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酰胺羧酸酯类作为潜在抗阿尔茨海默病药物的药理学评价:抗自由基、酶抑制、动物模型中的模拟和行为研究。

Pharmacological evaluations of amide carboxylates as potential anti-Alzheimer agents: anti-radicals, enzyme inhibition, simulation and behavioral studies in animal models.

机构信息

Department of Pharmaceutical Chemistry, College of Pharmacy, Najran University, Najran, Kingdom of Saudi Arabia.

Department of Chemistry, Quaid-i-Azam University, Islamabad, Pakistan.

出版信息

J Biomol Struct Dyn. 2024 Oct;42(17):9249-9268. doi: 10.1080/07391102.2023.2251052. Epub 2023 Aug 29.

Abstract

Alzheimer's disease (AD) is a neurological disorder that progresses gradually but irreversibly leading to dementia and is difficult to prevent and treat. There is a considerable time window in which the progression of the disease can be intervened. Scientific advances were required to help the researchers to identify the effective methods for the prevention and treatment of disease. This research was designed to investigate potential mediators for the remedy of AD, five new carboxylate amide zinc complexes (AAZ9-AAZ13) were synthesized and characterized by spectroscopic and physicochemical techniques. The biological evaluation was carried out based on the cholinesterase inhibitory mechanism. The preparation methodology provided the effective synthesis of targeted moieties. The pharmacological activities were evaluated involving AChE/BChE inhibition and antioxidant potential. All synthesized compounds displayed activity against both enzymes in higher or comparable to the standard drug Galantamine, a reversible inhibitor but the results displayed by compound AAZ10 indicated IC of 0.0013 µM (AChE) and 0.061 µM (BChE) as high values for dual AChE/BChE inhibition with potent anti-oxidant results. Structure activity relationship (SAR) indicated that the potent activity of compound AAZ10 appeared due to the presence of nitro clusters at the ortho position of an aromatic ring. The potent synthesized compound AAZ10 was also explored for the in-vivo Anti-Alzheimer activity and anti-oxidant activity. Binding approaches of all synthesized compounds were revealed through molecular docking studies concerning binding pockets of enzymes that analyzed the best posture interaction with amino acid (AA) residues providing an appreciable understanding of enzyme inhibitory mechanisms. Results indicate that synthesized zinc (II) amide carboxylates can behave as an effective remedy in the treatment of Alzheimer's disease.Communicated by Ramaswamy H. Sarma.

摘要

阿尔茨海默病(AD)是一种神经退行性疾病,其进展逐渐但不可逆转地导致痴呆,且难以预防和治疗。在疾病进展过程中有相当长的时间窗口可以进行干预。需要科学进步来帮助研究人员确定预防和治疗疾病的有效方法。本研究旨在探索阿尔茨海默病治疗的潜在介质,合成并通过光谱和物理化学技术对 5 种新的羧酸盐酰胺锌配合物(AAZ9-AAZ13)进行了表征。基于胆碱酯酶抑制机制进行了生物评价。该制备方法为靶向部分的有效合成提供了条件。药理学活性评估涉及 AChE/BChE 抑制和抗氧化潜力。所有合成化合物均显示出对两种酶的活性,其活性高于或与标准药物加兰他敏相当,加兰他敏是一种可逆抑制剂,但化合物 AAZ10 的结果表明对 AChE 的 IC 为 0.0013 µM(BChE)和 0.061 µM(BChE),作为双重 AChE/BChE 抑制的高值,具有很强的抗氧化效果。构效关系(SAR)表明,由于在芳环的邻位存在硝基簇,化合物 AAZ10 表现出很强的活性。还对具有潜在活性的合成化合物 AAZ10 进行了体内抗阿尔茨海默病活性和抗氧化活性研究。通过分子对接研究揭示了所有合成化合物的结合方法,研究了酶的结合口袋,分析了与氨基酸(AA)残基的最佳立体相互作用,提供了对酶抑制机制的理解。结果表明,合成的锌(II)酰胺羧酸盐可作为治疗阿尔茨海默病的有效方法。由 Ramaswamy H. Sarma 传达。

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