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公开(公告)号:US6034089A
公开(公告)日:2000-03-07
申请号:US163033
申请日:1998-09-28
申请人: Yongxin Han , Andre Giroux , Dwight MacDonald , Robert N. Young , Helene Perrier , Carole Lepine
发明人: Yongxin Han , Andre Giroux , Dwight MacDonald , Robert N. Young , Helene Perrier , Carole Lepine
IPC分类号: C07D333/24 , C07D409/04 , C07D409/12 , C07D409/14 , C07D417/14 , A61K31/505 , A61K31/38 , A61K31/44 , C07D403/00 , C07D409/00
CPC分类号: C07D409/14 , C07D333/24 , C07D409/04 , C07D409/12 , C07D417/14
摘要: The invention encompasses the novel compound of Formula I useful in the treatment of diseases, including asthma, by raising the level of cyclic adenosine-3',5'-monophosphate (cAMP) through the inhibition of phosphodiesterase IV (PDE IV). ##STR1## The invention also encompasses certain pharmaceutical compositions and methods for treatment of diseases by inhibition of PDE IV, resulting in an elevation of cAMP, comprising the use of compounds of Formula I.
摘要翻译: 本发明包括通过抑制磷酸二酯酶IV(PDE IV)提高环腺苷-3',5'-单磷酸(cAMP)的水平,可用于治疗包括哮喘在内的疾病的新型式I化合物。 本发明还包括通过抑制PDE IV治疗疾病的某些药物组合物和方法,导致cAMP升高,包括使用式I化合物。
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公开(公告)号:US6020339A
公开(公告)日:2000-02-01
申请号:US163032
申请日:1998-09-28
申请人: Helene Perrier , Yongxin Han , Christopher Bayly , Dwight Mac Donald , Andre Giroux , Robert N. Young
发明人: Helene Perrier , Yongxin Han , Christopher Bayly , Dwight Mac Donald , Andre Giroux , Robert N. Young
IPC分类号: A61K31/341 , A61K31/4164 , A61K31/4178 , A61K31/4184 , A61K31/423 , A61K31/428 , A61K31/443 , A61K31/4525 , A61K31/4709 , A61K31/496 , A61K31/506 , A61K31/52 , A61K31/5355 , A61P11/06 , A61P43/00 , C07D307/38 , C07D307/42 , C07D307/46 , C07D307/54 , C07D307/56 , C07D307/64 , C07D307/66 , C07D405/04 , C07D405/06 , C07D405/12 , C07D413/12 , C07D417/12 , C07D473/38 , C07F7/08 , A61K31/505 , A61K31/34 , C07D277/62 , C07D401/00
CPC分类号: C07D307/42 , C07D307/46 , C07D307/54 , C07D405/04 , C07D405/12 , C07D413/12 , C07D417/12 , C07F7/0814
摘要: The invention encompasses the novel compound of Formula I useful in the treatment of diseases, including asthma, by raising the level of cyclic adenosine-3',5'-monophosphate (cAMP) through the inhibition of phosphodiesterase IV (PDE IV). ##STR1## The invention also encompasses certain pharmaceutical compositions and methods for treatment of diseases by inhibition of PDE IV, resulting in an elevation of cAMP, comprising the use of compounds of Formula I.
