1,3,4 -恶二唑类抗菌抗真菌药物的研究

B. Revanasiddappa, E. Subrahmanyam
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引用次数: 1

摘要

在POCl3的存在下,通过INH(1)和取代芳香酸(2)的反应合成了一系列新的1,3,4 -恶二唑(3a-j)。根据IR、1H NMR和质谱数据确定了新化合物。对所获化合物进行了体外抗菌和抗真菌活性测定,并与标准药物进行了比较。第4位的给电子和吸电子基团的存在是表现出良好活性的主要原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study on 1, 3, 4-Oxadiazole Derivatives as an Antibacterial and Antifungal Agents
In the present investigation a new series of 1, 3, 4-oxadiazoles (3a-j) were synthesized by reacting INH (1) and substituted aromatic acids (2) in presence of POCl3. The new compounds were established on the basis of IR, 1H NMR and Mass spectral data. The compounds were subjected for In-vitro antibacterial and antifungal activities and compared with the standard drugs Some of the tested compounds showed good activity against all the organisms. The presence of electron donating and withdrawing groups at the fourth position is mainly responsible for showing the good activity.
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