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Assay Detail

CHEMBL929004

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

Binding
Inhibition of CDK4
21
Total Activities
21
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Cyclin-dependent kinase 4 (CHEMBL331)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and biological evaluation of 3,5-diaminoindazoles as cyclin-dependent kinase inhibitors.
Lee J, Choi H, Kim KH, Jeong S, Park JW, Baek CS, Lee SH.
Bioorg Med Chem Lett (2008) 18 : 2292 -2295
PubMed 18353638 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 21 5.81 6.68

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL257831 1 6.68
CHEMBL255262 1 6.15
CHEMBL258040 1 6.12
CHEMBL255463 1 6.05
CHEMBL404504 1 5.98
CHEMBL415789 1 5.89
CHEMBL254171 1 5.88
CHEMBL254170 1 5.85
CHEMBL254979 1 5.80
CHEMBL255718 1 5.76
CHEMBL256558 1 5.75
CHEMBL402158 1 5.75
CHEMBL402370 1 5.70
CHEMBL402157 1 5.70
CHEMBL255932 1 5.66
CHEMBL402759 1 5.66
CHEMBL254367 1 5.52
CHEMBL255263 1 5.52
CHEMBL255255 1 5.43
CHEMBL403605 1 5.40
CHEMBL258039 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL257831 IC50 = 210.0 nM 6.68
CHEMBL255262 IC50 = 710.0 nM 6.15
CHEMBL258040 IC50 = 750.0 nM 6.12
CHEMBL255463 IC50 = 890.0 nM 6.05
CHEMBL404504 IC50 = 1050.0 nM 5.98
CHEMBL415789 IC50 = 1300.0 nM 5.89
CHEMBL254171 IC50 = 1330.0 nM 5.88
CHEMBL254170 IC50 = 1400.0 nM 5.85
CHEMBL254979 IC50 = 1600.0 nM 5.80
CHEMBL255718 IC50 = 1750.0 nM 5.76
CHEMBL256558 IC50 = 1800.0 nM 5.75
CHEMBL402158 IC50 = 1800.0 nM 5.75
CHEMBL402370 IC50 = 2000.0 nM 5.70
CHEMBL402157 IC50 = 2000.0 nM 5.70
CHEMBL255932 IC50 = 2200.0 nM 5.66
CHEMBL402759 IC50 = 2200.0 nM 5.66
CHEMBL254367 IC50 = 3000.0 nM 5.52
CHEMBL255263 IC50 = 3000.0 nM 5.52
CHEMBL255255 IC50 = 3700.0 nM 5.43
CHEMBL403605 IC50 = 4000.0 nM 5.40
CHEMBL258039 IC50 > 1000.0 nM -