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Assay Detail

CHEMBL960041

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

Binding
Inhibition of human HDAC11
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 11 (CHEMBL3310)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

N-Hydroxy-(4-oxime)-cinnamide: a versatile scaffold for the synthesis of novel histone deacetylase [correction of deacetilase] (HDAC) inhibitors.
Giannini G, Marzi M, Pezzi R, Brunetti T, Battistuzzi G, Marzo MD, Cabri W, Vesci L, Pisano C.
Bioorg Med Chem Lett (2009) 19 : 2346 -2349
PubMed 19285395 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 5.81 7.82

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL99 TRICHOSTATIN 1.0 1 7.82
CHEMBL471042 1 6.10
CHEMBL472631 1 5.51
CHEMBL471041 1 5.26
CHEMBL470843 1 5.20
CHEMBL471043 1 4.97

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL99 TRICHOSTATIN IC50 = 15.0 nM 7.82
CHEMBL471042 IC50 = 790.0 nM 6.10
CHEMBL472631 IC50 = 3060.0 nM 5.51
CHEMBL471041 IC50 = 5480.0 nM 5.26
CHEMBL470843 IC50 = 6260.0 nM 5.20
CHEMBL471043 IC50 = 10800.0 nM 4.97