Assay Detail
Functional
CHEMBL959248
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Cytotoxicity against human LNCAP cells
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | LNCaP |
| Confidence | 1 — Organism |
| Curated By | Autocuration |
Publication
Discovery of 5-pyrrolopyridinyl-2-thiophenecarboxamides as potent AKT kinase inhibitors.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 13 | 6.83 | 7.75 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL523586 | — | — | 1 | 7.75 |
| CHEMBL470597 | — | — | 1 | 7.68 |
| CHEMBL520788 | — | — | 1 | 7.62 |
| CHEMBL498052 | — | — | 1 | 7.41 |
| CHEMBL469590 | — | — | 1 | 7.35 |
| CHEMBL496690 | — | — | 1 | 7.18 |
| CHEMBL482536 | — | — | 1 | 7.11 |
| CHEMBL470598 | — | — | 1 | 6.36 |
| CHEMBL482537 | — | — | 1 | 6.36 |
| CHEMBL524998 | — | — | 1 | 6.14 |
| CHEMBL512135 | — | — | 1 | 6.12 |
| CHEMBL498051 | — | — | 1 | 6.12 |
| CHEMBL513728 | — | — | 1 | 5.57 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL523586 | — | IC50 | = | 18.0 | nM | 7.75 |
| CHEMBL470597 | — | IC50 | = | 21.0 | nM | 7.68 |
| CHEMBL520788 | — | IC50 | = | 24.0 | nM | 7.62 |
| CHEMBL498052 | — | IC50 | = | 39.0 | nM | 7.41 |
| CHEMBL469590 | — | IC50 | = | 45.0 | nM | 7.35 |
| CHEMBL496690 | — | IC50 | = | 66.0 | nM | 7.18 |
| CHEMBL482536 | — | IC50 | = | 78.0 | nM | 7.11 |
| CHEMBL470598 | — | IC50 | = | 440.0 | nM | 6.36 |
| CHEMBL482537 | — | IC50 | = | 440.0 | nM | 6.36 |
| CHEMBL524998 | — | IC50 | = | 720.0 | nM | 6.14 |
| CHEMBL512135 | — | IC50 | = | 750.0 | nM | 6.12 |
| CHEMBL498051 | — | IC50 | = | 750.0 | nM | 6.12 |
| CHEMBL513728 | — | IC50 | = | 2700.0 | nM | 5.57 |