Assay Detail
Functional
CHEMBL2380108
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Cytotoxicity against human SK-BR-3 cells after 72 hrs by resazurin/resorufin-based fluorescence assay
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | SK-BR-3 |
| Confidence | 1 — Organism |
| Curated By | Autocuration |
Publication
Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 7 | 5.98 | 7.05 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL53463 | DOXORUBICIN | 4.0 | 1 | 7.05 |
| CHEMBL2377825 | — | — | 1 | 6.31 |
| CHEMBL2377823 | — | — | 1 | 5.92 |
| CHEMBL2377820 | — | — | 1 | 5.39 |
| CHEMBL2377685 | — | — | 1 | 5.21 |
| CHEMBL2103840 | DINACICLIB | 3.0 | 1 | - |
| CHEMBL2377821 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL53463 | DOXORUBICIN | IC50 | = | 90.0 | nM | 7.05 |
| CHEMBL2377825 | — | IC50 | = | 490.0 | nM | 6.31 |
| CHEMBL2377823 | — | IC50 | = | 1200.0 | nM | 5.92 |
| CHEMBL2377820 | — | IC50 | = | 4100.0 | nM | 5.39 |
| CHEMBL2377685 | — | IC50 | = | 6100.0 | nM | 5.21 |
| CHEMBL2103840 | DINACICLIB | IC50 | < | 5.0 | nM | - |
| CHEMBL2377821 | — | IC50 | > | 10000.0 | nM | - |