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Assay Detail

CHEMBL5716488

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

Binding
Inhibition of HDAC1 (unknown origin) using acetyl-Gly-Ala-(N-acetyl-Lys)-amino-4-methylcoumarin as substrate incubated for 15 mins by fluorescence plate reader analysis
3
Total Activities
3
Compounds Tested
1
Activity Types
2
Assay Parameters

Assay Information

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

Target

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

Publication

A novel histone deacetylase 8 (HDAC8)-specific inhibitor PCI-34051 induces apoptosis in T-cell lymphomas.
Balasubramanian S, Ramos J, Luo W, Sirisawad M, Verner E, Buggy JJ.
Leukemia (2008) 22 : 1026 -1034
PubMed 18256683 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 7.08 8.30

Assay Parameters

Parameter Type Value Units Text
EFO_ID EFO_ID - MONDO:0015760
EFO_TERM EFO_TERM - t-cell non-hodgkin lymphoma

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2105727 ABEXINOSTAT HYDROCHLORIDE -1.0 1 8.30
CHEMBL98 VORINOSTAT 4.0 1 7.55
CHEMBL2170177 1 5.40

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2105727 ABEXINOSTAT HYDROCHLORIDE IC50 = 5.0 nM 8.30
CHEMBL98 VORINOSTAT IC50 = 28.0 nM 7.55
CHEMBL2170177 IC50 = 4000.0 nM 5.40