Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL4838110

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

Binding
Inhibition of human N-terminal GST-fusion tagged VEGFR2 cytoplasmic domain (790 to 1356 end residues) expressed in Sf21 insect cells
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type Sf21
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Vascular endothelial growth factor receptor 2 (CHEMBL279)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, synthesis and biological evaluations of a series of Pyrido[1,2-a]pyrimidinone derivatives as novel selective FGFR inhibitors.
Ran K, Zeng J, Wan G, He X, Feng Z, Xiang W, Wei W, Hu X, Wang N, Liu Z, Yu L.
Eur J Med Chem (2021) 220 : 113499 -113499
PubMed 33940465 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 7.84 7.84

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4862576 1 7.84

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4862576 IC50 = 14.4 nM 7.84