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Design and Synthesis of New N-(5-Trifluoromethyl)-1H-1,2,4-triazol-3-yl Benzenesulfonamides as Possible Antimalarial Prototypes
A rational approach was used to synthesize a new set of 15 1H-1,2,4-triazol-3-yl benzenesulfonamide derivatives with the aim of developing new antimalarial lead compounds. These derivatives were prepared in yields between 50% and 62%, and their structures were elucidated using IR, (1)H-, (13)C-, (19...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264137/ https://www.ncbi.nlm.nih.gov/pubmed/21934646 http://dx.doi.org/10.3390/molecules16098083 |
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author | Boechat, Nubia Pinheiro, Luiz C.S. Santos-Filho, Osvaldo A. Silva, Isabor C. |
author_facet | Boechat, Nubia Pinheiro, Luiz C.S. Santos-Filho, Osvaldo A. Silva, Isabor C. |
author_sort | Boechat, Nubia |
collection | PubMed |
description | A rational approach was used to synthesize a new set of 15 1H-1,2,4-triazol-3-yl benzenesulfonamide derivatives with the aim of developing new antimalarial lead compounds. These derivatives were prepared in yields between 50% and 62%, and their structures were elucidated using IR, (1)H-, (13)C-, (19)F-NMR, MS and elemental analysis. A docking study based on sulfonamides previously used against malaria identified trifluoromethyl-substituted derivatives to be the best lead compounds for new antimalarial drug development. |
format | Online Article Text |
id | pubmed-6264137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62641372018-12-10 Design and Synthesis of New N-(5-Trifluoromethyl)-1H-1,2,4-triazol-3-yl Benzenesulfonamides as Possible Antimalarial Prototypes Boechat, Nubia Pinheiro, Luiz C.S. Santos-Filho, Osvaldo A. Silva, Isabor C. Molecules Article A rational approach was used to synthesize a new set of 15 1H-1,2,4-triazol-3-yl benzenesulfonamide derivatives with the aim of developing new antimalarial lead compounds. These derivatives were prepared in yields between 50% and 62%, and their structures were elucidated using IR, (1)H-, (13)C-, (19)F-NMR, MS and elemental analysis. A docking study based on sulfonamides previously used against malaria identified trifluoromethyl-substituted derivatives to be the best lead compounds for new antimalarial drug development. MDPI 2011-09-20 /pmc/articles/PMC6264137/ /pubmed/21934646 http://dx.doi.org/10.3390/molecules16098083 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Boechat, Nubia Pinheiro, Luiz C.S. Santos-Filho, Osvaldo A. Silva, Isabor C. Design and Synthesis of New N-(5-Trifluoromethyl)-1H-1,2,4-triazol-3-yl Benzenesulfonamides as Possible Antimalarial Prototypes |
title | Design and Synthesis of New N-(5-Trifluoromethyl)-1H-1,2,4-triazol-3-yl Benzenesulfonamides as Possible Antimalarial Prototypes |
title_full | Design and Synthesis of New N-(5-Trifluoromethyl)-1H-1,2,4-triazol-3-yl Benzenesulfonamides as Possible Antimalarial Prototypes |
title_fullStr | Design and Synthesis of New N-(5-Trifluoromethyl)-1H-1,2,4-triazol-3-yl Benzenesulfonamides as Possible Antimalarial Prototypes |
title_full_unstemmed | Design and Synthesis of New N-(5-Trifluoromethyl)-1H-1,2,4-triazol-3-yl Benzenesulfonamides as Possible Antimalarial Prototypes |
title_short | Design and Synthesis of New N-(5-Trifluoromethyl)-1H-1,2,4-triazol-3-yl Benzenesulfonamides as Possible Antimalarial Prototypes |
title_sort | design and synthesis of new n-(5-trifluoromethyl)-1h-1,2,4-triazol-3-yl benzenesulfonamides as possible antimalarial prototypes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264137/ https://www.ncbi.nlm.nih.gov/pubmed/21934646 http://dx.doi.org/10.3390/molecules16098083 |
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