cT1 | KWCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | MCF-7 | Breast Cancer | CC50 = 6.4 ± 0.6 µM |
| dbacp07809 | cT1 | KWCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | HeLa | Cervical Cancer | CC50 = 6.7 ± 0.6 µM |
| dbacp07810 | [R/K]cT1 | KWCFKVCYKGICYKKCKG | Synthetic | Not Available | Resazurin dye assay | WM164 | Skin Cancer | CC50 = 4.3 ± 0.3 µM |
| dbacp07811 | [R/K]cT1 | KWCFKVCYKGICYKKCKG | Synthetic | Not Available | Resazurin dye assay | MDA-MB-435S | Skin Cancer | CC50 = 3.5 ± 0.4 µM |
| dbacp07812 | [R/K]cT1 | KWCFKVCYKGICYKKCKG | Synthetic | Not Available | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 2.5 ± 0.1 µM |
| dbacp07813 | [R/K]cT1 | KWCFKVCYKGICYKKCKG | Synthetic | Not Available | Resazurin dye assay | HeLa | Cervical Cancer | CC50 = 13.4 ± 1.9 µM |
| dbacp07814 | [W2S]cT1 | KSCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 2.0 ± 0.1 µM |
| dbacp07815 | [W2S]cT1 | KSCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | HT-144 | Skin Cancer | CC50 = 3.0 ± 0.2 µM |
| dbacp07816 | [W2S]cT1 | KSCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | WM164 | Skin Cancer | CC50 = 3.9 ± 0.2 µM |
| dbacp07817 | [W2S]cT1 | KSCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | MDA-MB-435S | Skin Cancer | CC50 = 18.9 ± 0.9 µM |
| dbacp07818 | [W2S]cT1 | KSCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 2.7 ± 0.2 µM |
| dbacp07819 | [W2S]cT1 | KSCFRVCYRGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | HeLa | Cervical Cancer | CC50 = 22.5 ± 2.1 µM |
| dbacp07820 | [Y8S-I11S]cT1 | KWCFRVCSRGSCYRRCRG | Synthetic | Not Available | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 17.3 ± 1.0 µM |
| dbacp07821 | [Y8S-I11S]cT1 | KWCFRVCSRGSCYRRCRG | Synthetic | Not Available | Resazurin dye assay | HT-144 | Skin Cancer | CC50 = 27.8 ± 2.2 µM |
| dbacp07822 | [Y8S-I11S]cT1 | KWCFRVCSRGSCYRRCRG | Synthetic | Not Available | Resazurin dye assay | WM164 | Skin Cancer | CC50 = 28.2 ± 2.0 µM |
| dbacp07823 | [Y8S-I11S]cT1 | KWCFRVCSRGSCYRRCRG | Synthetic | Not Available | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 13.2 ± 0.9 µM |
| dbacp07824 | [R9S]cT1 | KWCFRVCYSGICYRRCRG | Synthetic | Not Available | Resazurin dye assay | MDA-MB-435S | Skin Cancer | CC50 = 5.3 ± 0.6 µM |
| dbacp07825 | [R14S]cT1 | KWCFRVCYRGICYSRCRG | Synthetic | Not Available | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 1.7 ± 0.1 µM |
| dbacp07826 | [R14S]cT1 | KWCFRVCYRGICYSRCRG | Synthetic | Not Available | Resazurin dye assay | HT-144 | Skin Cancer | CC50 = 2.3 ± 0.2 µM |
| dbacp07827 | [R14S]cT1 | KWCFRVCYRGICYSRCRG | Synthetic | Not Available | Resazurin dye assay | WM164 | Skin Cancer | CC50 = 2.7 ± 0.1 µM |
| dbacp07828 | [R14S]cT1 | KWCFRVCYRGICYSRCRG | Synthetic | Not Available | Resazurin dye assay | MDA-MB-435S | Skin Cancer | CC50 = 3.5 ± 0.3 µM |
| dbacp07829 | [R14S]cT1 | KWCFRVCYRGICYSRCRG | Synthetic | Not Available | Resazurin dye assay | HeLa | Cervical Cancer | CC50 = 7.5 ± 0.3 µM |
| dbacp07830 | [R17S]cT1 | KWCFRVCYRGICYRRCSG | Synthetic | Not Available | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 1.8 ± 0.1 µM |
| dbacp07831 | [R17S]cT1 | KWCFRVCYRGICYRRCSG | Synthetic | Not Available | Resazurin dye assay | HT-144 | Skin Cancer | CC50 = 1.2 ± 0.1 µM |
| dbacp07832 | [R17S]cT1 | KWCFRVCYRGICYRRCSG | Synthetic | Not Available | Resazurin dye assay | WM164 | Skin Cancer | CC50 = 1.8 ± 0.1 µM |
| dbacp07833 | [R17S]cT1 | KWCFRVCYRGICYRRCSG | Synthetic | Not Available | Resazurin dye assay | MDA-MB-435S | Skin Cancer | CC50 = 4.5 ± 0.3 µM |
| dbacp07834 | [R17S]cT1 | KWCFRVCYRGICYRRCSG | Synthetic | Not Available | Resazurin dye assay | HeLa | Cervical Cancer | CC50 = 12.2 ± 0.4 µM |
| dbacp07835 | [R9S-R14S-R17S]cT1 | KWCFRVCYSGICYSRCSG | Synthetic | Not Available | Resazurin dye assay | HT-144 | Skin Cancer | CC50 = 11.8 ± 0.9 µM |
| dbacp07836 | [R9S-R14S-R17S]cT1 | KWCFRVCYSGICYSRCSG | Synthetic | Not Available | Resazurin dye assay | WM164 | Skin Cancer | CC50 = 11.1 ± 0.9 µM |
| dbacp07837 | [R9S-R14S-R17S]cT1 | KWCFRVCYSGICYSRCSG | Synthetic | Not Available | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 4.8 ± 0.3 µM |
| dbacp07838 | [G18K]cT1 | KWCFRVCYRGICYRRCRK | Synthetic | Not Available | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 1.0 ± 0.1 µM |
| dbacp07839 | [G18K]cT1 | KWCFRVCYRGICYRRCRK | Synthetic | Not Available | Resazurin dye assay | HT-144 | Skin Cancer | CC50 = 3.2 ± 0.1 µM |
| dbacp07840 | [G18K]cT1 | KWCFRVCYRGICYRRCRK | Synthetic | Not Available | Resazurin dye assay | WM164 | Skin Cancer | CC50 = 2.7 ± 0.2 µM |
| dbacp07841 | [G18K]cT1 | KWCFRVCYRGICYRRCRK | Synthetic | Not Available | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 1.7 ± 0.1 µM |
| dbacp07842 | [G18K]cT1 | KWCFRVCYRGICYRRCRK | Synthetic | Not Available | Resazurin dye assay | HeLa | Cervical Cancer | CC50 = 6.7 ± 1.1 µM |
| dbacp07843 | [I11F-G18K]cT1 | KWCFRVCYRGFCYRRCRK | Synthetic | Not Available | Resazurin dye assay | MM96L | Skin Cancer | CC50 = 1.3 ± 0.1 µM |
| dbacp07844 | [I11F-G18K]cT1 | KWCFRVCYRGFCYRRCRK | Synthetic | Not Available | Resazurin dye assay | HT-144 | Skin Cancer | CC50 = 3.2 ± 0.1 µM |
| dbacp07845 | [I11F-G18K]cT1 | KWCFRVCYRGFCYRRCRK | Synthetic | Not Available | Resazurin dye assay | WM164 | Skin Cancer | CC50 = 2.9 ± 0.2 µM |
| dbacp07846 | [I11F-G18K]cT1 | KWCFRVCYRGFCYRRCRK | Synthetic | Not Available | Resazurin dye assay | K-562 | Leukemia Cancer | CC50 = 1.9 ± 0.1 µM |
| dbacp07847 | [I11F-G18K]cT1 | KWCFRVCYRGFCYRRCRK | Synthetic | Not Available | Resazurin dye assay | HeLa | Cervical Cancer | CC50 = 5.1 ± 0.3 µM |
| dbacp07854 | K8, 23-DPT9 | GLWSKIKKAAKTAGKAALGFVNKMV | Synthetic | Membrane disruption and cationic enhancement | MTT assay | MCF-7 | Breast Cancer | IC50 = 8.64 µM |
| dbacp07855 | K8, 23-DPT9 | GLWSKIKKAAKTAGKAALGFVNKMV | Synthetic | Membrane disruption and cationic enhancement | MTT assay | U251-MG | Brain Tumor | IC50 = 18.51 µM |
| dbacp07856 | K8, 23-DPT9 | GLWSKIKKAAKTAGKAALGFVNKMV | Synthetic | Membrane disruption and cationic enhancement | MTT assay | H-157 | Lung Cancer | IC50 = 9.88 µM |
| dbacp07857 | K8, 23-DPT9 | GLWSKIKKAAKTAGKAALGFVNKMV | Synthetic | Membrane disruption and cationic enhancement | MTT assay | PC-3 | Prostate Cancer | IC50 = 9.97 µM |
| dbacp07858 | K8, 23-DPT9 | GLWSKIKKAAKTAGKAALGFVNKMV | Synthetic | Membrane disruption and cationic enhancement | MTT assay | PANC-1 | Pancreatic Cancer | IC50 = 11.17 µM |
| dbacp07882 | 0Dap | GIKKWLHSAKKFGKKFVKKIZNS | Synthetic | Not Available | WST-1 assay | PANC-1 | Pancreatic Cancer | EC50 = 9.1±0.3 μM |
| dbacp07883 | 2Dap | GIKXWLHSAKKFGXKFVKKIZNS | Synthetic | Not Available | WST-1 assay | PANC-1 | Pancreatic Cancer | EC50 = 14.7±0.6 μM |
| dbacp07884 | 4Dap | GIKXWLHSAXKFGXKFVKXIZNS | Synthetic | Not Available | WST-1 assay | PANC-1 | Pancreatic Cancer | EC50 = 35.7±0.7 μM |
| dbacp07885 | 6Dap | GIKXWLHSAXXFGXKFVXXIZNS | Synthetic | Not Available | WST-1 assay | PANC-1 | Pancreatic Cancer | EC50 = 55.0±1.8 μM |
| dbacp07886 | 8Dap | GIXXWLHSAXXFGXXFVXXIZNS | Synthetic | Not Available | WST-1 assay | PANC-1 | Pancreatic Cancer | EC50 = 61.4±0.7 μM |
| dbacp07889 | H-58 | IKLSKKTKKNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 0.62 ± 0.12 μM |
| dbacp07890 | H-58 | IKLSKKTKKNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HCT-116 | Colon Cancer | IC50 = 1.29 ± 0.08 μM |
| dbacp07891 | H-58 | IKLSKKTKKNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HepG-2 | Liver Cancer | IC50 = 2.13 ± 0.07 μM |
| dbacp07892 | H-57 | IKLSKKTKKNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 0.62 ± 0.12 μM |
| dbacp07893 | H-57 | IKLSKKTKKNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HCT-116 | Colon Cancer | IC50 = 1.29 ± 0.08 μM |
| dbacp07894 | H-57 | IKLSKKTKKNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HepG-2 | Liver Cancer | IC50 = 2.13 ± 0.07 μM |
| dbacp07895 | H-18 | IKLSKKTKKNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 0.89 ± 0.21 μM |
| dbacp07896 | H-18 | IKLSKKTKKNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HCT-116 | Colon Cancer | IC50 = 1.11 ± 0.21 μM |
| dbacp07897 | H-18 | IKLSKKTKKNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HepG-2 | Liver Cancer | IC50 = 1.61 ± 0.21 μM |
| dbacp07898 | H-21 | IKLSKS5TKKS5LKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 3.26 ± 0.36 μM |
| dbacp07899 | H-21 | IKLSKS5TKKS5LKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HCT-116 | Colon Cancer | IC50 = 3.05 ± 0.21 μM |
