Key Laboratory of Beibu Gulf Environment Change and Resources Utilization (Guangxi Teachers Education University), Ministry of Education, Nanning, China.
Inorg Chem. 2013 Nov 4;52(21):12440-9. doi: 10.1021/ic401362s. Epub 2013 Oct 21.
A series of ketone-N(4)-substituted thiosemicarbazone (TSC) compounds (L1-L9) and their corresponding (η(6)-p-cymene)Ru(II)(TSC)Cl complexes (1-9) were synthesized and characterized by NMR, IR, elemental analysis, and HR-ESI-mass spectrometry. The molecular structures of L4, L9, 1-6, and 9 were determined by single-crystal X-ray diffraction analysis. The compounds were further evaluated for their in vitro antiproliferative activities against the SGC-7901 human gastric cancer, BEL-7404 human liver cancer, and HEK-293T noncancerous cell lines. Furthermore, the interactions of the compounds with DNA were followed by electrophoretic mobility spectrometry studies.
一系列酮-N(4)-取代的硫代缩氨基脲(TSC)化合物(L1-L9)及其相应的(η(6)-p-枯烯)Ru(II)(TSC)Cl配合物(1-9)被合成并通过 NMR、IR、元素分析和高分辨率电喷雾质谱(HR-ESI-mass spectrometry)进行了表征。L4、L9、1-6 和 9 的分子结构通过单晶 X 射线衍射分析确定。进一步评估了这些化合物对 SGC-7901 人胃癌、BEL-7404 人肝癌和 HEK-293T 非癌细胞系的体外抗增殖活性。此外,通过电泳迁移率谱研究跟踪了化合物与 DNA 的相互作用。