Chemistry of heterocycles as carbonic anhydrase inhibitors: A pathway to novel research in medicinal chemistry review

Author:

Bendi Anjaneyulu1,Taruna 2,Rajni 2,Kataria Sweety2,Singh Lakhwinder2,Kennedy John F.3,Supuran Claudiu T.4,Raghav Neera5ORCID

Affiliation:

1. Department of Chemistry Presidency University Bengaluru Karnataka India

2. Department of Chemistry Faculty of Science SGT University Gurugram Haryana India

3. Chembiotech Laboratories Ltd Tenbury Wells UK

4. Neurofarba Department, Pharmaceutical and Neutraceutical Section University of Florence Florence Italy

5. Department of Chemistry Kurukshetra University Kurukshetra Haryana India

Abstract

AbstractNowadays, the scientific community has focused on dealing with different kinds of diseases by exploring the chemistry of various heterocycles as novel drugs. In this connection, medicinal chemists identified carbonic anhydrases (CA) as one of the biologically active targets for curing various diseases. The widespread distribution of these enzymes and the high degree of homology shared by the different isoforms offer substantial challenges to discovering potential drugs. Medicinal and synthetic organic chemists have been continuously involved in developing CA inhibitors. This review explored the chemistry of different heterocycles as CA inhibitors using the last 11 years of published research work. It provides a pathway for young researchers to further explore the chemistry of a variety of synthetic as well as natural heterocycles as CA inhibitors.

Publisher

Wiley

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Exploring the Chemistry of Dihydropyrimidinone Derived Heterocycles: A Comprehensive Review;Journal of Molecular and Engineering Materials;2024-08-29

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