Vincent Luzet , Florentin Allemand , Chloé Richet , Barbara Dehecq , Alexandre Bonet , Dominique Harakat , Bernard Refouvelet , Hélène Martin , Bruno Cardey , Marc Pudlo
{"title":"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。","authors":"Vincent Luzet , Florentin Allemand , Chloé Richet , Barbara Dehecq , Alexandre Bonet , Dominique Harakat , Bernard Refouvelet , Hélène Martin , Bruno Cardey , Marc Pudlo","doi":"10.1016/j.bmcl.2024.129938","DOIUrl":null,"url":null,"abstract":"<div><p>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 <em>O</em>-desmethyldonepezil. As compounds <strong>5</strong> and <strong>6</strong> display a high inhibition of acetylcholinesterase (IC<sub>50</sub> = 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 <em>O</em>-desmethyldonepezil could serve as a platform for the straightforward design of donepezil hybrids.</p></div>","PeriodicalId":256,"journal":{"name":"Bioorganic & Medicinal Chemistry Letters","volume":"112 ","pages":"Article 129938"},"PeriodicalIF":2.5000,"publicationDate":"2024-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0960894X24003408/pdfft?md5=8d09dfee3840bb50751162e260ccafc4&pid=1-s2.0-S0960894X24003408-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Synthesis and evaluation of lipoic acid – donepezil hybrids for Alzheimer’s disease using a straightforward strategy\",\"authors\":\"Vincent Luzet , Florentin Allemand , Chloé Richet , Barbara Dehecq , Alexandre Bonet , Dominique Harakat , Bernard Refouvelet , Hélène Martin , Bruno Cardey , Marc Pudlo\",\"doi\":\"10.1016/j.bmcl.2024.129938\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>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 <em>O</em>-desmethyldonepezil. As compounds <strong>5</strong> and <strong>6</strong> display a high inhibition of acetylcholinesterase (IC<sub>50</sub> = 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 <em>O</em>-desmethyldonepezil could serve as a platform for the straightforward design of donepezil hybrids.</p></div>\",\"PeriodicalId\":256,\"journal\":{\"name\":\"Bioorganic & Medicinal Chemistry Letters\",\"volume\":\"112 \",\"pages\":\"Article 129938\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-08-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S0960894X24003408/pdfft?md5=8d09dfee3840bb50751162e260ccafc4&pid=1-s2.0-S0960894X24003408-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioorganic & Medicinal Chemistry Letters\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0960894X24003408\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioorganic & Medicinal Chemistry Letters","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0960894X24003408","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Synthesis and evaluation of lipoic acid – donepezil hybrids for Alzheimer’s disease using a straightforward strategy
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.
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.