Assay Detail
Binding
CHEMBL862178
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Inhibition of p38alpha
13
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Organism | Homo sapiens |
| Confidence | 9 — Direct single protein target |
| Curated By | Expert |
Publication
Design and synthesis of 2'-anilino-4,4'-bipyridines as selective inhibitors of c-Jun N-terminal kinase-3.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 13 | 6.84 | 7.43 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL203225 | — | — | 1 | 7.43 |
| CHEMBL202676 | — | — | 1 | 7.40 |
| CHEMBL202639 | — | — | 1 | 7.30 |
| CHEMBL202666 | — | — | 1 | 6.79 |
| CHEMBL206466 | — | — | 1 | 6.77 |
| CHEMBL203535 | — | — | 1 | 6.75 |
| CHEMBL205078 | — | — | 1 | 6.70 |
| CHEMBL203059 | — | — | 1 | 6.60 |
| CHEMBL203839 | — | — | 2 | 6.38 |
| CHEMBL383678 | — | — | 1 | - |
| CHEMBL203631 | — | — | 1 | - |
| CHEMBL204757 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL203225 | — | IC50 | = | 37.0 | nM | 7.43 |
| CHEMBL202676 | — | IC50 | = | 40.0 | nM | 7.40 |
| CHEMBL202639 | — | IC50 | = | 50.0 | nM | 7.30 |
| CHEMBL202666 | — | IC50 | = | 162.0 | nM | 6.79 |
| CHEMBL206466 | — | IC50 | = | 171.0 | nM | 6.77 |
| CHEMBL203535 | — | IC50 | = | 180.0 | nM | 6.75 |
| CHEMBL205078 | — | IC50 | = | 199.0 | nM | 6.70 |
| CHEMBL203059 | — | IC50 | = | 251.0 | nM | 6.60 |
| CHEMBL203839 | — | IC50 | = | 421.0 | nM | 6.38 |
| CHEMBL203839 | — | IC50 | = | 581.0 | nM | 6.24 |
| CHEMBL383678 | — | IC50 | - | — | - | |
| CHEMBL203631 | — | IC50 | - | — | - | |
| CHEMBL204757 | — | IC50 | - | — | - |