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Assay Detail

CHEMBL4842907

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

Binding
Inhibition of HDAC8 (unknown origin)
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 8 (CHEMBL3192)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, synthesis and biological evaluation of 3, 4-disubstituted-imidazolidine-2, 5-dione derivatives as HDAC6 selective inhibitors.
Liang T, Xue J, Yao Z, Ye Y, Yang X, Hou X, Fang H.
Eur J Med Chem (2021) 221 : 113526 -113526
PubMed 33992929 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 5.95 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2364628 RICOLINOSTAT 2.0 1 7.00
CHEMBL2018302 TUBASTATIN A 1 6.07
CHEMBL2179618 NEXTURASTAT A 1 6.02
CHEMBL356769 TUBACIN 1 5.90
CHEMBL4066043 1 5.55
CHEMBL4876454 1 5.16

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2364628 RICOLINOSTAT IC50 = 100.0 nM 7.00
CHEMBL2018302 TUBASTATIN A IC50 = 854.0 nM 6.07
CHEMBL2179618 NEXTURASTAT A IC50 = 954.0 nM 6.02
CHEMBL356769 TUBACIN IC50 = 1270.0 nM 5.90
CHEMBL4066043 IC50 = 2800.0 nM 5.55
CHEMBL4876454 IC50 = 6851.0 nM 5.16