Suppr超能文献

[M(dmphen)(CO3)].H2O [M=Pt(II), Pd(II)]配合物的合成、表征、与 DNA 的相互作用及体外细胞毒性

Synthesis, characterization, interaction with DNA and cytotoxicity in vitro of the complexes [M(dmphen)(CO3)].H2O [M=Pt(II), Pd(II)].

机构信息

Laboratory of Coordination Chemistry, Shenyang Institute of Chemical Technology, Shenyang 110142, China.

出版信息

Eur J Med Chem. 2010 Jan;45(1):311-6. doi: 10.1016/j.ejmech.2009.10.014. Epub 2009 Oct 22.

Abstract

The complexes [Pt(dmphen)CO3].H2O (1), [Pd(dmphen)CO3].H2O (2) (dmphen is 2,9-dimethyl-1,10-phenanthroline) have been synthesized and characterized. The binding of the complexes with FS-DNA was investigated by UV spectrum and fluorescence spectrum, showing that the complexes have the ability of interaction with DNA of intercalative mode. The intrinsic binding constant K of the complexes with FS-DNA is 1.8 x 10(5) M(-1) (1) and 1.6 x 10(4) M(-1) (2), respectively. Gel electrophoresis assay demonstrated the ability of the complexes to cleave the pBR 322 plasmid DNA. Evaluation of cytotoxic activity of the complexes against four different cancer cell lines proved that the complexes exhibited cytotoxic specificity and significant cancer cell inhibitory rate.

摘要

标题

[Pt(dmphen)CO3].H2O 和 [Pd(dmphen)CO3].H2O 配合物与 FS-DNA 的作用机制及细胞毒活性研究

复合物 [Pt(dmphen)CO3].H2O (1) 和 [Pd(dmphen)CO3].H2O (2)(dmphen 是 2,9-二甲基-1,10-菲咯啉)已经被合成并进行了结构鉴定。通过紫外光谱和荧光光谱研究了复合物与 FS-DNA 的结合,结果表明复合物以嵌入模式与 DNA 相互作用。复合物与 FS-DNA 的内在结合常数 K 分别为 1.8 x 10(5) M(-1) (1) 和 1.6 x 10(4) M(-1) (2)。凝胶电泳实验证明了复合物切割 pBR 322 质粒 DNA 的能力。对四种不同癌细胞系的细胞毒性活性评价表明,复合物具有细胞毒性特异性和显著的癌细胞抑制率。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验