利索-全球专利检索

  1. 登录
  2. 注册

搜索结果

24 条记录 (耗时 0.052 秒)

    Heterocycle-substituted 3-alkyl azetidine derivatives
    3.
    发明授权
    Heterocycle-substituted 3-alkyl azetidine derivatives 失效
    杂环取代的3-烷基氮杂环丁烷衍生物

    公开(公告)号：US07906652B2

    公开(公告)日：2011-03-15

    申请号：US11602577

    申请日：2006-11-21

    申请人： Robert K. Baker ,  Jeffrey J. Hale ,  Shouwu Miao ,  Kathleen M. Rupprecht

    发明人： Robert K. Baker ,  Jeffrey J. Hale ,  Shouwu Miao ,  Kathleen M. Rupprecht

    IPC分类号： C07D271/10 ,  C07D205/04

    CPC分类号： C07D257/04 ,  C07D271/06 ,  C07D271/07 ,  C07D271/10 ,  C07D271/113 ,  C07D403/10 ,  C07D413/10 ,  C07D417/04 ,  C07D417/06 ,  C07D417/14

    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), and non-alcoholic steatohepatitis (NASH).

    摘要翻译： 结构式（I）的新型化合物是大麻素-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治疗精神病，记忆缺陷，认知障碍，阿尔茨海默病，偏头痛，神经病，包括多发性硬化症和神经 - 巴利综合征的神经炎症性疾病以及病毒性脑炎的炎症性后遗症的中枢作用药物 脑血管意外，头部创伤，焦虑障碍，压力，癫痫，帕金森病，运动障碍和精神分裂症。 这些化合物还可用于治疗药物滥用障碍，治疗肥胖或进食障碍，以及治疗哮喘，便秘，慢性肠假性梗阻，肝硬化，非酒精性脂肪性肝病（NAFLD ），非酒精性脂肪性肝炎（NASH）。

    Substituted 3-alkyl and 3-alkenyl azetidine derivatives
    4.
    发明申请
    Substituted 3-alkyl and 3-alkenyl azetidine derivatives 失效
    取代的3-烷基和3-烯基氮杂环丁烷衍生物

    公开(公告)号：US20090069284A1

    公开(公告)日：2009-03-12

    申请号：US12288518

    申请日：2008-10-21

    申请人： Robert K. Baker ,  Jianming Bao ,  Shouwu Miao ,  Kathleen M. Rupprecht

    发明人： Robert K. Baker ,  Jianming Bao ,  Shouwu Miao ,  Kathleen M. Rupprecht

    IPC分类号： A61K31/397 ,  C07D205/04 ,  C07D401/06 ,  A61K31/4427 ,  A61K31/4178 ,  A61K31/4196 ,  C07D205/06 ,  C07D403/06

    CPC分类号： C07D205/04 ,  C07D205/06 ,  C07D401/06 ,  C07D403/06 ,  C07D403/10 ,  C07D405/06 ,  C07D409/06

    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, 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, and cirrhosis of the liver.

    摘要翻译： 结构式（I）的新型化合物是大麻素-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治疗精神病，记忆缺陷，认知障碍，偏头痛，神经病，包括多发性硬化和神经 - 巴利综合征的神经炎症性疾病以及病毒性脑炎的炎症性后遗症，脑血管 事故和头部创伤，焦虑症，压力，癫痫，帕金森病，运动障碍和精神分裂症。 这些化合物还可用于治疗药物滥用障碍，治疗肥胖或进食障碍，以及治疗哮喘，便秘，慢性肠假性梗阻和肝硬化。

    Substituted 3-alkyl and 3-alkenyl azetidine derivatives
    9.
    发明授权
    Substituted 3-alkyl and 3-alkenyl azetidine derivatives 失效
    取代的3-烷基和3-烯基氮杂环丁烷衍生物

    公开(公告)号：US07906503B2

    公开(公告)日：2011-03-15

    申请号：US12288518

    申请日：2008-10-21

    申请人： Robert K. Baker ,  Jianming Bao ,  Shouwu Miao ,  Kathleen M. Rupprecht

    发明人： Robert K. Baker ,  Jianming Bao ,  Shouwu Miao ,  Kathleen M. Rupprecht

    IPC分类号： A61K31/397 ,  A61K31/4427 ,  A61K31/4178 ,  A61K31/4196 ,  C07D205/04 ,  C07D401/06 ,  C07D205/06 ,  C07D403/06

    CPC分类号： C07D205/04 ,  C07D205/06 ,  C07D401/06 ,  C07D403/06 ,  C07D403/10 ,  C07D405/06 ,  C07D409/06

    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, 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, and cirrhosis of the liver.

    摘要翻译： 结构式（I）的新型化合物是大麻素-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治疗精神病，记忆缺陷，认知障碍，偏头痛，神经病，包括多发性硬化和神经 - 巴利综合征的神经炎症性疾病以及病毒性脑炎的炎症性后遗症，脑血管 事故和头部创伤，焦虑症，压力，癫痫，帕金森病，运动障碍和精神分裂症。 这些化合物还可用于治疗药物滥用障碍，治疗肥胖或进食障碍，以及治疗哮喘，便秘，慢性肠假性梗阻和肝硬化。