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混合配体铜(II)N2O2配合物:仿生合成、体外活性及生物学模型、理论计算

Mixed ligand Cu(II)N2O2 complexes: biomimetic synthesis, activities in vitro and biological models, theoretical calculations.

作者信息

Li Chen, Yin Bing, Kang Yifan, Liu Ping, Chen Liang, Wang Yaoyu, Li Jianli

机构信息

Ministry of Education Key Laboratory of Synthetic and Natural Functional Molecule Chemistry, College of Chemistry & Materials Science, Northwest University , Xi'an, Shaanxi 710069, P. R. China.

出版信息

Inorg Chem. 2014 Dec 15;53(24):13019-30. doi: 10.1021/ic5021548. Epub 2014 Dec 3.

Abstract

Three new mixed ligand Cu(II)N2O2 complexes, namely, [Cu(II)(2-A-6-MBT)2(m-NB)2] (1), [Cu(II)(2-ABT)2(m-NB)2] (2), and [Cu(II)(2-ABT)2(o-NB)2] (3), (2-A-6-MBT = 2-amino-6-methoxybenzothiazole, m-NB = m-nitrobenzoate, 2-ABT = 2-aminobenzothiazole, and o-NB = o-nitrobenzoate), have been prepared by the biomimetic synthesis strategy, and their structures were determined by X-ray crystallography studies and spectral methods. These complexes exhibited the effective superoxide dismutase (SOD) activity and catecholase activity. On the basis of the experimental data and computational studies, the structure-activity relationship for these complexes was investigated. The results reveal that electron-accepting abilities of these complexes and coordination geometries have significant effects on the SOD activity and catecholase activity. Then, we found that 1 and 2 exerted potent intracellular antioxidant capacity in the model of H2O2-induced oxidative stress based on HeLa cervical cancer cells, which were screened out by the cytotoxicity assays of different kinds of cells. Furthermore, 1-3 showed the favorable biocompatibility in two different biological models: Saccharomyces cerevisiae and human vascular endothelial cells. These biological experimental data are indicative of the promising application potential of these complexes in biology and pharmacology.

摘要

通过仿生合成策略制备了三种新型混合配体铜(II)N2O2配合物,即[Cu(II)(2 - A - 6 - MBT)2(间 - NB)2](1)、[Cu(II)(2 - ABT)2(间 - NB)2](2)和[Cu(II)(2 - ABT)2(邻 - NB)2](3),(2 - A - 6 - MBT = 2 - 氨基 - 6 - 甲氧基苯并噻唑,间 - NB = 间硝基苯甲酸酯,2 - ABT = 2 - 氨基苯并噻唑,邻 - NB = 邻硝基苯甲酸酯),并通过X射线晶体学研究和光谱方法确定了它们的结构。这些配合物表现出有效的超氧化物歧化酶(SOD)活性和儿茶酚酶活性。基于实验数据和计算研究,研究了这些配合物的构效关系。结果表明,这些配合物的电子接受能力和配位几何结构对SOD活性和儿茶酚酶活性有显著影响。然后,我们发现基于Hela宫颈癌细胞的H2O2诱导氧化应激模型中,1和2具有强大的细胞内抗氧化能力,这是通过对不同种类细胞的细胞毒性测定筛选出来的。此外,1 - 3在两种不同的生物学模型:酿酒酵母和人血管内皮细胞中表现出良好的生物相容性。这些生物学实验数据表明这些配合物在生物学和药理学方面具有广阔的应用潜力。

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