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

CHEMBL4310935

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

Binding
Inhibition of HDAC6 in human A549 cells using tubulin as substrate measured after 4 hrs by Western blot analysis
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type A549
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

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

Publication

Development and characterization of a CNS-penetrant benzhydryl hydroxamic acid class IIa histone deacetylase inhibitor.
Luckhurst CA, Aziz O, Beaumont V, Bürli RW, Breccia P, Maillard MC, Haughan AF, Lamers M, Leonard P, Matthews KL, Raphy G, Stott AJ, Munoz-Sanjuan I, Thomas B, Wall M, Wishart G, Yates D, Dominguez C.
Bioorg Med Chem Lett (2019) 29 : 83 -88
PubMed 30463802 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 4.77 4.77

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4456445 1 4.77
CHEMBL4437833 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4456445 IC50 = 17000.0 nM 4.77
CHEMBL4437833 IC50 - -