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Assay Detail

CHEMBL697288

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

Binding
In vitro for anti-HDAC1 (Histone deacetylase 1) activity in mouse A20 cells
5
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Mus musculus
Cell Type A20
Confidence 9 — Direct single protein target
Curated By Expert

Target

Histone deacetylase 1 (CHEMBL4001)
Type SINGLE PROTEIN
Organism Mus musculus

Publication

Binding mode analysis of 3-(4-benzoyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamide: a new synthetic histone deacetylase inhibitor inducing histone hyperacetylation, growth inhibition, and terminal cell differentiation.
Mai A, Massa S, Ragno R, Esposito M, Sbardella G, Nocca G, Scatena R, Jesacher F, Loidl P, Brosch G.
J Med Chem (2002) 45 : 1778 -1784
PubMed 11960489 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 6.34 8.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL99 TRICHOSTATIN 1.0 1 8.70
CHEMBL98 VORINOSTAT 4.0 1 6.95
CHEMBL51060 1 5.38
CHEMBL51356 1 5.35
CHEMBL13168 1 5.31

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL99 TRICHOSTATIN IC50 = 2.0 nM 8.70
CHEMBL98 VORINOSTAT IC50 = 112.0 nM 6.95
CHEMBL51060 IC50 = 4200.0 nM 5.38
CHEMBL51356 IC50 = 4500.0 nM 5.35
CHEMBL13168 IC50 = 4900.0 nM 5.31