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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >New palladium(II) and platinum(II) 5,5-diethylbarbiturate complexes with 2-phenylpyridine, 2,2 '-bipyridine and 2,2 '-dipyridylamine: synthesis, structures, DNA binding, molecular docking, cellular uptake, antioxidant activity and cytotoxicity
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New palladium(II) and platinum(II) 5,5-diethylbarbiturate complexes with 2-phenylpyridine, 2,2 '-bipyridine and 2,2 '-dipyridylamine: synthesis, structures, DNA binding, molecular docking, cellular uptake, antioxidant activity and cytotoxicity

机译:新的5,5-二乙基巴比妥酸钯(II)和铂(II)与2-苯基吡啶,2,2'-联吡啶和2,2'-二吡啶胺的络合物:合成,结构,DNA结合,分子对接,细胞吸收,抗氧化活性和细胞毒性

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摘要

Novel palladium(II) and platinum(II) complexes of 5,5-diethylbarbiturate (barb) with 2-phenylpyridine (Hppy), 2,2'-bipyridine (bpy) and 2,2'-dipyridylamine (dpya) have been prepared and characterized by elemental analysis, IR, UV-Vis, NMR and ESI-MS. Single-crystal diffraction measurements show that complex 1 consists of binuclear [Pd-2(mu-barb-kappa N,O)(2)(ppy-kappa N,C)(2)] moieties, while complexes 3-5 are mononuclear, [M(barb-.kappa)(2)(L-kappa N,N')] (L = bpy or dpya). 6 has a composition of [Pt(dpya-kappa N,N')(2)][Ag(barb-kappa N)(2)](2)center dot 4H(2)O and 2 was assumed to have a structure of [Pt(barb-kappa N)(Hppy-kappa N)(ppy-kappa N,C)]center dot 3H(2)O. The complexes were found to exhibit significant DNA binding affinity by a non-covalent binding mode, in accordance with molecular docking studies. In addition, complexes 1 and 2 displayed strong binding with supercoiled pUC19 plasmid DNA. Cellular uptake studies were performed to assess the subcellular localization of the selected complexes. A moderate radical scavenging activity of 1 and 2 was confirmed by DPPH and ABTS tests. Complexes 1, 2, and 5 showed selectivity against HT-29 (colon) cell line.
机译:制备了5,5-二乙基巴比妥酸酯(倒钩)与2-苯基吡啶(Hppy),2,2'-联吡啶(bpy)和2,2'-联吡啶胺(dpya)的新型钯(II)和铂(II)配合物并通过元素分析,IR,UV-Vis,NMR和ESI-MS进行表征。单晶衍射测量表明,配合物1由双核[Pd-2(mu-barb-kappa N,O)(2)(ppy-kappa N,C)(2)]部分组成,而配合物3-5为单核。 ,[M(barb-.kappa)(2)(L-kappa N,N')](L = bpy或dpya)。图6具有[Pt(dpya-kappa N,N')(2)] [Ag(倒钩-kappa N)(2)](2)中心点4H(2)O的组成,并且假设2具有结构中心点3H(2)O的[Pt(倒钩-κN)(Hppy-κN)(ppy-kappa N,C)]的中心。根据分子对接研究,发现该复合物通过非共价结合模式表现出显着的DNA结合亲和力。另外,复合物1和2显示出与超螺旋的pUC19质粒DNA的强结合。进行细胞摄取研究以评估所选复合物的亚细胞定位。 DPPH和ABTS测试确认了1和2的中等自由基清除活性。配合物1、2和5对HT-29(结肠)细胞系表现出选择性。

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