| dbacp07900 | H-21 | IKLSKS5TKKS5LKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HepG-2 | Liver Cancer | IC50 = 1.50 ± 0.28 μM |
| dbacp07901 | H-20 | IKLSPS5TKKS5LKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 2.10 ± 0.32 μM |
| dbacp07902 | H-20 | IKLSPS5TKKS5LKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HCT-116 | Colon Cancer | IC50 = 2.63 ± 0.35 μM |
| dbacp07903 | H-20 | IKLSPS5TKKS5LKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HepG-2 | Liver Cancer | IC50 = 4.93 ± 0.53 μM |
| dbacp07904 | H-19 | IKLSKETKKNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 1.00 ± 0.36 μM |
| dbacp07905 | H-19 | IKLSKETKKNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HCT-116 | Colon Cancer | IC50 = 1.78 ± 0.35 μM |
| dbacp07906 | H-19 | IKLSKETKKNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HepG-2 | Liver Cancer | IC50 = 1.64 ± 0.36 μM |
| dbacp07907 | H-17 | IKLSKS5TKKS5LKKVLKGAIKGAIAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 0.96 ± 0.33 μM |
| dbacp07908 | H-17 | IKLSKS5TKKS5LKKVLKGAIKGAIAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HCT-116 | Colon Cancer | IC50 = 1.49 ± 0.45 μM |
| dbacp07909 | H-17 | IKLSKS5TKKS5LKKVLKGAIKGAIAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HepG-2 | Liver Cancer | IC50 = 1.64 ± 0.47 μM |
| dbacp07910 | H-16 | IKLSPS5TKKS5LKKVLKGAIKGAIAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 1.85 ± 0.31 μM |
| dbacp07911 | H-16 | IKLSPS5TKKS5LKKVLKGAIKGAIAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HCT-116 | Colon Cancer | IC50 = 2.65 ± 0.35 μM |
| dbacp07912 | H-16 | IKLSPS5TKKS5LKKVLKGAIKGAIAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HepG-2 | Liver Cancer | IC50 = 3.14 ± 0.46 μM |
| dbacp07913 | H-15 | IKLSKS5TKDS5LKKVLKGAIKGAIAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 2.26 ± 0.24 μM |
| dbacp07914 | H-15 | IKLSKS5TKDS5LKKVLKGAIKGAIAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HCT-116 | Colon Cancer | IC50 = 2.95 ± 0.25 μM |
| dbacp07915 | H-15 | IKLSKS5TKDS5LKKVLKGAIKGAIAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HepG-2 | Liver Cancer | IC50 = 2.20 ± 0.27 μM |
| dbacp07916 | H-10 | IKLSPS5TKDS5LKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 3.59 ± 0.12 μM |
| dbacp07917 | H-10 | IKLSPS5TKDS5LKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HCT-116 | Colon Cancer | IC50 = 3.51 ± 0.37 μM |
| dbacp07918 | H-10 | IKLSPS5TKDS5LKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HepG-2 | Liver Cancer | IC50 = 1.50 ± 0.21 μM |
| dbacp07919 | H-5 | IKLSPETKDNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 7.35 ± 0.22 μM |
| dbacp07920 | H-5 | IKLSPETKDNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HCT-116 | Colon Cancer | IC50 = 4.16 ± 0.21 μM |
| dbacp07921 | H-5 | IKLSPETKDNLKKVLKGS5IKGS5IAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HepG-2 | Liver Cancer | IC50 = 2.82 ± 0.23 μM |
| dbacp07922 | H-2 | IKLSPS5TKDS5LKKVLKGAIKGAIAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | A-549 | Lung Cancer | IC50 = 4.26 ± 0.52 μM |
| dbacp07923 | H-2 | IKLSPS5TKDS5LKKVLKGAIKGAIAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HCT-116 | Colon Cancer | IC50 = 3.54 ± 0.72 μM |
| dbacp07924 | H-2 | IKLSPS5TKDS5LKKVLKGAIKGAIAVAKMV | Synthetic | Cell entry, DNA damage, apoptosis. | MTT assay | HepG-2 | Liver Cancer | IC50 = 1.60 ± 0.24 μM |
| dbacp07934 | LyeTx-I-b | IWLTALKFLGKNLGKLAKQQLAKL | Synthetic | Membrane disruption, necroptosis, limited apoptosis | MTT/Resazurin dye assay | U-87-MG | Brain Tumor | IC50 = 29.20 ± 7.96 µM |
| dbacp07935 | LyeTx-I-b | IWLTALKFLGKNLGKLAKQQLAKL | Synthetic | Membrane disruption, necroptosis, limited apoptosis | MTT/Resazurin dye assay | U-373-MG | Brain Tumor | IC50 = 20.94 ± 5.18 µM |
| dbacp07936 | LyeTx-I-b | IWLTALKFLGKNLGKLAKQQLAKL | Synthetic | Membrane disruption, necroptosis, limited apoptosis | MTT/Resazurin dye assay | SH-SY5Y | Brain Tumor | IC50 = 93.80 ± 2.17 µM |
| dbacp07937 | Pantinin-1 | GILGKLWEGFKSIV | Synthetic | Selective binding, membrane disruption, apoptosis | MTS assay | MDA-MB-231 | Breast Cancer | IC50 = 28.5 ± 1.0 µM |
| dbacp07938 | Pantinin-1 | GILGKLWEGFKSIV | Synthetic | Selective binding, membrane disruption, apoptosis | MTS assay | DU-145 | Prostate Cancer | IC50 = 47.5 ± 2.0 µM |
| dbacp07939 | Pantinin-2 | IFGAIWKGISSLL | Synthetic | Selective binding, membrane disruption, apoptosis | MTS assay | MDA-MB-231 | Breast Cancer | IC50 = 12.5 ± 1.0 µM |
| dbacp07940 | Pantinin-2 | IFGAIWKGISSLL | Synthetic | Selective binding, membrane disruption, apoptosis | MTS assay | DU-145 | Prostate Cancer | IC50 = 16.5 ± 1.0 µM |
| dbacp07941 | Pantinin-3 | FLSTIWNGIKSLL | Synthetic | Selective binding, membrane disruption, apoptosis | MTS assay | MDA-MB-231 | Breast Cancer | IC50 = 13.5 ± 2.0 µM |
| dbacp07942 | Pantinin-3 | FLSTIWNGIKSLL | Synthetic | Selective binding, membrane disruption, apoptosis | MTS assay | DU-145 | Prostate Cancer | IC50 = 17.3 ± 1.0 µM |
| dbacp07947 | IL13Rα2 D1 peptide | GSETWKTIITKN | Synthetic | IL13Rα2 blockade inhibits cancer metastasis | MTT assay | KM12SM | Colorectal Cancer | inhibited IL13-stimulated cell adhesion |
| dbacp07948 | IL13Rα2 D1 peptide | GSETWKTIITKN | Synthetic | IL13Rα2 blockade inhibits cancer metastasis | MTT assay | SW-620 | Colorectal Cancer | inhibited IL13-stimulated cell adhesion |
| dbacp07949 | IL13Rα2 D1 peptide | GSETWKTIITKN | Synthetic | IL13Rα2 blockade inhibits cancer metastasis | MTT assay | U-87 | Brain Cancer | inhibited IL13-stimulated cell adhesion |
| dbacp07950 | IL13Rα2 D1 peptide | GSETWKTIITKN | Synthetic | IL13Rα2 blockade inhibits cancer metastasis | MTT assay | U-118 | Brain Cancer | inhibited IL13-stimulated cell adhesion |
| dbacp07951 | S-24-R2PLx | GIMDTVKNAAKNLAGQLLDKLKCSITAC | Synthetic Analogue of Ranatuerin-2PLx | R2PLx induces caspase-dependent apoptosis | MTT assay | PC-3 | Prostate Cancer | IC50 = 792.60 µM |
| dbacp07952 | S-24-R2PLx | GIMDTVKNAAKNLAGQLLDKLKCSITAC | Synthetic Analogue of Ranatuerin-2PLx | R2PLx induces caspase-dependent apoptosis | MTT assay | H-157 | Lung Cancer | IC50 = 58.18 µM |
| dbacp07953 | S-24-R2PLx | GIMDTVKNAAKNLAGQLLDKLKCSITAC | Synthetic Analogue of Ranatuerin-2PLx | R2PLx induces caspase-dependent apoptosis | MTT assay | MDA-MB-435S | Skin Cancer | IC50 = 179.00 µM |
| dbacp07954 | S-24-R2PLx | GIMDTVKNAAKNLAGQLLDKLKCSITAC | Synthetic Analogue of Ranatuerin-2PLx | R2PLx induces caspase-dependent apoptosis | MTT assay | U-251-MG | Brain Tumor | IC50 = 278.30 µM |
| dbacp07955 | S-24-R2PLx | GIMDTVKNAAKNLAGQLLDKLKCSITAC | Synthetic Analogue of Ranatuerin-2PLx | R2PLx induces caspase-dependent apoptosis | MTT assay | MCF-7 | Breast Cancer | IC50 = 316.90 µM |
| dbacp07956 | DP-2 | GRKKRRQRRRGALWKSLLKNVGKA | Synthetic | DRS-DU-1 induces selective tumor cytotoxicity | MTT assay | H-157 | Lung Cancer | IC50 = 3.21 μM |
| dbacp07957 | DP-2 | GRKKRRQRRRGALWKSLLKNVGKA | Synthetic | DRS-DU-1 induces selective tumor cytotoxicity | MTT assay | PC-3 | Prostate Cancer | IC50 = 6.75 μM |
| dbacp07958 | Compound 2a | Structure in scheme 1 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | MCF-7 | Breast Cancer | IC50 = 31.64 ± 1.30 µM |
| dbacp07959 | Compound 2a | Structure in scheme 1 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 20.37 ± 1.36 µM |
| dbacp07960 | Compound 2b | Structure in scheme 1 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | MCF-7 | Breast Cancer | IC50 = 32.58 ± 1.50 µM |
| dbacp07961 | Compound 2b | Structure in scheme 1 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 15.80 ± 1.66 µM |
| dbacp07962 | Compound 2c | Structure in scheme 1 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 35.52 ± 1.83 µM |
| dbacp07963 | Compound 3a | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 26.01 ± 2.35 µM |
| dbacp07964 | Compound 3b | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | MCF-7 | Breast Cancer | IC50 = 25.33 ± 1.18 µM |
| dbacp07965 | Compound 3b | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 13.54 ± 1.45 µM |
| dbacp07966 | Compound 3c | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | MCF-7 | Breast Cancer | IC50 = 29.55 ± 2.06 µM |
| dbacp07967 | Compound 3c | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 26.64 ± 1.85 µM |
| dbacp07968 | Compound 4a | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 11.59 ± 2.70 µM |
| dbacp07969 | Compound 4b | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | MCF-7 | Breast Cancer | IC50 = 10.45 ± 1.33 µM |
| dbacp07970 | Compound 4b | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 10.25 ± 2.20 µM |
