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Assay Detail

CHEMBL881135

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

Binding
Inhibitory activity against c-src tyrosine kinase
8
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Expert

Target

Proto-oncogene tyrosine-protein kinase Src (CHEMBL267)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

1-Oxo-3-aryl-1H-indene-2-carboxylic acid derivatives as selective inhibitors of fibroblast growth factor receptor-1 tyrosine kinase
Barvian M, Panek R, Lu G, Kraker A, Amar A, Hartl B, Hamby J, Showalter H
Bioorg Med Chem Lett (1997) 7 : 2903 -2908
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 8 5.00 5.44

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL329706 1 5.44
CHEMBL101457 1 5.40
CHEMBL98447 1 5.12
CHEMBL85589 1 5.08
CHEMBL99724 1 5.02
CHEMBL316567 1 4.89
CHEMBL317768 1 4.60
CHEMBL323564 1 4.48

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL329706 IC50 = 3600.0 nM 5.44
CHEMBL101457 IC50 = 4000.0 nM 5.40
CHEMBL98447 IC50 = 7600.0 nM 5.12
CHEMBL85589 IC50 = 8300.0 nM 5.08
CHEMBL99724 IC50 = 9600.0 nM 5.02
CHEMBL316567 IC50 = 13000.0 nM 4.89
CHEMBL317768 IC50 = 25000.0 nM 4.60
CHEMBL323564 IC50 = 33000.0 nM 4.48