首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis and Antimicrobial Activity of Some New N-substituted-5- arylidene-thiazolidine-2,4-diones
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Synthesis and Antimicrobial Activity of Some New N-substituted-5- arylidene-thiazolidine-2,4-diones

机译:一些新的N-取代的5-亚芳基-噻唑烷-2,4-二酮的合成及抑菌活性

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摘要

A total of 17 new N-substituted derivatives (2b–k and 3b–h) of 5-((2-phenylthiazol-4-yl)methylene) thiazolidine-2,4-dione (2a) and 5-(2,6-dichloro- benzylidene)thiazolidine-2,4-dione (3a) were synthesized. The structural elucidation of the newly synthesized compounds was based on elemental analysis and spectroscopic data (MS, ~1H NMR, ~(13)C NMR), and their antimicrobial activities were assessed in vitro against several strains of Gram-positive and Gram-negative bacteria and one fungal strain (Candida albicans) as growth inhibition diameter. Some of them showed modest to good antibacterial activity against Gram-negative Escherichia coli and Salmonella typhimurium and Gram-positive Staphylococcus aureus, Bacillus cereus, and Enterococcus fecalis bacterial strains, whereas almost all the compounds were inactive against Listeria monocytogenes. All of the synthesized compounds showed moderate to very good activity against C. albicans.
机译:总共17种新的5-((2-苯基噻唑-4-基)亚甲基)噻唑烷-2,4-二酮(2a)和5-(2,6)的N-取代衍生物(2bk和3bh)合成了-二氯亚苄基)噻唑烷-2,4-二酮(3a)。基于元素分析和光谱数据(MS,〜1H NMR,〜(13)C NMR)对新合成化合物的结构进行了阐明,并在体外评估了它们对几种革兰氏阳性和革兰氏阴性菌株的抗菌活性细菌和一种真菌菌株(白色念珠菌)作为生长抑制直径。他们中的一些对革兰氏阴性大肠杆菌和鼠伤寒沙门氏菌和革兰氏阳性金黄色葡萄球菌,蜡状芽孢杆菌和费氏肠球菌细菌菌株显示出中等至良好的抗菌活性,而几乎所有化合物对单核细胞增生李斯特菌均无活性。所有合成的化合物均显示出对白色念珠菌的中等至非常好的活性。

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