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银(I)-杂环卡宾配合物的分子对接及抗癌研究

Molecular docking and anticancer studies of silver(I)--heterocyclic carbene complexes.

作者信息

Akkoç Mitat, Khan Siraj, Yüce Hande, Türkmen Neşe Başak, Yaşar Şeyma, Yaşar Sedat, Özdemir İsmail

机构信息

Malatya Turgut Özal University, Hekimhan Vocational College, Department of Property Protection and Security, Hekimhan, Malatya, Turkey.

Quaid-i-Azam University, Faculty of Biological Sciences, Department of Pharmacy, Islamabad, 45320, Pakistan.

出版信息

Heliyon. 2022 Aug 6;8(8):e10133. doi: 10.1016/j.heliyon.2022.e10133. eCollection 2022 Aug.

Abstract

A series of symmetric and unsymmetrical benzimidazolium-based N-heterocyclic carbene (NHC) precursors () and their silver complexes () have been synthesized. The Ag(I)-NHC complexes were characterized by H, C{H} NMR, FTIR, LC/MS-QTOF, and elemental analysis. Anticancer and cytotoxic activity of all Ag(I)-NHC complexes were tested against healthy fibroblast cell line (L929), breast cancer cell line (MCF-7), and neuroblastoma cell line (SH-SY5Y) by MTS [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4sulfophenyl)-2H-tetrazolium] assay. The , , , , and complexes showed higher cytotoxicity than cisplatin against SH-SY5Y and MCF-7 and lower cytotoxic activity against L929 cell lines. Because of their high cytotoxic activity against cancer cells and low cytotoxicity against healthy fibroblast cell lines, the , , , , , and are expected to be new lead compounds. In addition, molecular docking studies were performed to explore the binding interactions of silver complexes with the enzyme to explore new anticancer compounds. Furthermore, ADME properties of all complexes were predicted to explore lead-like characteristics and may be a potential drug candidate for cancer treatment.

摘要

一系列对称和不对称的基于苯并咪唑鎓的N-杂环卡宾(NHC)前体()及其银配合物()已被合成。通过氢谱、碳谱{氢}核磁共振、傅里叶变换红外光谱、液相色谱/质谱-四极杆飞行时间质谱以及元素分析对Ag(I)-NHC配合物进行了表征。通过MTS[3-(4,5-二甲基噻唑-2-基)-5-(3-羧基甲氧基苯基)-2-(4-磺基苯基)-2H-四唑]法测试了所有Ag(I)-NHC配合物对健康成纤维细胞系(L929)、乳腺癌细胞系(MCF-7)和神经母细胞瘤细胞系(SH-SY5Y)的抗癌和细胞毒性活性。配合物、、、、和对SH-SY5Y和MCF-7显示出比顺铂更高的细胞毒性,而对L929细胞系的细胞毒性活性较低。由于它们对癌细胞具有高细胞毒性活性且对健康成纤维细胞系具有低细胞毒性,预计、、、、、和将成为新的先导化合物。此外,进行了分子对接研究以探索银配合物与该酶的结合相互作用,从而探索新的抗癌化合物。此外,预测了所有配合物的吸收、分布、代谢和排泄性质以探索类先导物特征,并且可能是癌症治疗的潜在候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/457f/9396551/89d7b99eba7b/sc2.jpg

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