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

Nowadays, 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 diseas...

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Veröffentlicht in:Archiv der Pharmazie (Weinheim) 2024-07, Vol.357 (7), p.e2400073-n/a
Hauptverfasser: Bendi, Anjaneyulu, Taruna, Rajni, Kataria, Sweety, Singh, Lakhwinder, Kennedy, John F., Supuran, Claudiu T., Raghav, Neera
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Sprache:eng
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Zusammenfassung:Nowadays, 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. Nowadays, medicinal chemists have identified carbonic anhydrases (CA) as one of the biologically active targets for curing various diseases. This review explores the chemistry of different heterocycles as CA inhibitors, using the last 5 years of published research work.
ISSN:0365-6233
1521-4184
1521-4184
DOI:10.1002/ardp.202400073