Antimicrobial Activity of 5-membered Nitroheteroaromatic Compounds beyond Nitrofurans and Nitroimidazoles: Recent Progress.

2 4-triazoles Nitroaromatic heterocycles antimicrobial agents drug-resistant pathogens microbial enzymes. nitro-1 nitroisoxazoles nitropyrroles nitrothiazoles nitrothiophenes

Journal

Current medicinal chemistry
ISSN: 1875-533X
Titre abrégé: Curr Med Chem
Pays: United Arab Emirates
ID NLM: 9440157

Informations de publication

Date de publication:
2021
Historique:
received: 25 09 2020
revised: 29 12 2020
accepted: 05 01 2021
pubmed: 18 2 2021
medline: 28 9 2021
entrez: 17 2 2021
Statut: ppublish

Résumé

The last decade has been characterized by the development and approval of pretomanid and delamanid, which are nitroimidazole based drugs for multidrug -resistant tuberculosis. This attracted renewed attention to the nitroheterocyclic scaffolds as a source of safe and efficient antimicrobial agents. While the primary focus is still on nitrofurans and nitroimidazoles, well known as bioreducible prodrugs, a number of studies have been published on other 5-membered nitroheteroaromatic compounds. The latter not only show promising antimicrobial activity but also demonstrate modes of action different from the conventional reductive activation of the nitro group. Considering the potential of these efforts to impact the continuing race against drug-resistant pathogens, herein we review non-furan/imidazole-based 5-membered nitroheteroaromatics investigated as antimicrobial agents in 2010-2020.

Identifiants

pubmed: 33593249
pii: CMC-EPUB-114252
doi: 10.2174/0929867328666210216114838
doi:

Substances chimiques

Anti-Infective Agents 0
Antitubercular Agents 0
Nitrofurans 0
Nitroimidazoles 0
Prodrugs 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

5926-5982

Subventions

Organisme : Russian Federation Government Mega grant
ID : 14.W03.031.0025

Informations de copyright

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

Auteurs

Stanislav Kalinin (S)

Institute of Chemistry, St. Petersburg State University, St. Petersburg, Russian Federation.

Tatiana Vedekhina (T)

Institute of Chemistry, St. Petersburg State University, St. Petersburg, Russian Federation.

Polina Paramonova (P)

Institute of Chemistry, St. Petersburg State University, St. Petersburg, Russian Federation.

Mikhail Krasavin (M)

Institute of Chemistry, St. Petersburg State University, St. Petersburg, Russian Federation.

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Classifications MeSH