| dbacp07971 | Compound 4c | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | MCF-7 | Breast Cancer | IC50 = 29.15 ± 1.39 µM |
| dbacp07972 | Compound 4c | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 18.84 ± 1.47 µM |
| dbacp07973 | Compound 5a | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | MCF-7 | Breast Cancer | IC50 = 12.67 ± 2.40 µM |
| dbacp07974 | Compound 5a | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 11.19 ± 1.95 µM |
| dbacp07975 | Compound 5b | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | MCF-7 | Breast Cancer | IC50 = 11.32 ± 1.15 µM |
| dbacp07976 | Compound 5b | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 10.09 ± 2.05 µM |
| dbacp07977 | Compound 5c | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | MCF-7 | Breast Cancer | IC50 = 9.41 ± 1.25 µM |
| dbacp07978 | Compound 5c | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 7.53 ± 1.33 µM |
| dbacp07979 | Compound 6a | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | MCF-7 | Breast Cancer | IC50 = 11.83 ± 1.62 µM |
| dbacp07980 | Compound 6a | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 12.44 ± 1.3 µM |
| dbacp07981 | Compound 6b | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | MCF-7 | Breast Cancer | IC50 = 10.87 ± 1.10 µM |
| dbacp07982 | Compound 6b | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 11.53 ± 1.70 µM |
| dbacp07983 | Compound 6c | Structure in scheme 2 | Synthetic | 5c inhibits cancer via kinase blockade | Not Available | HepG-2 | Liver Cancer | IC50 = 12.07 ± 1.68 µM |
| dbacp07984 | SOR-C13 | KEFLHPSKVDLPR | Synthetic | TRPV6 inhibition suppresses ovarian tumors | IP | SKOV-3 | Ovarian Cancer | Effectively inhibited the growth of tumor |
| dbacp07986 | SmacN7-Arg8 fused peptide P4 | Ahx-AVPIAQK(KRRRRRRRRRE) | Synthetic | Apoptosis inducing | Cell Titer Blue Cell Viability assay | U-266 | Skin Cancer | Cell viability < 50% at 50 μM |
| dbacp07987 | SmacN7-Arg8 fused peptide P5 | Ahx-(KAVPIAQKE)RRRRRRRR | Synthetic | Apoptosis inducing | Cell Titer Blue Cell Viability assay | U-266 | Skin Cancer | Cell viability < 50% at 50 μM |
| dbacp07988 | SmacN7-Arg8 fused peptide P7 | Ahx-(KAVPIAQKE)GG(KRRRRRRRRE) | Synthetic | Apoptosis inducing | Cell Titer Blue Cell Viability assay | U-266 | Skin Cancer | Cell viability < 50% at 50 μM |
| dbacp07993 | [G10a]SHa | FLSGIVGMLaKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | MCF-7 | Breast Cancer | IC50 = 16.2 ± 2.2 µM |
| dbacp07994 | [G10a]SHa | FLSGIVGMLaKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | HeLa | Cervical Cancer | IC50 = 22.7 ± 0.86 µM |
| dbacp07995 | [G10a]SHa | FLSGIVGMLaKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | NCI-H-460 | Lung Cancer | IC50 =24.3 ± 0.8 µM |
| dbacp07996 | [G10a]SHa-BCTP | FLSGIVGMLaKLFLFKQYAELW | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | MCF-7 | Breast Cancer | IC50 = 26.85 ± 1.85 µM |
| dbacp07997 | [G10a]SHa-BCTP | FLSGIVGMLaKLFLFKQYAELW | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | HeLa | Cervical Cancer | IC50 >100 µM |
| dbacp07998 | [G10a]SHa-BCTP | FLSGIVGMLaKLFLFKQYAELW | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | NCI-H-460 | Lung Cancer | IC50 >100 µM |
| dbacp07999 | [G4a]SHa | FLSaIVGMLGKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | MCF-7 | Breast Cancer | IC50 = 17.9 ± 1.1 µM |
| dbacp08000 | [G4a]SHa | FLSaIVGMLGKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | HeLa | Cervical Cancer | IC50 >100 µM |
| dbacp08001 | [G4a]SHa | FLSaIVGMLGKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | NCI-H-460 | Lung Cancer | IC50 >100 µM |
| dbacp08002 | [G7a]SHa | FLSGIVaMLGKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | MCF-7 | Breast Cancer | IC50 =22.4 ± 2.2 µM |
| dbacp08003 | [G7a]SHa | FLSGIVaMLGKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | HeLa | Cervical Cancer | IC50 >100 µM |
| dbacp08004 | [G7a]SHa | FLSGIVaMLGKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | NCI-H-460 | Lung Cancer | IC50 >100 µM |
| dbacp08005 | [G4,7a]SHa | FLSaIVaMLGKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | MCF-7 | Breast Cancer | IC50 = 29.5 ± 6.03 µM |
| dbacp08006 | [G4,7a]SHa | FLSaIVaMLGKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | HeLa | Cervical Cancer | IC50 >100 µM |
| dbacp08007 | [G4,7a]SHa | FLSaIVaMLGKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | NCI-H-460 | Lung Cancer | IC50 = 37.3 ± 3.5 µM |
| dbacp08008 | [G4,7,10a]SHa | FLSaIVaMLaKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | MCF-7 | Breast Cancer | IC50 = 26.33 ± 5.8 µM |
| dbacp08009 | [G4,7,10a]SHa | FLSaIVaMLaKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | HeLa | Cervical Cancer | IC50 >100 µM |
| dbacp08010 | [G4,7,10a]SHa | FLSaIVaMLaKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | NCI-H-460 | Lung Cancer | IC50 >100 µM |
| dbacp08011 | [G7,10a]SHa | FLSGIVaMLaKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | MCF-7 | Breast Cancer | IC50 = 21.3 ± 1.13 µM |
| dbacp08012 | [G7,10a]SHa | FLSGIVaMLaKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | HeLa | Cervical Cancer | IC50 >100 µM |
| dbacp08013 | [G7,10a]SHa | FLSGIVaMLaKLF | Synthetic analogue of Temporin-1SHa | Enhanced cationicity/hydrophobicity increases cytotoxicity | MTT assay | NCI-H-460 | Lung Cancer | IC50 >100 µM |
| dbacp08014 | Ec-LDP-hBD1 | MANCVVGYIGERCQYRDLKWWELRGGGGSGGGGSAPAFSVSPASGLSDGQSVSVSVSGAAAGETYYIAQCAPVGGQDACNPATATSFTTDASGAASFSFVVRKSYTGSTPEGTPVGSVDCATAACNLGAGNSGLDLGHVALTFGGGGGSGGGGSDHYNCVSSGGQCLYSACPIFTKIQGTCYRGKAKCCKLEHHHHHH | Synthetic | EGFR-targeted defensin induces mitochondrial apoptosis | CCK-8 assay | A-431 | Skin Cancer | IC50 = 1.8 μM |
| dbacp08015 | Ec-LDP-hBD1 | MANCVVGYIGERCQYRDLKWWELRGGGGSGGGGSAPAFSVSPASGLSDGQSVSVSVSGAAAGETYYIAQCAPVGGQDACNPATATSFTTDASGAASFSFVVRKSYTGSTPEGTPVGSVDCATAACNLGAGNSGLDLGHVALTFGGGGGSGGGGSDHYNCVSSGGQCLYSACPIFTKIQGTCYRGKAKCCKLEHHHHHH | Synthetic | EGFR-targeted defensin induces mitochondrial apoptosis | CCK-8 assay | A-549 | Lung Cancer | IC50 = 11.9 μM |
| dbacp08016 | Ec-LDP-hBD1 | MANCVVGYIGERCQYRDLKWWELRGGGGSGGGGSAPAFSVSPASGLSDGQSVSVSVSGAAAGETYYIAQCAPVGGQDACNPATATSFTTDASGAASFSFVVRKSYTGSTPEGTPVGSVDCATAACNLGAGNSGLDLGHVALTFGGGGGSGGGGSDHYNCVSSGGQCLYSACPIFTKIQGTCYRGKAKCCKLEHHHHHH | Synthetic | EGFR-targeted defensin induces mitochondrial apoptosis | CCK-8 assay | H-460 | Lung Cancer | IC50 = 5.19 μM |
| dbacp08017 | Ec-LDP-hBD1 | MANCVVGYIGERCQYRDLKWWELRGGGGSGGGGSAPAFSVSPASGLSDGQSVSVSVSGAAAGETYYIAQCAPVGGQDACNPATATSFTTDASGAASFSFVVRKSYTGSTPEGTPVGSVDCATAACNLGAGNSGLDLGHVALTFGGGGGSGGGGSDHYNCVSSGGQCLYSACPIFTKIQGTCYRGKAKCCKLEHHHHHH | Synthetic | EGFR-targeted defensin induces mitochondrial apoptosis | CCK-8 assay | PG-BE1 | Lung Cancer | IC50 = 31.3 μM |
| dbacp08045 | R11-NLS-pep8 | RRRRRRRRRRRIKKKRKWEASALVCIRLVTSSKPRTVa | NKp44 derived synthetic peptide | NKp44-pep8 inhibits PCNA function | PrestoBlue assay | B-16 | Skin Cancer | ED50 = 7.1 μM |
| dbacp08046 | R11-NLS-pep8 | RRRRRRRRRRRIKKKRKWEASALVCIRLVTSSKPRTVa | NKp44 derived synthetic peptide | NKp44-pep8 inhibits PCNA function | PrestoBlue assay | PANC-1 | Pancreatic Cancer | ED50 = 7.8 μM |
| dbacp08047 | R11-NLS-pep8 | RRRRRRRRRRRIKKKRKWEASALVCIRLVTSSKPRTVa | NKp44 derived synthetic peptide | NKp44-pep8 inhibits PCNA function | PrestoBlue assay | HepG-2 | Liver Cancer | ED50 = 5.9 μM |
| dbacp08048 | R11-NLS-pep8 | RRRRRRRRRRRIKKKRKWEASALVCIRLVTSSKPRTVa | NKp44 derived synthetic peptide | NKp44-pep8 inhibits PCNA function | PrestoBlue assay | MDA-MD-231 | Breast Cancer | ED50 = 5.6 μM |
| dbacp08049 | Temporin-1Ga | SILPTIVSFLSKVF | Synthetic | Temporin-1OLa disrupts bacterial membranes | MTS assay | 4T1 | Breast Cancer | LC50 = 20 μM |
| dbacp08050 | Temporin-CPa | IPPFIKKVLTTVF | Synthetic | Temporin-1OLa disrupts bacterial membranes | MTS assay | 4T1 | Breast Cancer | LC50 = 80 μM |
| dbacp08051 | MEL-Pep | GIGAVLKKLTTGLKALISWIKRKRQQ | Synthetic analog of Melittin | MEL-pep disrupts membrane, inhibits P-gp | CCK-8 assay | BEL-7402/5-FU | Liver Cancer | IC50 = 4.36 μM |
| dbacp08055 | L-FP21-PEG-PEI/pGRO-α | YTRDLVYGDPARPGIQGTGTF | Synthetic | D-FP21 delivers gene, inhibits proliferation | CCK-8 assay | HO-8910 | Ovarian Cancer | IC50 = 23.4 μg/mL |
| dbacp08056 | D-FP21-PEG-PEI/pGRO-α | ytrdlvygdparpgiqgtgtf | Synthetic | D-FP21 delivers gene, inhibits proliferation | CCK-8 assay | HO-8910 | Ovarian Cancer | IC50 = 21.6 μg/mL |
| dbacp08057 | TAK-448 | ywNTF(AzGly)R(Me)W | Synthetic | TAK-448 reduces testosterone, inhibits tumor | Given i.h. | VCaP | Prostate Cancer | Had greater anti-tumor effects in VCaP xenograft model |
