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Assay Detail

CHEMBL4152099

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

Binding
Inhibition of human recombinant HDAC6 incubated for 90 mins using fluorogenic substrate ZMAL (Z-Lys(Ac)-AMC) by fluorescence based assay
4
Total Activities
4
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

Histone Deacetylase 6-Selective Inhibitors and the Influence of Capping Groups on Hydroxamate-Zinc Denticity.
Porter NJ, Osko JD, Diedrich D, Kurz T, Hooker JM, Hansen FK, Christianson DW.
J Med Chem (2018) 61 : 8054 -8060
PubMed 30118224 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 7.89 8.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4162282 1 8.52
CHEMBL4173361 1 7.96
CHEMBL4170198 1 7.85
CHEMBL4165724 1 7.22

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4162282 IC50 = 3.0 nM 8.52
CHEMBL4173361 IC50 = 11.0 nM 7.96
CHEMBL4170198 IC50 = 14.0 nM 7.85
CHEMBL4165724 IC50 = 60.0 nM 7.22