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含2,4-二羟基亚苄基配体的钌(II)配合物的DNA结合、DNA切割、蛋白质结合、自由基清除及体外细胞毒性活性评估。

Evaluation of DNA binding, DNA cleavage, protein binding, radical scavenging and in vitro cytotoxic activities of ruthenium(II) complexes containing 2,4-dihydroxy benzylidene ligands.

作者信息

Mohanraj Maruthachalam, Ayyannan Ganesan, Raja Gunasekaran, Jayabalakrishnan Chinnasamy

机构信息

Postgraduate and Research Department of Chemistry, Sri Ramakrishna Mission Vidyalaya College of Arts and Science, Coimbatore-641 020, Tamil Nadu, India.

Postgraduate and Research Department of Chemistry, Sri Ramakrishna Mission Vidyalaya College of Arts and Science, Coimbatore-641 020, Tamil Nadu, India.

出版信息

Mater Sci Eng C Mater Biol Appl. 2016 Dec 1;69:1297-306. doi: 10.1016/j.msec.2016.08.043. Epub 2016 Aug 18.

Abstract

The new ruthenium(II) complexes with hydrazone ligands, 4-Methyl-benzoic acid (2,4-dihydroxy-benzylidene)-hydrazide (HL(1)), 4-Methoxy-benzoic acid (2,4-dihydroxy-benzylidene)-hydrazide (HL(2)), 4-Bromo-benzoic acid (2,4-dihydroxy-benzylidene)-hydrazide (HL(3)), were synthesized and characterized by various spectro analytical techniques. The molecular structures of the ligands were confirmed by single crystal X-ray diffraction technique. The DNA binding studies of the ligands and complexes were examined by absorption, fluorescence, viscosity and cyclic voltammetry methods. The results indicated that the ligands and complexes could interact with calf thymus DNA (CT-DNA) through intercalation. The DNA cleavage activity of the complexes was evaluated by gel electrophoresis assay, which revealed that the complexes are good DNA cleaving agents. The binding interaction of the ligands and complexes with bovine serum albumin (BSA) was investigated using fluorescence spectroscopic method. Antioxidant studies showed that the complexes have a strong radical scavenging properties. Further, the cytotoxic effect of the complexes examined on cancerous cell lines showed that the complexes exhibit significant anticancer activity.

摘要

合成了新型含腙配体的钌(II)配合物,即4-甲基苯甲酸(2,4-二羟基苄叉)酰肼(HL(1))、4-甲氧基苯甲酸(2,4-二羟基苄叉)酰肼(HL(2))、4-溴苯甲酸(2,4-二羟基苄叉)酰肼(HL(3)),并通过各种光谱分析技术对其进行了表征。通过单晶X射线衍射技术确定了配体的分子结构。采用吸收光谱、荧光光谱、粘度和循环伏安法研究了配体和配合物与DNA的结合作用。结果表明,配体和配合物可通过嵌入作用与小牛胸腺DNA(CT-DNA)相互作用。通过凝胶电泳分析评估了配合物的DNA切割活性,结果表明这些配合物是良好的DNA切割剂。采用荧光光谱法研究了配体和配合物与牛血清白蛋白(BSA)的结合相互作用。抗氧化研究表明,这些配合物具有较强的自由基清除性能。此外,对癌细胞系进行的配合物细胞毒性研究表明,这些配合物具有显著的抗癌活性。

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