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Assay Detail

CHEMBL5344766

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

Binding
Inhibition of N-terminal GST-tagged full length human HDAC6 expressed in baculovirus system using FTS as substrate preincubated for 10 mins followed by substrate addition and measured after 2 hrs by fluorescence based analysis
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 6 (CHEMBL1865)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Histone deacetylases (HDACs) as the promising immunotherapeutic targets for hematologic cancer treatment.
Yang FF, Hu T, Liu JQ, Yu XQ, Ma LY.
Eur J Med Chem (2023) 245 : 114920 -114920
PubMed 36399875 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 8.38 8.77

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3655950 1 8.77
CHEMBL3693786 CITARINOSTAT 2.0 1 8.59
CHEMBL356769 TUBACIN 1 8.40
CHEMBL2364628 RICOLINOSTAT 2.0 1 8.33
CHEMBL2018302 TUBASTATIN A 1 7.82
CHEMBL5075729 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3655950 IC50 = 1.7 nM 8.77
CHEMBL3693786 CITARINOSTAT IC50 = 2.6 nM 8.59
CHEMBL356769 TUBACIN IC50 = 4.0 nM 8.40
CHEMBL2364628 RICOLINOSTAT IC50 = 4.7 nM 8.33
CHEMBL2018302 TUBASTATIN A IC50 = 15.0 nM 7.82
CHEMBL5075729 IC50 = 0.4 nM -