Assay Detail
Binding
CHEMBL897816
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Inhibition of P38 kinase
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Organism | Homo sapiens |
| Confidence | 0 — Uncurated / Unknown |
| Curated By | Autocuration |
Publication
Pyridinylimidazole inhibitors of Tie2 kinase.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 11 | 5.51 | 7.38 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL10 | SB-203580 | — | 1 | 7.38 |
| CHEMBL17023 | — | — | 1 | 6.52 |
| CHEMBL400840 | — | — | 1 | 6.13 |
| CHEMBL400839 | — | — | 1 | 5.34 |
| CHEMBL237358 | — | — | 1 | 4.80 |
| CHEMBL399410 | — | — | 1 | 4.80 |
| CHEMBL237351 | — | — | 1 | 4.78 |
| CHEMBL237352 | — | — | 1 | 4.30 |
| CHEMBL237565 | — | — | 1 | - |
| CHEMBL237564 | — | — | 1 | - |
| CHEMBL237353 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL10 | SB-203580 | IC50 | = | 42.0 | nM | 7.38 |
| CHEMBL17023 | — | IC50 | = | 300.0 | nM | 6.52 |
| CHEMBL400840 | — | IC50 | = | 741.0 | nM | 6.13 |
| CHEMBL400839 | — | IC50 | = | 4571.0 | nM | 5.34 |
| CHEMBL237358 | — | IC50 | = | 16000.0 | nM | 4.80 |
| CHEMBL399410 | — | IC50 | = | 16000.0 | nM | 4.80 |
| CHEMBL237351 | — | IC50 | = | 16500.0 | nM | 4.78 |
| CHEMBL237352 | — | IC50 | = | 50000.0 | nM | 4.30 |
| CHEMBL237565 | — | IC50 | > | 16000.0 | nM | - |
| CHEMBL237564 | — | IC50 | > | 16000.0 | nM | - |
| CHEMBL237353 | — | IC50 | > | 16000.0 | nM | - |