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作 者:盖爽爽 蓝峻峰 张鹏[1,2] 蒋才云 覃逸明[1,2] GAI Shuang-Shuang;LAN Jun-Feng;ZHANG Peng;JIANG Cai-Yun;QIN Yi-Ming(Key Laboratory for Research and Development of Characteristic Yao,Guangxi Science&Technology Normal University,Laibin,Guangxi 545004,China;School of Food and Biochemical Engineering,Guangxi Science&Technology Normal University,Laibin,Guangxi 545004,China)
机构地区:[1]广西科技师范学院,特色瑶药资源研究与开发校级重点实验室,来宾545004 [2]广西科技师范学院食品与生化工程学院,来宾545004
出 处:《无机化学学报》2021年第7期1277-1283,共7页Chinese Journal of Inorganic Chemistry
基 金:广西高校中青年教师科研基础能力提升项目(No.2019KY0853,2020KY23016)资助。
摘 要:为开发新型钌(Ru)抗肿瘤药物,以3-甲基-2-噻吩甲醛-4-羟基苯甲酰肼席夫碱配体(L)合成了[Ru(L)(DMSO)2Cl2](1)(DMSO=二甲基亚砜)。用X射线单晶衍射法测定了1的晶体结构。配合物1的结构由1个Ru(Ⅱ)中心离子与2个DMSO分子、2个氯离子、1个L配位而成。通过MTT实验分析,1对T24细胞表现出良好的抗肿瘤活性。同时,通过彗星实验、蛋白质印迹实验和DNA琼脂糖凝胶电泳实验结果证明1可以有效结合DNA,诱导DNA损伤,最终杀死肿瘤细胞。导致DNA损伤的原因很可能是由于细胞与1孵育后细胞内可以产生大量的活性氧。To develop a novel antitumor Ru agent,[Ru(L)(DMSO)2 Cl2](1)(DMSO=dimethyl sulfoxide) was synthesized by employing a Schiff base ligand 3-methyl-2-thiophenecarboxaldehyde-4-hydroxybenzhydrazide(L).The single crystal X-ray crystallographic study was carried out to determine the crystallographic structure of 1.The structure of complex 1 is composed of a central Ru(Ⅱ) ion,two DMSO molecules,two chloride ions,and a ligand L.In addition,1 possessed strong antitumor activity against T24 cells by MTT analysis.Furthermore,the potential antitumor mechanism of 1 was investigated by comet assays,western-blotting assays,and DNA agarose gel electrophoresis.These results indicate that 1 can effectively bind to DNA and induce DNA damage,and eventually kill the tumor cells.DNA damage may be caused by the production of reactive oxygen species.CCDC:2080249.
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