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11.(Methylsulfonyl)phenyl-2-(5H)-furanones as COX-2 inhibitors 失效
标题翻译: (甲基磺酰基)苯基-2-(5H) - 呋喃酮作为COX-2抑制剂公开(公告)号:US6020343A
公开(公告)日:2000-02-01
申请号:US97543
申请日:1998-06-15
申请人: Michel Belley , Jacques Yves Gauthier , Erich Grimm , Yves LeBlanc , Chun-Sing Li , Michel Therien , Cameron Black , Petpiboon Prasit , Cheuk-Kun Lau , Patrick Roy
发明人: Michel Belley , Jacques Yves Gauthier , Erich Grimm , Yves LeBlanc , Chun-Sing Li , Michel Therien , Cameron Black , Petpiboon Prasit , Cheuk-Kun Lau , Patrick Roy
IPC分类号: C07C317/24 , C07D307/58 , C07D307/60 , C07D307/62 , C07D307/64 , C07D307/66 , C07D307/68 , C07D307/83 , C07D307/94 , C07D405/12 , C07D409/12 , C07D417/12 , C07D471/04 , C07D491/04 , C07D495/04 , C07D498/04 , C07D513/04 , A61K31/665
CPC分类号: C07D405/12 , C07C317/24 , C07D307/58 , C07D307/60 , C07D307/62 , C07D307/64 , C07D307/66 , C07D307/68 , C07D307/83 , C07D307/94 , C07D409/12 , C07D417/12 , C07D471/04 , C07D491/04 , C07D495/04 , C07D513/04 , C07C2101/08
摘要: The invention encompasses the novel compound of Formula I useful in the treatment of cyclooxygenase-2 mediated diseases. ##STR1## The invention also encompasses certain pharmaceutical compositions for treatment of cyclooxygenase-2 mediated diseases comprising compounds of Formula I.
摘要翻译: 本发明包括可用于治疗环氧合酶-2介导的疾病的新颖的式I化合物。 本发明还包括用于治疗包含式I化合物的环氧合酶-2介导的疾病的某些药物组合物。
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12.(Methylsulfonyl)phenyl-2-(5H)-furanones as COX-2 inhibitors 失效
标题翻译: (甲基磺酰基)苯基-2-(5H) - 呋喃酮作为COX-2抑制剂公开(公告)号:US5981576A
公开(公告)日:1999-11-09
申请号:US97537
申请日:1998-06-15
申请人: Michel Belley , Jacques Yves Gauthier , Erich Grimm , Yves LeBlanc , Chun-Sing Li , Michel Therien , Cameron Black , Petpiboon Prasit , Cheuk-Kun Lau , Patrick Roy
发明人: Michel Belley , Jacques Yves Gauthier , Erich Grimm , Yves LeBlanc , Chun-Sing Li , Michel Therien , Cameron Black , Petpiboon Prasit , Cheuk-Kun Lau , Patrick Roy
IPC分类号: C07C317/24 , C07D307/58 , C07D307/60 , C07D307/62 , C07D307/64 , C07D307/66 , C07D307/68 , C07D307/83 , C07D307/94 , C07D405/12 , C07D409/12 , C07D417/12 , C07D471/04 , C07D491/04 , C07D495/04 , C07D498/04 , C07D513/04 , C07D307/02 , A61K31/34
CPC分类号: C07C317/24 , C07D307/58 , C07D307/60 , C07D307/62 , C07D307/64 , C07D307/66 , C07D307/68 , C07D307/83 , C07D307/94 , C07D405/12 , C07D409/12 , C07D417/12 , C07D471/04 , C07D491/04 , C07D495/04 , C07D513/04 , C07C2101/08
摘要: The invention encompasses the novel compound of Formula A that is useful in the treatment of cyclooxygenase-2 mediated diseases. ##STR1## The invention also encompasses certain pharmaceutical compositions for treatment of cyclooxygenase-2 mediated diseases comprising compounds of Formula A.
摘要翻译: 本发明包括可用于治疗环氧合酶-2介导的疾病的新颖的式A化合物。 本发明还包括用于治疗包含式A化合物的环氧合酶-2介导的疾病的某些药物组合物。
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公开(公告)号:US5767291A
公开(公告)日:1998-06-16
申请号:US738144
申请日:1996-10-25
申请人: Yves Ducharme , Jacques Yves Gauthier , Petpiboon Prasit , Yves Leblanc , Zhaoyin Wang , Serge Leger , Michel Therien
发明人: Yves Ducharme , Jacques Yves Gauthier , Petpiboon Prasit , Yves Leblanc , Zhaoyin Wang , Serge Leger , Michel Therien
摘要: The invention encompasses the novel compound of Formula I useful in the treatment of cyclooxygenase-2 mediated diseases. ##STR1## The invention also encompasses certain pharmaceutical compositions for treatment of cyclooxygenase-2 mediated diseases comprising compounds of Formula I.
