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具有抗菌和抗癌特性的新型基于肼甲酰胺的银(I)和镉(II)配合物的合成。

Synthesis of new Ag(i) and Cd(ii) hydrozanomide-based complexes with antibacterial and anticancer properties.

作者信息

Climova Alina, Pivovarova Ekaterina, Szczesio Małgorzata, Gobis Katarzyna, Korga-Plewko Agnieszka, Iwan Magdalena, Kordialik-Bogacka Edyta, Ścieszka Sylwia, Marek Jaromir, Czylkowska Agnieszka

机构信息

Institute of General and Ecological Chemistry, Faculty of Chemistry, Lodz University of Technology Zeromskiego 116 Lodz 90-924 Poland

Department of Organic Chemistry, Faculty of Pharmacy, Medical University of Gdańsk 107 Gen. Hallera Ave. Gdańsk 80-416 Poland.

出版信息

RSC Adv. 2025 Jun 10;15(25):19598-19609. doi: 10.1039/d5ra02001h.

DOI:10.1039/d5ra02001h
PMID:40503324
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12150283/
Abstract

A series of new Ag(i) and Cd(ii) hydrozanomide-based complexes have been prepared and studied. The synthesized compounds have undergone extensive spectroscopic and structural characterization, including F-AAS, FTIR, single crystal XRD and TGA analyses. Crystal structures of two representative complexes, 4 and 6, have revealed that the silver atom in complex 4 assumes a four-coordinate geometry with two ligands. Additionally, the stability of these complexes in DMSO has been determined using UV-vis spectroscopy. The biological activity of these metal complexes has been assessed, focusing on their antibacterial and anticancer properties against LN-229 and U87 cell lines. Among the tested compounds, silver-based complexes demonstrated significant antibacterial activity against a wide range of microorganisms. Moreover, cytotoxicity studies have shown that the metal complexes exhibit higher anticancer activity compared to their parent ligands. Notably, the Ag(i) complexes of L, L, and L have emerged as the most promising candidates for their selective toxicity against cancer cells, without harmful effects on normal human fibroblast cells. These findings highlight the potential of Ag(i) complexes as promising anticancer agents with selective toxicity and potent antibacterial properties.

摘要

已经制备并研究了一系列基于肼甲酰胺的新型银(I)和镉(II)配合物。合成的化合物经过了广泛的光谱和结构表征,包括火焰原子吸收光谱法(F-AAS)、傅里叶变换红外光谱法(FTIR)、单晶X射线衍射(XRD)和热重分析(TGA)。两种代表性配合物4和6的晶体结构表明,配合物4中的银原子与两个配体形成四配位几何结构。此外,使用紫外可见光谱法测定了这些配合物在二甲基亚砜(DMSO)中的稳定性。评估了这些金属配合物的生物活性,重点关注它们对LN-229和U87细胞系的抗菌和抗癌特性。在测试的化合物中,银基配合物对多种微生物表现出显著的抗菌活性。此外,细胞毒性研究表明,与母体配体相比,金属配合物表现出更高的抗癌活性。值得注意的是,L、L和L的银(I)配合物因其对癌细胞的选择性毒性而成为最有前途的候选物,对正常人类成纤维细胞没有有害影响。这些发现突出了银(I)配合物作为具有选择性毒性和强效抗菌特性的有前途的抗癌剂的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/98d65a4e934f/d5ra02001h-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/0c30bb17b26b/d5ra02001h-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/dd8569a6bef1/d5ra02001h-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/25656742a983/d5ra02001h-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/8ca10998c80d/d5ra02001h-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/9fc7a49f722e/d5ra02001h-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/70314ba74aae/d5ra02001h-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/907b49662768/d5ra02001h-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/8d366d669535/d5ra02001h-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/98d65a4e934f/d5ra02001h-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/0c30bb17b26b/d5ra02001h-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/dd8569a6bef1/d5ra02001h-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/25656742a983/d5ra02001h-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/8ca10998c80d/d5ra02001h-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/9fc7a49f722e/d5ra02001h-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/70314ba74aae/d5ra02001h-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/907b49662768/d5ra02001h-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/8d366d669535/d5ra02001h-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/12150283/98d65a4e934f/d5ra02001h-f9.jpg

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