Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/13791
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dc.contributor.authorDeng, Youchao-
dc.contributor.authorJiang, Yuren-
dc.contributor.authorZhao, Xiongjie-
dc.contributor.authorWang, Jinlian-
dc.date.accessioned2022-10-27T10:36:39Z-
dc.date.available2022-10-27T10:36:39Z-
dc.date.issued2019-09-15-
dc.identifier.citationDeng, Y., Jiang, Y., Zhao, X., & Wang, J. (2019). Design, synthesis and biological Evaluation of Dual acetyl cholinesterase and beta-secretase inhibitors in treatment for alzheimer's Disease. Pakistan Journal of Pharmaceutical Sciences, 32(5).en_US
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/13791-
dc.description.abstractWith the recent research advances in molecular biology and technology multiple credible hypotheses about the progress of Alzheimer’s disease (AD) have been proposed, among which the amyloid and cholinergic hypotheses are commonly used to develop reliable therapeutic agents. The multitarget-directed ligand (MTDL) approach was taken in this work to develop muilti-functional agents, which can mainly serve as dual beta-secretase (BACE 1) and Acetylcholinesterase (AChE) inhibitors. Series of new compounds were designed, synthesized and evaluated in this work, from which we identified 2-((4-(1,3-dioxoisoindolin-2-yl)benzyl)amino)-2-oxoethyl-2-(4-methoxyphenyl)acetate (1h) as a new dual cholinesterase and beta-secretase inhibitor without toxicity.en_US
dc.language.isoen_USen_US
dc.subjectBeta-Secretaseen_US
dc.subjectAcetylcholinesteraseen_US
dc.subjectInhibitoren_US
dc.subjectAlzheimer’s Disease.en_US
dc.titleDesign, synthesis and biological Evaluation of Dual acetyl cholinesterase and beta-secretase inhibitors in treatment for alzheimer’s Diseaseen_US
dc.typeArticleen_US
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