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公开(公告)号:US08772285B2
公开(公告)日:2014-07-08
申请号:US13660045
申请日:2012-10-25
发明人: Florencio Zaragoza Dorwald , Rolf Hohlweg , Inge Thoger Christensen , Jane Marie Lundbeck , Knud Erik Andersen
IPC分类号: A61K31/535 , A61K31/497 , C07D417/00 , C07D413/00 , C07D419/00
CPC分类号: C07D471/04 , C07D263/58 , C07D277/82 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/06 , C07D417/14
摘要: Certain novel benzothiazoles and benzoxazoles, e.g., 2-(piperazin-1-yl)benzothiazoles and 2-(piperazin-1-yl)benzoxazoles, optionally substituted in the 3 and/or 4 positions of the piperazine rings, having histamine H3 antagonistic activity can be used in pharmaceutical compositions.
摘要翻译: 某些新的苯并噻唑和苯并恶唑,例如2-(哌嗪-1-基)苯并噻唑和2-(哌嗪-1-基)苯并恶唑,任选在哌嗪环的3和/或4位被取代,具有组胺H3拮抗活性 可用于药物组合物。
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公开(公告)号:US20130079340A1
公开(公告)日:2013-03-28
申请号:US13660045
申请日:2012-10-25
申请人: Florencio Zaragoza Dorwald , Rolf Hohlweg , Inge Thoger Christensen , Jane Marie Lundbeck , Knud Erik Andersen
发明人: Florencio Zaragoza Dorwald , Rolf Hohlweg , Inge Thoger Christensen , Jane Marie Lundbeck , Knud Erik Andersen
IPC分类号: C07D471/04 , C07D417/14 , C07D413/14 , C07D417/04
CPC分类号: C07D471/04 , C07D263/58 , C07D277/82 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/06 , C07D417/14
摘要: Certain novel benzothiazoles and benzoxazoles, e.g., 2-(piperazin-1-yl)benzothiazoles and 2-(piperazin-1-yl)benzoxazoles, optionally substituted in the 3 and/or 4 positions of the piperazine rings, having histamine H3 antagonistic activity can be used in pharmaceutical compositions.
摘要翻译: 某些新的苯并噻唑和苯并恶唑,例如2-(哌嗪-1-基)苯并噻唑和2-(哌嗪-1-基)苯并恶唑,任选在哌嗪环的3和/或4位被取代,具有组胺H3拮抗活性 可用于药物组合物。
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公开(公告)号:US08394842B2
公开(公告)日:2013-03-12
申请号:US12294756
申请日:2007-03-22
申请人: Florencio Zaragoza Dorwald , Rolf Hohlweg , Inge Thoger Christensen , Jane Marie Lundbeck , Knud Erik Andersen
发明人: Florencio Zaragoza Dorwald , Rolf Hohlweg , Inge Thoger Christensen , Jane Marie Lundbeck , Knud Erik Andersen
IPC分类号: A01N43/78 , A61K31/425 , C07D277/82
CPC分类号: C07D471/04 , C07D263/58 , C07D277/82 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/06 , C07D417/14
摘要: Certain novel benzothiazoles and benzoxazoles, e.g., 2-(piperazin-1-yl)benzothiazoles and 2-(piperazin-1-yl)benzoxazoles, optionally substituted in the 3 and/or 4 positions of the piperazine rings,! of the general formula (1): having histamine H3 antagonistic activity can be used in pharmaceutical compositions.
