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首页> 外文期刊>Scientific reports. >Heteroleptic Copper(I) Complexes of “Scorpionate” Bis-pyrazolyl Carboxylate Ligand with Auxiliary Phosphine as Potential Anticancer Agents: An Insight into Cytotoxic Mode
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Heteroleptic Copper(I) Complexes of “Scorpionate” Bis-pyrazolyl Carboxylate Ligand with Auxiliary Phosphine as Potential Anticancer Agents: An Insight into Cytotoxic Mode

机译:“蝎子”双吡唑基羧酸盐配体的异铜铜(I)复合物,其具有辅助膦的潜在抗癌剂:对细胞毒性模式的洞察力

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New copper(I) complexes [CuCl(PPh3)(L)] (1: L?=?LA?=?4-carboxyphenyl)bis(3,5-dimethylpyrazolyl)methane; (2: L?=?LB?=?3-carboxyphenyl)bis(3,5-dimethylpyrazolyl)methane) were prepared and characterised by elemental analysis and various spectroscopic techniques such as FT-IR, NMR, UV–Vis, and ESI-MS. The molecular structures of complexes 1 and 2 were analyzed by theoretical B3LYP/DFT method. Furthermore, in vitro DNA binding studies were carried out to check the ability of complexes 1 and 2 to interact with native calf thymus DNA (CT-DNA) using absorption titration, fluorescence quenching and circular dichroism, which is indicative of more avid binding of the complex 1. Moreover, DNA mobility assay was also conducted to study the concentration-dependent cleavage pattern of pBR322 DNA by complex 1, and the role of ROS species to have a mechanistic insight on the cleavage pattern, which ascertained substantial roles by both hydrolytic and oxidative pathways. Additionally, we analyzed the potential of the interaction of complex 1 with DNA and enzyme (Topo I and II) with the aid of molecular modeling. Furthermore, cytotoxic activity of complex 1 was tested against HepG2 cancer cell lines. Thus, the potential of the complex 1 is promising though further in vivo investigations may be required before subjecting it to clinical trials.
机译:新型铜(I)配合物[CuCl(PPH3)(L)](1:L?=α1a≤α4-羧基苯基)双(3,5-二甲基吡唑基)甲烷; (2:l?=Δ=α=α= 3-羧基)双(3,5-二甲基吡唑基)甲烷,并通过元素分析和各种光谱技术,例如FT-IR,NMR,UV-Vis和ESI -小姐。通过理论B3LYP / DFT方法分析复合物1和2的分子结构。此外,进行体外DNA结合研究以检查复合物1和2的能力,使用吸收滴定,荧光猝灭和圆形二色性与天然小牛胸腺DNA(CT-DNA)相互作用,所述荧光猝灭和圆形二色性相互作用,所述荧光猝灭和圆形二色性表现出更多的狂热结合此外,还进行了DNA迁移率测定以研究复合物1的PBR322 DNA的浓度依赖性切割模式,以及ROS种类对裂解图案的作用,该方法通过水解和含水溶解和氧化途径。另外,借助于分子建模,我们分析了复合物1与DNA和酶(Topo I和II)的相互作用的潜力。此外,复合物1的细胞毒性活性对HepG2癌细胞系进行了测试。因此,复合物1的潜力是有前途的,但在使其进行临床试验之前可能需要进一步研究。

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