名称:
Discovery of γ-secretase inhibitors efficacious in a transgenic animal model of Alzheimer’s disease
摘要:
Attachment of the cyclopropylcarbamate group to the piperidine core of gamma-secretase inhibitors leads to a dramatic increase of their in vitro potency. Strategies for subsequent improvement of the in vivo pharmacokinetic profile of the series are discussed. Resulting compounds significantly reduce A beta levels in TgCRND8 mice after a single PO dosing at 30 mpk. (c) 2006 Elsevier Ltd. All rights reserved.
DOI:
10.1016/j.bmcl.2006.10.011