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

CHEMBL658935

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

Binding
Inhibition of cyclin A activated Cyclin-dependent kinase 2 (CDK2)
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Structure-based design and synthesis of 2-benzylidene-benzofuran-3-ones as flavopiridol mimics.
Schoepfer J, Fretz H, Chaudhuri B, Muller L, Seeber E, Meijer L, Lozach O, Vangrevelinghe E, Furet P.
J Med Chem (2002) 45 : 1741 -1747
PubMed 11960485 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 6.25 7.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL48362 1 7.52
CHEMBL418203 1 6.66
CHEMBL45477 1 6.51
CHEMBL51709 1 5.89
CHEMBL46181 1 5.53
CHEMBL48614 1 5.40

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL48362 IC50 = 30.0 nM 7.52
CHEMBL418203 IC50 = 220.0 nM 6.66
CHEMBL45477 IC50 = 310.0 nM 6.51
CHEMBL51709 IC50 = 1280.0 nM 5.89
CHEMBL46181 IC50 = 2980.0 nM 5.53
CHEMBL48614 IC50 = 3970.0 nM 5.40