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

CHEMBL806427

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

Binding
Inhibition of recombinant human Src kinase
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

7-Alkoxy-4-phenylamino-3-quinolinecar-bonitriles as dual inhibitors of Src and Abl kinases.
Boschelli DH, Wang YD, Johnson S, Wu B, Ye F, Barrios Sosa AC, Golas JM, Boschelli F.
J Med Chem (2004) 47 : 1599 -1601
PubMed 15027848 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 7.75 8.57

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL290921 1 8.57
CHEMBL288441 BOSUTINIB 4.0 1 8.42
CHEMBL42136 1 8.15
CHEMBL41465 1 8.11
CHEMBL40557 1 8.05
CHEMBL290664 1 7.92
CHEMBL41633 1 7.89
CHEMBL43577 1 7.68
CHEMBL290308 1 7.62
CHEMBL440847 1 7.46
CHEMBL40912 1 7.20
CHEMBL296844 1 7.06
CHEMBL291297 1 6.64

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL290921 IC50 = 2.7 nM 8.57
CHEMBL288441 BOSUTINIB IC50 = 3.8 nM 8.42
CHEMBL42136 IC50 = 7.0 nM 8.15
CHEMBL41465 IC50 = 7.7 nM 8.11
CHEMBL40557 IC50 = 9.0 nM 8.05
CHEMBL290664 IC50 = 12.0 nM 7.92
CHEMBL41633 IC50 = 13.0 nM 7.89
CHEMBL43577 IC50 = 21.0 nM 7.68
CHEMBL290308 IC50 = 24.0 nM 7.62
CHEMBL440847 IC50 = 35.0 nM 7.46
CHEMBL40912 IC50 = 63.0 nM 7.20
CHEMBL296844 IC50 = 87.0 nM 7.06
CHEMBL291297 IC50 = 230.0 nM 6.64