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Assay Detail

CHEMBL3889134

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

Binding
Biochemical Kinase Assay : Recombinant FGFR1 (2.5 nM), or FGFR4 (12 nM) was prepared as a mixture with substrate KKKSPGEYVNIEFG (SEQ ID NO:1) (20 μM, FGFR1 substrate); Poly [E,Y]4:1 (0.2 mg/ml, FGFR2,3,4 substrate)] in kinase reaction buffer (20 mM HEPES-HCl, pH 7.5, 10 mM MgCl2, 2 mM MnCl2, 1 mM EGTA, 0.02% Brij35, 0.1 mM Na3VO4, 0.02 mg/ml BSA, 2 mM DTT, and 1% DMSO). Compound was added to the enzyme/substrate mixture using acoustic technology and pre-incubated for 0, 15, or 60 minutes at room temperature. After compound pre-incubation, 33P-γ-ATP was added at a final concentration of 10 μM to initiate kinase reactions. Reactions were incubated for 120 minutes at room temperature.
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Fibroblast growth factor receptor 1 (CHEMBL3650)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Pyrimidine FGFR4 inhibitors
(2016)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 7.65 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1852688 INFIGRATINIB 4.0 1 9.00
CHEMBL3939295 H3B-6527 1.0 1 6.29

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1852688 INFIGRATINIB IC50 = 1.0 nM 9.00
CHEMBL3939295 H3B-6527 IC50 = 513.0 nM 6.29