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锌(II)配合物与 N'-(吡啶-2-基亚甲基)烟酰基肼:合成、晶体结构、计算和细胞毒性研究。

Zinc(II) coordination compound with N'-(pyridin-2-ylmethylene)nicotinohydrazide: Synthesis, crystal structure, computational and cytotoxicity studies.

机构信息

Department of Chemistry, Govt. Degree College, Dharmanagar, Tripura(N) 799253, India.

Department of Chemistry, Govt. Degree College, Dharmanagar, Tripura(N) 799253, India.

出版信息

J Inorg Biochem. 2024 Aug;257:112598. doi: 10.1016/j.jinorgbio.2024.112598. Epub 2024 May 8.

DOI:10.1016/j.jinorgbio.2024.112598
PMID:38763101
Abstract

In this work, we report on the synthesis of a novel zinc(II) coordination compound [ZnL] (1), which was readily obtained from the reaction of Zn(OAc)·2HO and N'-(pyridin-2-ylmethylene)nicotinohydrazide (HL) in methanol. Recrystallization of 1 from dimethylformamide under ambient conditions allowed to produce yellow block-like crystals of 1·HO. Complex 1·HO was characterized by FT-IR and H NMR spectroscopy, while its optical properties were studied by UV-vis and spectrofluorimetry in methanol. The crystal structure of the title complex was revealed by single crystal X-ray diffraction and further explored in detail by the Hirshfeld surface analysis. Theoretical investigations based on the DFT calculations have also been applied to show the electronic properties of complex 1. The antitumor activities of the parent ligand HL and complex 1 were studied using Dalton's lymphoma malignant cancer model. Both compounds were found to induce concentration-dependent cytotoxicity and apoptotic cell death, leading to a decrease in cell viability, body weight, and tumor volume in mice with the superior activity of complex 1 over HL. Mice treated with complex 1 demonstrated an increase in life span with a survival period of 23 days. Finally, using a molecular docking approach, we have probed complex 1 to inhibit the recombinant mouse tumor-necrosis factor alpha (mTNF).

摘要

在这项工作中,我们报告了一种新型锌(II)配合物[ZnL](1)的合成,该配合物可通过在甲醇中反应 Zn(OAc)·2HO 和 N'-(吡啶-2-亚甲基)烟酰基肼(HL)轻易得到。在环境条件下从二甲基甲酰胺中重结晶 1 得到 1·HO 的黄色块状晶体。配合物 1·HO 通过 FT-IR 和 H NMR 光谱进行了表征,同时通过甲醇中的 UV-vis 和荧光光谱法研究了其光学性质。标题配合物的晶体结构通过单晶 X 射线衍射揭示,并通过 Hirshfeld 表面分析进一步详细研究。还应用基于 DFT 计算的理论研究来显示配合物 1 的电子性质。使用道尔顿淋巴瘤恶性癌症模型研究了母体配体 HL 和配合物 1 的抗肿瘤活性。发现这两种化合物都能诱导浓度依赖性细胞毒性和细胞凋亡,导致小鼠的细胞活力、体重和肿瘤体积下降,而配合物 1 的活性优于 HL。用配合物 1 治疗的小鼠表现出寿命延长,存活期为 23 天。最后,通过分子对接方法,我们探测了配合物 1 抑制重组小鼠肿瘤坏死因子 alpha(mTNF)的能力。

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