首页> 美国卫生研究院文献>ACS Omega >Synthesis and Antimicrobial Studies of 4-3-(3-Fluorophenyl)-4-formyl-1H-pyrazol-1-ylbenzoic Acid and 4-3-(4-Fluorophenyl)-4-formyl-1H-pyrazol-1-ylbenzoic Acid as Potent Growth Inhibitorsof Drug-Resistant Bacteria
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Synthesis and Antimicrobial Studies of 4-3-(3-Fluorophenyl)-4-formyl-1H-pyrazol-1-ylbenzoic Acid and 4-3-(4-Fluorophenyl)-4-formyl-1H-pyrazol-1-ylbenzoic Acid as Potent Growth Inhibitorsof Drug-Resistant Bacteria

机译:4- 3-(3-氟苯基)-4-甲酰基-1H-吡唑-1-基苯甲酸和4- 3-(4-氟苯基)-4-甲酰基-1H-吡唑- 1-基苯甲酸作为有效的生长抑制剂耐药菌

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摘要

Microbial resistance to antibiotics is an urgent and worldwide concern. Several pyrazole-derived hydrazones were synthesized by using benign reaction conditions. Several of these molecules are potent growth inhibitors of drug-resistant strains of Staphylococcus aureus and Acinetobacter baumannii with minimum inhibitory concentration values as low as 0.39 μg/mL. Furthermore, these molecules are nontoxic to human cells at high concentrations. Some of these molecules were tested for their ability to disrupt the bacterial membrane by using the SYTO-9/propidium iodide (BacLight) assay.
机译:微生物对抗生素的耐药性是迫切和全世界关注的问题。利用良性反应条件合成了几种吡唑衍生的azo。这些分子中的几种是金黄色葡萄球菌和鲍曼不动杆菌的耐药菌株的有效生长抑制剂,最低抑菌浓度值低至0.39μg/ mL。此外,这些分子在高浓度下对人细胞无毒。通过使用SYTO-9 /碘化丙啶(BacLight)分析测试了其中一些分子破坏细菌膜的能力。

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