首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, cellular uptake, apopotosis, cytotoxicity, cell cycle arrest, interaction with DNA and antioxidant activity of ruthenium(II) complexes.
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Synthesis, cellular uptake, apopotosis, cytotoxicity, cell cycle arrest, interaction with DNA and antioxidant activity of ruthenium(II) complexes.

机译:钌(II)配合物的合成,细胞摄取,凋亡,细胞毒性,细胞周期停滞,与DNA的相互作用和抗氧化活性。

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摘要

A new ligand and two ruthenium(II) complexes [Ru(bpy)(2)(DNPIP)](ClO(4))(2)1 and [Ru(bpy)(2)(DAPIP)](ClO(4))(2)2 were synthesized and characterized. The DNA-binding constants for complexes 1 and 2 were determined to be 2.24 (+/-0.30) x 10(5) M(-1) (s = 1.29) and 6.34 (+/-0.32) x 10(4) M(-1) (s = 2.84). The photocleavage of pBR322 DNA by Ru(II) complexes was investigated. The cytotoxicity of complexes 1 and 2 were assessed against three tumor cell lines. The apoptosis and cellular uptake were studied. The retardation assay of pGL 3 plasmid DNA was explored. The cell cycle arrest was analysized by flow cytometry. The antioxidant activities of the ligand and complexes were also investigated.
机译:一个新的配体和两个钌(II)络合物[Ru(bpy)(2)(DNPIP)] [ClO(4))(2)1和[Ru(bpy)(2)(DAPIP)](ClO(4) )(2)2进行了合成和表征。确定复合物1和2的DNA结合常数为2.24(+/- 0.30)x 10(5)M(-1)(s = 1.29)和6.34(+/- 0.32)x 10(4)M (-1)(s = 2.84)。研究了Ru(II)配合物对pBR322 DNA的光裂解。针对三种肿瘤细胞系评估复合物1和2的细胞毒性。研究了细胞凋亡和细胞摄取。探索了pGL 3质粒DNA的阻滞测定。通过流式细胞术分析细胞周期停滞。还研究了配体和配合物的抗氧化活性。

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