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New 5-substituted-1,3,4-thiadiazole-2(3H)-thioneDerivatives: Synthesis and Their In vitroAntimicrobial Properties

机译:新的5-取代的1,3,4-噻二唑-2(3H)-硫酮衍生物:合成及其体外抗菌性能

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In this paper a new series of 1,3,4-thiadiazole derivatives have been designed, synthesized and evaluated as antimicrobial agents. New compounds were prepared by the reaction of 5-amino-1,3,4-thiadiazole-2(3 H )-thione with appropriate aldehydes. The structures of the obtained compounds were confirmed by means of ~(1)H NMR and ~(13)C NMR. All synthesized compounds were tested for their in vitro antibacterial and antifungal activities using the broth microdilution method. Our results showed that the three of synthesized compounds had bactericidal or fungicidal effect against reference strains of Gram-positive bacteria, mainly opportunistic S. epidermidis , M. luteus , Bacillus spp., and yeast belonging to Candida spp.
机译:本文设计,合成和评估了一系列新的1,3,4-噻二唑衍生物作为抗菌剂。通过使5-氨基-1,3,4-噻二唑-2(3 H)-硫酮与适当的醛反应来制备新化合物。借助〜(1)H NMR和〜(13)C NMR确认所获得的化合物的结构。使用肉汤微稀释法测试所有合成的化合物的体外抗菌和抗真菌活性。我们的结果表明,这三种合成的化合物对革兰氏阳性细菌的参考菌株(主要是机会表皮葡萄球菌,黄体分枝杆菌,芽孢杆菌和属于念珠菌的酵母菌)具有杀菌或杀真菌作用。

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