发明授权
US07999107B2 Substituted pyrano[2,3-B]pyridine derivatives as cannabinoid-1 receptor modulators
失效
取代的吡喃并[2,3-B]吡啶衍生物作为大麻素-1受体调节剂
- 专利标题: Substituted pyrano[2,3-B]pyridine derivatives as cannabinoid-1 receptor modulators
- 专利标题(中): 取代的吡喃并[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: US12009114申请日: 2008-01-16
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公开(公告)号: US07999107B2公开(公告)日: 2011-08-16
- 发明人: John S. Debenham , Jeffrey J. Hale , Pei Huo , Christina B. Madsen-Duggan , Thomas F. Walsh , Lin Yan
- 申请人: John S. Debenham , Jeffrey J. Hale , Pei Huo , Christina B. Madsen-Duggan , Thomas F. Walsh , Lin Yan
- 申请人地址: US NJ Rahway
- 专利权人: Merck Sharp & Dohme Corp.
- 当前专利权人: Merck Sharp & Dohme Corp.
- 当前专利权人地址: US NJ Rahway
- 代理商 Baerbel R. Brown; John C. Todaro
- 主分类号: C07D491/052
- IPC分类号: C07D491/052 ; A61K31/436
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, Huntington'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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