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首页> 外文期刊>Der Pharma Chemica: journal for medicinal chemistry, pharmaceutical chemistry and computational chemistry >Design, practical synthesis and biological evaluation of novel 1,3,4-oxadiazole derivatives incorporated with quinolone moiety as microbial agents
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Design, practical synthesis and biological evaluation of novel 1,3,4-oxadiazole derivatives incorporated with quinolone moiety as microbial agents

机译:结合喹诺酮部分作为微生物剂的新型1,3,4-恶二唑衍生物的设计,实用合成和生物学评估

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摘要

A series of novel 1,3,4-oxadiazole derivatives incorporated with quinolone moiety were designed and synthesized as biological compounds. In vitro antibacterial activity of the synthesized compounds (5a-g) was performed against Gram +ve microorganisms Staphylococcus aureus (MTCC No. 96), Pseudomonas aeruginosa (MTCC No. 1688), Bacillus subtillis (MTCC No. 121) and Gram -ve microorganisms Escherichia coli (MTCC No. 521). In vitro antifungal activity of compounds was screened against Candida albicans. The structure of all new compounds was confirmed by IR, 1H-NMR and Mass spectra.
机译:设计并合成了一系列与喹诺酮部分结合的新型1,3,4-恶二唑衍生物,并将其作为生物化合物合成。合成的化合物(5a-g)对革兰氏+ ve微生物金黄色葡萄球菌(MTCC编号96),铜绿假单胞菌(MTCC编号1688),枯草芽孢杆菌(MTCC编号121)和革兰氏大肠杆菌(MTCC 521)。筛选了化合物对白色念珠菌的体外抗真菌活性。所有新化合物的结构均通过IR,1H-NMR和质谱证实。

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