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Antimicrobial Activity of Pyrazinamide Coordination Frameworks Synthesized by Mechanochemistry

The urge for the development of a more efficient antibiotic crystalline forms led us to the disclosure of new antibiotic coordination frameworks of pyrazinamide, a well-known drug used for the treatment of tuberculosis, with some of the novel compounds unravelling improved antimycobacterial activity...

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Autores principales: Quaresma, Sílvia, Alves, Paula C., Rijo, Patrícia, Duarte, M. Teresa, André, Vânia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036749/
https://www.ncbi.nlm.nih.gov/pubmed/33800635
http://dx.doi.org/10.3390/molecules26071904
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author Quaresma, Sílvia
Alves, Paula C.
Rijo, Patrícia
Duarte, M. Teresa
André, Vânia
author_facet Quaresma, Sílvia
Alves, Paula C.
Rijo, Patrícia
Duarte, M. Teresa
André, Vânia
author_sort Quaresma, Sílvia
collection PubMed
description The urge for the development of a more efficient antibiotic crystalline forms led us to the disclosure of new antibiotic coordination frameworks of pyrazinamide, a well-known drug used for the treatment of tuberculosis, with some of the novel compounds unravelling improved antimycobacterial activity. Mechanochemistry was the preferred synthetic technique to yield novel compounds, allowing the reproduction of a 1D zinc framework, the synthesis of a novel hydrogen bonding manganese framework, and three new compounds with silver. The structural characterization of the novel forms is presented along with stability studies. The increased antimicrobial activity of the new silver-based frameworks against Escherichia coli, Staphylococcus aureus, and Mycobacterium smegmatis is particularly relevant.
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spelling pubmed-80367492021-04-12 Antimicrobial Activity of Pyrazinamide Coordination Frameworks Synthesized by Mechanochemistry Quaresma, Sílvia Alves, Paula C. Rijo, Patrícia Duarte, M. Teresa André, Vânia Molecules Article The urge for the development of a more efficient antibiotic crystalline forms led us to the disclosure of new antibiotic coordination frameworks of pyrazinamide, a well-known drug used for the treatment of tuberculosis, with some of the novel compounds unravelling improved antimycobacterial activity. Mechanochemistry was the preferred synthetic technique to yield novel compounds, allowing the reproduction of a 1D zinc framework, the synthesis of a novel hydrogen bonding manganese framework, and three new compounds with silver. The structural characterization of the novel forms is presented along with stability studies. The increased antimicrobial activity of the new silver-based frameworks against Escherichia coli, Staphylococcus aureus, and Mycobacterium smegmatis is particularly relevant. MDPI 2021-03-28 /pmc/articles/PMC8036749/ /pubmed/33800635 http://dx.doi.org/10.3390/molecules26071904 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Quaresma, Sílvia
Alves, Paula C.
Rijo, Patrícia
Duarte, M. Teresa
André, Vânia
Antimicrobial Activity of Pyrazinamide Coordination Frameworks Synthesized by Mechanochemistry
title Antimicrobial Activity of Pyrazinamide Coordination Frameworks Synthesized by Mechanochemistry
title_full Antimicrobial Activity of Pyrazinamide Coordination Frameworks Synthesized by Mechanochemistry
title_fullStr Antimicrobial Activity of Pyrazinamide Coordination Frameworks Synthesized by Mechanochemistry
title_full_unstemmed Antimicrobial Activity of Pyrazinamide Coordination Frameworks Synthesized by Mechanochemistry
title_short Antimicrobial Activity of Pyrazinamide Coordination Frameworks Synthesized by Mechanochemistry
title_sort antimicrobial activity of pyrazinamide coordination frameworks synthesized by mechanochemistry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036749/
https://www.ncbi.nlm.nih.gov/pubmed/33800635
http://dx.doi.org/10.3390/molecules26071904
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