Assay Detail
Functional
CHEMBL2185493
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Cytotoxicity against human SKBR3 cells incubated for 72 hrs by MTT assay
34
Total Activities
34
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | SK-BR-3 |
| Confidence | 1 — Organism |
| Curated By | Autocuration |
Publication
Repositioning HIV-1 integrase inhibitors for cancer therapeutics: 1,6-naphthyridine-7-carboxamide as a promising scaffold with drug-like properties.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 34 | 5.50 | 6.00 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL2180582 | — | — | 1 | 6.00 |
| CHEMBL2180577 | — | — | 1 | 6.00 |
| CHEMBL2180574 | — | — | 1 | 6.00 |
| CHEMBL2180576 | — | — | 1 | 6.00 |
| CHEMBL2180575 | — | — | 1 | 6.00 |
| CHEMBL2180581 | — | — | 1 | 6.00 |
| CHEMBL2180567 | — | — | 1 | 5.70 |
| CHEMBL2180584 | — | — | 1 | 5.70 |
| CHEMBL2180246 | — | — | 1 | 5.70 |
| CHEMBL2180249 | — | — | 1 | 5.55 |
| CHEMBL2180578 | — | — | 1 | 5.52 |
| CHEMBL2180583 | — | — | 1 | 5.52 |
| CHEMBL2180579 | — | — | 1 | 5.40 |
| CHEMBL2180247 | — | — | 1 | 5.38 |
| CHEMBL2180561 | — | — | 1 | 5.30 |
| CHEMBL2180568 | — | — | 1 | 5.22 |
| CHEMBL2177139 | — | — | 1 | 5.22 |
| CHEMBL2180562 | — | — | 1 | 5.22 |
| CHEMBL2180565 | — | — | 1 | 5.22 |
| CHEMBL2180245 | — | — | 1 | 5.16 |
| CHEMBL2180560 | — | — | 1 | 5.10 |
| CHEMBL2180559 | — | — | 1 | 5.07 |
| CHEMBL2180563 | — | — | 1 | 5.05 |
| CHEMBL2180570 | — | — | 1 | 5.00 |
| CHEMBL2180573 | — | — | 1 | - |
| CHEMBL2180598 | — | — | 1 | - |
| CHEMBL2180580 | — | — | 1 | - |
| CHEMBL2180558 | — | — | 1 | - |
| CHEMBL2180564 | — | — | 1 | - |
| CHEMBL2180566 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL2180582 | — | IC50 | = | 1000.0 | nM | 6.00 |
| CHEMBL2180581 | — | IC50 | = | 1000.0 | nM | 6.00 |
| CHEMBL2180575 | — | IC50 | = | 1000.0 | nM | 6.00 |
| CHEMBL2180576 | — | IC50 | = | 1000.0 | nM | 6.00 |
| CHEMBL2180574 | — | IC50 | = | 1000.0 | nM | 6.00 |
| CHEMBL2180577 | — | IC50 | = | 1000.0 | nM | 6.00 |
| CHEMBL2180246 | — | IC50 | = | 2000.0 | nM | 5.70 |
| CHEMBL2180584 | — | IC50 | = | 2000.0 | nM | 5.70 |
| CHEMBL2180567 | — | IC50 | = | 2000.0 | nM | 5.70 |
| CHEMBL2180249 | — | IC50 | = | 2800.0 | nM | 5.55 |
| CHEMBL2180578 | — | IC50 | = | 3000.0 | nM | 5.52 |
| CHEMBL2180583 | — | IC50 | = | 3000.0 | nM | 5.52 |
| CHEMBL2180579 | — | IC50 | = | 4000.0 | nM | 5.40 |
| CHEMBL2180247 | — | IC50 | = | 4200.0 | nM | 5.38 |
| CHEMBL2180561 | — | IC50 | = | 5000.0 | nM | 5.30 |
| CHEMBL2177139 | — | IC50 | = | 6000.0 | nM | 5.22 |
| CHEMBL2180562 | — | IC50 | = | 6000.0 | nM | 5.22 |
| CHEMBL2180568 | — | IC50 | = | 6000.0 | nM | 5.22 |
| CHEMBL2180565 | — | IC50 | = | 6000.0 | nM | 5.22 |
| CHEMBL2180245 | — | IC50 | = | 7000.0 | nM | 5.16 |
| CHEMBL2180560 | — | IC50 | = | 8000.0 | nM | 5.10 |
| CHEMBL2180559 | — | IC50 | = | 8500.0 | nM | 5.07 |
| CHEMBL2180563 | — | IC50 | = | 9000.0 | nM | 5.05 |
| CHEMBL2180570 | — | IC50 | = | 10000.0 | nM | 5.00 |
| CHEMBL2180248 | — | IC50 | - | — | - | |
| CHEMBL2180244 | — | IC50 | - | — | - | |
| CHEMBL2180243 | — | IC50 | - | — | - | |
| CHEMBL2180569 | — | IC50 | - | — | - | |
| CHEMBL2180566 | — | IC50 | - | — | - | |
| CHEMBL2180564 | — | IC50 | - | — | - | |
| CHEMBL2180558 | — | IC50 | > | 10000.0 | nM | - |
| CHEMBL2180580 | — | IC50 | > | 10000.0 | nM | - |
| CHEMBL2180598 | — | IC50 | - | — | - | |
| CHEMBL2180573 | — | IC50 | > | 10000.0 | nM | - |