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公开(公告)号:US06239148B1
公开(公告)日:2001-05-29
申请号:US09055574
申请日:1998-04-06
申请人: Florenzio Zaragossa Dörwald , Knud Erik Andersen , Rolf Hohlweg , Peter Madsen , Tine Krogh Jørgensen , Uffe Bang Olsen , Henrik Sune Andersen , Svend Treppendahl , Polivka Zdenék , Silhánková Alexandra , Sindelár Karel
发明人: Florenzio Zaragossa Dörwald , Knud Erik Andersen , Rolf Hohlweg , Peter Madsen , Tine Krogh Jørgensen , Uffe Bang Olsen , Henrik Sune Andersen , Svend Treppendahl , Polivka Zdenék , Silhánková Alexandra , Sindelár Karel
IPC分类号: A61K31451
CPC分类号: C07D207/16 , A61K31/44 , A61K31/451 , C07D211/60 , C07D211/62 , C07D401/06 , C07D403/06 , C07D413/06 , C07D453/02
摘要: The present invention relates to novel N-substituted azaheterocyclic carboxylic acids and esters thereof in which a substituted alkyl chain forms part of the N-substituent or salts thereof, to methods for their preparation, to compositions containing them, and to their use for the clinical treatment of painful, hyperalgesic and/or inflammatory conditions in which C-fibers play a pathophysiological role by eliciting neurogenic pain or inflammation.
摘要翻译: 本发明涉及新的N-取代的氮杂杂环羧酸及其酯,其中取代的烷基链形成N-取代基或其盐的一部分,其制备方法,含有它们的组合物及其用于临床的用途 治疗C型纤维通过引起神经源性疼痛或炎症而发挥病理生理作用的疼痛,痛觉过敏和/或炎性病症。
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公开(公告)号:US06613791B1
公开(公告)日:2003-09-02
申请号:US09640605
申请日:2000-08-17
申请人: Florenzio Zaragossa Dörwald , Enud Erik Andersen , Rolf Hohlweg , Peter Madsen , Tine Krogh Jørgensen , Uffe Bang Olsen , Henrik Sune Andersen , Svend Treppendahl , Polivka Zdenék , Silhánková Alexandra , Sindelár Karel
发明人: Florenzio Zaragossa Dörwald , Enud Erik Andersen , Rolf Hohlweg , Peter Madsen , Tine Krogh Jørgensen , Uffe Bang Olsen , Henrik Sune Andersen , Svend Treppendahl , Polivka Zdenék , Silhánková Alexandra , Sindelár Karel
IPC分类号: C07D20712
CPC分类号: C07D207/16 , A61K31/44 , A61K31/451 , C07D211/60 , C07D211/62 , C07D401/06 , C07D403/06 , C07D413/06 , C07D453/02
摘要: N-substituted azaheterocycyclic carboxylic acids and esters thereof of the formula I wherein Z, X, R1, R2 and r are defined in the specification. Compositions thereof and methods for preparing the compounds are disclosed. The compounds are useful for clinical treatment of painful, hyperalgesic and/or inflammatory conditions in which C-fibers play a pathophysiological role by eliciting neurogenic pain or inflammations.
摘要翻译: 在说明书中定义了式I中的N-取代的氮杂杂环羧酸及其酯,其中Z,X,R 1,R 2和r在本说明书中定义。 公开了其组合物及其制备方法。 该化合物可用于临床治疗疼痛,痛觉过敏和/或炎性疾病,其中C纤维通过引发神经源性疼痛或炎症而发挥病理生理学作用。
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