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首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis and In Vitro Antimicrobial Activity of 1,3,4-Oxadiazole-2-thiol and its Analogs
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Synthesis and In Vitro Antimicrobial Activity of 1,3,4-Oxadiazole-2-thiol and its Analogs

机译:1,3,4-恶二唑-2-硫醇及其类似物的合成及体外抗菌活性

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摘要

The present communication deals with the synthesis of 1,3,4-oxadiazole-2-thiol derivatives containing cyclic secondary amines such as morpholine, N-methyl piperizine, and piperizine. The structural elucidation is based on the spectral data (IR, H-1 NMR, and C-13 NMR) .The newly synthesized compounds were then tested for their antimicrobial activity against a representative panel of micro-organisms such as Bacillus subtilis, Escherichia coli and Candida albicans by using ciprofloxacin and fluconazole as reference drugs for bacteria and fungi, respectively. These synthesized compounds showed moderate to potential antibacterial and antifungal activity in the range of 6-50M against the selected bacteria and 12-50M against the most common fungi, respectively.
机译:本来文涉及1,3,4-恶二唑-2-硫醇衍生物的合成,该衍生物含有环状仲胺,如吗啉,N-甲基哌嗪和哌嗪。结构解析是基于光谱数据(IR,H-1 NMR和C-13 NMR)进行的,然后测试了新合成的化合物对诸如枯草芽孢杆菌,大肠杆菌等代表性微生物的抗菌活性。环丙沙星和氟康唑分别用作细菌和真菌的参考药物和白色念珠菌。这些合成的化合物对选定的细菌分别表现出中度至潜在的抗菌和抗真菌活性,范围为6-50M,对最常见的真菌为12-50M。

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