| Literature DB >> 27190595 |
Paola Costanzo1, Luca Cariati1, Doriana Desiderio2, Roberta Sgammato3, Anna Lamberti4, Rosaria Arcone3, Raffaele Salerno1, Monica Nardi5, Mariorosario Masullo3, Manuela Oliverio1.
Abstract
An ecofriendly synthetic pathway for the synthesis of donepezil precursors is described. Alternative energy sources were used for the total synthesis in order to improve yields, regioselectively, and rate of each synthetic step and to reduce the coproduction of waste at the same time. For all products, characterized by an improved structural rigidity respect to donepezil, the inhibitor activity on AChE, the selectivity vs BuChE, the side-activity on BACE-1, and the effect on SHSY-5Y neuroblastoma cells viability were tested. Two potential new lead compounds for a dual therapeutic strategy against Alzheimer's disease were envisaged.Entities:
Keywords: Alzheimer’s disease; acethylcholinesterase; aldol condensation; donepezil analogues; indanones
Year: 2016 PMID: 27190595 PMCID: PMC4867475 DOI: 10.1021/acsmedchemlett.5b00483
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345