首页> 外国专利> 1. Inhibitors from helix-1.3-oxalic acid and helix-1.4-oxalic acid, Bac 1 and/or Bac2; pharmacological synthesis; preparatory procedures; and uses for the treatment and/or prevention of Alzheimer's disease and diabetes.

1. Inhibitors from helix-1.3-oxalic acid and helix-1.4-oxalic acid, Bac 1 and/or Bac2; pharmacological synthesis; preparatory procedures; and uses for the treatment and/or prevention of Alzheimer's disease and diabetes.

机译:1.来自螺旋-[1.3]-草酸和螺旋-[1.4]-草酸,Bac 1和/或Bac2的抑制剂;药理合成筹备程序;以及用于治疗和/或预防阿尔茨海默氏病和糖尿病的用途。

摘要

The present invention provides spiro-[1,3]-oxazines and spiro-[1,4]-oxazepines of formula I having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful in the therapeutic and/or prophylactic treatment of e.g. Alzheimer's disease and type 2 diabetes.
机译:本发明提供了具有BACE1和/或BACE2抑制活性的式I的螺-[1,3]-恶嗪和螺-[1,4]-氧杂氮杂,它们的制备,含有它们的药物组合物以及它们作为治疗活性物质的用途。本发明的活性化合物可用于例如抗炎药的治疗和/或预防治疗。阿尔茨海默氏病和2型糖尿病。

著录项

  • 公开/公告号CL2013003372A1

    专利类型

  • 公开/公告日2014-07-25

    原文格式PDF

  • 申请/专利权人 F.HOFFMANN LA ROCHE AG;

    申请/专利号CL20130003372

  • 申请日2013-11-25

  • 分类号C07D498/10;A61K31/537;A61K31/553;A61P25/28;A61P3/10;

  • 国家 CL

  • 入库时间 2022-08-21 15:58:27

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