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Assay Detail

CHEMBL5374993

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

Binding
Inhibition of human recombinant HDAC6 using RHKKAc (379 to 382 residues) as substrate
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 6 (CHEMBL1865)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Development of First-in-Class Dual Sirt2/HDAC6 Inhibitors as Molecular Tools for Dual Inhibition of Tubulin Deacetylation.
Sinatra L, Vogelmann A, Friedrich F, Tararina MA, Neuwirt E, Colcerasa A, König P, Toy L, Yesiloglu TZ, Hilscher S, Gaitzsch L, Papenkordt N, Zhai S, Zhang L, Romier C, Einsle O, Sippl W, Schutkowski M, Gross O, Bendas G, Christianson DW, Hansen FK, Jung M, Schiedel M.
J Med Chem (2023) 66 : 14787 -14814
PubMed 37902787 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 8.11 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL356769 TUBACIN 1 8.40
CHEMBL5422921 1 7.82

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL356769 TUBACIN IC50 = 4.0 nM 8.40
CHEMBL5422921 IC50 = 15.0 nM 7.82