Assay Detail
Binding
CHEMBL5738873
Review assay metadata, readout intent, target linkage, and publication context from the same page.
HotSpot Assay: Table 3 and 4: The HotSpot kinase profiling and screening assays were carried out using the method of Anastassiadis et al., Nat. Biotechnol. (2011) Vol. 29, No. 11, pp. 1039-1045 (which is herein incorporated by reference in its entirety); 10 uM was the starting concentration with a 3-fold series dilution (10 doses) and the final ATP concentration was 10 uM.
12
Total Activities
4
Compounds Tested
3
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Confidence | 8 — Homologous single protein target |
| Curated By | Autocuration |
Target
Receptor-type tyrosine-protein kinase FLT3 (CHEMBL1974) ↗| Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
Publication
Substituted Imidazo[1,2-a]-pyridines as IRAK 1/4 and FLT3 inhibitors
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 4 | 9.54 | 9.63 |
| kon | 4 | - | - |
| k_off | 4 | - | - |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL576982 | QUIZARTINIB | 4.0 | 3 | 9.63 |
| CHEMBL256570 | — | — | 3 | 9.45 |
| CHEMBL5927784 | — | — | 3 | - |
| CHEMBL6002371 | — | — | 3 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL576982 | QUIZARTINIB | IC50 | = | 0.236 | nM | 9.63 |
| CHEMBL256570 | — | IC50 | = | 0.356 | nM | 9.45 |
| CHEMBL256570 | — | kon | = | - | — | - |
| CHEMBL256570 | — | k_off | = | - | s-1 | - |
| CHEMBL5927784 | — | IC50 | < | 0.508 | nM | - |
| CHEMBL5927784 | — | kon | = | - | — | - |
| CHEMBL5927784 | — | k_off | = | - | s-1 | - |
| CHEMBL6002371 | — | IC50 | < | 0.508 | nM | - |
| CHEMBL6002371 | — | kon | = | - | — | - |
| CHEMBL6002371 | — | k_off | = | - | s-1 | - |
| CHEMBL576982 | QUIZARTINIB | kon | = | - | — | - |
| CHEMBL576982 | QUIZARTINIB | k_off | = | - | s-1 | - |