Assay Detail
Binding
CHEMBL866013
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Inhibition of JNK2
14
Total Activities
14
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
Discovery of potent, highly selective, and orally bioavailable pyridine carboxamide c-Jun NH2-terminal kinase inhibitors.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 14 | 6.91 | 7.96 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL211584 | — | — | 1 | 7.96 |
| CHEMBL209534 | — | — | 1 | 7.39 |
| CHEMBL377408 | — | — | 1 | 7.28 |
| CHEMBL439323 | — | — | 1 | 7.17 |
| CHEMBL377383 | — | — | 1 | 7.13 |
| CHEMBL424872 | — | — | 1 | 6.92 |
| CHEMBL214212 | — | — | 1 | 6.92 |
| CHEMBL211195 | — | — | 1 | 6.72 |
| CHEMBL211605 | — | — | 1 | 6.21 |
| CHEMBL209397 | — | — | 1 | 5.36 |
| CHEMBL209740 | — | — | 1 | - |
| CHEMBL377991 | — | — | 1 | - |
| CHEMBL378955 | — | — | 1 | - |
| CHEMBL209049 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL211584 | — | IC50 | = | 11.0 | nM | 7.96 |
| CHEMBL209534 | — | IC50 | = | 41.0 | nM | 7.39 |
| CHEMBL377408 | — | IC50 | = | 53.0 | nM | 7.28 |
| CHEMBL439323 | — | IC50 | = | 68.0 | nM | 7.17 |
| CHEMBL377383 | — | IC50 | = | 74.0 | nM | 7.13 |
| CHEMBL424872 | — | IC50 | = | 120.0 | nM | 6.92 |
| CHEMBL214212 | — | IC50 | = | 120.0 | nM | 6.92 |
| CHEMBL211195 | — | IC50 | = | 190.0 | nM | 6.72 |
| CHEMBL211605 | — | IC50 | = | 610.0 | nM | 6.21 |
| CHEMBL209397 | — | IC50 | = | 4400.0 | nM | 5.36 |
| CHEMBL209740 | — | IC50 | - | — | - | |
| CHEMBL377991 | — | IC50 | - | — | - | |
| CHEMBL378955 | — | IC50 | > | 10000.0 | nM | - |
| CHEMBL209049 | — | IC50 | - | — | - |