Impact of Indazole Scaffold as Antibacterial and Antifungal Agent

Author:

Nanda Sitansu Sekhar1,Yi Dong Kee1,Panda Om Prakash2,Chigurupati Sridevi3,Mohapatra Tapas Kumar4,Hossain Md. Imran1

Affiliation:

1. Department of Chemistry, Myongji University, Yongin, 17058, South Korea

2. Centurion University of Technology and Management, Odisha, India

3. Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Qassim University, Buraydah, 52571, Kingdom of Saudi Arabia | Department of Biotechnology, Saveetha College of Engineering, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Saveetha Nagar, Thandalam, Chennai, 602105 India

4. Mayurbhanj Medical Academy, Indapahi, Baripada, Mayurbhanj, Odisha, 757107, India

Abstract

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.

Funder

Korean National Research Foundation

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,General Medicine

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