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Au2(phen2Me)2(μ-O)2(PF6)2 a Novel Dinuclear Gold(III) Complex Showing Excellent Antiproliferative Properties

机译:Au2(phen2Me)2(μ-O)2(PF6)2一种新型的双核金(III)配合物具有出色的抗增殖性能

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摘要

A novel dioxo-bridged dinuclear gold(III) complex with two 2,9-dimethylphenanthroline ligands was synthesized and thoroughly characterized. Its crystal structure was solved, and its solution behavior assessed. Remarkably, this compound revealed excellent antiproliferative properties in vitro against a wide panel of 36 cancer cell lines, combining a high cytotoxic potency to pronounced tumor selectivity. Very likely, these properties arise from an innovative mode of action (possibly involving histone deacetylase inhibition), as suggested by COMPARE analysis. In turn, electrospray ionization−mass spectrometry studies provided valuable insight into its molecular mechanisms of activation and of interaction with protein targets. Gold(III) reduction, dioxo bridge disruption, coordinative gold(I) binding to the protein, and concomitant release of the phenanthroline ligand were proposed to occur upon interaction with superoxide dismutase, used here as a model protein. Because of the reported results, this new gold(III) compound qualifies itself as an optimal candidate for further pharmacological testing.
机译:合成了具有两个2,9-二甲基菲咯啉配体的新型二氧桥联双核金(III)配合物,并对其进行了全面表征。解析其晶体结构,并评估其溶解行为。值得注意的是,该化合物在体外对36种癌细胞系具有优异的抗增殖特性,并具有高的细胞毒性和明显的肿瘤选择性。如COMPARE分析所建议的,这些特性很可能来自创新的作用方式(可能涉及组蛋白脱乙酰基酶抑制作用)。反过来,电喷雾电离质谱研究提供了对其激活和与蛋白质靶标相互作用的分子机制的宝贵见解。建议在与超氧化物歧化酶相互作用时发生金(III)还原,二氧代桥破坏,与蛋白质结合的配位金(I)以及伴随释放的菲咯啉配体,此处将其用作模型蛋白。由于报告的结果,这种新的金(III)化合物有资格成为进一步药理学测试的最佳候选者。

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