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Assay Detail

CHEMBL4422732

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

Binding
Inhibition of recombinant human GST-fused HDAC1 expressed in HEK293 cells Fluor-de-lys as substrate measured after 60 mins by fluorescence assay
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HEK293
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Histone deacetylase 1 (CHEMBL325)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

HDAC as onco target: Reviewing the synthetic approaches with SAR study of their inhibitors.
Sangwan R, Rajan R, Mandal PK.
Eur J Med Chem (2018) 158 : 620 -706
PubMed 30245394 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 7.43 8.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL98 VORINOSTAT 4.0 1 8.00
CHEMBL4562156 1 7.55
CHEMBL4438671 1 6.73

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL98 VORINOSTAT IC50 = 10.0 nM 8.00
CHEMBL4562156 IC50 = 28.0 nM 7.55
CHEMBL4438671 IC50 = 187.0 nM 6.73