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首页> 外文期刊>Bulletin of the Korean Chemical Society >Synthesis, Characterization and Antimicrobial Activity of New Thiadiazole Derivatives
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Synthesis, Characterization and Antimicrobial Activity of New Thiadiazole Derivatives

机译:新型噻二唑衍生物的合成,表征和抗菌活性

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摘要

A series of thiadiazole derivatives were synthesized with differently substituted benzoic acids which were cyclized to give differently substituted thiazolidin-4-one. Elemental analysis, IR, 1H NMR, 13C NMR and mass spectral data confirmed the structure of the newly synthesized compounds. The derivatives of these moieties were evaluated for antimicrobial activity. Most of the synthesized compounds showed good antimicrobial activity at 200 and 100 レg/mL. Compounds showed most significant antibacterial activity against gram negative test organism Escherichia coli and most significant antifungal activity against test organisms Aspergillus niger and Candida albicans. It was observed that compounds with OCH3 at 3, 4 position of phenyl ring [5(a-l)] were more potent against microbes as compared to compounds having unsubstituted phenyl ring [4(a-l)].
机译:用不同取代的苯甲酸合成了一系列噻二唑衍生物,将其环化以得到不同取代的噻唑烷丁-4-酮。元素分析,IR, 1 H NMR, 13 C NMR和质谱数据证实了新合成化合物的结构。评价这些部分的衍生物的抗微生物活性。大多数合成的化合物在200和100μg/ mL时显示出良好的抗菌活性。化合物对革兰氏阴性测试菌大肠杆菌显示最显着的抗菌活性,对黑曲霉白色念珠菌的测试菌显示最显着的抗菌活性。观察到在苯环[ 5 al )]的3、4位上带有OCH 3 的化合物对微生物的抵抗力更强具有未取代的苯环[ 4 al )]的化合物。

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