基于对异丙基甲苯和二甲基双胍的对称双核钌(Ⅱ)配合物的合成及其体外抗癌活性
Symmetrical Diruthenium(Ⅱ) Complex Based on 1-Isopropyl-4-methylbenzene and Dimethylbiguanide: Synthesis and Anticancer Activity in Vitro
作者单位E-mail
余群英 九江学院药学与生命科学学院, 九江 332000 qunyingyu@qq.com 
摘要: 在碱性水溶液中合成了一种对称双核桥联配合物(NH42[Ru(Cym)(L)]2Cl2·4H2O(1)(Cym=对异丙基甲苯,H2L=1,1-二甲基双胍)。采用红外光谱、核磁共振谱和X射线单晶衍射进行了结构表征,结晶水数目由热重分析法得出。采用MTT法测定了其对4种人癌细胞系HepG-2、A549、Hela、MCF-7的细胞毒性,以临床用药顺铂为对照,结果表明该配合物对HepG-2(肝细胞癌,HCC)的作用与顺铂相当。
关键词: 钌配合物  晶体结构  抗癌活性  顺铂
基金项目: 江西省教育厅科学技术基金(No.GJJ180907)和江西省卫生健康委科技计划项目(No.202131075)资助。
Abstract: A novel symmetrical dinuclear bridging complex (NH4)2[Ru(Cym)(L)]2Cl2·4H2O (1) (Cym=p-cymene=1-isopropyl-4-methylbenzene, H2L=1,1-dimethylbiguanide) was obtained by treatment of the precursor[Ru(Cym)Cl2]2 with metformin hydrochloride. In aqueous base solution, deprotonation of the proligand (1,1-dimethylbiguanide) occured and the corresponding neutral ruthenium complex 1 was obtained. The structure of complex 1 has been established by FT-IR and NMR spectroscopy and single-crystal X-ray diffraction analysis. The number of crystal water was obtained by thermogravimetric analysis. The inhibition of cell proliferation activity against four human cancer cell lines (HepG-2, A549, Hela, MCF-7) of complex 1 relative to cisplatin was measured by MTT method in vitro. Notably, the novel complex displayed comparable potency toward HepG-2 (hepatocellular carcinoma, HCC) compared to cisplatin.
Keywords: ruthenium complex  crystal structure  anticancer activity  cisplatin
投稿时间:2020-09-27 修订日期:2021-03-14
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余群英.基于对异丙基甲苯和二甲基双胍的对称双核钌(Ⅱ)配合物的合成及其体外抗癌活性[J].无机化学学报,2021,37(5):899-904.
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