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Efficient synthesis and antimicrobial activity of some novel S-β-d-glucosides of 5-aryl-1,2,4-triazole-3-thiones derivatives

机译:5-芳基-1,2,4-三唑-3-硫酮衍生物的一些新型S-β-d-糖苷的高效合成和抗菌活性

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摘要

A series of 3-S-β-d-glucosides-4-arylideneamino-5-aryl-1,2,4-triazoles were rationally designed and synthesized according to the principle of superposition of bioactive substructures by the combination of 1,2,4-triazole, Schiff base and glucosides. The structures of the target compounds have been characterized by 1H NMR, 13C NMR, IR, MS and HRMS. All the newly synthesized compounds have been evaluated for their antimicrobial activities in vitro against Staphylococcus aureus (ATCC 6538), Escherichia coli (ATCC 8099) as well as Monilia albican (ATCC 10231). The bioactive assay showed that most of the tested compounds displayed variable inhibitory effects on the growth of the Gram-positive bacterial strain (Staphylococcus aureus), Gram-negative bacterial strains (Escherichia coli) and fungal strains (Monilia albican). All the target compounds exhibited better antifungal activity than antibacterial activity. Especially, compounds 6b, 6c, 6f, 6j, 6k and 6l showed excellent activity against fungus Monilia albican with MIC values of 16 μg/mL.
机译:根据生物活性亚结构由1,2结合的原理,合理地设计和合成了一系列3-S-β-d-葡萄糖苷-4-芳基氨基-5-芳基-1,2,4-三唑。 4-三唑,席夫碱和葡萄糖苷。目标化合物的结构已通过1H NMR,13C NMR,IR,MS和HRMS进行了表征。已经评估了所有新合成的化合物在体外对金黄色葡萄球菌(ATCC 6538),大肠杆菌(ATCC 8099)和白色念珠菌(ATCC 10231)的抗菌活性。生物活性测定表明,大多数测试化合物对革兰氏阳性细菌菌株(金黄色葡萄球菌),革兰氏阴性细菌菌株(大肠杆菌)和真菌菌株(白色念珠菌)的生长均表现出不同的抑制作用。所有目标化合物均表现出比抗菌活性更好的抗真菌活性。特别地,化合物6b,6c,6f,6j,6k和6l显示出对真菌白念珠菌的优异活性,MIC值为16μg/ mL。

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