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首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Synthesis and in vitro antimicrobial activity of new 4-phenyl-5-methyl-4 H -1,2,4-triazole-3-thione derivatives
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Synthesis and in vitro antimicrobial activity of new 4-phenyl-5-methyl-4 H -1,2,4-triazole-3-thione derivatives

机译:新的4-苯基-5-甲基-4 H -1,2,4-三唑-3-硫酮衍生物的合成及其体外抗菌活性

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Abstract This study presents the synthesis, spectral analysis and antimicrobial evaluation of a new series of substituted 1,2,4-triazole ( 5a–i ) and 1,3,4-thiadiazole derivatives ( 9a, c, g, h ). New compounds were obtained by cyclization reaction of acyl thiosemicarbazide derivatives in the presence of alkaline and acidic media. All synthesized compounds were screened for their in vitro antimicrobial activities. Nine of the compounds had potential activity against Gram-positive bacteria (MIC?=?3.91–500 μg/mL). Some compounds showed good activity especially against: Micrococcus luteus ATCC 10240 (MIC?=?3.91?31.25 μg/mL), Bacillus subtilis ATCC 6633 (MIC?=?15.63? 62.5 μg/mL), and Staphylococcus aureus ATCC 25923 (MIC?=?15.63?125 μg/mL).
机译:摘要本研究介绍了一系列新的取代的1,2,4-三唑(5a–i)和1,3,4-噻二唑衍生物(9a,c,g,h)的合成,光谱分析和抗菌性能。在碱性和酸性介质存在下,通过酰基硫代氨基脲化合物的环化反应获得新化合物。筛选所有合成的化合物的体外抗菌活性。其中的9种化合物具有抗革兰氏阳性细菌的潜在活性(MIC≥3.91–500μg/ mL)。一些化合物表现出良好的活性,特别是对以下化合物:黄色微球菌ATCC 10240(MIC?=?3.91?31.25μg/ mL),枯草芽孢杆菌ATCC 6633(MIC?=?15.63?62.5μg/ mL)和金黄色葡萄球菌ATCC 25923(MIC? =≤15.63≤125μg/ mL)。

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