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Assay Detail

CHEMBL5628828

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

Binding
Inhibition of HDAC7 (unknown origin) using boc-(trifluoroacetyl)lysineAMC as substrate preincubated for 10 mins followed by substrate addition and measured after 30 mins by fluorescent based assay
2
Total Activities
2
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 7 (CHEMBL2716)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Rational discovery of dual FLT3/HDAC inhibitors as a potential AML therapy.
Wang Z, Wu D, Zhao X, Liu C, Jia S, He Q, Huang F, Cheng Z, Lu T, Chen Y, Chen Y, Yang P, Lu S.
Eur J Med Chem (2023) 260 : 115759 -115759
PubMed 37659198 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 7.18 7.18

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3110004 1 7.18
CHEMBL99 TRICHOSTATIN 1.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3110004 IC50 = 66.6 nM 7.18
CHEMBL99 TRICHOSTATIN IC50 - -