2-氨基-1,3,4-恶二唑n -氨基烷基化衍生物作为糖原合成酶激酶-3β抑制剂的分子对接研究

P. Zadorozhnii, Ihor O. Pokotylo
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引用次数: 0

摘要

阿尔茨海默病是一种神经退行性疾病,其病理特征是大脑皮层的神经原纤维缠结和β-淀粉样斑块。在阿尔茨海默病中,tau蛋白经历过度磷酸化,因此它的线开始合并并在神经细胞内形成神经原纤维缠结。研究表明,糖原合成酶激酶-3β是tau蛋白磷酸化的关键因素,其活性的增加导致神经原纤维缠结的病理,从而导致大脑的神经退行性改变。因此,寻找GSK-3β的有效抑制剂是一项非常重要和紧迫的任务,以进一步将其用于阿尔茨海默病的治疗。研究目的。本研究的目的是通过分子对接方法在2-氨基-1,3,4-恶二唑n -氨基烷基化衍生物中寻找新的GSK-3β抑制剂。材料和方法。我们使用ArgusLab 4.0.1软件对PM3半经验方法和GSK-3β分子对接进行了分析结构的几何优化。共结晶剂GSK-3β和抑制剂的三维晶体结构已从蛋白质分子数据库(PDB ID: 3F7Z)中加载。结果。在这项研究中已经表明,与已知的抑制剂相比,所研究的结构主要与酶形成更强的配合物。根据分子对接的结果,选择了先导化合物N-((5-(2-溴苯基)-1,3,4-恶二唑-2-基)氨基)甲基)苯酰胺和2,4-二氯-N-(2,2,2-三氯-1-((5-(对甲苯基)-1,3,4-恶二唑-2-基)氨基)乙基)苯酰胺。化合物先导化合物的结构已经过测试,符合利宾斯基标准。结论。提出的先导化合物可以推荐用于阿尔茨海默病治疗的进一步研究。尽管在硅分析中获得了良好的结果,但必须在体外和体内进行生物试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MOLECULAR DOCKING STUDIES OF SOME N-AMIDOALKYLATED DERIVATIVES OF 2-AMINO-1,3,4-OXADIAZOLE AS POTENTIAL INHIBITORS OF GLYCOGEN SYNTHASE KINASE-3β
Alzheimer's disease is a neurodegenerative disease characterized by pathological features of neurofibrillary tangles and β-amyloid plaques in the cerebral cortex. In Alzheimer's disease, tau protein undergoes excess phosphorylation, due to which its threads begin to merge and form neurofibrillary tangles within nerve cells. It has been shown that glycogen synthase kinase-3β is a key factor in the phosphorylation of tau protein, its increased activity leading to pathologies of neurofibrillary tangles and, consequently, to neurodegenerative changes in the brain. In this connection, the search for effective inhibitors of GSK-3β is a very important and urgent task, for their further use in the treatment of Alzheimer's disease. Aim of research.The aim of this study is to search new inhibitors of GSK-3β among N-amidoalkylated derivatives of 2-amino-1,3,4-oxadiazole by molecular docking methods. Materials and methods. We have carried out geometry optimization of analyzed structures within PM3 semi-empirical method, and GSK-3β molecular docking using software ArgusLab 4.0.1. The three-dimensional crystal structure of co-crystallizer GSK-3β and inhibitor has been loaded from the data bank of protein molecules (PDB ID: 3F7Z). Results. In this study it has been shown that the structures being studied mainly form stronger complexes with the enzyme compared to the known inhibitor. Based on the results of molecular docking, the compounds leaders N-(((5-(2-bromophenyl)-1,3,4-oxadiazol-2-yl)amino)methyl)benzamide and 2,4-dichloro-N-(2,2,2-trichloro-1-((5-(p-tolyl)-1,3,4-oxadiazol-2-yl)amino)ethyl)benzamide have been chosen. The structures of the compounds leaders have been tested for compliance with Lipinski criteria. Conclusions. Proposed compounds leaders can be recommended for further studies in the treatment of Alzheimer's disease. Despite the good results obtained in silico analysis, it is mandatory to perform biological tests in vitro and in vivo.
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