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Biscarbene gold(i) complexes: structure–activity-relationships regarding antibacterial effects cytotoxicity TrxR inhibition and cellular bioavailability

机译:Biscarbene gold(i)复合物:关于抗菌作用细胞毒性TrxR抑制和细胞生物利用度的结构-活性-关系

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摘要

A series of gold(i) complexes with two N-heterocyclic carbene ligands (biscarbene gold complexes) were prepared and evaluated for their effects against cancer cells and pathogenic bacteria. Proliferation inhibition was observed in cancer cells and in Gram-positive bacteria, whereas Gram-negative bacteria were less sensitive towards the compounds. The protein binding and cellular uptake were quantified and the combined results indicated a strong correlation between cellular bioavailability and antiproliferative effects. The biscarbene gold complexes inhibited bacterial and mammalian TrxRs with low to moderate potency. However, based on the obtained structure–activity-relationships and the high cellular accumulation levels, TrxR inhibition can be considered as a relevant contributor to the cellular pharmacology of biscarbene gold(i) complexes.
机译:制备了具有两个N-杂环卡宾配体的一系列金(i)配合物(双卡宾金配合物),并评估了它们对癌细胞和病原菌的作用。在癌细胞和革兰氏阳性细菌中观察到增殖抑制,而革兰氏阴性细菌对化合物的敏感性较低。定量蛋白质结合和细胞摄取,合并结果表明细胞生物利用度和抗增殖作用之间有很强的相关性。双卡宾金络合物以低至中等的效力抑制细菌和哺乳动物的TrxR。但是,基于获得的结构-活性关系和高细胞积累水平,TrxR抑制作用可以被认为是双卡宾金(i)配合物的细胞药理作用的相关因素。

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