4.7 Article

Dissecting Histone Deacetylase 3 in Multiple Disease Conditions: Selective Inhibition as a Promising Therapeutic Strategy

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 64, Issue 13, Pages 8827-8869

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.0c01676

Keywords

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Funding

  1. Council of Scientific and Industrial Research [CSIR-37(1722)/19/EMR-II]
  2. RUSA 2.0 of UGC, New Delhi, India
  3. Council of Scientific and Industrial Research (CSIR), New Delhi, India [09/096(0966)/2019EMR-I]

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Acetylation of histone and non-histone proteins has been linked to various disease states, making histone deacetylase 3 (HDAC3) an important drug target. Despite efforts, few selective inhibitors for HDAC3 have been reported, with research discussing its role in different diseases and various potential inhibitors. This could lead to the discovery of newer, more effective, and selective HDAC3 inhibitors.
The acetylation of histone and non-histone proteins has been implicated in several disease states. Modulation of such epigenetic modifications has therefore made histone deacetylases (HDACs) important drug targets. HDAC3, among various class I HDACs, has been signified as a potentially validated target in multiple diseases, namely, cancer, neurodegenerative diseases, diabetes, obesity, cardiovascular disorders, autoimmune diseases, inflammatory diseases, parasitic infections, and HIV. However, only a handful of HDAC3-selective inhibitors have been reported in spite of continuous efforts in design and development of HDAC3-selective inhibitors. In this Perspective, the roles of HDAC3 in various diseases as well as numerous potent and HDAC3-selective inhibitors have been discussed in detail. It will surely open up a new vista in the discovery of newer, more effective, and more selective HDAC3 inhibitors.

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