Assay Detail
Binding
CHEMBL959246
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Inhibition of AKT3
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Confidence | 8 — Homologous single protein target |
| Curated By | Intermediate |
Target
RAC-gamma serine/threonine-protein kinase (CHEMBL4816) ↗| Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
Publication
Discovery of 5-pyrrolopyridinyl-2-thiophenecarboxamides as potent AKT kinase inhibitors.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 13 | 8.49 | 9.00 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL482536 | — | — | 1 | 9.00 |
| CHEMBL470597 | — | — | 1 | 8.70 |
| CHEMBL524998 | — | — | 1 | 8.70 |
| CHEMBL523586 | — | — | 1 | 8.70 |
| CHEMBL496690 | — | — | 1 | 8.70 |
| CHEMBL520788 | — | — | 1 | 8.70 |
| CHEMBL498052 | — | — | 1 | 8.70 |
| CHEMBL469590 | — | — | 1 | 8.52 |
| CHEMBL470598 | — | — | 1 | 8.52 |
| CHEMBL482537 | — | — | 1 | 8.52 |
| CHEMBL512135 | — | — | 1 | 7.70 |
| CHEMBL513728 | — | — | 1 | 7.40 |
| CHEMBL498051 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL482536 | — | IC50 | = | 1.0 | nM | 9.00 |
| CHEMBL470597 | — | IC50 | = | 2.0 | nM | 8.70 |
| CHEMBL524998 | — | IC50 | = | 2.0 | nM | 8.70 |
| CHEMBL523586 | — | IC50 | = | 2.0 | nM | 8.70 |
| CHEMBL496690 | — | IC50 | = | 2.0 | nM | 8.70 |
| CHEMBL520788 | — | IC50 | = | 2.0 | nM | 8.70 |
| CHEMBL498052 | — | IC50 | = | 2.0 | nM | 8.70 |
| CHEMBL469590 | — | IC50 | = | 3.0 | nM | 8.52 |
| CHEMBL470598 | — | IC50 | = | 3.0 | nM | 8.52 |
| CHEMBL482537 | — | IC50 | = | 3.0 | nM | 8.52 |
| CHEMBL512135 | — | IC50 | = | 20.0 | nM | 7.70 |
| CHEMBL513728 | — | IC50 | = | 40.0 | nM | 7.40 |
| CHEMBL498051 | — | IC50 | - | — | - |