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一系列酮-N(4)-取代的硫代缩氨基脲及其钌(II)芳基配合物的合成、表征及抗癌活性。

Synthesis, characterization, and anticancer activity of a series of ketone-N(4)-substituted thiosemicarbazones and their ruthenium(II) arene complexes.

机构信息

Key Laboratory of Beibu Gulf Environment Change and Resources Utilization (Guangxi Teachers Education University), Ministry of Education, Nanning, China.

出版信息

Inorg Chem. 2013 Nov 4;52(21):12440-9. doi: 10.1021/ic401362s. Epub 2013 Oct 21.

Abstract

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.

摘要

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。

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