Cited by 44Histone Deacetylase Inhibitors ResearchEnzyme function and inhibitionEpigenetics and DNA Methylation

The DOI matches its Crossref record.

HDAC Inhibitors-New Generation of Target Specific Treatment

V. Chavan, A., R. Somani, R.·2010·Mini-Reviews in Medicinal Chemistry

Abstract

Histone Deacetylases (HDACs) enzymes are critical in regulating gene expression and transcription. They also play a fundamental role in regulating cellular activities such as cell proliferation, survival and differentiation. Inhibition of HDACs has generated many fascinating results including a new strategy in human cancer therapy. HDAC Inhibitors (HDACIs) like SAHA, TSA are emerging as new promising drugs for various anti-inflammatory and CNS-disorders. This review, along with chemical classification, emphasizes on the therapeutic potential of various HDACIs against different diseases. Keywords: Histone Deacetylase, HDAC inhibitor, chemistry, therapeutic applications, Enzyme Histone acetyltransferases, HAT, Class III HDACs, sirtuins, nu-clear receptor co-repressor, N-coR, Silencing Mediator, Thyroid receptors, SMRT, HDAC enzyme, aliphatic chain, Large hydrophobic region, Hydroxamic acids, trichostatin, TSA, suberoylanilide hydroxamic acid, SAHA, oxamflatin, Cyclic tetrapeptides, Benzamides, MS-27-275, Short-chain fatty acids, butyrates, Streptomyces hygro-scopicus, NVP-LAQ824, LAQ824, PDX 101, LDH589, Depsipeptide FK228, Chromobacterium violaceum, Apicidin, tubacin, Vorinostat, suberoylanilide hy-droxamic acid, Valproic acid, VPA, Trichostatin A

Overview

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Crossref · 10.2174/13895575110091263

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Metadata

Authors
V. Chavan, A., & R. Somani, R.
Venue
Mini-Reviews in Medicinal Chemistry
Published
2010-11-01
Volume
10
Issue
13
Pages
1263-1276
ISSN
1389-5575 (ISSN-L)
OpenAlex
W2057646700
Cited by
40
References
0
Citations by year
2025: 2 · 2023: 1 · 2022: 1 · 2021: 3 · 2020: 3 · 2018: 3 · 2017: 4 · 2016: 5 · 2015: 1 · 2014: 3 · 2013: 5 · 2012: 4
FWCI
1.95
Type
journal article
Language
en
Open access
closed
Locations
  • Mini-Reviews in Medicinal Chemistry (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Histone Deacetylase Inhibitors Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Enzyme function and inhibition
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
Keywords
histone deacetylase inhibitors, histone deacetylase, histone acetyltransferase, sirtuins, NCoR, SMRT, trichostatin A, vorinostat, valproic acid, butyrate, hydroxamic acids, cancer therapy, anti-inflammatory agents, central nervous system disorders
MeSH terms
Acylation, Animals, Central Nervous System Diseases, Histones, Humans, Structure-Activity Relationship, Histone Deacetylase Inhibitors

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CoChat. (2026). Citation check: HDAC Inhibitors-New Generation of Target Specific Treatment. https://app.cochat.ai/papers/10.2174/13895575110091263
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V. Chavan, A., & R. Somani, R. (2010). HDAC Inhibitors-New Generation of Target Specific Treatment. Mini-Reviews in Medicinal Chemistry. https://doi.org/10.2174/13895575110091263