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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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公开(公告)号:US07973037B2
公开(公告)日:2011-07-05
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: A61K31/535 , A61K31/497 , A61K31/435 , A61K31/385 , C07D265/30 , C07D241/04 , C07D211/08 , C07D333/02 , C07D255/03
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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公开(公告)号:US07375134B2
公开(公告)日:2008-05-20
申请号:US10505796
申请日:2003-02-28
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
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
IPC分类号: A01N37/34
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.
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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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公开(公告)号:US20050240023A1
公开(公告)日:2005-10-27
申请号:US10505796
申请日:2003-02-28
申请人: Christopher Bayly , Cameron Black , Serge Leger , Chun Ku , Dan McKay , Christophe Mellon , Jacques Gauthier , Vouy-Linh Truong , Cheuk Lau , Michel Therien
发明人: Christopher Bayly , Cameron Black , Serge Leger , Chun Ku , Dan McKay , Christophe Mellon , Jacques Gauthier , Vouy-Linh Truong , Cheuk Lau , Michel Therien
IPC分类号: C07D295/12 , A61K31/275 , A61K31/381 , A61K31/404 , A61K31/417 , A61K31/42 , A61K31/4245 , A61K31/426 , A61K31/427 , A61K31/44 , A61K31/4406 , A61K31/4409 , A61K31/4465 , A61K31/47 , A61K31/495 , A61K31/505 , A61K31/5375 , A61K45/00 , A61P1/02 , A61P3/14 , A61P19/02 , A61P19/08 , A61P19/10 , A61P29/00 , A61P35/00 , A61P43/00 , C07C255/25 , C07C255/29 , C07C255/46 , C07C255/58 , C07C255/60 , C07C259/10 , C07C311/37 , C07C317/32 , C07C317/36 , C07D209/08 , C07D211/26 , C07D211/38 , C07D213/36 , C07D213/38 , C07D213/57 , C07D213/61 , C07D213/64 , C07D213/70 , C07D213/71 , C07D213/74 , C07D213/89 , C07D215/12 , C07D231/12 , C07D233/54 , C07D233/64 , C07D239/06 , C07D239/26 , C07D241/12 , C07D261/08 , C07D263/32 , C07D271/06 , C07D277/28 , C07D295/135 , C07D295/22 , C07D307/52 , C07D333/20 , C07D401/04 , C07D417/04
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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公开(公告)号:US07687524B2
公开(公告)日:2010-03-30
申请号:US10581692
申请日:2004-12-09
申请人: Michael Boyd , Cheuk Lau , Christophe Mellon , Bruno Roy , John Scheigetz , Vouy Linh Truong
发明人: Michael Boyd , Cheuk Lau , Christophe Mellon , Bruno Roy , John Scheigetz , Vouy Linh Truong
IPC分类号: A61K31/44 , A61K31/275 , C07D211/70 , C07C255/46
CPC分类号: C07D213/56 , A61K31/277 , A61K31/397 , A61K31/426 , A61K31/44 , A61K31/663 , A61K45/06 , C07C255/46 , C07C2601/02 , A61K2300/00
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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公开(公告)号:US07407959B2
公开(公告)日:2008-08-05
申请号:US11282536
申请日:2005-11-18
IPC分类号: A61K31/497 , A61K31/425 , C07D241/04 , C07D211/84 , C07D277/30
CPC分类号: C07C255/46 , C07C2601/02
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.
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公开(公告)号:US08518964B2
公开(公告)日:2013-08-27
申请号:US12085331
申请日:2006-11-17
申请人: Jean-Francois Truchon , Nicolas Lachance , Cheuk Lau , Yves Leblanc , Christophe Mellon , Patrick Roy , Elise Isabel , Ryan D Otte , Jonathan R Young
发明人: Jean-Francois Truchon , Nicolas Lachance , Cheuk Lau , Yves Leblanc , Christophe Mellon , Patrick Roy , Elise Isabel , Ryan D Otte , Jonathan R Young
IPC分类号: A61K31/437 , A61K31/444
CPC分类号: C07D491/10 , C07D471/04
摘要: The present invention provides inhibitors of kinases, specifically IκB kinases, JAK1, JAK2, JAK3 and TYK2. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting said kinase activity by administering the compound to a patient in need of treatment for myeloproliferative disorders, cancer or NF-κB-mediated diseases.
摘要翻译: 本发明提供激酶抑制剂,特别是IkappaB激酶,JAK1,JAK2,JAK3和TYK2。 本发明还提供了包含这种抑制化合物的组合物和通过将该化合物施用于需要治疗骨髓增生性疾病,癌症或NF-κB介导的疾病的患者来抑制所述激酶活性的方法。
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公开(公告)号:US20070099893A1
公开(公告)日:2007-05-03
申请号:US10581692
申请日:2004-12-09
申请人: Michael Boyd , Cheuk Lau , Christophe Mellon , Bruno Roy , John Scheigetz , Vouy Truong
发明人: Michael Boyd , Cheuk Lau , Christophe Mellon , Bruno Roy , John Scheigetz , Vouy Truong
IPC分类号: A61K31/44 , A61K31/426 , A61K31/397 , A61K31/277
CPC分类号: C07D213/56 , A61K31/277 , A61K31/397 , A61K31/426 , A61K31/44 , A61K31/663 , A61K45/06 , C07C255/46 , C07C2601/02 , A61K2300/00
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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公开(公告)号:US20100048551A1
公开(公告)日:2010-02-25
申请号:US12085331
申请日:2006-11-17
申请人: Jean-Francois Truchon , Nicolas Lachance , Cheuk Lau , Yves Leblanc , Christophe Mellon , Patrick Roy , Elise Isabel , Ryan D. Otte , Jonathan R. Young
发明人: Jean-Francois Truchon , Nicolas Lachance , Cheuk Lau , Yves Leblanc , Christophe Mellon , Patrick Roy , Elise Isabel , Ryan D. Otte , Jonathan R. Young
IPC分类号: A61K31/437 , A61K31/5377 , A61K31/4365 , C07D491/107 , C07D495/04 , C07D471/04 , A61P17/00 , A61K31/444 , A61P35/00 , A61P11/00 , A61P11/06 , A61P29/00 , A61P27/02 , A61P9/12 , A61P9/10 , A61P25/00
CPC分类号: C07D491/10 , C07D471/04
摘要: The present invention provides inhibitors of kinases, specifically IκB kinases, JAK1, JAK2, JAK3 and TYK2. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting said kinase activity by administering the compound to a patient in need of treatment for myeloproliferative disorders, cancer or NF-κB-mediated diseases.
摘要翻译: 本发明提供激酶抑制剂,特别是I&Kgr B激酶,JAK1,JAK2,JAK3和TYK2。 本发明还提供了包含这种抑制性化合物的组合物和通过将该化合物施用于需要治疗骨髓增生性疾病,癌症或NF-和κB介导的疾病的患者来抑制所述激酶活性的方法。
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