| dbacp08063 | E5 | GGRSFFLLRRIQGCRFRNTVDD | Synthetic | E5 inhibits CXCR4–CXCL12 signaling | CCK-8 assay | 4T1 | Breast Cancer | 49% cell viability at 100 μM |
| dbacp08068 | temporin-PEa | FLYIVAKLLSGLL | Synthetic analog of Temporin-PE | Modulates membrane interactions | MTT assay | NCI-H-157 | Lung Cancer | IC50 = 3.398 μM |
| dbacp08069 | temporin-PEa | FLYIVAKLLSGLL | Synthetic analog of Temporin-PE | Modulates membrane interactions | MTT assay | U251-MG | Brain Tumor | IC50 = 3.520 μM |
| dbacp08070 | temporin-PEa | FLYIVAKLLSGLL | Synthetic analog of Temporin-PE | Modulates membrane interactions | MTT assay | PC-3 | Prostate Cancer | IC50 = 27.62 μM |
| dbacp08071 | temporin-PEa | FLYIVAKLLSGLL | Synthetic analog of Temporin-PE | Modulates membrane interactions | MTT assay | MDA-MB-435S | Skin Cancer | IC50 = 9.864 μM |
| dbacp08072 | temporin-PEb | FLPIVAKLLSGLLGRKKRRQRRR | Synthetic analog of Temporin-PE | Modulates membrane interactions | MTT assay | NCI-H-157 | Lung Cancer | IC50 = 3.464 μM |
| dbacp08073 | temporin-PEb | FLPIVAKLLSGLLGRKKRRQRRR | Synthetic analog of Temporin-PE | Modulates membrane interactions | MTT assay | U251-MG | Brain Tumor | IC50 = 3.087 μM |
| dbacp08074 | temporin-PEb | FLPIVAKLLSGLLGRKKRRQRRR | Synthetic analog of Temporin-PE | Modulates membrane interactions | MTT assay | PC-3 | Prostate Cancer | IC50 = 3.051 μM |
| dbacp08075 | temporin-PEb | FLPIVAKLLSGLLGRKKRRQRRR | Synthetic analog of Temporin-PE | Modulates membrane interactions | MTT assay | MDA-MB-435S | Skin Cancer | IC50 = 3.483 μM |
| dbacp08081 | Peptide 3a | YD | Synthetic | Inhibit COX-2 enzyme | MTT assay | MCF-7 | Breast Cancer | IC50 = 17.5 ± 0.04 µM |
| dbacp08082 | Peptide 3a | YD | Synthetic | Inhibit COX-2 enzyme | MTT assay | HepG-2 | Liver Cancer | IC50 = 4.8 ± 0.12 µM |
| dbacp08083 | Peptide 3a | YD | Synthetic | Inhibit COX-2 enzyme | MTT assay | A-549 | Lung Cancer | IC50 = 5.7 ± 0.04 µM |
| dbacp08084 | Peptide 3b | YD | Synthetic | Inhibit COX-2 enzyme | MTT assay | HepG-2 | Liver Cancer | IC50 = 62.3 ± 0.02 µM |
| dbacp08085 | Peptide 3b | YD | Synthetic | Inhibit COX-2 enzyme | MTT assay | A-549 | Lung Cancer | IC50 = 5.8 ± 0.02 µM |
| dbacp08112 | FR-15 | FRRFFKWFRRFFKFF | Synthetic | Proline-substituted AMP triggers mitochondrial apoptosis | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 3.15 μM |
| dbacp08113 | FR-15 | FRRFFKWFRRFFKFF | Synthetic | Proline-substituted AMP triggers mitochondrial apoptosis | MTT assay | HeLa | Cervical Cancer | IC50 = 4.9 μM |
| dbacp08114 | FR-15 | FRRFFKWFRRFFKFF | Synthetic | Proline-substituted AMP triggers mitochondrial apoptosis | MTT assay | DLD-1 | Colon Cancer | IC50 = 6.7 μM |
| dbacp08115 | FR-15 | FRRFFKWFRRFFKFF | Synthetic | Proline-substituted AMP triggers mitochondrial apoptosis | MTT assay | HepG-2 | Liver Cancer | IC50 = 2.5 μM |
| dbacp08143 | MccJ25-18-4 | GGAGHVPEYFVGIGTPISFYG-WxEAAYQrFL | Synthetic | Apoptosis inducing | MTT assay | MCF-7 | Breast Cancer | IC50 = 14.2 ± 1.5 μM |
| dbacp08144 | MccJ25-18-4 | GGAGHVPEYFVGIGTPISFYG-WxEAAYQrFL | Synthetic | Apoptosis inducing | MTT assay | MDA-MB-435 | Breast Cancer | IC50 = 20.0 ± 0.5 μM |
| dbacp08145 | MccJ25-18-4 | GGAGHVPEYFVGIGTPISFYG-WxEAAYQrFL | Synthetic | Apoptosis inducing | MTT assay | MDA-MB-435-MDR | Breast Cancer | IC50 = 25.0 ± 0.5 μM |
| dbacp08146 | LfcinB-P13 | KCRRWLKRMKKLG | Synthetic analog of LFcinB | LfcinB-P13 induces liver cancer apoptosis | MTT assay | SMMC-7721 | Liver Cancer | IC50 = 41.8 µg/ml |
| dbacp08150 | CIGB-552 | HARIKpTFRRlKWKYKGKFW | Synthetic | Not Available | Sulforhodamine B assay | MCF-7 | Breast Cancer | IC50 = 379.1 ± 8.6 µM |
| dbacp08151 | ZXR-2 | FKIGGFIKKLWRSLLA | Synthetic | Ile/Leu residues crucially mediate cytolysis | LDH leakage assay | HeLa | Cervical Cancer | 40% LDH release at 32 μM |
| dbacp08152 | IL-1 | FKAGGFIKKLWRSLLA | Synthetic | Ile/Leu residues crucially mediate cytolysis | MTT assay | HeLa | Cervical Cancer | IC50 = 73.9 ± 13.6 μM |
| dbacp08153 | IL-1 | FKAGGFIKKLWRSLLA | Synthetic | Ile/Leu residues crucially mediate cytolysis | MTT assay | PC-3 | Prostate Cancer | IC50 = 58.4 ± 13.7 μM |
| dbacp08154 | IL-1 | FKAGGFIKKLWRSLLA | Synthetic | Ile/Leu residues crucially mediate cytolysis | LDH leakage assay | HeLa | Cervical Cancer | 30% LDH release at 32 μM |
| dbacp08155 | IL-2 | FKIGGFAKKLWRSLLA | Synthetic | Ile/Leu residues crucially mediate cytolysis | MTT assay | HeLa | Cervical Cancer | IC50 = 52.0 ± 5.8 μM |
| dbacp08156 | IL-2 | FKIGGFAKKLWRSLLA | Synthetic | Ile/Leu residues crucially mediate cytolysis | MTT assay | PC-3 | Prostate Cancer | IC50 = 43.6 ± 7.9 μM |
| dbacp08157 | IL-2 | FKIGGFAKKLWRSLLA | Synthetic | Ile/Leu residues crucially mediate cytolysis | LDH leakage assay | HeLa | Cervical Cancer | 30% LDH release at 32 μM |
| dbacp08158 | IL-3 | FKIGGFIKKAWRSLLA | Synthetic | Ile/Leu residues crucially mediate cytolysis | MTT assay | HeLa | Cervical Cancer | IC50 = 93.5 ± 19.4 μM |
| dbacp08159 | IL-3 | FKIGGFIKKAWRSLLA | Synthetic | Ile/Leu residues crucially mediate cytolysis | MTT assay | PC-3 | Prostate Cancer | IC50 = 74.9 ± 13.3 μM |
| dbacp08160 | IL-3 | FKIGGFIKKAWRSLLA | Synthetic | Ile/Leu residues crucially mediate cytolysis | LDH leakage assay | HeLa | Cervical Cancer | 35% LDH release at 32 μM |
| dbacp08161 | IL-4 | FKIGGFIKKLWRSALA | Synthetic | Ile/Leu residues crucially mediate cytolysis | MTT assay | HeLa | Cervical Cancer | IC50 = 54.4 ± 3.0 μM |
| dbacp08162 | IL-4 | FKIGGFIKKLWRSALA | Synthetic | Ile/Leu residues crucially mediate cytolysis | MTT assay | PC-3 | Prostate Cancer | IC50 = 35.5 ± 3.9 μM |
| dbacp08163 | IL-4 | FKIGGFIKKLWRSALA | Synthetic | Ile/Leu residues crucially mediate cytolysis | LDH leakage assay | HeLa | Cervical Cancer | 28% LDH release at 32 μM |
| dbacp08164 | IL-5 | FKIGGFIKKLWRSLAA | Synthetic | Ile/Leu residues crucially mediate cytolysis | MTT assay | HeLa | Cervical Cancer | IC50 = 28.0 ± 4.6 μM |
| dbacp08165 | IL-5 | FKIGGFIKKLWRSLAA | Synthetic | Ile/Leu residues crucially mediate cytolysis | MTT assay | PC-3 | Prostate Cancer | IC50 = 22.0 ± 2.6 μM |
| dbacp08166 | IL-5 | FKIGGFIKKLWRSLAA | Synthetic | Ile/Leu residues crucially mediate cytolysis | LDH leakage assay | HeLa | Cervical Cancer | 35% LDH release at 32 μM |
| dbacp08169 | Peptide - 1 | GF(A6c)G(A6c)KK(A6c)G(A6c)F(A6c)G(A6c)GKK(A6c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | CPFAC-1 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08170 | Peptide - 1 | GF(A6c)G(A6c)KK(A6c)G(A6c)F(A6c)G(A6c)GKK(A6c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | MCF-7 | Breast Cancer | IC50 = 6.2 µM |
| dbacp08171 | Peptide - 1 | GF(A6c)G(A6c)KK(A6c)G(A6c)F(A6c)G(A6c)GKK(A6c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | IGROV-1 | Ovarian Cancer | IC50 > 7.5 µM |
| dbacp08172 | Peptide - 1 | GF(A6c)G(A6c)KK(A6c)G(A6c)F(A6c)G(A6c)GKK(A6c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | COLO-205 | Colon Cancer | IC50 = 5.4 µM |
| dbacp08173 | Peptide - 1 | GF(A6c)G(A6c)KK(A6c)G(A6c)F(A6c)G(A6c)GKK(A6c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | DLD-1 | Colon Cancer | IC50 > 7.5 µM |
| dbacp08174 | Peptide - 1 | GF(A6c)G(A6c)KK(A6c)G(A6c)F(A6c)G(A6c)GKK(A6c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | UACC-62 | Skin Cancer | IC50 = 2.6 µM |
| dbacp08175 | Peptide - 1 | GF(A6c)G(A6c)KK(A6c)G(A6c)F(A6c)G(A6c)GKK(A6c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | MiaPaCa.2 | Pancreatic Cancer | IC50 = 7.3 µM |
| dbacp08176 | Peptide - 1 | GF(A6c)G(A6c)KK(A6c)G(A6c)F(A6c)G(A6c)GKK(A6c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | A-498 | Renal Cancer | IC50 = 3.0 µM |
| dbacp08177 | Peptide - 1 | GF(A6c)G(A6c)KK(A6c)G(A6c)F(A6c)G(A6c)GKK(A6c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | PC-3 | Prostate Cancer | Not Available |
| dbacp08178 | Peptide - 1 | GF(A6c)G(A6c)KK(A6c)G(A6c)F(A6c)G(A6c)GKK(A6c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | A-549 | Lung Cancer | Not Available |
| dbacp08179 | Peptide - 1 | GF(A6c)G(A6c)KK(A6c)G(A6c)F(A6c)G(A6c)GKK(A6c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | NCI-H69 | Lung Cancer | Not Available |
| dbacp08180 | Peptide - 1 | GF(A6c)G(A6c)KK(A6c)G(A6c)F(A6c)G(A6c)GKK(A6c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | RL | Lymphoma Cancer | Not Available |
| dbacp08181 | Peptide - 2 | GF(A6c)G(A6c)R(A6c)G(A6c)F(A6c)G(A6c)GR(A6c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | CPFAC-1 | Pancreatic Cancer | IC50 = 2.6 µM |
