Assay Detail
Binding
CHEMBL914868
Review assay metadata, readout intent, target linkage, and publication context from the same page.
Inhibition of Src kinase
11
Total Activities
11
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 |
Target
Proto-oncogene tyrosine-protein kinase Src (CHEMBL267) ↗| Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
Publication
Identification of 7-phenylaminothieno- [3,2-b]pyridine-6-carbonitriles as a new class of Src kinase inhibitors.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 11 | 6.83 | 7.89 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL375844 | — | — | 1 | 7.89 |
| CHEMBL222548 | — | — | 1 | 7.68 |
| CHEMBL426990 | — | — | 1 | 7.47 |
| CHEMBL425371 | — | — | 1 | 7.30 |
| CHEMBL224856 | — | — | 1 | 6.62 |
| CHEMBL373582 | — | — | 1 | 6.60 |
| CHEMBL413418 | — | — | 1 | 6.24 |
| CHEMBL375012 | — | — | 1 | 6.08 |
| CHEMBL222035 | — | — | 1 | 5.60 |
| CHEMBL222806 | — | — | 1 | - |
| CHEMBL390943 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL375844 | — | IC50 | = | 13.0 | nM | 7.89 |
| CHEMBL222548 | — | IC50 | = | 21.0 | nM | 7.68 |
| CHEMBL426990 | — | IC50 | = | 34.0 | nM | 7.47 |
| CHEMBL425371 | — | IC50 | = | 50.0 | nM | 7.30 |
| CHEMBL224856 | — | IC50 | = | 240.0 | nM | 6.62 |
| CHEMBL373582 | — | IC50 | = | 250.0 | nM | 6.60 |
| CHEMBL413418 | — | IC50 | = | 580.0 | nM | 6.24 |
| CHEMBL375012 | — | IC50 | = | 830.0 | nM | 6.08 |
| CHEMBL222035 | — | IC50 | = | 2500.0 | nM | 5.60 |
| CHEMBL222806 | — | IC50 | > | 10000.0 | nM | - |
| CHEMBL390943 | — | IC50 | > | 10000.0 | nM | - |