Assay Detail
Functional
CHEMBL959247
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Cytotoxicity against human BT474 cells
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | BT-474 |
| 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 | 6.25 | 7.22 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL520788 | — | — | 1 | 7.22 |
| CHEMBL482536 | — | — | 1 | 7.22 |
| CHEMBL498052 | — | — | 1 | 6.92 |
| CHEMBL469590 | — | — | 1 | 6.70 |
| CHEMBL470597 | — | — | 1 | 6.64 |
| CHEMBL523586 | — | — | 1 | 6.62 |
| CHEMBL496690 | — | — | 1 | 6.30 |
| CHEMBL482537 | — | — | 1 | 5.92 |
| CHEMBL524998 | — | — | 1 | 5.72 |
| CHEMBL498051 | — | — | 1 | 5.64 |
| CHEMBL470598 | — | — | 1 | 5.58 |
| CHEMBL512135 | — | — | 1 | 5.40 |
| CHEMBL513728 | — | — | 1 | 5.35 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL520788 | — | IC50 | = | 60.0 | nM | 7.22 |
| CHEMBL482536 | — | IC50 | = | 60.0 | nM | 7.22 |
| CHEMBL498052 | — | IC50 | = | 120.0 | nM | 6.92 |
| CHEMBL469590 | — | IC50 | = | 200.0 | nM | 6.70 |
| CHEMBL470597 | — | IC50 | = | 230.0 | nM | 6.64 |
| CHEMBL523586 | — | IC50 | = | 240.0 | nM | 6.62 |
| CHEMBL496690 | — | IC50 | = | 500.0 | nM | 6.30 |
| CHEMBL482537 | — | IC50 | = | 1200.0 | nM | 5.92 |
| CHEMBL524998 | — | IC50 | = | 1900.0 | nM | 5.72 |
| CHEMBL498051 | — | IC50 | = | 2300.0 | nM | 5.64 |
| CHEMBL470598 | — | IC50 | = | 2600.0 | nM | 5.58 |
| CHEMBL512135 | — | IC50 | = | 4000.0 | nM | 5.40 |
| CHEMBL513728 | — | IC50 | = | 4500.0 | nM | 5.35 |