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Substituted pyrano2,3-Bpyridine derivatives as cannabinoid-1 receptor modulators

机译:取代吡喃并[2,3-B]吡啶衍生物作为大麻素-1受体调节剂

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.
机译:结构式(I)的新化合物是大麻素-1(CB1)受体的拮抗剂和/或反向激动剂,可用于治疗,预防和抑制由CB1受体介导的疾病。本发明的化合物可用作中枢性药物,用于治疗精神病,记忆力减退,认知障碍,阿尔茨海默氏病,偏头痛,神经病,神经炎性疾病,包括多发性硬化症和格林-巴利综合征以及病毒性脑炎的炎症后遗症。 ,脑血管意外和头部外伤,焦虑症,压力,癫痫,帕金森氏病,亨廷顿氏病运动障碍和精神分裂症。该化合物还可用于治疗药物滥用疾病,肥胖症或进食障碍,以及治疗哮喘,便秘,慢性肠假性阻塞,肝硬化,非酒精性脂肪肝(NAFLD) ),非酒精性脂肪性肝炎(NASH)和促进清醒。

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