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Assay Detail

CHEMBL4422757

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

Binding
Inhibition of recombinant human HDAC6 using 7-AMC-labelled HDAC substrate measured after 30 mins by fluorescence assay
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Histone deacetylase 6 (CHEMBL1865)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

HDAC as onco target: Reviewing the synthetic approaches with SAR study of their inhibitors.
Sangwan R, Rajan R, Mandal PK.
Eur J Med Chem (2018) 158 : 620 -706
PubMed 30245394 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 7.37 7.50

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL98 VORINOSTAT 4.0 1 7.50
CHEMBL4066043 1 7.24

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL98 VORINOSTAT IC50 = 32.0 nM 7.50
CHEMBL4066043 IC50 = 58.0 nM 7.24