Literature DB >> 33673069

Nitroaromatic Antibiotics as Nitrogen Oxide Sources.

Allison M Rice1, Yueming Long1, S Bruce King1.   

Abstract

pan class="Chemical">n class="Chemical">Nitroaromatic antibiotics show activity against anaerobic bacteria and pan>rasitpan class="Chemical">es, finding use in the treatment of Heliobacter pan class="Species">pylori infections, tuberculosis, trichomoniasis, human African trypanosomiasis, Chagas disease and leishmaniasis. Despite this activity and a clear need for the development of new treatments for these conditions, the associated toxicity and lack of clear mechanisms of action have limited their therapeutic development. Nitroaromatic antibiotics require reductive bioactivation for activity and this reductive metabolism can convert the nitro group to nitric oxide (NO) or a related reactive nitrogen species (RNS). As nitric oxide plays important roles in the defensive immune response to bacterial infection through both signaling and redox-mediated pathways, defining controlled NO generation pathways from these antibiotics would allow the design of new therapeutics. This review focuses on the release of nitrogen oxide species from various nitroaromatic antibiotics to portend the increased ability for these compounds to positively impact infectious disease treatment.

Entities:  

Keywords:  infectious diseases; metronidazole; nitric oxide (NO); nitrite; nitroaromatic antibiotics; nitroxyl (HNO); reactive nitrogen species (RNS)

Year:  2021        PMID: 33673069      PMCID: PMC7918234          DOI: 10.3390/biom11020267

Source DB:  PubMed          Journal:  Biomolecules        ISSN: 2218-273X


  107 in total

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Journal:  J Med Chem       Date:  2017-08-28       Impact factor: 7.446

5.  Synthesis, Biological Evaluation, Structure-Activity Relationship, and Mechanism of Action Studies of Quinoline-Metronidazole Derivatives Against Experimental Visceral Leishmaniasis.

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10.  Development of (6 R)-2-Nitro-6-[4-(trifluoromethoxy)phenoxy]-6,7-dihydro-5 H-imidazo[2,1- b][1,3]oxazine (DNDI-8219): A New Lead for Visceral Leishmaniasis.

Authors:  Andrew M Thompson; Patrick D O'Connor; Andrew J Marshall; Adrian Blaser; Vanessa Yardley; Louis Maes; Suman Gupta; Delphine Launay; Stephanie Braillard; Eric Chatelain; Baojie Wan; Scott G Franzblau; Zhenkun Ma; Christopher B Cooper; William A Denny
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Authors:  Saúl Noriega; Jaime Cardoso-Ortiz; Argelia López-Luna; Ma Del Refugio Cuevas-Flores; Juan Armando Flores De La Torre
Journal:  Pharmaceuticals (Basel)       Date:  2022-06-05

3.  Exploration of Nitroaromatic Antibiotics via Sanger's Reagent: Synthesis, In Silico, and Antimicrobial Evaluation.

Authors:  Mohammed Salah Ayoup; Ahmed R Rabee; Hamida Abdel-Hamid; Marwa F Harras; Nagwan G El Menofy; Magda M F Ismail
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4.  The zebrafish embryo as an in vivo model for screening nanoparticle-formulated lipophilic anti-tuberculosis compounds.

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Journal:  Dis Model Mech       Date:  2022-01-26       Impact factor: 5.758

5.  Bioactive Nitrosylated and Nitrated N-(2-hydroxyphenyl)acetamides and Derived Oligomers: An Alternative Pathway to 2-Amidophenol-Derived Phytotoxic Metabolites.

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