Issue 40, 2022

Synthesis and pharmacological activities of azo dye derivatives incorporating heterocyclic scaffolds: a review

Abstract

Nowadays, there is significant interest in the synthesis of heterocycle-incorporated azo dye derivatives as potential scaffolds in the pharmaceutical sector. The pharmaceutical or drug industries need a simplistic synthesis approach that can afford a wide range of azo dye derivatives. The incorporation of the heterocyclic moiety into the azo dye scaffold has improved the bioactive properties of the target derivatives. The various biological and pharmacological applications of drugs such as anti-fungal, anti-tuberculosis, anti-viral, anti-inflammatory, anti-cancer, anti-bacterial, DNA binding, and analgesic properties can be easily tuned by introducing heterocyclic moieties. To date, continuous efforts are being made in the search for more potent, new, and safe synthetic methodologies for azo dye derivatives. This review presents a brief discussion of the facile synthetic approaches and the relevance of the title compound and its derivatives towards various biological activities. Thus, the synthesis of azo dye derivatives incorporating heterocyclic scaffolds such as imidazole, pyrazole, thiazole, oxazolone, thiophene, pyrrole, benzothiazole and quinoline moieties and their pharmacological applications are discussed briefly.

Graphical abstract: Synthesis and pharmacological activities of azo dye derivatives incorporating heterocyclic scaffolds: a review

Article information

Article type
Review Article
Submitted
08 Aug 2022
Accepted
30 Aug 2022
First published
13 Sep 2022
This article is Open Access
Creative Commons BY license

RSC Adv., 2022,12, 25932-25946

Synthesis and pharmacological activities of azo dye derivatives incorporating heterocyclic scaffolds: a review

K. Mezgebe and E. Mulugeta, RSC Adv., 2022, 12, 25932 DOI: 10.1039/D2RA04934A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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