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14.Use of inhibitors of cyclooxygenase in the treatment of neurodegenerative diseases 失效
标题翻译: 使用环氧合酶抑制剂治疗神经变性疾病公开(公告)号:US5840746A
公开(公告)日:1998-11-24
申请号:US926291
申请日:1997-09-05
申请人: Yves Ducharme , Jacques Yves Gauthier , Petpiboon Prasit , Yves Leblanc , Zhaoyin Wang , Serge Leger , Michel Therien
发明人: Yves Ducharme , Jacques Yves Gauthier , Petpiboon Prasit , Yves Leblanc , Zhaoyin Wang , Serge Leger , Michel Therien
IPC分类号: A61K31/10 , A61K31/341 , A61K31/381 , A61K31/425 , A61K31/426 , C07C311/08 , C07C311/29 , C07C311/46 , C07C311/49 , C07C317/24 , C07C323/49 , C07D209/26 , C07D275/02 , C07D277/26 , C07D307/38 , C07D307/58 , C07D333/18 , C07D333/38 , C07D405/04 , A61K31/38 , A61K31/27 , A61K31/34
CPC分类号: C07D275/02 , A61K31/10 , A61K31/341 , A61K31/381 , A61K31/425 , A61K31/426 , C07C311/08 , C07C311/29 , C07C311/46 , C07C311/49 , C07C317/24 , C07C323/49 , C07D209/26 , C07D277/26 , C07D307/38 , C07D307/58 , C07D333/18 , C07D333/38 , C07D405/04 , C07C2101/08 , C07C2102/08
摘要: The present invention provides a method of treating a neurodegenerative disease and in particular Alzheimers disease which comprises administering to a human in need thereof a therapeutically effective amount of a non-steroid COX-II inhibitor. Although a wide range of COX-II inhibitors may be employed but it is preferred to employ compounds of the Formula I: ##STR1##
摘要翻译: 本发明提供治疗神经变性疾病,特别是阿尔茨海默病的方法,其包括向有需要的人施用治疗有效量的非类固醇COX-II抑制剂。 尽管可以使用大范围的COX-II抑制剂,但优选使用式I的化合物:
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15.Use of inhibitors of cyclooxygenase in the treatment of neurodegenerative diseases 失效
标题翻译: 使用环氧合酶抑制剂治疗神经变性疾病公开(公告)号:US06486194B2
公开(公告)日:2002-11-26
申请号:US09796211
申请日:2001-02-28
申请人: Yves Ducharme , Jacques Yves Gauthier , Petpiboon Prasit , Yves Leblanc , Zhaoyin Wang , Serge Leger , Michel Therien
发明人: Yves Ducharme , Jacques Yves Gauthier , Petpiboon Prasit , Yves Leblanc , Zhaoyin Wang , Serge Leger , Michel Therien
IPC分类号: A61K3138
CPC分类号: C07D275/02 , A61K31/10 , A61K31/341 , A61K31/381 , A61K31/425 , A61K31/426 , C07C311/29 , C07C311/46 , C07C311/49 , C07C317/24 , C07C2601/08 , C07D277/26 , C07D307/38 , C07D307/58 , C07D333/18 , C07D333/38 , C07D405/04
摘要: The present invention provides a method of treating a neurodegenerative disease and in particular Alzheimers disease which comprises administering to a human in need thereof a therapeutically effective amount of a non-steroid COX-II inhibitor. Although a wide range of COX-II inhibitors may be employed but it is preferred to employ compounds of the Formula I:
摘要翻译: 本发明提供治疗神经变性疾病,特别是阿尔茨海默病的方法,其包括向有需要的人施用治疗有效量的非类固醇COX-II抑制剂。 尽管可以使用大范围的COX-II抑制剂,但优选使用式I的化合物:
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公开(公告)号:US5710140A
公开(公告)日:1998-01-20
申请号:US699142
