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Assay Detail

CHEMBL1680140

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

Binding
Inhibition of human recombinant HDAC6
6
Total Activities
6
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

Effect of Inhibiting Histone Deacetylase with Short-Chain Carboxylic Acids and Their Hydroxamic Acid Analogs on Vertebrate Development and Neuronal Chromatin.
Fass DM, Shah R, Ghosh B, Hennig K, Norton S, Zhao WN, Reis SA, Klein PS, Mazitschek R, Maglathlin RL, Lewis TA, Haggarty SJ.
ACS Med Chem Lett (2011) 2 : 39 -42
PubMed 21874153 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 5.60 6.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL55895 PHENYLBUTYRYLHYDROXAMIC ACID 1 6.30
CHEMBL1672332 BUTYRYLHYDROXAMIC ACID 1 5.70
CHEMBL186311 VALPROPYLHYDROXAMIC ACID 1 4.80
CHEMBL14227 BUTYRIC ACID 2.0 1 -
CHEMBL1469 PHENYLBUTANOIC ACID 4.0 1 -
CHEMBL109 VALPROIC ACID 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL55895 PHENYLBUTYRYLHYDROXAMIC ACID IC50 = 500.0 nM 6.30
CHEMBL1672332 BUTYRYLHYDROXAMIC ACID IC50 = 2000.0 nM 5.70
CHEMBL186311 VALPROPYLHYDROXAMIC ACID IC50 = 16000.0 nM 4.80
CHEMBL14227 BUTYRIC ACID IC50 > 2000000.0 nM -
CHEMBL1469 PHENYLBUTANOIC ACID IC50 = 240000.0 nM -
CHEMBL109 VALPROIC ACID IC50 > 2000000.0 nM -