| dbacp08182 | Peptide - 2 | GF(A6c)G(A6c)R(A6c)G(A6c)F(A6c)G(A6c)GR(A6c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | MCF-7 | Breast Cancer | IC50 = 7.0 µM |
| dbacp08183 | Peptide - 2 | GF(A6c)G(A6c)R(A6c)G(A6c)F(A6c)G(A6c)GR(A6c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | IGROV-1 | Ovarian Cancer | IC50 = 6.0 µM |
| dbacp08184 | Peptide - 2 | GF(A6c)G(A6c)R(A6c)G(A6c)F(A6c)G(A6c)GR(A6c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | COLO-205 | Colon Cancer | IC50 = 6.6 µM |
| dbacp08185 | Peptide - 2 | GF(A6c)G(A6c)R(A6c)G(A6c)F(A6c)G(A6c)GR(A6c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | DLD-1 | Colon Cancer | IC50 = 6.4 µM |
| dbacp08186 | Peptide - 2 | GF(A6c)G(A6c)R(A6c)G(A6c)F(A6c)G(A6c)GR(A6c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | UACC-62 | Skin Cancer | IC50 = 6.4 µM |
| dbacp08187 | Peptide - 2 | GF(A6c)G(A6c)R(A6c)G(A6c)F(A6c)G(A6c)GR(A6c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | MiaPaCa.2 | Pancreatic Cancer | IC50 = 5.0 µM |
| dbacp08188 | Peptide - 2 | GF(A6c)G(A6c)R(A6c)G(A6c)F(A6c)G(A6c)GR(A6c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | A-498 | Renal Cancer | IC50 = 5.6 µM |
| dbacp08189 | Peptide - 3 | GF(A6c)G(A6c)Orn(A6c)G(A6c)F(A6c)G(A6c)GOrn(A6c)Orn-Orn- Orn- Orn | Synthetic | Not Available | CellTiter-Glo assay | CPFAC-1 | Pancreatic Cancer | IC50 = 5.9 µM |
| dbacp08190 | Peptide - 3 | GF(A6c)G(A6c)Orn(A6c)G(A6c)F(A6c)G(A6c)GOrn(A6c)Orn-Orn- Orn- Orn | Synthetic | Not Available | CellTiter-Glo assay | MCF-7 | Breast Cancer | IC50 = 4.6 µM |
| dbacp08191 | Peptide - 3 | GF(A6c)G(A6c)Orn(A6c)G(A6c)F(A6c)G(A6c)GOrn(A6c)Orn-Orn- Orn- Orn | Synthetic | Not Available | CellTiter-Glo assay | IGROV-1 | Ovarian Cancer | IC50 = 5.4 µM |
| dbacp08192 | Peptide - 3 | GF(A6c)G(A6c)Orn(A6c)G(A6c)F(A6c)G(A6c)GOrn(A6c)Orn-Orn- Orn- Orn | Synthetic | Not Available | CellTiter-Glo assay | COLO-205 | Colon Cancer | IC50 = 3.2 µM |
| dbacp08193 | Peptide - 3 | GF(A6c)G(A6c)Orn(A6c)G(A6c)F(A6c)G(A6c)GOrn(A6c)Orn-Orn- Orn- Orn | Synthetic | Not Available | CellTiter-Glo assay | DLD-1 | Colon Cancer | IC50 = 6.2 µM |
| dbacp08194 | Peptide - 3 | GF(A6c)G(A6c)Orn(A6c)G(A6c)F(A6c)G(A6c)GOrn(A6c)Orn-Orn- Orn- Orn | Synthetic | Not Available | CellTiter-Glo assay | UACC-62 | Skin Cancer | IC50 = 3.1 µM |
| dbacp08195 | Peptide - 3 | GF(A6c)G(A6c)Orn(A6c)G(A6c)F(A6c)G(A6c)GOrn(A6c)Orn-Orn- Orn- Orn | Synthetic | Not Available | CellTiter-Glo assay | MiaPaCa.2 | Pancreatic Cancer | IC50 = 3.6 µM |
| dbacp08196 | Peptide - 3 | GF(A6c)G(A6c)Orn(A6c)G(A6c)F(A6c)G(A6c)GOrn(A6c)Orn-Orn- Orn- Orn | Synthetic | Not Available | CellTiter-Glo assay | A-498 | Renal Cancer | IC50 = 4.7 µM |
| dbacp08197 | Peptide - 4 | GF(A6c)G(A6c)Dab(A6c)G(A6c)F(A6c)G(A6c)GDab(A6c)Dab-Dab-Dab-Dab | Synthetic | Not Available | CellTiter-Glo assay | CPFAC-1 | Pancreatic Cancer | IC50 = 2.7 µM |
| dbacp08198 | Peptide - 4 | GF(A6c)G(A6c)Dab(A6c)G(A6c)F(A6c)G(A6c)GDab(A6c)Dab-Dab-Dab-Dab | Synthetic | Not Available | CellTiter-Glo assay | MCF-7 | Breast Cancer | IC50 = 3.0 µM |
| dbacp08199 | Peptide - 4 | GF(A6c)G(A6c)Dab(A6c)G(A6c)F(A6c)G(A6c)GDab(A6c)Dab-Dab-Dab-Dab | Synthetic | Not Available | CellTiter-Glo assay | IGROV-1 | Ovarian Cancer | IC50 = 2.3 µM |
| dbacp08200 | Peptide - 4 | GF(A6c)G(A6c)Dab(A6c)G(A6c)F(A6c)G(A6c)GDab(A6c)Dab-Dab-Dab-Dab | Synthetic | Not Available | CellTiter-Glo assay | COLO-205 | Colon Cancer | IC50 = 6.4 µM |
| dbacp08201 | Peptide - 4 | GF(A6c)G(A6c)Dab(A6c)G(A6c)F(A6c)G(A6c)GDab(A6c)Dab-Dab-Dab-Dab | Synthetic | Not Available | CellTiter-Glo assay | DLD-1 | Colon Cancer | IC50 = 2.6 µM |
| dbacp08202 | Peptide - 4 | GF(A6c)G(A6c)Dab(A6c)G(A6c)F(A6c)G(A6c)GDab(A6c)Dab-Dab-Dab-Dab | Synthetic | Not Available | CellTiter-Glo assay | UACC-62 | Skin Cancer | IC50 = 1.9 µM |
| dbacp08203 | Peptide - 4 | GF(A6c)G(A6c)Dab(A6c)G(A6c)F(A6c)G(A6c)GDab(A6c)Dab-Dab-Dab-Dab | Synthetic | Not Available | CellTiter-Glo assay | MiaPaCa.2 | Pancreatic Cancer | IC50 = 4.4 µM |
| dbacp08204 | Peptide - 4 | GF(A6c)G(A6c)Dab(A6c)G(A6c)F(A6c)G(A6c)GDab(A6c)Dab-Dab-Dab-Dab | Synthetic | Not Available | CellTiter-Glo assay | A-498 | Renal Cancer | IC50 = 2.1 µM |
| dbacp08205 | Peptide - 6 | GF(A5c)G(A5c)K(A5c)G(A5c)F(A5c)G(A5c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | CPFAC-1 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08206 | Peptide - 6 | GF(A5c)G(A5c)K(A5c)G(A5c)F(A5c)G(A5c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | MCF-7 | Breast Cancer | IC50 > 7.5 µM |
| dbacp08207 | Peptide - 6 | GF(A5c)G(A5c)K(A5c)G(A5c)F(A5c)G(A5c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | IGROV-1 | Ovarian Cancer | IC50 > 7.5 µM |
| dbacp08208 | Peptide - 6 | GF(A5c)G(A5c)K(A5c)G(A5c)F(A5c)G(A5c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | COLO-205 | Colon Cancer | IC50 > 7.5 µM |
| dbacp08209 | Peptide - 6 | GF(A5c)G(A5c)K(A5c)G(A5c)F(A5c)G(A5c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | DLD-1 | Colon Cancer | IC50 > 7.5 µM |
| dbacp08210 | Peptide - 6 | GF(A5c)G(A5c)K(A5c)G(A5c)F(A5c)G(A5c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | UACC-62 | Skin Cancer | IC50 > 7.5 µM |
| dbacp08211 | Peptide - 6 | GF(A5c)G(A5c)K(A5c)G(A5c)F(A5c)G(A5c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | MiaPaCa.2 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08212 | Peptide - 6 | GF(A5c)G(A5c)K(A5c)G(A5c)F(A5c)G(A5c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | A-498 | Renal Cancer | IC50 > 7.5 µM |
| dbacp08213 | Peptide - 7 | GF(A5c)G(A5c)R(A5c)G(A5c)F(A5c)G(A5c)GR(A5c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | CPFAC-1 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08214 | Peptide - 7 | GF(A5c)G(A5c)R(A5c)G(A5c)F(A5c)G(A5c)GR(A5c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | MCF-7 | Breast Cancer | IC50 > 7.5 µM |
| dbacp08215 | Peptide - 7 | GF(A5c)G(A5c)R(A5c)G(A5c)F(A5c)G(A5c)GR(A5c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | IGROV-1 | Ovarian Cancer | IC50 > 7.5 µM |
| dbacp08216 | Peptide - 7 | GF(A5c)G(A5c)R(A5c)G(A5c)F(A5c)G(A5c)GR(A5c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | COLO-205 | Colon Cancer | IC50 > 7.5 µM |
| dbacp08217 | Peptide - 7 | GF(A5c)G(A5c)R(A5c)G(A5c)F(A5c)G(A5c)GR(A5c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | DLD-1 | Colon Cancer | IC50 > 7.5 µM |
| dbacp08218 | Peptide - 7 | GF(A5c)G(A5c)R(A5c)G(A5c)F(A5c)G(A5c)GR(A5c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | UACC-62 | Skin Cancer | IC50 > 7.5 µM |
| dbacp08219 | Peptide - 7 | GF(A5c)G(A5c)R(A5c)G(A5c)F(A5c)G(A5c)GR(A5c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | MiaPaCa.2 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08220 | Peptide - 7 | GF(A5c)G(A5c)R(A5c)G(A5c)F(A5c)G(A5c)GR(A5c)RRRR | Synthetic | Not Available | CellTiter-Glo assay | A-498 | Renal Cancer | IC50 > 7.5 µM |
| dbacp08221 | Peptide - 8 | GF(A6c)G(Tic)K(A6c)G(Tic)F(A6c)G(Tic)GK(Tic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | CPFAC-1 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08222 | Peptide - 8 | GF(A6c)G(Tic)K(A6c)G(Tic)F(A6c)G(Tic)GK(Tic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | MCF-7 | Breast Cancer | IC50 > 7.5 µM |
| dbacp08223 | Peptide - 8 | GF(A6c)G(Tic)K(A6c)G(Tic)F(A6c)G(Tic)GK(Tic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | IGROV-1 | Ovarian Cancer | IC50 > 7.5 µM |
| dbacp08224 | Peptide - 8 | GF(A6c)G(Tic)K(A6c)G(Tic)F(A6c)G(Tic)GK(Tic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | COLO-205 | Colon Cancer | IC50 > 7.5 µM |
| dbacp08225 | Peptide - 8 | GF(A6c)G(Tic)K(A6c)G(Tic)F(A6c)G(Tic)GK(Tic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | DLD-1 | Colon Cancer | IC50 > 7.5 µM |
| dbacp08226 | Peptide - 8 | GF(A6c)G(Tic)K(A6c)G(Tic)F(A6c)G(Tic)GK(Tic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | UACC-62 | Skin Cancer | IC50 > 7.5 µM |
| dbacp08227 | Peptide - 8 | GF(A6c)G(Tic)K(A6c)G(Tic)F(A6c)G(Tic)GK(Tic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | MiaPaCa.2 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08228 | Peptide - 8 | GF(A6c)G(Tic)K(A6c)G(Tic)F(A6c)G(Tic)GK(Tic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | A-498 | Renal Cancer | IC50 > 7.5 µM |
| dbacp08229 | Peptide - 9 | GF(A6c)G(Oic)K(A6c)G(Oic)F(A6c)G(Oic)GK(Oic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | CPFAC-1 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08230 | Peptide - 9 | GF(A6c)G(Oic)K(A6c)G(Oic)F(A6c)G(Oic)GK(Oic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | MCF-7 | Breast Cancer | IC50 > 7.5 µM |
