M. Lin, L. Hsin, Hui‐Bing ‐B Tsai, M. Tsai, C. Cheng
{"title":"Synthesis of 1,4-dihydro-2-phenyl-4,4-bis(4-pyridinylmethyl)-2H-isoquinolin-3-one and related compounds as acetylcholine release enhancers","authors":"M. Lin, L. Hsin, Hui‐Bing ‐B Tsai, M. Tsai, C. Cheng","doi":"10.7019/CPJ.200208.0271","DOIUrl":null,"url":null,"abstract":"Acetylcholine release enhancers may have therapeutic value in the treatment of Alzheimer's disease. A series of 1 ,4-dihydro-4,4-bis(pyridinylmethyl)-2H-isoquinolin-3-ones (2-l3) was synthesized as analogs of the known acetylcholine-release enhancer linopirdine (1). Their cholinergic activity was measured as the enhancement of indirectly-elicited twitch tension of the mouse diaphragm. Among the target compounds, 2-phenyl-4, 4-bis (4-pyridinylmethyl)-4H-isoquinolineI, 3-dione (2) and 7-bromo-1, 4-dihydro-2-phenyl-4, 4-bis {{} 4-pyridinylmethyl}-2H-isoquinolin3-one (11) were found to be more potent than 1.","PeriodicalId":22409,"journal":{"name":"The Chinese Pharmaceutical Journal","volume":"20 1","pages":"271-281"},"PeriodicalIF":0.0000,"publicationDate":"2002-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Chinese Pharmaceutical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7019/CPJ.200208.0271","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Acetylcholine release enhancers may have therapeutic value in the treatment of Alzheimer's disease. A series of 1 ,4-dihydro-4,4-bis(pyridinylmethyl)-2H-isoquinolin-3-ones (2-l3) was synthesized as analogs of the known acetylcholine-release enhancer linopirdine (1). Their cholinergic activity was measured as the enhancement of indirectly-elicited twitch tension of the mouse diaphragm. Among the target compounds, 2-phenyl-4, 4-bis (4-pyridinylmethyl)-4H-isoquinolineI, 3-dione (2) and 7-bromo-1, 4-dihydro-2-phenyl-4, 4-bis {{} 4-pyridinylmethyl}-2H-isoquinolin3-one (11) were found to be more potent than 1.