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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, characterization, interaction with DNA and cytotoxicity in vitro of the complexes (M(dmphen)(CO3)).H2O (M=Pt(II), Pd(II)).
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Synthesis, characterization, interaction with DNA and cytotoxicity in vitro of the complexes (M(dmphen)(CO3)).H2O (M=Pt(II), Pd(II)).

机译:配合物(M(dmphen)(CO3))。H2O(M = Pt(II),Pd(II))的合成,表征,与DNA的相互作用和体外细胞毒性。

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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.
机译:已合成并表征了[Pt(dmphen)CO3] .H2O(1),[Pd(dmphen)CO3] .H2O(2)(dmphen为2,9-二甲基-1,10-菲咯啉)的配合物。通过紫外光谱和荧光光谱研究了配合物与FS-DNA的结合,表明配合物具有与嵌入模式DNA相互作用的能力。与FS-DNA配合物的固有结合常数K分别为1.8 x 10(5)M(-1)(1)和1.6 x 10(4)M(-1)(2)。凝胶电泳分析证明了复合物切割pBR 322质粒DNA的能力。评价该复合物对四种不同癌细胞系的细胞毒性活性证明该复合物表现出细胞毒性特异性和显着的癌细胞抑制率。

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