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.

Original languageEnglish
Pages (from-to)5926-5982
Number of pages57
JournalCurrent Medicinal Chemistry
Volume28
Issue number29
DOIs
StatePublished - 16 Feb 2021

    Scopus subject areas

  • Drug Discovery
  • Molecular Medicine
  • Biochemistry
  • Pharmacology
  • Organic Chemistry

    Research areas

  • 1,3,4-OXADIAZOLE DERIVATIVES, 2, 2-COMPONENT SIGNAL-TRANSDUCTION, 4-triazoles, DRUGS, GIARDICIDAL ACTIVITY, HELICOBACTER-PYLORI, IN-VITRO, Nitroaromatic heterocycles, OLD ANTIBIOTICS, REDUCTIVE ACTIVATION, RESEARCH-AND-DEVELOPMENT, TRICHOMONAS-VAGINALIS, antimicrobial agents, drug-resistant pathogens, microbial enzymes, nitro-1, nitro-thiazoles, nitroisoxazoles, nitropyrroles, nitrothiophenes, Humans, Nitroimidazoles/pharmacology, Nitrofurans/pharmacology, Anti-Infective Agents/pharmacology, Prodrugs, Tuberculosis, Multidrug-Resistant, Antitubercular Agents/pharmacology

ID: 85062562