首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and antimicrobial activities of some 3-arylamino-5-(2-(substituted 1-imidazolyl)ethyl)-1,2,4-triazole derivatives.
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Synthesis and antimicrobial activities of some 3-arylamino-5-(2-(substituted 1-imidazolyl)ethyl)-1,2,4-triazole derivatives.

机译:某些3-芳基氨基-5-(2-(取代的1-咪唑基)乙基)-1,2,4-三唑衍生物的合成和抑菌活性。

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摘要

In this study, some 3-arylamino-5-[2-(substituted imidazol-1-yl or benzimidazol-1-yl)ethyl]-1,2,4-triazole derivatives were synthesised by reacting 3-(substituted imidazol-1-yl)propionyl hydrazides, with S-methyl-N'-arylisothiouronium iodide salts. Their structures were elucidated by IR, 1H-NMR and mass spectroscopic data and elemental analyses results. Antimicrobial activities of the compounds were observed against Staphylococcus aureus NRRL B-767, Micrococcus luteus NRRL B-4375, Escherichia coli B, Pseudomonas aeroginosa NRRL B-23 and the fungi Candida albicans and Candida glabrata by using the tube dilution technique. Remarkable activity was obtained.
机译:在这项研究中,通过使3-(取代的咪唑-1)反应,合成了一些3-芳基氨基-5- [2-(取代的咪唑-1-基或苯并咪唑-1-基)乙基] -1,2,4-三唑衍生物。 (-基)丙酰肼,与S-甲基-N'-芳基异硫脲碘化物盐。通过IR,1 H-NMR和质谱数据以及元素分析结果阐明了它们的结构。通过使用管稀释技术,观察到该化合物对金黄色葡萄球菌NRRL B-767,黄褐微球菌NRRL B-4375,大肠杆菌B,铜绿假单胞菌NRRL B-23和真菌白色念珠菌和光滑念珠菌的抗菌活性。获得了显着的活性。

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