MedicineChemistry
DOI: 10.1007/7355_2019_68

tlooto Summary

This review focuses on the typical zinc-binding groups employed in HDAC inhibitors and the major advances within each class in terms of potency, isoform selectivity, and clinical applications.

Abstract

Abstract is not available.

Citation format

GANESAN, A. Targeting the zinc-dependent histone deacetylases (hdacs) for drug discovery. Topics in Medicinal Chemistry, 2019.