Synthesis, characterization and crystal structure of cobalt(III) complexes containing 2-acetylpyridine thiosemicarbazones: DNA/protein interaction, radical scavenging and cytotoxic activities

被引:78
|
作者
Manikandan, Rajendran [1 ]
Viswanathamurthi, Periasamy [1 ]
Velmurugan, Krishnaswamy [2 ]
Nandhakumar, Raju [2 ]
Hashimoto, Takeshi [3 ]
Endo, Akira [3 ]
机构
[1] Periyar Univ, Dept Chem, Salem 636011, Tamil Nadu, India
[2] Karunya Univ, Dept Chem, Coimbeitore 641114, India
[3] Sophia Univ, Dept Mat & Life Sci, Tokyo 1028554, Japan
关键词
Cobalt(III) complexes; DNA binding; DNA cleavage; Protein binding; Antioxidant activity; Cytotoxicity; TRANSITION-METAL-COMPLEXES; X-RAY-STRUCTURE; DNA-BINDING; BIOLOGICAL EVALUATION; COORDINATING AGENTS; ANTITUMOR-ACTIVITY; LIGANDS; ACID; IRON; SUBSTITUTION;
D O I
10.1016/j.jphotobiol.2013.11.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The synthesis, structure and biological studies of cobalt(III) complexes supported by NNS-tridentate ligands are reported. Reactions of 2-acetylpyridine N-substituted thiosemicarbazone (HL1-3) with [CoCl2(PPh3)(2)] resulted [Co(L1-3)(2)]Cl (1-3) which were characterized by elemental analysis and various spectral studies. The molecular structure of the complex 1 has been determined by single crystal X-ray diffraction studies. In vitro DNA binding studies of complexes 1-3 carried out by fluorescence studies and the results revealed the binding of complexes to DNA via intercalation. The binding constant (K-b) values of complexes 1-3 from fluorescence experiments showed that the complex 3 has greater binding propensity for DNA. The DNA cleavage activity of the complexes 1 and 3 were ascertained by gel electrophoresis assay which revealed that the complexes are good DNA cleavage agents. Further, the interactions of the complexes with bovine serum albumin (BSA) were also investigated using fluorescence spectroscopic method, which showed that the complexes 1-3 could bind strongly with BSA. The antioxidant property of the complexes was evaluated to test their free-radical scavenging ability. Furthermore, in vitro cytotoxicity of the complexes against MCF-7 and A431 cell lines was assayed which showed higher activity and efficiently vanished the cancer cells even at low concentrations. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:205 / 216
页数:12
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