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    SUBSTITUTED FURO [2,3-B] PYRIDINE DERIVATIVES
    2.
    发明申请
    SUBSTITUTED FURO [2,3-B] PYRIDINE DERIVATIVES 审中-公开
    取代的FURO [2,3-B]吡啶衍生物

    公开(公告)号：WO2004012671A2

    公开(公告)日：2004-02-12

    申请号：PCT/US2003/024280

    申请日：2003-08-01

    申请人： MERCK & CO., INC. ,  TOUPENCE, Richard, B. ,  DEBENHAM, John, S. ,  GOULET, Mark, T. ,  MADSEN-DUGGAN, Christina, B. ,  WALSH, Thomas, F. ,  SHAH, Shrenik, K.

    发明人： TOUPENCE, Richard, B. ,  DEBENHAM, John, S. ,  GOULET, Mark, T. ,  MADSEN-DUGGAN, Christina, B. ,  WALSH, Thomas, F. ,  SHAH, Shrenik, K.

    IPC分类号： A61K

    CPC分类号： C07D491/04 ,  C07D453/06

    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，慢性肠假性梗阻和肝硬化。

    SUBSTITUTED PYRIDO[2,3-D]PYRIMIDINE DERIVATIVES AS CANNABINOID-1 RECEPTOR MODULATORS
    4.
    发明申请
    SUBSTITUTED PYRIDO[2,3-D]PYRIMIDINE DERIVATIVES AS CANNABINOID-1 RECEPTOR MODULATORS 审中-公开
    作为CANNABINOID-1受体调节剂的取代的吡咯并[2,3-D]吡啶衍生物

    公开(公告)号：WO2008121257A1

    公开(公告)日：2008-10-09

    申请号：PCT/US2008/003848

    申请日：2008-03-24

    申请人： MERCK & CO., INC. ,  DEBENHAM, John, S. ,  MADSEN-DUGGAN, Christina, B. ,  WALSH, Thomas, F.

    发明人： DEBENHAM, John, S. ,  MADSEN-DUGGAN, Christina, B. ,  WALSH, Thomas, F.

    IPC分类号： A01N43/90 ,  A61K31/519

    CPC分类号： C07D471/04

    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.

    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炎症后遗症的中枢作用药物 脑炎，脑血管意外和头部创伤，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，肝硬化，非酒精性脂肪性肝病（NAFLD ），非酒精性脂肪性肝炎（NASH），以及促进觉醒。

    SUBSTITUTED PYRIDO[3,2-E][1,2,4]TRIAZOLO[4,3-C]PYRIMIDINE DERIVATIVES AS CANNABINOID-1 RECEPTOR MODULATORS
    10.
    发明申请
    SUBSTITUTED PYRIDO[3,2-E][1,2,4]TRIAZOLO[4,3-C]PYRIMIDINE DERIVATIVES AS CANNABINOID-1 RECEPTOR MODULATORS 审中-公开
    取代的吡咯并[3,2-E] [1,2,4]三唑并[4,3-C]吡啶衍生物作为CANNABINOID-1受体调节剂

    公开(公告)号：WO2008118414A1

    公开(公告)日：2008-10-02

    申请号：PCT/US2008/003847

    申请日：2008-03-24

    申请人： MERCK & CO., INC. ,  DEBENHAM, John, S. ,  MADSEN-DUGGAN, Christina, B. ,  HALE, Jeffrey, J. ,  WALSH, Thomas, F.

    发明人： DEBENHAM, John, S. ,  MADSEN-DUGGAN, Christina, B. ,  HALE, Jeffrey, J. ,  WALSH, Thomas, F.

    IPC分类号： A01N43/90 ,  A61K31/519

    CPC分类号： C07D487/14

    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), non-alcoholic steatohepatitis (NASH), and the promotion of wakefulness.

    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炎症后遗症的中枢作用药物 脑炎，脑血管意外和头部创伤，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，肝硬化，非酒精性脂肪性肝病（NAFLD ），非酒精性脂肪性肝炎（NASH），以及促进觉醒。