申请日:1996-08-16
申请人: Yves Ducharme , Jacques Yves Gauthier , Petpiboon Prasit , Yves Leblanc , Zhaoyin Wang , Serge Leger , Michel Therien
发明人: Yves Ducharme , Jacques Yves Gauthier , Petpiboon Prasit , Yves Leblanc , Zhaoyin Wang , Serge Leger , Michel Therien
IPC分类号: C07D333/06 , A61K31/00 , A61K31/10 , A61K31/12 , A61K31/122 , A61K31/18 , A61K31/19 , A61K31/255 , A61K31/34 , A61K31/341 , A61K31/35 , A61K31/351 , A61K31/365 , A61K31/38 , A61K31/381 , A61K31/395 , A61K31/40 , A61K31/4015 , A61K31/425 , A61K31/426 , A61K31/66 , A61P1/00 , A61P1/02 , A61P1/04 , A61P7/04 , A61P11/06 , A61P15/00 , A61P17/02 , A61P19/00 , A61P19/02 , A61P21/00 , A61P25/28 , A61P29/00 , A61P31/12 , A61P31/16 , A61P35/00 , A61P43/00 , C07C20060101 , C07C13/08 , C07C13/10 , C07C305/18 , C07C307/02 , C07C311/15 , C07C311/16 , C07C311/29 , C07C311/37 , C07C311/46 , C07C311/49 , C07C311/51 , C07C317/10 , C07C317/24 , C07C323/29 , C07D207/26 , C07D207/333 , C07D207/38 , C07D207/444 , C07D207/448 , C07D275/02 , C07D277/02 , C07D277/22 , C07D277/24 , C07D277/26 , C07D307/33 , C07D307/38 , C07D307/58 , C07D309/32 , C07D333/04 , C07D333/12 , C07D333/16 , C07D333/18 , C07D333/24 , C07D333/38 , C07D333/40 , C07D405/04 , C07D407/04 , C07D409/04 , C07D413/04 , C07D417/04 , C07D503/04 , C07F9/40 , C07F9/547 , C07F9/572 , C07F9/6506 , C07F9/653 , C07F9/6539 , C07F9/655 , A61K31/675 , C07F9/02
CPC分类号: C07D275/02 , C07C311/29 , C07C311/46 , C07C311/49 , C07C317/24 , C07D277/26 , C07D307/38 , C07D307/58 , C07D333/18 , C07D333/38 , C07D405/04 , C07C2101/08
摘要: The invention encompasses the novel compound of Formula I useful in the treatment of cyclooxygenase-2 mediated diseases. ##STR1## The invention also encompasses certain pharmaceutical compositions for treatment of cyclooxygenase-2 mediated diseases comprising compounds of Formula I.
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17.5-hydroxy-2,3-dihydrobenzofuran analogs as leukotriene biosynthesis inhibitors 失效
标题翻译: 5-羟基-2,3-二氢苯并呋喃类似物作为紫苏酮生物合成抑制剂公开(公告)号:US5091533A
公开(公告)日:1992-02-25
申请号:US491799
申请日:1990-03-12
申请人: Patrice C. Belanger , Claude Dufresne , Brian Fitzsimmons, deceased , Maryann Fitzsimmons, Heir , Yvan Guindon , Cheuk K. Lau , Joshua Rokach , John Schiegetz , Michel Therien , Robert N. Young
发明人: Patrice C. Belanger , Claude Dufresne , Brian Fitzsimmons, deceased , Maryann Fitzsimmons, Heir , Yvan Guindon , Cheuk K. Lau , Joshua Rokach , John Schiegetz , Michel Therien , Robert N. Young
IPC分类号: A61K31/34 , A61K31/343 , A61P9/00 , A61P11/00 , A61P17/00 , A61P29/00 , A61P37/08 , C07D307/79 , C07D307/80 , C07D307/83 , C07D405/12 , C07D417/12
CPC分类号: C07D307/79 , C07D307/80 , C07D405/12 , C07D417/12
摘要: Compounds of the formula: ##STR1## where R.sup.2 contains certain aryls or heteroaryls are effective leukotriene inhibitors.