| dbacp08231 | Peptide - 9 | GF(A6c)G(Oic)K(A6c)G(Oic)F(A6c)G(Oic)GK(Oic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | IGROV-1 | Ovarian Cancer | IC50 > 7.5 µM |
| dbacp08232 | Peptide - 9 | GF(A6c)G(Oic)K(A6c)G(Oic)F(A6c)G(Oic)GK(Oic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | COLO-205 | Colon Cancer | IC50 > 7.5 µM |
| dbacp08233 | Peptide - 9 | GF(A6c)G(Oic)K(A6c)G(Oic)F(A6c)G(Oic)GK(Oic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | DLD-1 | Colon Cancer | IC50 > 7.5 µM |
| dbacp08234 | Peptide - 9 | GF(A6c)G(Oic)K(A6c)G(Oic)F(A6c)G(Oic)GK(Oic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | UACC-62 | Skin Cancer | IC50 > 7.5 µM |
| dbacp08235 | Peptide - 9 | GF(A6c)G(Oic)K(A6c)G(Oic)F(A6c)G(Oic)GK(Oic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | MiaPaCa.2 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08236 | Peptide - 9 | GF(A6c)G(Oic)K(A6c)G(Oic)F(A6c)G(Oic)GK(Oic)KKKK | Synthetic | Not Available | CellTiter-Glo assay | A-498 | Renal Cancer | IC50 > 7.5 µM |
| dbacp08237 | Peptide - 10 | GF(A5c)G(A6c)K(A5c)G(A6c)F(A5c)G(A6c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | CPFAC-1 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08238 | Peptide - 10 | GF(A5c)G(A6c)K(A5c)G(A6c)F(A5c)G(A6c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | MCF-7 | Breast Cancer | IC50 > 7.5 µM |
| dbacp08239 | Peptide - 10 | GF(A5c)G(A6c)K(A5c)G(A6c)F(A5c)G(A6c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | IGROV-1 | Ovarian Cancer | IC50 > 7.5 µM |
| dbacp08240 | Peptide - 10 | GF(A5c)G(A6c)K(A5c)G(A6c)F(A5c)G(A6c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | COLO-205 | Colon Cancer | IC50 > 7.5 µM |
| dbacp08241 | Peptide - 10 | GF(A5c)G(A6c)K(A5c)G(A6c)F(A5c)G(A6c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | DLD-1 | Colon Cancer | IC50 > 7.5 µM |
| dbacp08242 | Peptide - 10 | GF(A5c)G(A6c)K(A5c)G(A6c)F(A5c)G(A6c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | UACC-62 | Skin Cancer | IC50 > 7.5 µM |
| dbacp08243 | Peptide - 10 | GF(A5c)G(A6c)K(A5c)G(A6c)F(A5c)G(A6c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | MiaPaCa.2 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08244 | Peptide - 10 | GF(A5c)G(A6c)K(A5c)G(A6c)F(A5c)G(A6c)GK(A5c)KKKK | Synthetic | Not Available | CellTiter-Glo assay | A-498 | Renal Cancer | IC50 > 7.5 µM |
| dbacp08245 | Peptide - 11 | KKKKGF(A6c)G(A6c)K(A6c)G(A6c)F(A6c)G(A6c)GK(A6c) | Synthetic | Not Available | CellTiter-Glo assay | CPFAC-1 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08246 | Peptide - 11 | KKKKGF(A6c)G(A6c)K(A6c)G(A6c)F(A6c)G(A6c)GK(A6c) | Synthetic | Not Available | CellTiter-Glo assay | MCF-7 | Breast Cancer | IC50 = 7.3 µM |
| dbacp08247 | Peptide - 11 | KKKKGF(A6c)G(A6c)K(A6c)G(A6c)F(A6c)G(A6c)GK(A6c) | Synthetic | Not Available | CellTiter-Glo assay | IGROV-1 | Ovarian Cancer | IC50 > 7.5 µM |
| dbacp08248 | Peptide - 11 | KKKKGF(A6c)G(A6c)K(A6c)G(A6c)F(A6c)G(A6c)GK(A6c) | Synthetic | Not Available | CellTiter-Glo assay | COLO-205 | Colon Cancer | IC50 = 6.7 µM |
| dbacp08249 | Peptide - 11 | KKKKGF(A6c)G(A6c)K(A6c)G(A6c)F(A6c)G(A6c)GK(A6c) | Synthetic | Not Available | CellTiter-Glo assay | DLD-1 | Colon Cancer | IC50 > 7.5 µM |
| dbacp08250 | Peptide - 11 | KKKKGF(A6c)G(A6c)K(A6c)G(A6c)F(A6c)G(A6c)GK(A6c) | Synthetic | Not Available | CellTiter-Glo assay | UACC-62 | Skin Cancer | IC50 = 6.4 µM |
| dbacp08251 | Peptide - 11 | KKKKGF(A6c)G(A6c)K(A6c)G(A6c)F(A6c)G(A6c)GK(A6c) | Synthetic | Not Available | CellTiter-Glo assay | MiaPaCa.2 | Pancreatic Cancer | IC50 > 7.5 µM |
| dbacp08252 | Peptide - 11 | KKKKGF(A6c)G(A6c)K(A6c)G(A6c)F(A6c)G(A6c)GK(A6c) | Synthetic | Not Available | CellTiter-Glo assay | A-498 | Renal Cancer | IC50 = 4.2 µM |
| dbacp08266 | ZXR-2 | FKIGGFIKKLWRSLLA | Synthetic | Not Available | MTT assay | HeLa | Cervical Cancer | IC50 = 8.1 ± 1.6 μM |
| dbacp08267 | ZXR-2 | FKIGGFIKKLWRSLLA | Synthetic | Not Available | MTT assay | SACC-83 | Salivary Cancer | IC50 = 9.9 ± 1.7 μM |
| dbacp08268 | ZXR-2 | FKIGGFIKKLWRSLLA | Synthetic | Not Available | MTT assay | HepG-2 | Liver Cancer | IC50 = 7.5 ± 1.2 μM |
| dbacp08269 | ZXR-2 | FKIGGFIKKLWRSLLA | Synthetic | Not Available | MTT assay | Huh-7 | Liver Cancer | IC50 = 8.4 ± 1.1 μM |
| dbacp08270 | ZXR-2 | FKIGGFIKKLWRSLLA | Synthetic | Not Available | MTT assay | PC-3 | Prostate Cancer | IC50 = 14.2 ± 0.5 μM |
| dbacp08271 | ZXR-2 | FKIGGFIKKLWRSLLA | Synthetic | Not Available | MTT assay | 293T | Kidney Cancer | IC50 = 6.3 ± 0.7 μM |
| dbacp08291 | L-Carnosine | Beta-AH | Synthetic | Not Available | MTT assay | A-2780 | Ovarian Cancer | IC50 = 165 mM |
| dbacp08292 | L-Carnosine | Beta-AH | Synthetic | Not Available | MTT assay | OVCAR-3 | Ovarian Cancer | IC50 = 125 mM |
| dbacp08293 | L-Carnosine | Beta-AH | Synthetic | Not Available | MTT assay | SK-OV-3 | Ovarian Cancer | IC50 = 485 mM |
| dbacp08294 | CA4 | CGPCFTTDHNMARKCDECCGGKGRGKCFGPQCLCR | Synthetic | Not Available | MTT assay | U-251 | Brain Tumor | Graph Figure 2 |
| dbacp08295 | CTX-23 | VCMPCFTTDQQMARKCSDCCGGKGRGKCYGPQCLCR | Synthetic | Not Available | MTT assay | U-251 | Brain Tumor | Graph Figure 2 |
| dbacp08297 | DN1 | ILGKIVKKLVSDF | Synthetic | Not Available | MTT assay | HepG-2 | Liver Cancer | 152.17 ± 7.73 μM |
| dbacp08298 | DN4 | ILGKIWKGIVSDF | Synthetic | Not Available | MTT assay | HepG-2 | Liver Cancer | 191.67 ± 12.02 μM |
| dbacp08299 | SKACP003 | FPLPCAYKGTYC | Synthetic | Not Available | MTT assay | MCF-7 | Breast Cancer | IC50 = 193 ± 0.5 µM |
| dbacp08300 | SKACP003 | FPLPCAYKGTYC | Synthetic | Not Available | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 212 ± 0.5 µM |
| dbacp08301 | SKACP003 | FPLPCAYKGTYC | Synthetic | Not Available | MTT assay | MDA-MB-453 | Breast Cancer | IC50 = 156 ± 0.5 µM |
| dbacp08303 | ATRA1-R3W2 - HYD | RRWKRFFKRWKGGVIGVTFPF | Synthetic | Not Available | Cytotoxicity assay | H-358 | Lung Cancer | LD50 ~24.5 μM |
| dbacp08304 | MAD1 | KRWHWWRRHWVVW | Synthetic | Not Available | MTT assay | OVCAR-3 | Ovarian Cancer | IC50 = 14.2 μM |
| dbacp08305 | MAD1 | KRWHWWRRHWVVW | Synthetic | Not Available | MTT assay | A-549 | Lung Cancer | IC50 = 36.2 μM |
| dbacp08306 | MAD1 | KRWHWWRRHWVVW | Synthetic | Not Available | MTT assay | NCI/ADR-RES | Ovarian Cancer | IC50 = 85.6 μM |
| dbacp08307 | DAP1 | LWKRWVGVWRKWL | Synthetic | Not Available | MTT assay | A-549 | Lung Cancer | IC50 = 11.9 μM |
| dbacp08308 | DAP1 | LWKRWVGVWRKWL | Synthetic | Not Available | MTT assay | OVCAR-3 | Ovarian Cancer | IC50 = 8.6 μM |
| dbacp08309 | DAP1 | LWKRWVGVWRKWL | Synthetic | Not Available | MTT assay | NCI/ADR-RES | Ovarian Cancer | IC50 = 14.0 μM |
| dbacp08310 | DAP1 | LWKRWVGVWRKWL | Synthetic | Not Available | MTT assay | T-24 | Bladder Cancer | IC50 = 15.3 μM |
| dbacp08311 | AMP1 | WKWLKKWIK | Synthetic | Not Available | MTT assay | OVCAR-3 | Ovarian Cancer | IC50 = 51.1 μM |
| dbacp08312 | AMP2 | KRWWKWWRR | Synthetic | Not Available | MTT assay | OVCAR-3 | Ovarian Cancer | IC50 = 53.5 μM |
| dbacp08313 | P1C | YKSIEFC | Synthetic | Not Available | Cell Proliferation assay | BXPC-3 | Pancreatic Cancer | ~40% reduction in cell growth at 20 μM |
| dbacp08314 | P1A | YKSIEFC | Synthetic | Not Available | Cell Proliferation assay | BXPC-4 | Pancreatic Cancer | ~50% reduction in cell growth at 20 μM |
| dbacp08315 | P1B | YKSVEFC | Synthetic | Not Available | Cell Proliferation assay | BXPC-5 | Pancreatic Cancer | ~50% reduction in cell growth at 20 μM |
| dbacp08316 | Sample Peptide 1 from US011339203B2 | LTSVVFILICCFHLENIFVLLKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 assay | CAKI-2 | Renal Cancer | Cell Viability = 48% at 25 μM |
| dbacp08317 | Sample Peptide 2 from US011339203B2 | FIGNLALSDLLAGVAYTANLLLKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 assay | CAKI-2 | Renal Cancer | Cell Viability = 0.4% at 25 μM |
| dbacp08318 | Sample Peptide 2 from US011339203B2 | FIGNLALSDLLAGVAYTANLLLKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 assay | PC-3 | Prostate Cancer | Cell Viability = 2.5% at 25 μM |
| dbacp08319 | Sample Peptide 2 from US011339203B2 | FIGNLALSDLLAGVAYTANLLLKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 assay | A-2058 | Skin Cancer | Cell Viability = 0.2% at 25 μM |
| dbacp08320 | Sample Peptide 2 from US011339203B2 | FIGNLALSDLLAGVAYTANLLLKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 assay | NCI-H2444 | Lung Cancer | Cell Viability = 0.6% at 25 μM |
