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Assay Detail

CHEMBL872274

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

Binding
Inhibition of Histone deacetylase 1 (HDAC1) of HeLa nuclear extracts
8
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Expert

Target

Histone deacetylase 1 (CHEMBL325)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, synthesis, and activity of HDAC inhibitors with a N-formyl hydroxylamine head group.
Wu TY, Hassig C, Wu Y, Ding S, Schultz PG.
Bioorg Med Chem Lett (2004) 14 : 449 -453
PubMed 14698179 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 8 5.74 6.80

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL140525 1 6.80
CHEMBL336935 1 6.75
CHEMBL98 VORINOSTAT 4.0 1 6.32
CHEMBL141909 1 6.09
CHEMBL343717 1 5.89
CHEMBL137875 1 5.24
CHEMBL337584 1 4.52
CHEMBL141885 1 4.31

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL140525 IC50 = 160.0 nM 6.80
CHEMBL336935 IC50 = 180.0 nM 6.75
CHEMBL98 VORINOSTAT IC50 = 480.0 nM 6.32
CHEMBL141909 IC50 = 810.0 nM 6.09
CHEMBL343717 IC50 = 1300.0 nM 5.89
CHEMBL137875 IC50 = 5700.0 nM 5.24
CHEMBL337584 IC50 = 30000.0 nM 4.52
CHEMBL141885 IC50 = 49000.0 nM 4.31