AZA-BICYLOALKYL ETHERS AND THEIR USE AS ALPHA7-NACHR AGONISTS
    11.
    发明申请
    AZA-BICYLOALKYL ETHERS AND THEIR USE AS ALPHA7-NACHR AGONISTS 有权
    AZA-BICYLOALKYL ETHERS及其作为ALPHA7-NACHR AGONISTS的用途

    公开(公告)号:US20150183794A1

    公开(公告)日:2015-07-02

    申请号:US14643275

    申请日:2015-03-10

    Applicant: Novartis AG

    CPC classification number: A61K31/439 A61K9/20 A61K31/444 C07D453/02 C07D487/08

    Abstract: The present invention relates to 1-aza-bicycloalkyl derivatives of formula I, wherein X is CH2 or a single bond; Y is a group of formula and wherein R has the meanings as defined in the specification, which compounds are alpha 7 nicotinic acetylcholine receptor (nAChR) agonists; to processes for their production, their use as pharmaceuticals and to pharmaceutical compositions comprising them.

    Abstract translation: 本发明涉及式I的1-氮杂 - 双环烷基衍生物,其中X是CH 2或单键; Y是一组式,其中R具有本说明书中定义的含义,该化合物是α7烟碱型乙酰胆碱受体(nAChR)激动剂; 其制备方法,它们作为药物的用途以及包含它们的药物组合物。

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