摘要翻译: 本发明包括通过抑制磷酸二酯酶IV(PDE IV)提高环腺苷-3',5'-单磷酸(cAMP)的水平,可用于治疗包括哮喘在内的疾病的新型式I化合物。 本发明还包括通过抑制PDE IV治疗疾病的某些药物组合物和方法,导致cAMP升高,包括使用式I化合物。
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公开(公告)号:US20110003815A1
公开(公告)日:2011-01-06
申请号:US12682150
申请日:2008-10-06
申请人: Anthony Ogawa , Feroze Ujjainwalla , Bing Li , Lin Chu , Minal Patel , Helen M. Armstrong , Hyun O. Ok , Rosemary Sisco , Dwight MacDonald , John Hutchinson , Helene Perrier
发明人: Anthony Ogawa , Feroze Ujjainwalla , Bing Li , Lin Chu , Minal Patel , Helen M. Armstrong , Hyun O. Ok , Rosemary Sisco , Dwight MacDonald , John Hutchinson , Helene Perrier
IPC分类号: A61K31/5377 , C07D401/14 , C07D413/12 , C07D211/68 , C07D417/12 , C07D403/12 , A61K31/4439 , A61K31/444 , A61K31/501 , A61P9/10
CPC分类号: C07D401/12 , C07D213/30 , C07D213/55 , C07D213/56 , C07D237/20 , C07D239/26 , C07D277/24 , C07D401/14 , C07D403/04 , C07D403/12 , C07D403/14 , C07D413/10 , C07D413/12 , C07D413/14 , C07D417/10 , C07D417/12 , C07D417/14 , C07D453/02
摘要: The present invention provides compounds of Formula I which are FLAP inhibitors useful as anti-atherosclerotic, anti-asthmatic, anti-allergic, anti-inflammatory and cytoprotective agents.
摘要翻译: 本发明提供了可用作抗动脉粥样硬化,抗哮喘,抗过敏,抗炎和细胞保护作用的FLAP抑制剂的式I化合物。
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公开(公告)号:US06740666B2
公开(公告)日:2004-05-25
申请号:US10040993
申请日:2001-11-09
申请人: Dwight Macdonald , Helene Perrier , Roch Thibert , Guo-Jie Ho , Anant Vailaya , David Conlon , Elizabeth Kwong , Sophie-Dorothee Clas
发明人: Dwight Macdonald , Helene Perrier , Roch Thibert , Guo-Jie Ho , Anant Vailaya , David Conlon , Elizabeth Kwong , Sophie-Dorothee Clas
IPC分类号: A61K3147
CPC分类号: C07D401/10 , C07D215/12 , C07D215/14 , C07D413/10 , C07D417/10
摘要: Novel sulfuric acid, methanesulfonic acid, p-toluenesulfonic acid, 2-naphthalenesulfonic acid, hydrochloride acid, or benzenesulfonic acid salts of substituted 8-arylquinolines, wherein the aryl group at the 8-position contains a substituent substituted-alkenyl group, are PDE4 inhibitors.
摘要翻译: 其中8位的芳基含有取代的取代的链烯基的取代的8-芳基喹啉的新型硫酸,甲磺酸,对甲苯磺酸,2-萘磺酸,盐酸或苯磺酸盐是PDE4抑制剂 。
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5.
公开(公告)号:US20060040981A1
公开(公告)日:2006-02-23
申请号:US10536250
申请日:2003-11-19
申请人: Daniel Dube , Michel Gallant , Patrick Lacombe , Yves Girard , Dwight Macdonald , Richard Friesen , Yves Ducharme , Bernard Cote , Marc Blouin , Evelyn Martins , Daniel Guay , Pierre Hamel , Mario Girard , Richard Frenette , Sebastien Laliberte , Annette Robichaud , Anthony Mastracchio , Helene Perrier
发明人: Daniel Dube , Michel Gallant , Patrick Lacombe , Yves Girard , Dwight Macdonald , Richard Friesen , Yves Ducharme , Bernard Cote , Marc Blouin , Evelyn Martins , Daniel Guay , Pierre Hamel , Mario Girard , Richard Frenette , Sebastien Laliberte , Annette Robichaud , Anthony Mastracchio , Helene Perrier
IPC分类号: A61K31/4709 , A61K31/47
CPC分类号: A61K31/4709 , A61K31/277 , A61K31/4375 , A61K31/44 , A61K31/47
摘要: The present invention is directed to a method of enhancing cognition in a healthy subject comprising administering a safe cognition enhancing amount of a phosphodiesterase-4 inhibitor. In particular, this invention is directed to a method of enhancing memory, learning, retention, recall, awareness and judgement in health subjects comprising administering a safe and effective amount of a phosphodiesterase-4 inhibitor.
