Hydrazides as Potential HDAC Inhibitors: Structure-activity Relationships and Biological Implications

Author:

Banerjee Suvankar1,Baidya Sandip Kumar2,Adhikari Nilanjan3,Jha Tarun1,Ghosh Balaram4ORCID

Affiliation:

1. Natural Science Laboratory, Division of Medicinal and Pharmaceutical Chemistry, Department of Pharmaceutical Technology, P.O. Box 17020, Jadavpur University, Kolkata, 700032, West Bengal, India

2. Natural Science Laboratory, Division of Medicinal and Pharmaceutical Chemistry, Department of Pharmaceutical Technology, P.O. Box 17020, Jadavpur University, Kolkata, 700032, West Bengal, India;

3. Natural Science Laboratory, Division of Medicinal and Pharmaceutical Chemistry, Department of Pharmaceutical Technology, P.O. Box 17020, Jadavpur University, Kolkata, 700032, West Bengal, India

4. Epigenetic Research Laboratory, Department of Pharmacy, Birla Institute of Technology and Science-Pilani, Hyderabad Campus, Shamirpet, Hyderabad, 500078, India

Abstract

Abstract: Epigenetic modulations by HDACs are associated with multiple disease conditions. In this context, HDACs play vital roles in the progression of diseases including several cancers, neu-rodegenerative diseases, inflammatory diseases, and metabolic disorders. Though several HDAC inhibitors have been established as drug candidates, their usage has been restricted because of broad-spectrum inhibition, highly toxic character, and off-target adverse effects. Therefore, specific HDAC selectivity is essential to get rid of such adverse effects. Hydrazide-based compounds have already been proven to exert higher inhibitory efficacy and specific HDAC selectivity. In this arti-cle, the detailed structure-activity relationship (SAR) of the existing hydrazide-based HDAC inhibi-tors has been elucidated to gather crucial information that can be utilized further for the develop-ment of promising drug candidates for combating diverse diseases in the future.

Funder

Council of Scientific and Industrial Research

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,General Medicine

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