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双核铜(II)配合物的合成及晶体结构,该配合物由 N-(2-羟基苯基)-N'-[3-(二乙氨基)丙基]氧酰胺桥连:体外抗癌活性及与 DNA 和蛋白质的反应性。

Synthesis and crystal structure of binuclear copper(II) complex bridged by N-(2-hydroxyphenyl)-N'-[3-(diethylamino)propyl]oxamide: in vitro anticancer activity and reactivity toward DNA and protein.

机构信息

Marine Drug & Food Institute, Ocean University of China, Qingdao, Shandong, People's Republic of China.

出版信息

J Biochem Mol Toxicol. 2013 Aug;27(8):412-24. doi: 10.1002/jbt.21504. Epub 2013 Jun 18.

DOI:10.1002/jbt.21504
PMID:23780852
Abstract

A new oxamido-bridged bicopper(II) complex, Cu2(pdpox)(bpy)(CH3OH), where H3pdpox and bpy stand for N-(2-hydroxyphenyl)-N'-[3-(diethylamino)propyl]oxamide and 2,2'-bipyridine, respectively, has been synthesized and characterized by elemental analyses, molar conductivity measurements, infrared and electronic spectra studies, and X-ray single crystal diffraction. In the crystal structure, the pdpox(3-) ligand bridges two copper(II) ions as cisoid conformation. The inner copper(II) ion has a {N3O} square-planar coordination geometry, while the exo- one is in a {N2O3} square-pyramidal environment. There are two sets of interpenetrating two-dimensional hydrogen bonding networks parallel to the planes (2 1 0) and (21¯0), respectively, to form a three-dimensional supramolecular structure. The bicopper(II) complex exhibits cytotoxic activity against the SMMC7721 and A549 cell lines. The reactivity toward herring sperm DNA and bovine serum albumin revealed that the bicopper(II) complex can interact with the DNA by intercalation mode, and the complex binds to protein BSA responsible for quenching of tryptophan fluorescence by static quenching mechanism.

摘要

一种新型的氧肟酸桥联双铜(II)配合物,Cu2(pdpox)(bpy)(CH3OH),其中 H3pdpox 和 bpy 分别代表 N-(2-羟基苯基)-N'-[3-(二乙氨基)丙基]氧酰胺和 2,2'-联吡啶,通过元素分析、摩尔电导率测量、红外和电子光谱研究以及 X 射线单晶衍射进行了合成和表征。在晶体结构中,pdpox(3-)配体以顺式构象桥联两个铜(II)离子。内铜(II)离子具有{ N3O } 正方形平面配位几何形状,而外铜(II)离子则处于{ N2O3 } 正方形金字塔环境中。有两组相互穿插的二维氢键网络,分别平行于(210)和(21¯0)平面,形成三维超分子结构。双铜(II)配合物对 SMMC7721 和 A549 细胞系表现出细胞毒性活性。与鲱鱼精 DNA 和牛血清白蛋白的反应表明,双铜(II)配合物可以通过嵌入模式与 DNA 相互作用,并且该配合物通过静态猝灭机制与负责色氨酸荧光猝灭的蛋白质 BSA 结合。

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