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Assay Detail

CHEMBL4684787

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Functional
Antiproliferative activity against human A375 cells assessed as inhibition of cell growth incubated for 72 hrs by CCK-8 assay
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type A-375
Confidence 1 — Organism
Curated By Autocuration

Target

A-375 (CHEMBL613859)
Type CELL-LINE
Organism Homo sapiens

Publication

Discovery of novel cyclin-dependent kinase (CDK) and histone deacetylase (HDAC) dual inhibitors with potent in vitro and in vivo anticancer activity.
Cheng C,Yun F,Ullah S,Yuan Q
Eur J Med Chem (2020) 189 : 112073 -112073
PubMed 31991336 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 5.55 5.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4761880 1 5.92
CHEMBL4787723 1 5.92
CHEMBL4750839 1 5.80
CHEMBL4745240 1 5.80
CHEMBL4741275 1 5.77
CHEMBL4784610 1 5.68
CHEMBL4800383 1 5.64
CHEMBL4757496 1 5.58
CHEMBL98 VORINOSTAT 4.0 1 5.57
CHEMBL4798528 1 5.54
CHEMBL4759239 1 5.53
CHEMBL4798305 1 5.52
CHEMBL4087968 1 5.39
CHEMBL4782264 1 5.34
CHEMBL4758936 1 5.30
CHEMBL4752270 1 5.19
CHEMBL518383 1 4.87

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4761880 IC50 = 1200.0 nM 5.92
CHEMBL4787723 IC50 = 1200.0 nM 5.92
CHEMBL4750839 IC50 = 1590.0 nM 5.80
CHEMBL4745240 IC50 = 1600.0 nM 5.80
CHEMBL4741275 IC50 = 1700.0 nM 5.77
CHEMBL4784610 IC50 = 2110.0 nM 5.68
CHEMBL4800383 IC50 = 2270.0 nM 5.64
CHEMBL4757496 IC50 = 2660.0 nM 5.58
CHEMBL98 VORINOSTAT IC50 = 2680.0 nM 5.57
CHEMBL4798528 IC50 = 2890.0 nM 5.54
CHEMBL4759239 IC50 = 2970.0 nM 5.53
CHEMBL4798305 IC50 = 3010.0 nM 5.52
CHEMBL4087968 IC50 = 4110.0 nM 5.39
CHEMBL4782264 IC50 = 4610.0 nM 5.34
CHEMBL4758936 IC50 = 5050.0 nM 5.30
CHEMBL4752270 IC50 = 6420.0 nM 5.19
CHEMBL518383 IC50 = 13380.0 nM 4.87