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首页> 外文期刊>Inorganica Chimica Acta >Design, synthesis, molecular docking studies of organotin-drug derivatives as multi-target agents against antibacterial, antifungal, alpha-amylase, alpha-glucosidase and butyrylcholinesterase
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Design, synthesis, molecular docking studies of organotin-drug derivatives as multi-target agents against antibacterial, antifungal, alpha-amylase, alpha-glucosidase and butyrylcholinesterase

机译:有机素 - 药物衍生物作为针对抗菌,抗菌,α-淀粉酶,α-葡糖苷酶和丁酰胆碱酯酶的多目标试剂的设计,合成,分子对接研究

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摘要

A series of organotin esters has been synthesized using a diverse array of drugs containing carboxylic function with triphenyl/tributyltin. The synthesized derivatives were bioevaluated for antibacterial, anti fungal and enzyme inhibition (alpha-amylase, alpha-glucosidase and butyrylcholinesterase) activities. Interestingly, compound 3c was found to be most potent in all bioassay and showed higher activity than the standards in case of antibacterial and antifungal activity.
机译:已经使用含有羧基功能的多样化药物合成了一系列有机汀酯,其具有与三烯基/枝丁基锡的羧基功能。 合成的衍生物为抗菌,抗真菌和酶抑制(α-淀粉酶,α-葡糖苷酶和丁酰基胆管酶)活性的生物预测。 有趣的是,在所有生物测定中发现化合物3C最有效,并且在抗菌和抗真菌活性的情况下表现出比标准更高的活性。

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