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Synthesis, interaction with double-helical DNA and biological activity of new Pt(II) and Pd(II) complexes with phenylglycine

机译:新型Pt(II)和Pd(II)与苯基甘氨酸配合物的合成,与双螺旋DNA的相互作用以及生物学活性

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The mononuclear palladium(II) (1) and platinum(II) (2) complexes containing phenylglycine have been synthesized and characterized by elemental analysis, IR spectra, and 1H NMR spectra. The structure of 1 was determined by X-ray diffractometry. The interaction between the complexes and fish sperm DNA (FS-DNA), adenosine-5′-triphosphate (ATP), and adenine (Ade) were investigated by UV absorption spectra, the interaction mode of the complex binding to DNA was studied by fluorescence spectra and viscometry. The results indicate that the two complexes have different binding affinities to DNA, complex 2 complex 1. Gel electrophoresis assay demonstrates that the two complexes have the ability to cleave pBR322 plasmid DNA. Cytotoxicity experiments were carried out toward four different cancer cell lines, and 1 shows lower inhibitory efficiency than 2, consistent with the binding affinities towards DNA.View full textDownload full textKeywordsPlatinum and palladium complexes, DNA intercalation, Spectroscopy, Cleavage, Cytotoxic activityRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/00958970903093678
机译:合成了含苯基甘氨酸的单核钯(II)(1)和铂(II)(2)配合物,并通过元素分析,IR光谱和 1 1 H NMR光谱对其进行了表征。 1的结构通过X射线衍射法确定。通过紫外吸收光谱研究了配合物与鱼精DNA(FS-DNA),5'-腺苷三磷酸(ATP)和腺嘌呤(Ade)之间的相互作用,并研究了配合物与DNA的相互作用方式。荧光光谱和粘度测定。结果表明,两种复合物对DNA的结合亲和力不同,复合物2>复合物1。凝胶电泳分析表明这两种复合物具有切割pBR322质粒DNA的能力。对四种不同的癌细胞系进行了细胞毒性实验,其中1种抑制作用比2种抑制作用要低,这与对DNA的结合亲和力一致。查看全文下载全文关键词铂和钯配合物,DNA嵌入,光谱学,裂解,细胞毒性活性相关var addthis_config = {ui_cobrand:“ Taylor&Francis Online”,servicescompact:“ citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,更多”,发布:“ ra-4dff56cd6bb1830b”};添加到收藏夹链接永久链接http://dx.doi.org/10.1080/00958970903093678

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