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首页> 外文期刊>Journal of Biomolecular Structure and Dynamics >Synthesis and characterization of heterobimetallic Sn-IV-Cu-II/Zn-II complexes: DFT studies, cleavage potential and cytotoxic activity
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Synthesis and characterization of heterobimetallic Sn-IV-Cu-II/Zn-II complexes: DFT studies, cleavage potential and cytotoxic activity

机译:杂二种Sn-IV-Cu-II / Zn-II复合物的合成与表征:DFT研究,切割潜力和细胞毒性活性

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摘要

Heterobimetallic complexes [Cu(L)Sn(CH3)(2)(H2O)(Cl)] (3) and [Zn(L)Sn(CH3)(2)(H2O)(Cl)] (4) have been synthesized from their monometallic analogs [Cu(L)(H2O)(Cl)] (1) and [Zn(L)(H2O)(Cl)] (2) of Schiff base ligand (L) which were characterized by various spectroscopic and analytical methods. DFT calculations were carried out to simulate the vibrational spectra to support the anticipated structures. The interaction studies of ligand (L) and complexes (1-4) with CT-DNA were performed by employing UV-vis, and fluorescence spectroscopic techniques which revealed that heterobimetallic complexes 3 and 4 showed higher affinity with DNA due to dual mode of action as compared to monometallic complexes 1 and 2. Further, validation of the interaction studies was accomplished by carrying out molecular docking studies with DNA. Gel assay displayed that both the complexes have ability to cleave DNA efficiently and are specific minor groove binders. Cu-II-Sn-IV complex 3 cleaved pBR322 DNA via oxidative mechanism, while Zn-II-Sn-IV complex 4 followed hydrolytic cleavage pathway. In vitro cytotoxicity evaluation of complex 3 was tested on a different cancer cell lines showing promising antitumor activity.
机译:异质物络合物[Cu(1)Sn(CH 3)(2)(2)(H 2 O)(Cl)](3)和[Zn(1)Sn(2)(2)(2)(H 2 O)(Cl)](4)已经合成了合成从它们的单金属剂类似物[Cu(1)(H 2 O)(Cl)](1)和席克夫碱配体(L)的[Zn(L)(H 2 O)(Cl)](2),其特征在于各种光谱和分析方法。进行DFT计算以模拟振动光谱以支持预期的结构。通过采用UV-Vis和荧光光谱技术进行CT-DNA的配体(L)和复合物(1-4)的相互作用研究,并透露荧光光谱技术由于双重作用而言,偏移量络合物3和4显示出与DNA具有更高的亲和力与单金属络合物1和2相比,通过用DNA进行分子对接研究来实现相互作用研究的验证。凝胶测定显示,复合物的能力有效地切割DNA,并且是特异性较小槽粘合剂。 Cu-II-Sn-IV复合物3通过氧化机制切割PBR322 DNA,而Zn-II-Sn-IV复合物4遵循水解裂解途径。在不同的癌细胞系上测试复合物3的体外细胞毒性评估,所述癌细胞系显示出现有前途的抗肿瘤活性。

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