Impact of Indazole Scaffold as Antibacterial and Antifungal Agent.
Antifungal
Antimicrobial
Chalcone
Indazole
cox-1
cox-2
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
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
1152-1159Subventions
Organisme : Korean National Research Foundation
ID : 2021R1F1A1048388, 2021R1F1A1063636
Informations de copyright
Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.