| dbacp08321 | Sample Peptide 2 from US011339203B2 | FIGNLALSDLLAGVAYTANLLLKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 assay | A-549 | Lung Cancer | Cell Viability = 1.4% at 25 μM |
| dbacp08322 | Sample Peptide 3 from US011339203B2 | WFLREGSMFVALSASVFSLLAIKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 assay | CAKI-2 | Renal Cancer | Cell Viability = 45.8% at 25 μM |
| dbacp08323 | Sample Peptide 4 from US011339203B2 | FLLISACWVISLILGGLPIMGWKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 assay | CAKI-2 | Renal Cancer | Cell Viability = 85.6% at 25 μM |
| dbacp08324 | Sample Peptide 5 from US011339203B2 | LYHKHYILECTTVFTLLLLSIVILYCRIKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 assay | CAKI-2 | Renal Cancer | Cell Viability = 77.6% at 25 μM |
| dbacp08325 | Sample Peptide 6 from US011339203B2 | VIIVLSVFIACWAPLFILLLLKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 assay | CAKI-2 | Renal Cancer | Cell Viability = 59.7% at 25 μM |
| dbacp08326 | Sample Peptide 7 from US011339203B2 | LFRAEYFLVLAVLNSGTNPIIKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 assay | CAKI-2 | Renal Cancer | Cell Viability = 66.3% at 25 μM |
| dbacp08327 | Sample Peptide 1 from EP3604345B1 | MQIPQAPWPVVWAVLQLGWRKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 / WST-8 | NCI-H2444 | Lung Cancer | Cell Viability = 6.8% at 25 μM |
| dbacp08328 | Sample Peptide 1 from EP3604345B1 | MQIPQAPWPVVWAVLQLGWRKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 / WST-8 | HCC-827 | Lung Cancer | Cell Viability = 11.8% at 25 μM |
| dbacp08329 | Sample Peptide 1 from EP3604345B1 | MQIPQAPWPVVWAVLQLGWRKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 / WST-8 | NCI-H446 | Lung Cancer | Cell Viability = 0.5% at 25 μM |
| dbacp08330 | Sample Peptide 1 from EP3604345B1 | MQIPQAPWPVVWAVLQLGWRKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 / WST-8 | A-2058 | Skin Cancer | Cell Viability = 6.7% at 25 μM |
| dbacp08331 | Sample Peptide 1 from EP3604345B1 | MQIPQAPWPVVWAVLQLGWRKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 / WST-8 | MDA-MB-231 | Breast Cancer | Cell Viability = 62.3% at 25 μM |
| dbacp08332 | Sample Peptide 2 from EP3604345B1 | MQIPQAPWPVVWAVLQLGWRRKKRRQRRR | Synthetic | Not Available | CCK-8 / WST-8 | NCI-H2444 | Lung Cancer | Cell Viability = 3.6% at 25 μM |
| dbacp08333 | Sample Peptide 2 from EP3604345B1 | MQIPQAPWPVVWAVLQLGWRRKKRRQRRR | Synthetic | Not Available | CCK-8 / WST-8 | HCC-827 | Lung Cancer | Cell Viability = 4.9% at 25 μM |
| dbacp08334 | Sample Peptide 2 from EP3604345B1 | MQIPQAPWPVVWAVLQLGWRRKKRRQRRR | Synthetic | Not Available | CCK-8 / WST-8 | A-549 | Lung Cancer | Cell Viability = 9.1% at 25 μM |
| dbacp08335 | Sample Peptide 3 from EP3604345B1 | MRIFAVFIFMTYWHLLNAKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 / WST-8 | NCI-H2444 | Lung Cancer | Cell Viability = 87.7% at 25 μM |
| dbacp08336 | Sample Peptide 3 from EP3604345B1 | MRIFAVFIFMTYWHLLNAKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 / WST-8 | HCC-827 | Lung Cancer | Cell Viability = 120.6% at 25 μM |
| dbacp08337 | Sample Peptide 3 from EP3604345B1 | MRIFAVFIFMTYWHLLNAKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 / WST-8 | NCI-H446 | Lung Cancer | Cell Viability = 56.7% at 25 μM |
| dbacp08338 | Sample Peptide 3 from EP3604345B1 | MRIFAVFIFMTYWHLLNAKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 / WST-8 | A-2058 | Skin Cancer | Cell Viability = 87.5% at 25 μM |
| dbacp08339 | Sample Peptide 3 from EP3604345B1 | MRIFAVFIFMTYWHLLNAKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 / WST-8 | MDA-MB-231 | Breast Cancer | Cell Viability = 81.7% at 25 μM |
| dbacp08340 | Sample Peptide 4 from EP3604345B1 | PWWWPPVVVQQQMILLIGAARKKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 / WST-8 | HCC-827 | Lung Cancer | Cell Viability = 102.6% at 25 μM |
| dbacp08341 | Sample Peptide 5 from EP3604345B1 | KKRTLRKNDRKKR | Synthetic | Not Available | CCK-8 / WST-8 | HCC-827 | Lung Cancer | Cell Viability = 106.5% at 25 μM |
| dbacp08349 | LPSBD-0 | CQYSVNPKIKRFELYFKGRMW | Synthetic | Not Available | Not Available | THP-1 | Leukemia Cancer | Not Available |
| dbacp08350 | LPSBD-2 | CHYRVKPKIKRFEKYKGRMW | Synthetic | Not Available | Not Available | THP-1 | Leukemia Cancer | Not Available |
| dbacp08351 | Seq ID No. 15 from patent ID US202000079827A1 | LKKWWKKVKGLLGGLLGKVTSVIK | Synthetic | Not Available | Tetrazolium-based assay | HOP-062 | Lung Cancer | Cell viability ~ 50% at 20 μM |
| dbacp08352 | Seq ID No. 15 from patent ID US202000079827A1 | LKKWWKKVKGLLGGLLGKVTSVIK | Synthetic | Not Available | Tetrazolium-based assay | NCI-H460 | Lung Cancer | Cell viability < 25% at 20 μM |
| dbacp08353 | Seq ID No. 15 from patent ID US202000079827A1 | LKKWWKKVKGLLGGLLGKVTSVIK | Synthetic | Not Available | Tetrazolium-based assay | Calu-1 | Lung Cancer | Cell viability < 50% at 20 μM |
| dbacp08354 | Seq ID No. 16 from patent ID US202000079827A1 | LKKWWKKVKGLLGGLLGKVKSVIK | Synthetic | Not Available | Tetrazolium-based assay | HOP-062 | Lung Cancer | Cell viability > 50% at 20 μM |
| dbacp08355 | Seq ID No. 16 from patent ID US202000079827A1 | LKKWWKKVKGLLGGLLGKVKSVIK | Synthetic | Not Available | Tetrazolium-based assay | NCI-H460 | Lung Cancer | Cell viability > 50% at 20 μM |
| dbacp08356 | Seq ID No. 16 from patent ID US202000079827A1 | LKKWWKKVKGLLGGLLGKVKSVIK | Synthetic | Not Available | Tetrazolium-based assay | Calu-1 | Lung Cancer | Cell viability > 50% at 20 μM |
| dbacp08357 | Seq ID No. 17 from patent ID US202000079827A1 | LKKWWKKVKGLLGGLLGKVKKVIK | Synthetic | Not Available | Tetrazolium-based assay | HOP-062 | Lung Cancer | Cell viability > 50% at 20 μM |
| dbacp08358 | Seq ID No. 17 from patent ID US202000079827A1 | LKKWWKKVKGLLGGLLGKVKKVIK | Synthetic | Not Available | Tetrazolium-based assay | NCI-H460 | Lung Cancer | Cell viability > 50% at 20 μM |
| dbacp08359 | Seq ID No. 17 from patent ID US202000079827A1 | LKKWWKKVKGLLGGLLGKVKKVIK | Synthetic | Not Available | Tetrazolium-based assay | Calu-1 | Lung Cancer | Cell viability > 50% at 20 μM |
| dbacp08360 | Seq ID No. 26 from patent ID US202000079827A1 | RRWVRRVRRVWRRVVRVVRRWVRR | Synthetic | Not Available | Tetrazolium-based assay | H-460 | Lung Cancer | Cell viability < 50% at 20 μM |
| dbacp08361 | Seq ID No. 26 from patent ID US202000079827A1 | RRWVRRVRRVWRRVVRVVRRWVRR | Synthetic | Not Available | Tetrazolium-based assay | Calu-1 | Lung Cancer | Cell viability > 50% at 20 μM |
| dbacp08362 | Seq ID No. 34 from patent ID US202000079827A1 | RRWvRRvRRvWRRvvRvvRRWvRR | Synthetic | Not Available | Tetrazolium-based assay | NCI-H460 | Lung Cancer | Cell viability < 25% at 20 μM |
| dbacp08363 | Seq ID No. 34 from patent ID US202000079827A1 | RRWvRRvRRvWRRvvRvvRRWvRR | Synthetic | Not Available | Tetrazolium-based assay | Calu-1 | Lung Cancer | Cell viability > 50% at 20 μM |
| dbacp08364 | IDP-NS10 | AALVVILKKATEYVHS | Synthetic | Not Available | AlamarBlue assay | RG1 | Glioblastoma | EC50 ~ 7 μM |
| dbacp08365 | IDP-NS10 | AALVVILKKATEYVHS | Synthetic | Not Available | AlamarBlue assay | GMB-27 | Glioblastoma | EC50 ~ 7.5 μM |
| dbacp08366 | IDP-NS10 | AALVVILKKATEYVHS | Synthetic | Not Available | AlamarBlue assay | 12015 | Glioblastoma | EC50 ~ 10 μM |
| dbacp08367 | IDP-NS10 | AALVVILKKATEYVHS | Synthetic | Not Available | AlamarBlue assay | 12089 | Glioblastoma | EC50 ~ 4 μM |
| dbacp08368 | IDP-NS10 | AALVVILKKATEYVHS | Synthetic | Not Available | AlamarBlue assay | RG6 | Glioblastoma | EC50 ~ 5 μM |
| dbacp08369 | IDP-NS10 | AALVVILKKATEYVHS | Synthetic | Not Available | AlamarBlue assay | RG4 | Glioblastoma | EC50 ~ 5 μM |
| dbacp08370 | IDP-NS10 | AALVVILKKATEYVHS | Synthetic | Not Available | AlamarBlue assay | RG5 | Glioblastoma | EC50 ~ 7 μM |
| dbacp08371 | IDP-NS10 | AALVVILKKATEYVHS | Synthetic | Not Available | AlamarBlue assay | 12053 | Glioblastoma | EC50 ~ 50 μM |
| dbacp08372 | IDP-NS02 | RQRRNDLRSSFLTLRDH | Synthetic | Not Available | AlamarBlue assay | NCI-H524 | Lung Cancer | EC50 ~ 5 μM |
| dbacp08373 | IDP-NS16 | RQRRNDLRSSFLTLRDH | Synthetic | Not Available | AlamarBlue assay | RG1 | Glioblastoma | EC50 ~ 15 μM |
| dbacp08374 | IDP-NS16 | RQRRNDLRSSFLTLRDH | Synthetic | Not Available | AlamarBlue assay | 12053 | Glioblastoma | EC50 ~ 10 μM |
| dbacp08375 | IDP-Na05 | RRNDLRSSFLTLRDHVP | Synthetic | Not Available | AlamarBlue assay | RG1 | Glioblastoma | EC50 ~ 10 μM |
| dbacp08376 | IDP-NLCa02 | RQIKIWFQNRRMKWKKRQRRNDLRSSFLTLRDHVP | Synthetic | Not Available | AlamarBlue assay | RG1 | Glioblastoma | EC50 ~ 5 μM |