摘要翻译: 某些新的苯并噻唑和苯并恶唑,例如2-(哌嗪-1-基)苯并噻唑和2-(哌嗪-1-基)苯并恶唑,任选在哌嗪环的3位和/或4位取代, 具有组胺H3拮抗活性的通式(1)的化合物可用于药物组合物中。
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公开(公告)号:US20100298316A1
公开(公告)日:2010-11-25
申请号:US12294756
申请日:2007-03-22
申请人: Florencio Zaragoza Dorwald , Rolf Hohlweg , Inge Thoger Christensen , Jane Marie Lundbeck , Erik Knud Andersen
发明人: Florencio Zaragoza Dorwald , Rolf Hohlweg , Inge Thoger Christensen , Jane Marie Lundbeck , Erik Knud Andersen
IPC分类号: A61K31/496 , C07D417/04 , C07D417/14 , C07D413/04 , C07D413/14 , A61K31/4985 , A61K31/5377 , A61P25/00 , A61P9/00 , A61P11/00 , A61P1/00 , A61P5/00 , A61P3/04 , A61P35/00
CPC分类号: C07D471/04 , C07D263/58 , C07D277/82 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/06 , C07D417/14
摘要: Certain novel benzothiazoles and benzoxazoles, e.g., 2-(piperazin-1-yl)benzothiazoles and 2-(piperazin-1-yl)benzoxazoles, optionally substituted in the 3 and/or 4 positions of the piperazine rings,! of the general formula (1): having histamine H3 antagonistic activity can be used in pharmaceutical compositions.
摘要翻译: 某些新的苯并噻唑和苯并恶唑,例如2-(哌嗪-1-基)苯并噻唑和2-(哌嗪-1-基)苯并恶唑,任选在哌嗪环的3位和/或4位取代, 具有组胺H3拮抗活性的通式(1)的化合物可用于药物组合物中。
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公开(公告)号:US20090264435A1
公开(公告)日:2009-10-22
申请号:US12367952
申请日:2009-02-09
申请人: Rolf Hohlweg , Florencio Zaragoza Dorwald , Henrik Stephensen , Ingrid Pettersson , Bernd Peschke
发明人: Rolf Hohlweg , Florencio Zaragoza Dorwald , Henrik Stephensen , Ingrid Pettersson , Bernd Peschke
IPC分类号: A61K31/495 , C07D241/04 , C07D401/04 , C07D403/04 , A61K31/496 , A61K31/501 , C07D471/00
CPC分类号: C07D213/74 , C07D213/82 , C07D215/38 , C07D237/20 , C07D241/26 , C07D241/44 , C07D295/03 , C07D295/033 , C07D295/073 , C07D295/088 , C07D295/096 , C07D295/112 , C07D401/04 , C07D471/04 , C07D491/04
摘要: Novel aryl- and heteroarylpiperazines, use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds, and a method of treatment employing these compounds and compositions. The compounds show a high and selective binding affinity to the histamine H3 receptor indicating histamine H3 receptor antagonistic, inverse agonistic or agonistic activity. As a result, the compounds are useful for the treatment of diseases and disorders related to the histamine H3 receptor.
摘要翻译: 新的芳基和杂芳基哌嗪,这些化合物用作药物组合物,包含该化合物的药物组合物,以及使用这些化合物和组合物的治疗方法。 化合物对组胺H3受体表现出高且选择性的结合亲和力,表明组胺H3受体拮抗,反向激动或激动活性。 结果,这些化合物可用于治疗与组胺H3受体相关的疾病和病症。
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公开(公告)号:US06673829B2
公开(公告)日:2004-01-06
申请号:US10242968
申请日:2002-09-12
IPC分类号: A61K3140
CPC分类号: C07D401/12 , A61K31/40 , A61K31/445 , A61K31/4523 , C07D207/14 , C07D211/56 , C07D211/58 , C07D405/12 , C07D409/12 , C07D413/12
摘要: Novel aminoazetidine, -pyrrolidine, and -piperidine derivatives, use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds, and a method of treatment employing these compounds and compositions. The compounds show a high and selective binding affinity to the histamine H3 receptor indicating histamine H3 receptor antagonistic, inverse agonistic or agonistic activity. As a result, the compounds are useful for the treatment of diseases and disorders related to the histamine H3 receptor.
摘要翻译: 新型氨基氮杂环丁烷,吡咯烷和哌啶衍生物,这些化合物用作药物组合物,包含该化合物的药物组合物,以及使用这些化合物和组合物的治疗方法。 化合物对组胺H3受体表现出高且选择性的结合亲和力,表明组胺H3受体拮抗,反向激动或激动活性。 结果,这些化合物可用于治疗与组胺H3受体相关的疾病和病症。
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