摘要翻译: 本发明涉及增强健康受试者的认知的方法,其包括施用安全认知增加量的磷酸二酯酶-4抑制剂。 特别地,本发明涉及增加健康受试者的记忆,学习,保留,召回,意识和判断的方法,包括施用安全有效量的磷酸二酯酶-4抑制剂。
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公开(公告)号:US06410563B1
公开(公告)日:2002-06-25
申请号:US09741517
申请日:2000-12-20
申请人: Denis Deschenes , Daniel Dube , Michel Gallant , Yves Girard , Patrick Lacombe , Dwight MacDonald , Anthony Mastracchio , Helene Perrier
发明人: Denis Deschenes , Daniel Dube , Michel Gallant , Yves Girard , Patrick Lacombe , Dwight MacDonald , Anthony Mastracchio , Helene Perrier
IPC分类号: A61K314709
CPC分类号: C07D401/10 , C07D215/12 , C07D215/14 , C07D401/14 , C07D405/12 , C07D409/10 , C07D413/10 , C07D413/14 , C07D417/10 , C07D417/12 , C07D417/14
摘要: Novel substituted 8-arylquinolines, wherein the aryl group at the 8-position contains a substituent substituted-alkenyl group, are PDE4 inhibitors.
摘要翻译: 新的取代的8-芳基喹啉,其中8位的芳基含有取代的取代的烯基,是PDE4抑制剂。
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7.
公开(公告)号:US5453443A
公开(公告)日:1995-09-26
申请号:US277854
申请日:1994-07-20
申请人: Helene Perrier , Petpiboon Prasit , Ian Street , Zhaoyin Wang
发明人: Helene Perrier , Petpiboon Prasit , Ian Street , Zhaoyin Wang
IPC分类号: C07C59/90 , C07C323/52 , C07C323/53 , A61K31/19
CPC分类号: C07C59/90 , C07C323/52 , C07C323/53 , C07C2101/02
摘要: Compounds having the formula I: ##STR1## are inhibitors of the PLA.sub.2 s enzymes. These compounds are useful as anti-allergic, anti-asthmatic, they are also useful in treating various inflammatory diseases such as rheumatoid arthritis, osteoarthritis, bursitis, psoriasis; immunoinflammatory disorders such as contact dermatitis, irritable bowel disease and the like.
摘要翻译: 具有式I的化合物:其为PLA2酶的抑制剂。 这些化合物可用作抗过敏,抗哮喘,它们也可用于治疗各种炎性疾病如类风湿性关节炎,骨关节炎,滑囊炎,牛皮癣; 免疫炎性疾病如接触性皮炎,肠易激综合征等。
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公开(公告)号:US06180650B2
公开(公告)日:2001-01-30
申请号:US09525600
申请日:2000-03-14
申请人: Richard Frenette , Richard Friesen , Mario Girard , Yves Girard , Cedrickx Godbout , Daaniel Guay , Pierre Hamel , Helene Perrier
发明人: Richard Frenette , Richard Friesen , Mario Girard , Yves Girard , Cedrickx Godbout , Daaniel Guay , Pierre Hamel , Helene Perrier
IPC分类号: C07D40102
CPC分类号: C07D213/64 , C07D213/76 , C07D213/79 , C07D213/89 , C07D405/14 , C07D409/14 , C07D417/14
摘要: The invention encompasses the novel compound of Formula I useful in the treatment of diseases, including asthma, by raising the level of cyclic adenosine-3′,5′-monophosphate (cAMP) through the inhibition of phosphodiesterase IV (PDE 4). The invention also encompasses pharmaceutical compositions and methods for treatment.
摘要翻译: 本发明包括通过抑制磷酸二酯酶IV(PDE 4)提高环腺苷-3',5'-单磷酸(cAMP)的水平,可用于治疗包括哮喘在内的疾病的新颖化合物。本发明 还包括用于治疗的药物组合物和方法。
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