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首页> 外文期刊>Quimica nova >In vitro antibacterial activity and toxicity toward Artemia salina Leach of some triazene compounds
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In vitro antibacterial activity and toxicity toward Artemia salina Leach of some triazene compounds

机译:对一些三氮杂化合物的Artemia Salina Leach的体外抗菌活性和毒性

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摘要

Bacterial resistance to antibacterial agents is currently a major concern. We report the synthesis, in vitro antibacterial activity and toxicity toward Artemia salina of six diaryltriazene compounds bearing different substituent groups. Minimal Inhibitory Concentration (MIC) and Minimal Bactericidal Concentration (MBC) values against standard strains (ATCC) and clinical isolates (including ESBL, MBL and AmpC strains) were good to very good, in the range 8 to 128 mg mL-1. Results suggest that hydroxyl, 4-carboxyl and 4-phenyldiazenil groups attached to the diaryltriazenes provide enhanced activity. Toxicity results showed very low LC50 values for three compounds (10-fold lower than DTIC).
机译:对抗菌剂的细菌性是目前是一个主要问题。我们向携带不同取代基的六个二芳基化合物的蒿属盐沼报告合成,体外抗菌活性和毒性。对标准菌株(ATCC)和临床分离株(包括ESBL,MBL和AMPC菌株在内的临床分离株(包括ESBL,MBL和AMPC菌株)的最小抑制浓度(MIC)和最小的杀菌浓度(MBC)值良好,在8-128mg ML-1的范围内。结果表明,附着于二芳基氮的羟基,4-羧基和4-苯基二亚硝尼尔基团提供增强的活性。毒性结果显示出三种化合物的LC50值非常低(低于DTIC)。

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