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Assay Detail

CHEMBL5734832

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

Binding
Kinase Activity Inhibition Assay: Recombinant FGFR1 (2.5 nM), FGFR2 (1 nM), FGFR3 (5 nM), or FGFR4 (12 nM) was prepared as a mixture with substrate KKKSPGEYVNIEFG (SEQ ID NO:1) (20 μM, FGFR1 substrate); and 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 (Labcyte® Echo 550, Sunnyvale, Calif.)(see, Olechno et al., 2006, Improving IC50 results with acoustic droplet ejection. JALA 11, 240-246) and pre-incubated for 0, 15, or 60 minutes at room temperature. After compound pre-incubation, a mixture of ATP (Sigma-Aldrich®) and 33P-γ-ATP (PerkinElmer) was added to a final concentration of 10 μM to initiate kinase reactions. Reactions were incubated for 120 minutes at room temperature and then spotted onto Whatman™ P81 ion exchange filter paper.
6
Total Activities
2
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Fibroblast growth factor receptor 2 (CHEMBL4142)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Pyrimidine FGFR4 inhibitors
(2020)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 5.54 5.70
kon 2 - -
k_off 2 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3939295 H3B-6527 1.0 3 5.70
CHEMBL3961994 3 5.38

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3939295 H3B-6527 IC50 = 1980.0 nM 5.70
CHEMBL3961994 IC50 = 4180.0 nM 5.38
CHEMBL3961994 kon = - -
CHEMBL3961994 k_off = - s-1 -
CHEMBL3939295 H3B-6527 kon = - -
CHEMBL3939295 H3B-6527 k_off = - s-1 -