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Assay Detail

CHEMBL666097

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

Binding
Inhibition of Cyclin-dependent kinase 4 (CDK4/cyclin Dl)
11
Total Activities
11
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 4 (CHEMBL331)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

5-Arylamino-2-methyl-4,7-dioxobenzothiazoles as inhibitors of cyclin-dependent kinase 4 and cytotoxic agents.
Ryu CK, Kang HY, Lee SK, Nam KA, Hong CY, Ko WG, Lee BH.
Bioorg Med Chem Lett (2000) 10 : 461 -464
PubMed 10743948 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 5.06 5.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL142789 1 5.52
CHEMBL143570 1 5.25
CHEMBL290904 1 5.22
CHEMBL38693 1 5.22
CHEMBL40326 1 5.20
CHEMBL140584 1 5.17
CHEMBL142788 1 5.17
CHEMBL38694 1 5.16
CHEMBL40362 1 4.70
CHEMBL14762 SELICICLIB 2.0 1 4.00
CHEMBL280074 OLOMOUCINE 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL142789 IC50 = 3000.0 nM 5.52
CHEMBL143570 IC50 = 5600.0 nM 5.25
CHEMBL290904 IC50 = 6000.0 nM 5.22
CHEMBL38693 IC50 = 6000.0 nM 5.22
CHEMBL40326 IC50 = 6300.0 nM 5.20
CHEMBL140584 IC50 = 6700.0 nM 5.17
CHEMBL142788 IC50 = 6700.0 nM 5.17
CHEMBL38694 IC50 = 7000.0 nM 5.16
CHEMBL40362 IC50 = 20000.0 nM 4.70
CHEMBL14762 SELICICLIB IC50 = 100000.0 nM 4.00
CHEMBL280074 OLOMOUCINE IC50 > 200000.0 nM -