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

CHEMBL661114

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

Binding
Inhibition of Cyclin-dependent kinase 1-cyclin B1
12
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 7 — Homologous single protein target
Curated By Autocuration

Target

Cyclin-dependent kinase 1/cyclin B1 (CHEMBL1907602)
Type PROTEIN COMPLEX
Organism Homo sapiens

Publication

Thio- and oxoflavopiridols, cyclin-dependent kinase 1-selective inhibitors: synthesis and biological effects.
Kim KS, Sack JS, Tokarski JS, Qian L, Chao ST, Leith L, Kelly YF, Misra RN, Hunt JT, Kimball SD, Humphreys WG, Wautlet BS, Mulheron JG, Webster KR.
J Med Chem (2000) 43 : 4126 -4134
PubMed 11063609 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 6.11 7.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL428690 ALVOCIDIB 3.0 1 7.52
CHEMBL112582 1 7.10
CHEMBL334881 2 6.96
CHEMBL133498 1 6.89
CHEMBL112050 1 6.36
CHEMBL326843 1 6.34
CHEMBL1242973 BUTYROLACTONE I 1 6.22
CHEMBL132888 1 5.60
CHEMBL323015 1 5.19
CHEMBL280074 OLOMOUCINE 1 5.16
CHEMBL130395 1 4.79

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL428690 ALVOCIDIB IC50 = 30.0 nM 7.52
CHEMBL112582 IC50 = 80.0 nM 7.10
CHEMBL334881 IC50 = 110.0 nM 6.96
CHEMBL133498 IC50 = 130.0 nM 6.89
CHEMBL112050 IC50 = 440.0 nM 6.36
CHEMBL326843 IC50 = 460.0 nM 6.34
CHEMBL1242973 BUTYROLACTONE I IC50 = 600.0 nM 6.22
CHEMBL132888 IC50 = 2500.0 nM 5.60
CHEMBL334881 IC50 = 6100.0 nM 5.21
CHEMBL323015 IC50 = 6400.0 nM 5.19
CHEMBL280074 OLOMOUCINE IC50 = 7000.0 nM 5.16
CHEMBL130395 IC50 = 16300.0 nM 4.79