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某些5-(4-联苯基)-7-芳基[3,4-d][1,2,3]-苯并噻二唑的合成与抗菌活性

Synthesis and antibacterial activity of some 5-(4-biphenylyl)-7-aryl[3,4-d] [1,2,3]-benzothiadiazoles.

作者信息

Balasankar T, Gopalakrishnan M, Nagarajan S

机构信息

Department of Chemistry, Annamalai University, Annamalainagar 608002, Tamil Nadu, India.

出版信息

Eur J Med Chem. 2005 Jul;40(7):728-31. doi: 10.1016/j.ejmech.2005.01.005. Epub 2005 Mar 2.

Abstract

A series of 5-(4-biphenylyl)-7-aryl[3,4-d] [1,2,3]-benzothiadiazoles were synthesized, characterized by IR, NMR and elemental analysis and evaluated for in vitro antibacterial activity against some Gram-positive and Gram-negative bacteria. The antibacterial data revealed that compounds 7a-j had better activity against tested Gram-positive organisms than the reference ciprofloxacin and norfloxacin. However, the compounds were nearly inactive against Gram-negative bacteria. Compound 7c and 7d were the most active compounds against Gram-positive bacteria.

摘要

合成了一系列5-(4-联苯基)-7-芳基[3,4-d][1,2,3]-苯并噻二唑,通过红外光谱、核磁共振和元素分析对其进行了表征,并评估了它们对一些革兰氏阳性菌和革兰氏阴性菌的体外抗菌活性。抗菌数据表明,化合物7a-j对测试的革兰氏阳性菌的活性优于对照品环丙沙星和诺氟沙星。然而,这些化合物对革兰氏阴性菌几乎没有活性。化合物7c和7d是对革兰氏阳性菌活性最强的化合物。

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