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Assay Detail

CHEMBL866819

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

Binding
Inhibition of CDK2
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 Expert

Target

Cyclin-dependent kinase 2 (CHEMBL301)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery and evaluation of N-cyclopropyl- 2,4-difluoro-5-((2-(pyridin-2-ylamino)thiazol-5- ylmethyl)amino)benzamide (BMS-605541), a selective and orally efficacious inhibitor of vascular endothelial growth factor receptor-2.
Borzilleri RM, Bhide RS, Barrish JC, D'Arienzo CJ, Derbin GM, Fargnoli J, Hunt JT, Jeyaseelan R, Kamath A, Kukral DW, Marathe P, Mortillo S, Qian L, Tokarski JS, Wautlet BS, Zheng X, Lombardo LJ.
J Med Chem (2006) 49 : 3766 -3769
PubMed 16789733 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 7.30 7.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL379495 1 7.30
CHEMBL377734 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL379495 IC50 = 50.0 nM 7.30
CHEMBL377734 IC50 > 10000.0 nM -