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N-[4-(4-取代苯基)-1,3-噻唑-2-基]-1,3,5-三嗪-2-胺的合成与抗菌评估

Synthesis and Antibacterial Assessment of N-[4-(4-substituted phenyl)-1,3-thiazol-2-yl]-1,3,5-triazin-2-amine.

作者信息

Gahtori P, Das A, Bhatt H

机构信息

Department of Pharmacy, Kumaun University, Bhimtal-263 136, India.

出版信息

Indian J Pharm Sci. 2009 Jan;71(1):79-82. doi: 10.4103/0250-474X.51960.

Abstract

In a wide search program towards new and efficient antibacterial agents, we assessed the extent to which physicochemical properties can be exploited to promote antibacterial activity associated with a series of substituted s-triazine. The synthesized compounds (1a-12b) were subsequently screened for their in vitro antibacterial activity against three gram positive (Bacillus subtilis, Bacillus cereus, Staphylococcus aureus) and three Gram-negative microorganism (Salmonella typhi, Escherichia coli, Klebsiella aerogenes) by the broth dilution technique, recommended by European Committee for antimicrobial susceptibility testing with reference to streptomycin.

摘要

在一项针对新型高效抗菌剂的广泛研究计划中,我们评估了利用物理化学性质来促进一系列取代 s-三嗪的抗菌活性的程度。随后,通过肉汤稀释技术,参照链霉素,按照欧洲抗菌药物敏感性试验委员会推荐的方法,对合成的化合物(1a - 12b)针对三种革兰氏阳性菌(枯草芽孢杆菌、蜡样芽孢杆菌、金黄色葡萄球菌)和三种革兰氏阴性菌(伤寒沙门氏菌、大肠杆菌、产气克雷伯菌)进行了体外抗菌活性筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/320f/2810059/43ec65bb0fa3/IJPhS-71-79-g001.jpg

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