首页> 外文期刊>Research communications in molecular pathology and pharmacology >Novel compounds, 1,3-selenazine derivatives, as antibacterial agents against Escherichia coli and Staphylococcus aureus.
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Novel compounds, 1,3-selenazine derivatives, as antibacterial agents against Escherichia coli and Staphylococcus aureus.

机译:新型化合物1,3-selenazine衍生物,作为针对大肠杆菌和金黄色葡萄球菌的抗菌剂。

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摘要

The antibacterial activities of several kinds of novel 4H-5,6-dihydro-1,3-selenazine derivatives against Escherichia coli and Staphylococcus aureus were investigated. 4-Hydroxy-4-methyl-2-p-tolyl-4H-5,6-dihydro-1,3-selenazine (TS-1), 4-ethyl-4-hydroxy-2-p-tolyl-4H-5,6-dihydro-1,3-selenazine (TS-2), and 4-hydroxy-4-methyl-2-pentyl-4H-5,6-dihydro-1,3-selenazine (PS-1) exhibited strong inhibitory activity against E. coli, and TS-1, TS-2, PS-1, 4-hydroxy-4-methyl-2-pentyl-6-propyl-4H-5,6-dihydro-1,3-selenazine (PS-6) and 4-hydroxy-4-methyl-2-pentyl-6-phenyl-4H-5,6-dihydro-1,3-selenazine (PS-8) also showed inhibitory activity against S. aureus. 4H-5,6-dihydro-1,3-thiazines and 1,3-selenazole had no inhibitory activities against both bacteria. TS-1, TS-2, and PS-1 exhibited marked antibacterial activities against both Gram-negative and Gram-positive bacteria.
机译:研究了几种新型的4H-5,6-二氢-1,3-硒嗪衍生物对大肠杆菌和金黄色葡萄球菌的抗菌活性。 4-羟基-4-甲基-2-对甲苯基-4H-5,6-二氢-1,3-硒嗪(TS-1),4-乙基-4-羟基-2-对甲苯基-4H-5 ,6-二氢-1,3-硒嗪(TS-2)和4-羟基-4-甲基-2-戊基-4H-5,6-二氢-1,3-硒嗪(PS-1)具有较强的抑制作用对大肠杆菌和TS-1,TS-2,PS-1、4-羟基-4-甲基-2-戊基-6-丙基-4H-5,6-二氢-1,3-硒硒嗪(PS -6)和4-羟基-4-甲基-2-戊基-6-苯基-4H-5,6-二氢-1,3-硒嗪(PS-8)也表现出对金黄色葡萄球菌的抑制活性。 4H-5,6-二氢-1,3-噻嗪和1,3-硒代唑对两种细菌均无抑制活性。 TS-1,TS-2和PS-1对革兰氏阴性和革兰氏阳性细菌均显示出显着的抗菌活性。

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