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Antimicrobial Activities and In silico Analysis of Methoxy Amino Chalcone Derivatives

机译:抗菌活性和甲氧基氨基氨基酮衍生物的硅分析

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A series of methoxy-4'-amino chalcone derivatives were tested for their antimicrobial activities against Escherichia coli ATCC 25923, Staphylococcus aureus ATCC 25922 and Candida albicans ATCC 10231. Furthermore, their molecular interactions with dihydropteroate synthase (DHPS) of E. coli and S. aureus were studied with a docking experiment. Compound 4 ((E)-1-(4-aminophenyl)-3-(2,3-dimethoxyphenyl)prop-2-en-l-one) exhibited the strongest activity, in which its activity was equal to sulfamerazine and sulfadiazine used as positive controls. In addition, it showed a good potential to be used as a wide spectrum antimicrobial agent. The in silico experiment showed that the prepared compounds had higher affinity to DHPS of S. aureus than to DHPS of E. coli. The tested compounds showed high similarity interaction with hydroxymethylpterin pyrophosphate (natural substrate of DHPS) in building intermolecular interactions.
机译:测试一系列甲氧基-4'-氨基胆酮衍生物,用于对来自大肠杆菌ATCC 25923,葡萄球菌ATCC 25922和Candida albicans ATCC 10231的抗菌活性进行抗微生物活性。此外,它们与大肠杆菌和S的二氢酯合酶(DHPS)的分子相互作用。 。使用对接实验研究了金黄色葡萄球菌。化合物4((e)-1-(4-氨基苯基)-3-(2,3-二甲氧基苯基)PR-2-EN-L-ON)表现出最强的活性,其中其活性等于磺胺嘧啶和磺胺扎氨酸作为阳性对照。此外,它表明用作宽谱抗微生物剂的良好潜力。在硅实验表明,制备的化合物对DHPS的S.UUREUS的亲和力较高而不是大肠杆菌的DHP。测试化合物显示出高度相似性与构建分子间相互作用的与羟甲基甲基酯蛋白焦磷酸酯(DHPS天然底物)相互作用。

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