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Impact of Indazole Scaffold as Antibacterial and Antifungal Agent

journal contribution
posted on 2024-07-08, 03:26 authored by Sitansu Sekhar Nanda, Dong Kee Yi, Om Prakash Panda, Sridevi Chigurupati, Tapas Kumar Mohapatra, Md Imran Hossain
Abstract: Heterocycles consisting of nitrogen atom, Indazole, is a pungent, biological, heterocyclic, bicyclic compounds possessing electron rich portions. Indazole composed of two nitrogen atoms put under the azoles family, further called as isoindazolone. It is a colorless solid nitrogen–containing heterocyclics with atomic formula C7H6N2 are extraordinary scaffolds, still identified as isoindazole. So, analogs of Indazole have experienced expert approach in later times because of its special biological properties, such as antimicrobial, anti-inflammatory, anticancer, anti-HIV, and antihypertensive actions. 1H-indazole and 2H-indazole are two toutomeric forms of Indazole. Sometimes, indazole produced three tautomeric forms that are 1H, 2H and 3H tautomers of indazole. 1H-indazole is reliable than 2H-indazole. We should note that a series of derivatives of indazole having 2H toutomers follow hybridization of cyclic systems and act as anti-inflammatory as well as antimicrobial compounds. It formed Indazole itself and derivatives of Indazole in natural products. A sequence of N-methyl-3-aryl inazoles has dominant against bacterial strains like xanthomon as campstris, Baillus cereus, Escherichia coli, Bacillus megaterium and a fungal strain candida albicans found by in-vitro antimicrobial study of indazole derivatives.

History

Journal

Current Topics in Medicinal Chemistry

Volume

22

Pagination

1152-1159

Location

Sharjah, United Arab Emirates

Open access

  • No

ISSN

1568-0266

eISSN

1873-4294

Language

eng

Publication classification

C1.1 Refereed article in a scholarly journal

Issue

14

Publisher

Bentham Science Publishers