Université de Franche-Comté, FEMTO-ST, F-25000 Besançon, France.
Université de Franche-Comté, Chrono-environnement UMR6249, CNRS, F-25000 Besançon, France.
Bioorg Med Chem Lett. 2024 Nov 1;112:129938. doi: 10.1016/j.bmcl.2024.129938. Epub 2024 Aug 31.
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 (IC = 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.
阿尔茨海默病与胆碱能系统中神经元和突触连接的进行性丧失有关。氧化应激导致神经元损伤,并导致淀粉样斑块和神经原纤维缠结的形成。因此,抗氧化剂已被广泛研究用于减轻阿尔茨海默病的进展,其中,硫辛酸已显示出神经保护作用。在这里,我们介绍了基于 O-去甲丹酚的硫辛酸-多奈哌齐杂合物的合成、分子建模和评价。由于化合物 5 和 6 对乙酰胆碱酯酶的抑制作用很强(IC = 7.6 nM 和 9.1 nM,分别),对丁酰胆碱酯酶具有选择性,并且具有显著的神经保护作用,略优于硫辛酸,本研究表明 O-去甲丹酚可作为设计多奈哌齐杂合物的简单平台。