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Assay Detail

CHEMBL3707777

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
In Vitro Kinase Activity Assay: Compounds to be tested were dissolved in 100% DMSO in a range of concentrations from 10-8 to 10-3 M including negative control (DMSO), then diluted with Kinase Buffer (50 mM HEPES, pH 7.5, 1 mM EGTA, 10 mM MgCl2, 0.01% Tween-20, and 2 mM DTT, added fresh) to 4x the final concentration. The final curve included 11 concentrations (10-11 to 10-5 M) plus negative control DMSO tested in triplicate.Kinase and ATP concentrations necessary for optimal activity were determined in separate experiments. (Table 2). Briefly, increasing concentrations of kinase were incubated in a fixed concentration of ATP (200 uM) in Kinase Buffer to determine maximal activity at various time points (30-120 min). The concentration of kinase that resulted in maximal activity with the shortest incubation time was then incubated in Kinase Buffer with increasing concentrations of ATP.
7
Total Activities
7
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

Target

Hepatocyte growth factor receptor (CHEMBL3717)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Tyrosine kinase inhibitors
(2014)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 6.84 7.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3671310 1 7.85
CHEMBL1980995 1 6.97
CHEMBL3671318 1 5.70
CHEMBL3671314 1 -
CHEMBL3671313 1 -
CHEMBL3671315 1 -
CHEMBL3671316 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3671310 IC50 = 14.03 nM 7.85
CHEMBL1980995 IC50 = 107.4 nM 6.97
CHEMBL3671318 IC50 = 2000.0 nM 5.70
CHEMBL3671314 IC50 > 10000.0 nM -
CHEMBL3671313 IC50 > 10000.0 nM -
CHEMBL3671315 IC50 > 10000.0 nM -
CHEMBL3671316 IC50 > 10000.0 nM -