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Assay Detail

CHEMBL5119802

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

Binding
Inhibition of HDAC6 (unknown origin) using FTS as substrate preincubated for 6 mins followed by substrate addition measured after 60 secs
1
Total Activities
1
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

First-in-Class Hydrazide-Based HDAC6 Selective Inhibitor with Potent Oral Anti-Inflammatory Activity by Attenuating NLRP3 Inflammasome Activation.
Yue K, Sun S, Jia G, Qin M, Hou X, Chou CJ, Huang C, Li X.
J Med Chem (2022) 65 : 12140 -12162
PubMed 36073117 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 8.33 8.33

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2364628 RICOLINOSTAT 2.0 1 8.33

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2364628 RICOLINOSTAT IC50 = 4.7 nM 8.33