Synthesis and evaluation of lipoic acid – donepezil hybrids for Alzheimer’s disease using a straightforward strategy

IF 2.5 4区 医学 Q3 CHEMISTRY, MEDICINAL Bioorganic & Medicinal Chemistry Letters Pub Date : 2024-08-31 DOI:10.1016/j.bmcl.2024.129938
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Abstract

Alzheimer’s disease is associated with a progressive loss of neurons and synaptic connections in the cholinergic system. Oxidative stress contributes to neuronal damages and to the development of amyloid plaques and neurofibrillary tangles. Therefore, antioxidants have been widely studied to mitigate the progression of Alzheimer’s disease, and among these, lipoic acid has demonstrated a neuroprotective effect. Here, we present the synthesis, the molecular modelling, and the evaluation of lipoic acid–donepezil hybrids based on O-desmethyldonepezil. As compounds 5 and 6 display a high inhibition of acetylcholinesterase (IC50 = 7.6 nM and 9.1 nM, respectively), selective against butyrylcholinesterase, and a notable neuroprotective effect, slightly better than that of lipoic acid, the present study suggests that O-desmethyldonepezil could serve as a platform for the straightforward design of donepezil hybrids.

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采用直接策略合成和评估治疗阿尔茨海默病的硫辛酸-多奈哌齐混合物。
阿尔茨海默病与胆碱能系统中神经元和突触连接的逐渐丧失有关。氧化应激是造成神经元损伤以及形成淀粉样蛋白斑块和神经纤维缠结的原因之一。因此,人们广泛研究抗氧化剂以缓解阿尔茨海默病的进展,其中硫辛酸已证明具有神经保护作用。在此,我们介绍了基于 O-去甲基多奈哌齐的硫辛酸-多奈哌齐混合物的合成、分子建模和评估。由于化合物 5 和 6 对乙酰胆碱酯酶有较高的抑制作用(IC50 分别为 7.6 nM 和 9.1 nM),对丁酰胆碱酯酶有选择性抑制作用,并且具有显著的神经保护作用,略优于硫辛酸,因此本研究认为 O-去甲基多奈哌齐可以作为直接设计多奈哌齐杂交化合物的平台。
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来源期刊
CiteScore
5.70
自引率
3.70%
发文量
463
审稿时长
27 days
期刊介绍: Bioorganic & Medicinal Chemistry Letters presents preliminary experimental or theoretical research results of outstanding significance and timeliness on all aspects of science at the interface of chemistry and biology and on major advances in drug design and development. The journal publishes articles in the form of communications reporting experimental or theoretical results of special interest, and strives to provide maximum dissemination to a large, international audience.
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