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3-(1,3,4-恶二唑-2-基)喹唑啉-4(3H)-酮的合成与抗菌活性

Synthesis and antimicrobial activity of 3-(1,3,4-Oxadiazol-2-yl)quinazolin-4(3H)-ones.

作者信息

Patel Navin B, Patel Jaymin C

机构信息

Department of Chemistry, Veer Narmad South Gujarat University, Surat 395007, Gujarat, India.

出版信息

Sci Pharm. 2010 Apr-Jun;78(2):171-93. doi: 10.3797/scipharm.0912-16. Epub 2010 Apr 26.

Abstract

In attempt to find new pharmacologically active molecules, we report here the synthesis and in vitro antimicrobial activity of various 3-(1,3,4-oxadiazol-2-yl)-quinazolin-4(3H)-ones. The antimicrobial activity of title compounds were examined against two gram positive bacteria (S. aureus, S. pyogenes), two gram negative bacteria (E. coli, P. aeruginosa) and three fungi (C. albicans, A. niger, A. clavatus) using the broth microdilution method. Some derivatives bearing a bromo or iodo group exhibited very good antimicrobial activity.

摘要

为了寻找新的具有药理活性的分子,我们在此报告各种3-(1,3,4-恶二唑-2-基)-喹唑啉-4(3H)-酮的合成及其体外抗菌活性。采用肉汤微量稀释法检测了目标化合物对两种革兰氏阳性菌(金黄色葡萄球菌、化脓性链球菌)、两种革兰氏阴性菌(大肠杆菌、铜绿假单胞菌)和三种真菌(白色念珠菌、黑曲霉、棒曲霉)的抗菌活性。一些带有溴或碘基团的衍生物表现出非常好的抗菌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e3d/3002796/edb2a8c6c6c4/scipharm.2010.78.171f1.jpg

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