Assay Detail
Functional
CHEMBL862168
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Antiproliferative activity against K562 cells
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | K562 |
| Confidence | 1 — Organism |
| Curated By | Expert |
Publication
Design and synthesis of 3-substituted benzamide derivatives as Bcr-Abl kinase inhibitors.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 12 | 7.91 | 8.40 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL206034 | — | — | 1 | 8.40 |
| CHEMBL205723 | — | — | 1 | 8.40 |
| CHEMBL203343 | — | — | 1 | 8.30 |
| CHEMBL383010 | — | — | 1 | 8.15 |
| CHEMBL383711 | — | — | 1 | 8.05 |
| CHEMBL203071 | — | — | 1 | 8.00 |
| CHEMBL382605 | — | — | 1 | 8.00 |
| CHEMBL383710 | — | — | 1 | 7.96 |
| CHEMBL206834 | BAFETINIB | 2.0 | 1 | 7.96 |
| CHEMBL206319 | — | — | 1 | 7.77 |
| CHEMBL205409 | — | — | 1 | 7.20 |
| CHEMBL941 | IMATINIB | 4.0 | 1 | 6.74 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL206034 | — | IC50 | = | 4.0 | nM | 8.40 |
| CHEMBL205723 | — | IC50 | = | 4.0 | nM | 8.40 |
| CHEMBL203343 | — | IC50 | = | 5.0 | nM | 8.30 |
| CHEMBL383010 | — | IC50 | = | 7.0 | nM | 8.15 |
| CHEMBL383711 | — | IC50 | = | 9.0 | nM | 8.05 |
| CHEMBL203071 | — | IC50 | = | 10.0 | nM | 8.00 |
| CHEMBL382605 | — | IC50 | = | 10.0 | nM | 8.00 |
| CHEMBL383710 | — | IC50 | = | 11.0 | nM | 7.96 |
| CHEMBL206834 | BAFETINIB | IC50 | = | 11.0 | nM | 7.96 |
| CHEMBL206319 | — | IC50 | = | 17.0 | nM | 7.77 |
| CHEMBL205409 | — | IC50 | = | 63.0 | nM | 7.20 |
| CHEMBL941 | IMATINIB | IC50 | = | 182.0 | nM | 6.74 |