首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >New copper(I) and heteronuclear copper(I)-ruthenium(II) complexes: Synthesis, structural characterization and cytotoxicity
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New copper(I) and heteronuclear copper(I)-ruthenium(II) complexes: Synthesis, structural characterization and cytotoxicity

机译:新的铜(I)和异核铜(I) - 钌(II)复合物:合成,结构表征和细胞毒性

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A new family of copper(I) complexes of general formula [Cu(dppe)(NN)](+) have been synthesized and fully characterized, with dppe = 1.2-bis(diphenylphosphino)ethane and NN representing several bidentate heteroaromatic ligands: 22'-bipy = 2.2'-bipyridine (1), Me(2)bpy = 4.4'-dimethyl-2,2'-bipyridine (2), dpytz = 3-(2-pyridyl)-5,6-diphenyl-1,2,4-triazine (3), dpp = 2.3-bis(2-pyridyl)pyrazine (4), and the metallaligand [Ru(eta(5)-C5H5)(PPh3)(dpp)](+) (5), yielding the bimetallic copper(l)-ruthenium(II) complex [Cu( dppe)( mu-dpp)Ru(eta(5)-O5H5)(PPh3)](2+) (6). The single crystal structures of complexes (2) and (4) were determined by Xray diffraction studies. All the complexes exhibit high cytotoxicity against the human cancer cells A2780 and MCF7 with IC50 values far lower than those found for the antitumor drug cisplatin in the same cell lines and even surpassing cisplatin resistance in the A2780cisR cells. They display IC50 values on the human embryonic kidney HEK293 non-tumoral cells of the same order of magnitude as those found for the tumoral cells. In the ovarian cells the compounds induce rapid production of reactive oxygen species (ROS) probably through mitochondrial pathways. According to the results reported here, these compounds can be considered as prospective antitumoral agents that deserve further evaluation. (C) 2017 Elsevier Inc. All rights reserved.
机译:合成了一类新的通式[Cu(dppe)(NN)](+)铜(I)配合物,并对其进行了充分表征,其中dppe=1.2-双(二苯基膦)乙烷和NN代表几种双齿杂芳香配体:22'-bipy=2.2'-bipyridine(1),Me(2)bpy=4.4'-dimethyl-2,2'-bipyridine(2),dpytz=3-(2-吡啶基)-5,6-二苯基-1,2,4-三嗪(3),dpp=2.3-双(2-吡啶基)吡嗪(4),以及金属配体[Ru(eta(5)-C5H5)(PPh3)(dpp)](+)(5),产生双金属铜(l)-钌(II)络合物[Cu(dppe)(mu-dpp)Ru(eta(5)-O5H5)(PPh3)](2+(6)。通过X射线衍射研究确定了配合物(2)和(4)的单晶结构。所有复合物对人类癌细胞A2780和MCF7都表现出很高的细胞毒性,IC50值远低于在同一细胞系中发现的抗肿瘤药物顺铂,甚至超过A2780cisR细胞对顺铂的耐药性。它们在人类胚胎肾HEK293非肿瘤细胞上显示IC50值,其数量级与肿瘤细胞相同。在卵巢细胞中,这些化合物可能通过线粒体途径诱导活性氧(ROS)的快速产生。根据本文报道的结果,这些化合物可以被认为是值得进一步评估的潜在抗肿瘤药物。(C) 2017爱思唯尔公司版权所有。

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