Suppr超能文献

镍(II)配合物与席夫碱配体的制备、表征、DNA/蛋白质相互作用及细胞毒性研究。

Ni(II) Complexes with Schiff Base Ligands: Preparation, Characterization, DNA/Protein Interaction and Cytotoxicity Studies.

机构信息

Guangxi Key Laboratory of Chemistry and Engineering of Forest Products, School of Chemistry and Chemical Engineering, Guangxi University for Nationalities, Nanning 530008, China.

Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), School of Chemistry and Pharmacy, Guangxi Normal University, Guilin 541004, China.

出版信息

Molecules. 2017 Oct 24;22(10):1772. doi: 10.3390/molecules22101772.

Abstract

In this study, two Ni(II) complexes, namely [Ni(HL1)₂(OAc)₂] () and [Ni(L2)₂] () (where HL1 and HL2 are ()-1-((1-(2-hydroxyethyl)-1-pyrazol-5-ylimino)methyl)-naphthalen-2-ol) and ()-ethyl-5-((2-hydroxynaphthalen-1-yl)methyleneamino)-1-methyl-1-pyrazole-4-carboxylate, respectively), were synthesized and characterized by X-ray crystallography, Electrospray Ionization Mass Spectrometry (ESI-MS), elemental analysis, and IR. Their uptake in biological macromolecules and cancer cells were preliminarily investigated through electronic absorption (UV-Vis), circular dichroism (CD) and fluorescence quenching measurements. Bovine serum albumin (BSA) interaction experiments were investigated by spectroscopy which showed that the complexes and ligands could quench the intrinsic fluorescence of BSA through an obvious static quenching process. The spectroscopic studies indicated that these complexes could bind to DNA via groove, non-covalent, and electrostatic interactions. Furthermore, in vitro methyl thiazolyl tetrazolium (MTT) assays and Annexin V/PI flow cytometry experiments were performed to assess the antitumor capacity of the complexes against eight cell lines. The results show that both of the complexes possess reasonable cytotoxicities.

摘要

在这项研究中,合成并通过 X 射线晶体学、电喷雾电离质谱 (ESI-MS)、元素分析和红外光谱对两个 Ni(II) 配合物进行了表征,分别为[Ni(HL1)₂(OAc)₂] ()和[Ni(L2)₂] ()(其中 HL1 和 HL2 分别为()-1-((1-(2-羟乙基)-1-吡唑-5-基亚氨基)甲基)萘-2-醇)和()-乙基-5-((2-羟基萘-1-基)亚甲基氨基)-1-甲基-1-吡唑-4-羧酸酯)。通过电子吸收(UV-Vis)、圆二色性(CD)和荧光猝灭测量初步研究了它们在生物大分子和癌细胞中的摄取情况。通过光谱研究了牛血清白蛋白 (BSA) 的相互作用实验,结果表明配合物和配体能通过明显的静态猝灭过程猝灭 BSA 的固有荧光。光谱研究表明,这些配合物可以通过沟、非共价和静电相互作用与 DNA 结合。此外,还进行了体外甲基噻唑基四唑 (MTT) 测定和 Annexin V/PI 流式细胞术实验,以评估这些配合物对八种细胞系的抗肿瘤能力。结果表明,两种配合物均具有合理的细胞毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98ed/6151616/58ce6863bcbb/molecules-22-01772-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验