Assay Detail
Functional
CHEMBL4391799
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Cytotoxicity against human MCF7 cells assessed as cell growth inhibition incubated for 72 hrs by MTT assay
25
Total Activities
25
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | MCF7 |
| Confidence | 1 — Organism |
| Curated By | Autocuration |
Publication
Design, synthesis and biological evaluation of novel α-acyloxy carboxamides via Passerini reaction as caspase 3/7 activators.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 25 | 7.24 | 8.30 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL4572642 | — | — | 1 | 8.30 |
| CHEMBL4452355 | — | — | 1 | 8.19 |
| CHEMBL4470597 | — | — | 1 | 8.11 |
| CHEMBL4483079 | — | — | 1 | 8.06 |
| CHEMBL4582711 | — | — | 1 | 8.01 |
| CHEMBL4542198 | — | — | 1 | 7.85 |
| CHEMBL4581075 | — | — | 1 | 7.83 |
| CHEMBL4457138 | — | — | 1 | 7.82 |
| CHEMBL4444346 | — | — | 1 | 7.77 |
| CHEMBL53463 | DOXORUBICIN | 4.0 | 1 | 7.63 |
| CHEMBL4517018 | — | — | 1 | 7.59 |
| CHEMBL4587937 | — | — | 1 | 7.57 |
| CHEMBL4451006 | — | — | 1 | 7.46 |
| CHEMBL4531962 | — | — | 1 | 7.45 |
| CHEMBL4474493 | — | — | 1 | 7.38 |
| CHEMBL4476481 | — | — | 1 | 7.24 |
| CHEMBL4455197 | — | — | 1 | 6.62 |
| CHEMBL4474327 | — | — | 1 | 6.41 |
| CHEMBL4464653 | — | — | 1 | 6.39 |
| CHEMBL4452570 | — | — | 1 | 6.35 |
| CHEMBL4561108 | — | — | 1 | 6.29 |
| CHEMBL3194066 | — | — | 1 | 6.22 |
| CHEMBL4451398 | — | — | 1 | 6.21 |
| CHEMBL4516932 | — | — | 1 | 6.18 |
| CHEMBL4457766 | — | — | 1 | 6.04 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL4572642 | — | IC50 | = | 5.01 | nM | 8.30 |
| CHEMBL4452355 | — | IC50 | = | 6.5 | nM | 8.19 |
| CHEMBL4470597 | — | IC50 | = | 7.7 | nM | 8.11 |
| CHEMBL4483079 | — | IC50 | = | 8.7 | nM | 8.06 |
| CHEMBL4582711 | — | IC50 | = | 9.8 | nM | 8.01 |
| CHEMBL4542198 | — | IC50 | = | 14.1 | nM | 7.85 |
| CHEMBL4581075 | — | IC50 | = | 14.7 | nM | 7.83 |
| CHEMBL4457138 | — | IC50 | = | 15.0 | nM | 7.82 |
| CHEMBL4444346 | — | IC50 | = | 16.9 | nM | 7.77 |
| CHEMBL53463 | DOXORUBICIN | IC50 | = | 23.4 | nM | 7.63 |
| CHEMBL4517018 | — | IC50 | = | 25.4 | nM | 7.59 |
| CHEMBL4587937 | — | IC50 | = | 27.1 | nM | 7.57 |
| CHEMBL4451006 | — | IC50 | = | 34.9 | nM | 7.46 |
| CHEMBL4531962 | — | IC50 | = | 35.4 | nM | 7.45 |
| CHEMBL4474493 | — | IC50 | = | 41.2 | nM | 7.38 |
| CHEMBL4476481 | — | IC50 | = | 57.6 | nM | 7.24 |
| CHEMBL4455197 | — | IC50 | = | 237.0 | nM | 6.62 |
| CHEMBL4474327 | — | IC50 | = | 393.0 | nM | 6.41 |
| CHEMBL4464653 | — | IC50 | = | 403.0 | nM | 6.39 |
| CHEMBL4452570 | — | IC50 | = | 444.0 | nM | 6.35 |
| CHEMBL4561108 | — | IC50 | = | 516.0 | nM | 6.29 |
| CHEMBL3194066 | — | IC50 | = | 597.0 | nM | 6.22 |
| CHEMBL4451398 | — | IC50 | = | 619.0 | nM | 6.21 |
| CHEMBL4516932 | — | IC50 | = | 664.0 | nM | 6.18 |
| CHEMBL4457766 | — | IC50 | = | 903.0 | nM | 6.04 |