| dbacp08377 | IDP-wtL05 | RKRRNDLRSRFLALRDQ | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | RPMI | Leukemia Cancer | EC50 ~ 10 μM |
| dbacp08378 | IDP-LS05 | RKRRNDLRSRFLALRDQ | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | HL-60 | Leukemia Cancer | EC50 ~ 5 μM |
| dbacp08379 | IDP-LS05 | RKRRNDLRSRFLALRDQ | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | RPMI | Leukemia Cancer | EC50 ~ 6 μM |
| dbacp08380 | IDP-LS13 | RKRRNDLRSRFLALRDQ | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | MCF-7 | Breast Cancer | EC50 ~ 10 μM |
| dbacp08381 | IDP-LS13 | RKRRNDLRSRFLALRDQ | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | HL-60 | Leukemia Cancer | EC50 ~ 7 μM |
| dbacp08382 | IDP-LS13 | RKRRNDLRSRFLALRDQ | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | RPMI | Leukemia Cancer | EC50 ~ 9 μM |
| dbacp08383 | IDP-LS13 | RKRRNDLRSRFLALRDQ | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | U266 | Lymphoma Cancer | EC50 ~ 10 μM |
| dbacp08384 | IDP-LS15 | RKRRNDLRSRFLALRDQ | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | RPMI | Leukemia Cancer | EC50 ~ 7 μM |
| dbacp08385 | IDP-LS15 | RKRRNDLRSRFLALRDQ | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | U266 | Lymphoma Cancer | EC50 ~ 8 μM |
| dbacp08386 | IDP-LS16 | APKVVILSKALEYLQA | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | RPMI | Leukemia Cancer | EC50 ~ 15 μM |
| dbacp08387 | IDP-LS16 | APKVVILSKALEYLQA | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | U266 | Lymphoma Cancer | EC50 ~ 10 μM |
| dbacp08388 | IDP-LS17 | APKVVILSKALEYLQA | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | RPMI | Leukemia Cancer | EC50 ~ 10 μM |
| dbacp08389 | IDP-LS17 | APKVVILSKALEYLQA | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | U266 | Lymphoma Cancer | EC50 ~ 16 μM |
| dbacp08390 | IDP-LLCb01 | RRRRRRRSKAPKVVILSKALEYLQA | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H187 | Lung Cancer | EC50 ~ 5 μM |
| dbacp08391 | IDP-LLCb01 | RRRRRRRSKAPKVVILSKALEYLQA | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H82 | Lung Cancer | EC50 ~ 2.5 μM |
| dbacp08392 | IDP-LLCb01 | RRRRRRRSKAPKVVILSKALEYLQA | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H510A | Lung Cancer | EC50 ~ 5 μM |
| dbacp08393 | IDP-LLCb02 | RQIKWFQNRRMKWKKSKAPKVVILSKALEYLQA | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H187 | Lung Cancer | EC50 ~ 7.5 μM |
| dbacp08394 | IDP-LLCb02 | RQIKWFQNRRMKWKKSKAPKVVILSKALEYLQA | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H82 | Lung Cancer | EC50 ~ 10 μM |
| dbacp08395 | IDP-LLCb02 | RQIKWFQNRRMKWKKSKAPKVVILSKALEYLQA | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H510A | Lung Cancer | EC50 ~ 15 μM |
| dbacp08396 | IDP-Lb01 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H187 | Lung Cancer | EC50 ~ 22.5 μM |
| dbacp08397 | IDP-Lb01 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H82 | Lung Cancer | EC50 ~ 12.5 μM |
| dbacp08398 | IDP-Lb01 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H510A | Lung Cancer | EC50 ~ 22.5 μM |
| dbacp08399 | IDP-Lb02 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H187 | Lung Cancer | EC50 ~ 22.5 μM |
| dbacp08400 | IDP-Lb02 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H82 | Lung Cancer | EC50 ~ 7.5 μM |
| dbacp08401 | IDP-Lb02 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H510A | Lung Cancer | EC50 ~ 15 μM |
| dbacp08402 | IDP-Lb03 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H187 | Lung Cancer | EC50 ~ 22.5 μM |
| dbacp08403 | IDP-Lb03 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H82 | Lung Cancer | EC50 ~ 5 μM |
| dbacp08404 | IDP-Lb03 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H510A | Lung Cancer | EC50 ~ 15 μM |
| dbacp08405 | IDP-Lb04 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H187 | Lung Cancer | EC50 > 30 μM |
| dbacp08406 | IDP-Lb04 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H82 | Lung Cancer | EC50 ~ 12.5 μM |
| dbacp08407 | IDP-Lb04 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H510A | Lung Cancer | EC50 > 30 μM |
| dbacp08408 | IDP-Lb05 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H187 | Lung Cancer | EC50 ~ 10 μM |
| dbacp08409 | IDP-Lb05 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H82 | Lung Cancer | EC50 ~ 7.5 μM |
| dbacp08410 | IDP-Lb05 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H510A | Lung Cancer | EC50 ~ 12.5 μM |
| dbacp08411 | IDP-Lb06 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H187 | Lung Cancer | EC50 ~ 12.5 μM |
| dbacp08412 | IDP-Lb06 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H82 | Lung Cancer | EC50 ~ 7.5 μM |
| dbacp08413 | IDP-Lb06 | SKAPKVVILSKALEYL | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H510A | Lung Cancer | EC50 ~ 12.5 μM |
| dbacp08414 | IDP-La05 | RRNDLRSRFLALRDQVP | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H187 | Lung Cancer | EC50 ~ 22.5 μM |
| dbacp08415 | IDP-La05 | RRNDLRSRFLALRDQVP | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H82 | Lung Cancer | EC50 ~ 15 μM |
| dbacp08416 | IDP-La05 | RRNDLRSRFLALRDQVP | Synthetic | Not Available | MTT/Alamamar-Blue/Hexosaminidase activity test | NCl-H510A | Lung Cancer | EC50 ~ 10 μM |
| dbacp08417 | 5-2C | NYPQRPCRGDKGPDC | Synthetic | Not Available | MTT assay | U343 | Glioblastoma | IC50 = 0.781 μM |
| dbacp08418 | 5-2C | NYPQRPCRGDKGPDC | Synthetic | Not Available | MTT assay | U373MG | Glioblastoma | IC50 = 0.8717 μM |
| dbacp08419 | 5-2C | NYPQRPCRGDKGPDC | Synthetic | Not Available | MTT assay | U251 | Glioblastoma | IC50 = 0.7607 μM |
| dbacp08420 | 5-2C | NYPQRPCRGDKGPDC | Synthetic | Not Available | MTT assay | U87-MG | Glioblastoma | IC50 = 0.9164 μM |
| dbacp08421 | 5-2C | NYPQRPCRGDKGPDC | Synthetic | Not Available | MTT assay | HepG-2 | Liver Cancer | IC50 = 3.064 μM |
| dbacp08422 | 5-2C | NYPQRPCRGDKGPDC | Synthetic | Not Available | MTT assay | Hep3B | Liver Cancer | IC50 = 0.7847 μM |
| dbacp08423 | 5-2C | NYPQRPCRGDKGPDC | Synthetic | Not Available | MTT assay | 293T | Renal Cancer | IC50 = 1.107 μM |
| dbacp08424 | 5-2C | NYPQRPCRGDKGPDC | Synthetic | Not Available | MTT assay | MCF-7 | Breast Cancer | IC50 = 9.74 μM |
| dbacp08425 | 5-2C | NYPQRPCRGDKGPDC | Synthetic | Not Available | MTT assay | MDA-MB-231 | Breast Cancer | IC50 = 0.8061 μM |
| dbacp08426 | 5-2C | NYPQRPCRGDKGPDC | Synthetic | Not Available | MTT assay | HL-60 | Blood Cancer | IC50 = 1.111 μM |
| dbacp08427 | 5-2C | NYPQRPCRGDKGPDC | Synthetic | Not Available | MTT assay | K-562 | Blood Cancer | IC50 = 1.103 μM |
| dbacp08428 | 5-2C | NYPQRPCRGDKGPDC | Synthetic | Not Available | MTT assay | Hel | Blood Cancer | IC50 = 1.055 μM |
| dbacp08429 | hBD3-3 M1 | GKCSTRGRKCMRRKK | Synthetic | Not Available | Cell Proliferation assay | MDA-MB-231 | Breast Cancer | Concentration dependent reduction in colony formation between 100 μM and 200 μM. |
| dbacp08430 | hBD3-3 M1 | GKCSTRGRKCMRRKK | Synthetic | Not Available | Annexin V/ PI staining assay | MDA-MB-231 | Breast Cancer | Inhibition in growth by apoptosis as cells positive for annexin V formed 50% of test group |
| dbacp08431 | hBD3-3 M2 | GKCSTRGRKMCRRKK | Synthetic | Not Available | Cell Proliferation assay | MDA-MB-231 | Breast Cancer | Concentration dependent reduction in colony formation between 100 μM and 200 μM. |
| dbacp08432 | hBD3-3 M2 | GKCSTRGRKMCRRKK | Synthetic | Not Available | Annexin V/ PI staining assay | MDA-MB-231 | Breast Cancer | Inhibition in growth by apoptosis as cells positive for annexin V formed 50% of test group |
| dbacp08433 | Alpha-gliadin peptide p31-43 | LGQQQPFPPQQPY | Synthetic | Not Available | MTT assay | A-549 | Lung Cancer | 9.4% growth inhibition at 70 μg/mL |
| dbacp08434 | Alpha-gliadin peptide p31-43 | LGQQQPFPPQQPY | Synthetic | Not Available | MTT assay | NCI-H1975 | Lung Cancer | 36.3% growth inhibition at 70 μg/mL |
| dbacp08435 | Alpha-gliadin peptide p31-43 | LGQQQPFPPQQPY | Synthetic | Not Available | MTT assay | PANC-1 | Pancreatic Cancer | 26.2% growth inhibition at 70 μg/mL |
| dbacp08436 | Alpha-gliadin peptide p31-43 | LGQQQPFPPQQPY | Synthetic | Not Available | TUNEL assay | A-549 | Lung Cancer | Mean apoptotic rate = 36% at 200 μg/mL |
| dbacp08437 | Balixafortide | ACSAp(Dab)RYCYQKpPYH | Synthetic | Not Available | HUVEC sprouting | Namalwa | Lymphoma | IC50< 10 nM |
| dbacp08438 | Balixafortide | ACSAp(Dab)RYCYQKpPYH | Synthetic | Not Available | HUVEC sprouting | Jurkat | Blood Cancer | IC50< 10 nM |
| dbacp08439 | Balixafortide | ACSAp(Dab)RYCYQKpPYH | Synthetic | Not Available | HUVEC sprouting | MDA-MB-231 | Breast Cancer | IC50< 20 nM |