合成的s -三嗪衍生物抑菌活性优化

G. Swami, K. Bothara
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引用次数: 0

摘要

新的传染病的出现、几种似乎已得到控制的感染的死灰复燃以及细菌耐药性的增加,使得有必要进行旨在开发新的潜在抗菌剂的研究。合成了一系列新型sTriazine,并对其抗菌活性进行了筛选。化合物R3和R10对金黄色葡萄球菌的抑菌活性最佳;在25ug/ml浓度下,化合物R5对铜绿假单胞菌的抑菌活性最佳,化合物R6对枯草芽孢杆菌、金黄色葡萄球菌的抑菌活性最佳,对大肠杆菌和铜绿假单胞菌的抑菌活性中等
本文章由计算机程序翻译,如有差异,请以英文原文为准。
OPTIMIZATION OF ANTIMICROBIAL ACTIVITY OF SYNTHESIZED S-TRIAZINE DERIVATIVES
The emergence of new infectious diseases, the resurgence of several infections that appeared to have been controlled and the increase in bacterial resistance have created the necessity for studies directed towards the development of new potential antimicrobials. A series of novel sTriazine has been synthesized and screened for antimicrobial activities. The compound R3 and R10 obtained optimum antibacterial activity against S. aureus; compound R5 obtained optimum antibacterial activity against Pseudomonas aeruginosa and compound R6 obtained optimum antibacterial activity against Bacillus substilis, S. aureus and moderate activity against E. coli and P. aeruginosa at 25ug/ml concentration
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