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Synthesis and investigation of antimicrobial activities of nitrofurazone analogues containing hydrazide-hydrazone moiety

In this research we synthesized and tested for in vitro antimicrobial activity 21 nitrofurazone analogues. The compounds we obtained were identified on the basis of (1)H NMR and (13)C NMR spectroscopy. The in vitro screening of antimicrobial properties of synthesized compounds revealed a wide spectr...

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Autores principales: Popiołek, Łukasz, Biernasiuk, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681330/
https://www.ncbi.nlm.nih.gov/pubmed/29158722
http://dx.doi.org/10.1016/j.jsps.2017.05.006
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author Popiołek, Łukasz
Biernasiuk, Anna
author_facet Popiołek, Łukasz
Biernasiuk, Anna
author_sort Popiołek, Łukasz
collection PubMed
description In this research we synthesized and tested for in vitro antimicrobial activity 21 nitrofurazone analogues. The compounds we obtained were identified on the basis of (1)H NMR and (13)C NMR spectroscopy. The in vitro screening of antimicrobial properties of synthesized compounds revealed a wide spectrum of antimicrobial activity. Compounds 28, 29, 32–43, and 45–48 showed very high bactericidal effect towards Staphylococcus spp. ATTC and Bacillus spp. ATTC (MIC = 0.002–7.81 µg/ml and MBC = 0.002–31.25 µg/ml). The levels of activity of several compounds were far better than those of nitrofurantoin, ciprofloxacin or cefuroxime.
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spelling pubmed-56813302017-11-20 Synthesis and investigation of antimicrobial activities of nitrofurazone analogues containing hydrazide-hydrazone moiety Popiołek, Łukasz Biernasiuk, Anna Saudi Pharm J Original Article In this research we synthesized and tested for in vitro antimicrobial activity 21 nitrofurazone analogues. The compounds we obtained were identified on the basis of (1)H NMR and (13)C NMR spectroscopy. The in vitro screening of antimicrobial properties of synthesized compounds revealed a wide spectrum of antimicrobial activity. Compounds 28, 29, 32–43, and 45–48 showed very high bactericidal effect towards Staphylococcus spp. ATTC and Bacillus spp. ATTC (MIC = 0.002–7.81 µg/ml and MBC = 0.002–31.25 µg/ml). The levels of activity of several compounds were far better than those of nitrofurantoin, ciprofloxacin or cefuroxime. Elsevier 2017-11 2017-05-26 /pmc/articles/PMC5681330/ /pubmed/29158722 http://dx.doi.org/10.1016/j.jsps.2017.05.006 Text en © 2017 King Saud University https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Popiołek, Łukasz
Biernasiuk, Anna
Synthesis and investigation of antimicrobial activities of nitrofurazone analogues containing hydrazide-hydrazone moiety
title Synthesis and investigation of antimicrobial activities of nitrofurazone analogues containing hydrazide-hydrazone moiety
title_full Synthesis and investigation of antimicrobial activities of nitrofurazone analogues containing hydrazide-hydrazone moiety
title_fullStr Synthesis and investigation of antimicrobial activities of nitrofurazone analogues containing hydrazide-hydrazone moiety
title_full_unstemmed Synthesis and investigation of antimicrobial activities of nitrofurazone analogues containing hydrazide-hydrazone moiety
title_short Synthesis and investigation of antimicrobial activities of nitrofurazone analogues containing hydrazide-hydrazone moiety
title_sort synthesis and investigation of antimicrobial activities of nitrofurazone analogues containing hydrazide-hydrazone moiety
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681330/
https://www.ncbi.nlm.nih.gov/pubmed/29158722
http://dx.doi.org/10.1016/j.jsps.2017.05.006
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