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Updated: Dec 25, 2025

Assays for Validating Histone Acetyltransferase Inhibitors
Published on: August 6, 2020
PROTAC-mediated degradation of class I histone deacetylase enzymes in corepressor complexes
Joshua P Smalley1, Grace E Adams2, Christopher J Millard3
1Leicester Institute of Structural and Chemical Biology and Department of Chemistry, University of Leicester, University Road, Leicester, LE1 7RH, UK. JTHodgkinson@le.ac.uk.
Abstract:
We have identified a proteolysis targeting chimera (PROTAC) of class I HDACs 1, 2 and 3. The most active degrader consists of a benzamide HDAC inhibitor, an alkyl linker, and the von Hippel-Lindau E3 ligand. Our PROTAC increased histone acetylation levels and compromised colon cancer HCT116 cell viability, establishing a degradation strategy as an alternative to class I HDAC inhibition.
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