发明申请
US20080269279A1 Substituted furo[2,3-B] pyridine derivatives as cannabinoid-1 receptor modulators
审中-公开
取代的呋喃并[2,3-B]吡啶衍生物作为大麻素-1受体调节剂
- 专利标题: Substituted furo[2,3-B] pyridine derivatives as cannabinoid-1 receptor modulators
- 专利标题(中): 取代的呋喃并[2,3-B]吡啶衍生物作为大麻素-1受体调节剂
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申请号: US12082013申请日: 2008-04-07
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公开(公告)号: US20080269279A1公开(公告)日: 2008-10-30
- 发明人: Matthew J. Clements , John S. Debenham , Jeffrey J. Hale , Christina B. Madsen-Duggan , Thomas F. Walsh , Andrey V. Peresypkin , Roy Helmy
- 申请人: Matthew J. Clements , John S. Debenham , Jeffrey J. Hale , Christina B. Madsen-Duggan , Thomas F. Walsh , Andrey V. Peresypkin , Roy Helmy
- 主分类号: A61K31/4355
- IPC分类号: A61K31/4355 ; C07D471/04 ; A61P25/00 ; A61P3/04
摘要:
Novel compounds of the structural formula (I) are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor. The compounds of the present invention are useful as centrally acting drugs in the treatment of psychosis, memory deficits, cognitive disorders, Alzheimer's disease, migraine, neuropathy, neuro-inflammatory disorders including multiple sclerosis and Guillain-Barre syndrome and the inflammatory sequelae of viral encephalitis, cerebral vascular accidents, and head trauma, anxiety disorders, stress, epilepsy, Parkinson's disease, movement disorders, and schizophrenia. The compounds are also useful for the treatment of substance abuse disorders, the treatment of obesity or eating disorders, as well as the treatment of asthma, constipation, chronic intestinal pseudo-obstruction, cirrhosis of the liver, non-alcoholic fatty liver disease (NAFLD), non-alcoholic steatohepatitis (NASH), and the promotion of wakefulness.
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