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钌(II) 多吡啶配合物的合成、DNA 结合、细胞毒性、光解、抗菌和对接研究。

Synthesis, DNA-binding, cytotoxicity, photo cleavage, antimicrobial and docking studies of Ru(II) polypyridyl complexes.

机构信息

Department of Chemistry, Osmania University, Hyderabad, India.

出版信息

J Fluoresc. 2013 Sep;23(5):897-908. doi: 10.1007/s10895-013-1209-7. Epub 2013 Apr 4.

Abstract

Three Ruthenium(II) polypyridine complexes, Ru(phen)2(mipc)(1), Ru(bpy)2(mipc) (2) and Ru(dmb)2(mipc)(3) [mipc = 2-(6-methyl-3-(1H-imidazo[4, 5-f][1,10]-phenanthroline-2-yl)-4H-chromene-4-one, phen = 1,10-phenanthroline,bpy = 2, 2'bipyridine,dmb = 4, 4'-dimethyl-2, 2'-bipyridine] have been synthesized and characterized by elemental analysis, IR, UV-Vis, (1)H& (13)C NMR and mass spectra. The DNA-binding properties of the Ruthenium(II) complexes were investigated by spectrophotometric methods, viscosity measurements and light switch studies. These three complexes have been focused on photo activated cleavage studies with pBR-322 and antimicrobial studies. Experimental results indicate that the three complexes intercalate into DNA base pairs and follows the order of 1 > 2 > 3 respectively. Molecular docking studies also support the DNA interactions with complexes through hydrogen bonding and vander Waal's interactions. Cytotoxicity studies with Hela cell lines has been revealing about anti tumor activity of these complexes.

摘要

三种钌(II)多吡啶配合物,[Ru(phen)2(mipc)]²⁺(1)、[Ru(bpy)2(mipc)]²⁺(2)和[Ru(dmb)2(mipc)]²⁺(3)[mipc = 2-(6-甲基-3-(1H-咪唑并[4,5-f][1,10]菲咯啉-2-基)-4H-色烯-4-酮,phen = 1,10-菲咯啉,bpy = 2,2′-联吡啶,dmb = 4,4′-二甲基-2,2′-联吡啶]已通过元素分析、红外、紫外-可见、(1)H 和(13)C NMR 和质谱进行了合成和表征。通过分光光度法、粘度测量和光开关研究研究了钌(II)配合物的 DNA 结合特性。这些配合物已集中在 pBR-322 的光激活断裂研究和抗菌研究上。实验结果表明,这三种配合物分别以 1>2>3 的顺序嵌入 DNA 碱基对中。分子对接研究也通过氢键和范德华相互作用支持配合物与 DNA 的相互作用。Hela 细胞系的细胞毒性研究揭示了这些配合物的抗肿瘤活性。

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