Impact of Indazole Scaffold as Antibacterial and Antifungal Agent.


Journal

Current topics in medicinal chemistry
ISSN: 1873-4294
Titre abrégé: Curr Top Med Chem
Pays: United Arab Emirates
ID NLM: 101119673

Informations de publication

Date de publication:
2022
Historique:
received: 07 10 2021
revised: 19 01 2022
accepted: 21 03 2022
pubmed: 14 5 2022
medline: 19 8 2022
entrez: 13 5 2022
Statut: ppublish

Résumé

Heterocycles consisting of a nitrogen atom, Indazole, is a pungent, biological, heterocyclic, bicyclic compound possessing electron-rich portions. Indazole is composed of two nitrogen atoms put under the azoles family, further called isoindazolone. It is colorless solid nitrogen- containing heterocyclics with atomic formula-C7H6N2 are extraordinary scaffolds, still identified as isoindazole. Therefore, analogs of Indazole have experienced expert approaches in later times because of its special biological properties, such as anti-microbial, anti-inflammatory, anticancer, anti- HIV and antihypertensive actions. 1H-indazole and 2H-indazole are two toutomeric forms of Indazole. Sometimes, indazole produces 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 anti-microbial 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 anti-microbial study of indazole derivatives.

Identifiants

pubmed: 35549876
pii: CTMC-EPUB-123451
doi: 10.2174/1568026622666220512145646
doi:

Substances chimiques

Anti-Bacterial Agents 0
Anti-Inflammatory Agents 0
Antifungal Agents 0
Indazoles 0
Nitrogen N762921K75

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1152-1159

Subventions

Organisme : Korean National Research Foundation
ID : 2021R1F1A1048388, 2021R1F1A1063636

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Sitansu Sekhar Nanda (SS)

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

Dong Kee Yi (DK)

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

Om Prakash Panda (OP)

Centurion University of Technology and Management, Odisha, India.

Sridevi Chigurupati (S)

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.

Tapas Kumar Mohapatra (TK)

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

Md Imran Hossain (MI)

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

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Classifications MeSH