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Assay Detail

CHEMBL660787

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

Binding
Inhibition of Cyclin-dependent kinase 2 (CDK2)
10
Total Activities
10
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

A computational model of binding thermodynamics: the design of cyclin-dependent kinase 2 inhibitors.
Sims PA, Wong CF, McCammon JA.
J Med Chem (2003) 46 : 3314 -3325
PubMed 12852762 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 5.76 7.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL48362 1 7.52
CHEMBL45477 1 6.51
CHEMBL112582 1 5.97
CHEMBL51709 1 5.89
CHEMBL113544 1 5.68
CHEMBL326275 1 5.68
CHEMBL326843 1 5.41
CHEMBL48614 1 5.40
CHEMBL112050 1 5.18
CHEMBL323015 1 4.39

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL48362 IC50 = 30.0 nM 7.52
CHEMBL45477 IC50 = 310.0 nM 6.51
CHEMBL112582 IC50 = 1070.0 nM 5.97
CHEMBL51709 IC50 = 1280.0 nM 5.89
CHEMBL113544 IC50 = 2100.0 nM 5.68
CHEMBL326275 IC50 = 2110.0 nM 5.68
CHEMBL326843 IC50 = 3930.0 nM 5.41
CHEMBL48614 IC50 = 3970.0 nM 5.40
CHEMBL112050 IC50 = 6590.0 nM 5.18
CHEMBL323015 IC50 = 40400.0 nM 4.39