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摘要:
Bacterial infections present a serious challenge to healthcare practitioners due to the emergence of resistance to numerous conventional antibacterial drugs. Therefore, new bacterial targets and new antimicrobials are unmet medical needs. Rhodanine derivatives are known to possess potent antimicrobial activities. In this study, we determined the activity spectrum of a series of new rhodanine derivatives against representative Gram-positive and Gram-negative bacterial strains. Compounds 3a and 5a had the highest activity with minimum inhibitory concentrations in the range of 1.12 - 2.5 μg/mL. Transmission electron microscope results confirmed that activities against bacteria occurred via rupturing of the cell wall. Molecular modeling results suggested that rhodanine derivatives have the potential to irreversibly bind to the penicillin-binding protein (PBP) Ser62 residue in the active site. Thus, our results suggested that these rhodanine derivatives could be potential antibacterial drug candidates with strong activity against Gram-negative bacteria.
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篇名 Design, Synthesis, <i>in Vitro</i>Antibacterial Activity, and Docking Studies of New Rhodanine Derivatives
来源期刊 药物化学期刊(英文) 学科 化学
关键词 RHODANINE Compounds PBP Β-LACTAMASE Enzyme DOCKING
年,卷(期) 2020,(1) 所属期刊栏目
研究方向 页码范围 15-34
页数 20页 分类号 O62
字数 语种
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研究主题发展历程
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RHODANINE
Compounds
PBP
Β-LACTAMASE
Enzyme
DOCKING
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期刊影响力
药物化学期刊(英文)
季刊
2164-3121
武汉市江夏区汤逊湖北路38号光谷总部空间
出版文献量(篇)
64
总下载数(次)
0
总被引数(次)
0
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