首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Exploring the DNA interactions, FGF growth receptor interaction and biological screening of metal(II) complexes of NNN donor ligand derived from 2-(aminomethyl)benzimidazole
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Exploring the DNA interactions, FGF growth receptor interaction and biological screening of metal(II) complexes of NNN donor ligand derived from 2-(aminomethyl)benzimidazole

机译:探索DNA相互作用,FGF生长受体相互作用和NNN供体配体的金属(II)络合物的生物学筛选衍生自2-(氨基甲基)苯并咪唑的苯并咪唑

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This work deals with a series of biologically important novel transition metal(II) Schiff base chelates containing terpyridine. Benzimidazole, a moiety found in broad spectrum of drugs is espoused in a Schiff base ligand system. Eight such metal(II) complexes are designed, synthesized and characterized. An octahedral geometry has been envisaged for all the complexes. DNA-binding behaviours are studied by absorption titration, electrochemical, viscosity, fluorescence and circular dichroism methods. The DNA cleavage ability is also evaluated by agarose gel electrophoresis method. These studies reveal that the complexes show an intercalative mode of binding to CT-DNA and also effectively cleave the supercoiled pBR322 DNA. The molecular docking studies of the complexes against FGF growth receptors indicate that they bind through electrostatic, van der Waals, hydrogen bonding and pi-pi interactions. The ligand and its complexes are screened for in vitro antimicrobial activities against a few microorganisms. The data exhibit that they are better antimicrobial agents than the ligand. The cytotoxic activity of the complexes is probed in four cell lines wherein the complex 5 has good cytotoxic activity and is partial to MCF-7 cell line which is comparable with the cisplatin drug which can be attributed to the presence of planar terpyridine co-ligand. (C) 2018 Elsevier B.V. All rights reserved.
机译:这项工作涉及一系列生物学上重要的新型过渡金属(II)Schiff碱基螯合物,其含有Terpyridine。 Benzimidazole,在秀碱配体系中施加了广谱中的一部分中发现的部分。设计,合成和表征,设计了八种这样的金属(II)配合物。所有复合物都设想了八面体几何形状。通过吸收滴定,电化学,粘度,荧光和圆形二色性方法研究了DNA结合行为。还通过琼脂糖凝胶电泳方法评估DNA裂解能力。这些研究表明,复合物显示与CT-DNA结合的插入模式,并且还有效地切割超硅酸钙PBR322 DNA。复合物对FGF生长受体的分子对接研究表明它们通过静电,范德瓦尔斯,氢键和PI-PI相互作用结合。对少量微生物的体外抗微生物活性筛选配体及其复合物。数据表明它们是比配体更好的抗微生物剂。复合物的细胞毒性活性在四种细胞系中探测,其中复合体5具有良好的细胞毒性活性,并且是MCF-7细胞系的部分,其与顺铂药物相当,其可归因于平面吡啶共配体的存在。 (c)2018年elestvier b.v.保留所有权利。

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