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Assay Detail

CHEMBL950125

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

Binding
Inhibition of human HDAC in HeLa cells
8
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HeLa
Confidence 5 — Multiple protein complex / RNA
Curated By Autocuration

Target

Histone deacetylase (CHEMBL2093865)
Type PROTEIN FAMILY
Organism Homo sapiens

Publication

New sulfurated derivatives of valproic acid with enhanced histone deacetylase inhibitory activity.
Perrino E, Cappelletti G, Tazzari V, Giavini E, Del Soldato P, Sparatore A.
Bioorg Med Chem Lett (2008) 18 : 1893 -1897
PubMed 18294844 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 8 5.10 6.35

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL402341 1 6.35
CHEMBL271677 1 5.02
CHEMBL257239 1 4.76
CHEMBL272134 1 4.25
CHEMBL109 VALPROIC ACID 4.0 1 -
CHEMBL271256 1 -
CHEMBL271923 1 -
CHEMBL255609 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL402341 IC50 = 450.0 nM 6.35
CHEMBL271677 IC50 = 9600.0 nM 5.02
CHEMBL257239 IC50 = 17500.0 nM 4.76
CHEMBL272134 IC50 = 56400.0 nM 4.25
CHEMBL109 VALPROIC ACID IC50 = 995000.0 nM -
CHEMBL271256 IC50 = 198000.0 nM -
CHEMBL271923 IC50 = 102000.0 nM -
CHEMBL255609 IC50 > 10000.0 nM -