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公开(公告)号:US08318748B2
公开(公告)日:2012-11-27
申请号:US13115462
申请日:2011-05-25
申请人: Christopher I. Bayly , Cameron Black , Serge Leger , Chun Sing Li , Dan McKay , Christophe Mellon , Jacques Yves Gauthier , Vouy-Linh Truong , Cheuk Lau , Michel Therien , Michael J. Green , Bernard L. Hirschbein , James William Janc , James T. Palmer , Chitra Baskaran
发明人: Christopher I. Bayly , Cameron Black , Serge Leger , Chun Sing Li , Dan McKay , Christophe Mellon , Jacques Yves Gauthier , Vouy-Linh Truong , Cheuk Lau , Michel Therien , Michael J. Green , Bernard L. Hirschbein , James William Janc , James T. Palmer , Chitra Baskaran
IPC分类号: A61K31/4965 , A61K31/66 , A61K31/44 , A61K31/445 , A61K31/425 , A61K31/415
CPC分类号: C07C237/20 , A61K31/165 , A61K31/18 , A61K31/4174 , A61K31/426 , A61K31/44 , A61K31/4418 , A61K31/495 , C07C255/25 , C07C255/29 , C07C255/46 , C07C255/58 , C07C259/10 , C07C311/37 , C07C317/32 , C07C2601/02 , C07C2601/14 , C07D209/08 , C07D213/38 , C07D213/57 , C07D213/64 , C07D213/70 , C07D213/89 , C07D215/12 , C07D231/12 , C07D233/64 , C07D239/26 , C07D241/12 , C07D261/08 , C07D263/32 , C07D271/06 , C07D277/28 , C07D277/30 , C07D295/135 , C07D295/155 , C07D307/52 , C07D333/20 , C07D401/04 , C07D417/04
摘要: This invention relates to a novel class of compounds which are cysteine protease inhibitors, including but not limited to, inhibitors of cathepsins K, L, S and B. These compounds are useful for treating diseases in which inhibition of bone resorption is indicated, such as osteoporosis.
摘要翻译: 本发明涉及一类新的化合物,它们是半胱氨酸蛋白酶抑制剂,包括但不限于组织蛋白酶K,L,S和B的抑制剂。这些化合物可用于治疗其中指示抑制骨吸收的疾病,例如 骨质疏松症
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19.Diphenyl-1,2,3-thiadiazol-3-oxides, compositions and methods of use 失效
标题翻译: 二苯基-1,2,3-噻二唑-3-氧化物,组合物和使用方法公开(公告)号:US06211210B1
公开(公告)日:2001-04-03
申请号:US09561565
申请日:2000-04-28
IPC分类号: C07D28506
CPC分类号: C07D285/06
摘要: The invention encompasses compounds of Formula I as well as a method of treating COX-2 mediated diseases comprising administration to a patient in need of such treatment of a non-toxic therapeutically effective amount of a compound of Formula I. The invention also encompasses certain pharmaceutical compositions for treatment of COX-2 mediated diseases comprising compounds of Formula I.
摘要翻译: 本发明包括式I化合物以及治疗COX-2介导的疾病的方法,其包括给予需要这种治疗无毒治疗有效量的式I化合物的患者。本发明还包括某些药物 用于治疗包含式I化合物的COX-2介导的疾病的组合物。
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公开(公告)号:US20080188529A1
公开(公告)日:2008-08-07
申请号:US12082104
申请日:2008-04-08
申请人: Christopher I. Bayly , Cameron Black , Serge Leger , Chun Sing Li , Dan McKay , Christophe Mellon , Jacques Yves Gauthier , Vouy-Linh Truong , Cheuk Lau , Michel Therien , Michael J. Green , Bernard L. Hirschbein , James William Janc , James T. Palmer , Chitra Baskaran
发明人: Christopher I. Bayly , Cameron Black , Serge Leger , Chun Sing Li , Dan McKay , Christophe Mellon , Jacques Yves Gauthier , Vouy-Linh Truong , Cheuk Lau , Michel Therien , Michael J. Green , Bernard L. Hirschbein , James William Janc , James T. Palmer , Chitra Baskaran
IPC分类号: A61K31/4418 , C07C233/40 , A61K31/165 , C07D213/57
CPC分类号: C07C237/20 , A61K31/165 , A61K31/18 , A61K31/4174 , A61K31/426 , A61K31/44 , A61K31/4418 , A61K31/495 , C07C255/25 , C07C255/29 , C07C255/46 , C07C255/58 , C07C259/10 , C07C311/37 , C07C317/32 , C07C2601/02 , C07C2601/14 , C07D209/08 , C07D213/38 , C07D213/57 , C07D213/64 , C07D213/70 , C07D213/89 , C07D215/12 , C07D231/12 , C07D233/64 , C07D239/26 , C07D241/12 , C07D261/08 , C07D263/32 , C07D271/06 , C07D277/28 , C07D277/30 , C07D295/135 , C07D295/155 , C07D307/52 , C07D333/20 , C07D401/04 , C07D417/04
摘要: This invention relates to a novel class of compounds which are cysteine protease inhibitors, including but not limited to, inhibitors of cathepsins K, L, S and B. These compounds are useful for treating diseases in which inhibition of bone resorption is indicated, such as osteoporosis.
摘要翻译: 本发明涉及一类新的化合物,它们是半胱氨酸蛋白酶抑制剂,包括但不限于组织蛋白酶K,L,S和B的抑制剂。这些化合物可用于治疗其中指示抑制骨吸收的疾病,例如 骨质疏松症
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