Inside HDACs with more selective HDAC inhibitors

Eur J Med Chem. 2016 Oct 4:121:451-483. doi: 10.1016/j.ejmech.2016.05.047. Epub 2016 May 25.

Abstract

Inhibitors of histone deacetylases (HDACs) are nowadays part of the therapeutic arsenal mainly against cancers, with four compounds approved by the Food and Drug Administration. During the last five years, several groups have made continuous efforts to improve this class of compounds, designing more selective compounds or compounds with multiple capacities. After a survey of the HDAC biology and structures, this review summarizes the results of the chemists working in this field, and highlights when possible the behavior of the molecules inside their targets.

Keywords: Epigenetics; HDAC inhibitors; Histone acetylation; Molecular modelling; Synthesis.

Publication types

  • Review

MeSH terms

  • Animals
  • Histone Deacetylase Inhibitors / chemistry
  • Histone Deacetylase Inhibitors / metabolism
  • Histone Deacetylase Inhibitors / pharmacology*
  • Histone Deacetylases / metabolism*
  • Humans
  • Organic Chemicals / chemistry
  • Organic Chemicals / metabolism
  • Organic Chemicals / pharmacology
  • Substrate Specificity

Substances

  • Histone Deacetylase Inhibitors
  • Organic Chemicals
  • Histone Deacetylases