Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL4707189

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

Binding
Inhibition of recombinant human N-terminal GST-tagged HDAC6 expressed in baculovirus infected Sf9 cells using fluorogenic HDAC substrate 3 measured after 30 mins by fluorescence based assay
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type Sf9
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

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

Publication

Design, Synthesis, and Preclinical Evaluation of Fused Pyrimidine-Based Hydroxamates for the Treatment of Hepatocellular Carcinoma.
Chen D,Soh CK,Goh WH,Wang H
J Med Chem (2018) 61 : 1552 -1575
PubMed 29360358 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 7.89 8.38

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4749655 1 8.38
CHEMBL4785064 1 8.34
CHEMBL4744689 1 8.18
CHEMBL98 VORINOSTAT 4.0 1 7.92
CHEMBL3622533 FIMEPINOSTAT 2.0 1 7.47
CHEMBL1851943 PRACINOSTAT 3.0 1 7.03
CHEMBL99 TRICHOSTATIN 1.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4749655 IC50 = 4.2 nM 8.38
CHEMBL4785064 IC50 = 4.6 nM 8.34
CHEMBL4744689 IC50 = 6.6 nM 8.18
CHEMBL98 VORINOSTAT IC50 = 12.0 nM 7.92
CHEMBL3622533 FIMEPINOSTAT IC50 = 34.0 nM 7.47
CHEMBL1851943 PRACINOSTAT IC50 = 93.0 nM 7.03
CHEMBL99 TRICHOSTATIN IC50 - -