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Assay Detail

CHEMBL832923

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

Binding
Inhibition of human cyclin-dependent kinase 6 complex with a virus-encoded cyclin from herpesvirus saimiri (Vcyclin)
7
Total Activities
7
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 6 (CHEMBL2508)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Crystal structure of a human cyclin-dependent kinase 6 complex with a flavonol inhibitor, fisetin.
Lu H, Chang DJ, Baratte B, Meijer L, Schulze-Gahmen U.
J Med Chem (2005) 48 : 737 -743
PubMed 15689157 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 5.57 7.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL428690 ALVOCIDIB 3.0 1 7.10
CHEMBL31574 FISETIN 2.0 1 6.07
CHEMBL28 APIGENIN 1 5.77
CHEMBL117 CHRYSIN 1 5.22
CHEMBL150 KAEMPFEROL 1.0 1 4.66
CHEMBL50 QUERCETIN 3.0 1 4.60
CHEMBL151 LUTEOLIN 2.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL428690 ALVOCIDIB IC50 = 80.0 nM 7.10
CHEMBL31574 FISETIN IC50 = 850.0 nM 6.07
CHEMBL28 APIGENIN IC50 = 1700.0 nM 5.77
CHEMBL117 CHRYSIN IC50 = 6000.0 nM 5.22
CHEMBL150 KAEMPFEROL IC50 = 22000.0 nM 4.66
CHEMBL50 QUERCETIN IC50 = 25000.0 nM 4.60
CHEMBL151 LUTEOLIN IC50 > 300000.0 nM -