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新型 N-(5-三氟甲基)-1H-1,2,4-三唑-3-基苯磺酰胺类抗疟原虫化合物的设计与合成。

Design and synthesis of new N-(5-trifluoromethyl)-1H-1,2,4-triazol-3-yl benzenesulfonamides as possible antimalarial prototypes.

机构信息

Departamento de Sintese Organica, Instituto de Tecnologia em Farmacos, Fundacao Oswaldo Cruz, Manguinhos, CEP 21041-250, Rio de Janeiro, RJ, Brazil.

出版信息

Molecules. 2011 Sep 20;16(9):8083-97. doi: 10.3390/molecules16098083.

Abstract

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, ¹H-, ¹³C-, ¹⁹F-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.

摘要

采用合理的方法合成了一组新的 15 个 1H-1,2,4-三唑-3-基苯磺酰胺衍生物,旨在开发新的抗疟先导化合物。这些衍生物的产率在 50%至 62%之间,其结构通过 IR、1H-NMR、13C-NMR、19F-NMR、MS 和元素分析得到阐明。基于先前用于抗疟疾的磺胺类药物的对接研究,确定三氟甲基取代衍生物是开发新的抗疟药物的最佳先导化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf8e/6264137/3b46d4cf26f2/molecules-16-08083-g005.jpg

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