Therapeutic pyrazolo[3,4-b]pyridines and indazoles
    2.
    发明授权
    Therapeutic pyrazolo[3,4-b]pyridines and indazoles 失效
    治疗性吡唑并[3,4-b]吡啶和吲唑

    公开(公告)号:US07485636B2

    公开(公告)日:2009-02-03

    申请号:US11446277

    申请日:2006-06-02

    申请人: Po-Wai Yuen

    发明人: Po-Wai Yuen

    IPC分类号: A61K31/535 C07D413/12

    摘要: The present invention provides for compounds of Formula I: wherein R2, R3, R4, R5, R6, R7, X, and L have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of central nervous disorders and conditions including attention deficit hyperactivity disorder, neuropathic pain, urinary incontinence, anxiety, depression, and schizophrenia and fibromyalgia. Also provided are pharmaceutical compositions comprising one or more compounds of Formula I.

    摘要翻译: 本发明提供式I化合物:其中R2,R3,R4,R5,R6,R7,X和L具有说明书中定义的任何值及其药学上可接受的盐,其可用作 治疗中枢神经障碍和包括注意力缺陷多动障碍,神经性疼痛,尿失禁,焦虑,抑郁和精神分裂症以及纤维肌痛的病症。 还提供了包含一种或多种式I化合物的药物组合物。

    Substituted phenols as novel calcium channel blockers
    4.
    发明授权
    Substituted phenols as novel calcium channel blockers 失效
    取代酚作为新的钙通道阻滞剂

    公开(公告)号:US6124280A

    公开(公告)日:2000-09-26

    申请号:US983633

    申请日:1998-01-23

    CPC分类号: C07D295/096 C07D295/135

    摘要: The present invention relates to novel substituted phenols and derivatives thereof useful in the treatment of neurological disorders. Methods of preparing the compounds, intermediates useful in the preparation and pharmaceutical compositions containing the compounds are also includes.

    摘要翻译: PCT No.PCT / US96 / 08064 Sec。 371日期1998年1月23日 102(e)日期1998年1月23日PCT提交1996年7月16日PCT公布。 公开号WO97 / 05125 日期:1997年2月13日本发明涉及用于治疗神经障碍的新型取代苯酚及其衍生物。 制备化合物的方法,可用于制备的中间体和含有这些化合物的药物组合物还包括。

    Therapeutic Pyrazolo[3,4-b]Pyridines and Indazoles
    8.
    发明申请
    Therapeutic Pyrazolo[3,4-b]Pyridines and Indazoles 审中-公开
    治疗性吡唑并[3,4-b]吡啶类和吲唑类

    公开(公告)号:US20080293715A1

    公开(公告)日:2008-11-27

    申请号:US12185419

    申请日:2008-08-04

    摘要: The present invention provides for compounds of Formula I: wherein R2, R3, R4, R5, R6, R7, X, and L have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of central nervous disorders and conditions including attention deficit hyperactivity disorder, neuropathic pain, urinary incontinence, anxiety, depression, and schizophrenia and fibromyalgia. Also provided are pharmaceutical compositions comprising one or more compounds of Formula I.

    摘要翻译: 本发明提供式I化合物:其中R2,R3,R4,R5,R6,R7,X和L具有说明书中定义的任何值及其药学上可接受的盐,其可用作 治疗中枢神经障碍和包括注意力缺陷多动障碍,神经性疼痛,尿失禁,焦虑,抑郁和精神分裂症以及纤维肌痛的病症。 还提供了包含一种或多种式I化合物的药物组合物。

    3-heteroarylalkyl substituted GABA analogs
    9.
    发明授权
    3-heteroarylalkyl substituted GABA analogs 失效
    3-杂芳基烷基取代的GABA类似物

    公开(公告)号:US06833385B2

    公开(公告)日:2004-12-21

    申请号:US10741116

    申请日:2003-12-19

    申请人: Po-Wai Yuen

    发明人: Po-Wai Yuen

    IPC分类号: C07D33310

    CPC分类号: C07D307/54 C07D333/24

    摘要: The invention is a novel series of compounds which are useful in the treatment of epilepsy, faintness attacks, neurodegenerative disorders, depression, anxiety, panic, pain, neuropathological disorders, gastrointestinal disorders such as irritable bowel syndrome (IBS), and inflammation, especially arthritis. A pharmaceutical composition containing a compound of the invention as well as methods of preparing the compounds and novel intermediates useful in the preparation of the final compounds are included.

    摘要翻译: 本发明是可用于治疗癫痫,微弱发作,神经退行性疾病,抑郁症,焦虑症,恐慌症,疼痛,神经病理学障碍,胃肠道疾病如肠易激综合征(IBS)和炎症,特别是关节炎的新一系列化合物 。 包括含有本发明化合物的药物组合物以及制备化合物的方法和用于制备最终化合物的新中间体。