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Assay Detail

CHEMBL3376044

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

Binding
Inhibition of human HDAC11 using RHKK(Ac) as substrate by fluorimetric analysis
7
Total Activities
7
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 11 (CHEMBL3310)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Hydroxamic acid based histone deacetylase inhibitors with confirmed activity against the malaria parasite.
Giannini G, Battistuzzi G, Vignola D.
Bioorg Med Chem Lett (2015) 25 : 459 -461
PubMed 25563890 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 7.44 7.89

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3098691 1 7.89
CHEMBL3353925 1 7.85
CHEMBL3098604 1 7.82
CHEMBL3098695 1 7.43
CHEMBL3353927 1 7.36
CHEMBL3098602 1 7.26
CHEMBL98 VORINOSTAT 4.0 1 6.44

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3098691 IC50 = 13.0 nM 7.89
CHEMBL3353925 IC50 = 14.0 nM 7.85
CHEMBL3098604 IC50 = 15.0 nM 7.82
CHEMBL3098695 IC50 = 37.0 nM 7.43
CHEMBL3353927 IC50 = 44.0 nM 7.36
CHEMBL3098602 IC50 = 55.0 nM 7.26
CHEMBL98 VORINOSTAT IC50 = 362.0 nM 6.44