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Assay Detail

CHEMBL900125

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

Binding
Inhibition of HDAC in 293T cells
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type 293T
Confidence 5 — Multiple protein complex / RNA
Curated By Autocuration

Target

Histone deacetylase (CHEMBL2093865)
Type PROTEIN FAMILY
Organism Homo sapiens

Publication

Novel aminophenyl benzamide-type histone deacetylase inhibitors with enhanced potency and selectivity.
Moradei OM, Mallais TC, Frechette S, Paquin I, Tessier PE, Leit SM, Fournel M, Bonfils C, Trachy-Bourget MC, Liu J, Yan TP, Lu AH, Rahil J, Wang J, Lefebvre S, Li Z, Vaisburg AF, Besterman JM.
J Med Chem (2007) 50 : 5543 -5546
PubMed 17941625 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 6.14 7.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL356066 DACINOSTAT 2.0 1 7.30
CHEMBL235210 1 6.82
CHEMBL235842 1 6.52
CHEMBL393242 1 6.05
CHEMBL236061 1 5.52
CHEMBL236060 1 5.52
CHEMBL235191 TACEDINALINE 3.0 1 5.22

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL356066 DACINOSTAT IC50 = 50.0 nM 7.30
CHEMBL235210 IC50 = 150.0 nM 6.82
CHEMBL235842 IC50 = 300.0 nM 6.52
CHEMBL393242 IC50 = 900.0 nM 6.05
CHEMBL236061 IC50 = 3000.0 nM 5.52
CHEMBL236060 IC50 = 3000.0 nM 5.52
CHEMBL235191 TACEDINALINE IC50 = 6000.0 nM 5.22