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Assay Detail

CHEMBL4426417

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

Binding
Inhibition of human FGFR2 using poly (Glu,Tyr)4:1 as substrate incubated for 60 mins by ELISA
2
Total Activities
2
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

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

Publication

Discovery of Substituted 1H-Pyrazolo[3,4-b]pyridine Derivatives as Potent and Selective FGFR Kinase Inhibitors.
Zhao B, Li Y, Xu P, Dai Y, Luo C, Sun Y, Ai J, Geng M, Duan W.
ACS Med Chem Lett (2016) 7 : 629 -634
PubMed 27326339 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 9.28 9.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3348846 FEXAGRATINIB 2.0 1 9.40
CHEMBL4447359 1 9.15

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3348846 FEXAGRATINIB IC50 = 0.4 nM 9.40
CHEMBL4447359 IC50 = 0.7 nM 9.15