Assay Detail
Binding
CHEMBL4018638
Review assay metadata, readout intent, target linkage, and publication context from the same page.
Inhibition of recombinant IR (unknown origin) using poly (Glu,Tyr) 4:1 as substrate after 60 mins by ELISA
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Organism | Homo sapiens |
| Confidence | 9 — Direct single protein target |
| Curated By | Autocuration |
Publication
Design, Synthesis, and Pharmacological Evaluation of Novel Multisubstituted Pyridin-3-amine Derivatives as Multitargeted Protein Kinase Inhibitors for the Treatment of Non-Small Cell Lung Cancer.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 4 | 6.46 | 7.04 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL4105329 | — | — | 1 | 7.04 |
| CHEMBL4062877 | — | — | 1 | 6.38 |
| CHEMBL4067871 | — | — | 1 | 6.37 |
| CHEMBL4075917 | — | — | 1 | 6.05 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL4105329 | — | IC50 | = | 91.6 | nM | 7.04 |
| CHEMBL4062877 | — | IC50 | = | 417.5 | nM | 6.38 |
| CHEMBL4067871 | — | IC50 | = | 431.2 | nM | 6.37 |
| CHEMBL4075917 | — | IC50 | = | 887.6 | nM | 6.05 |