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1.
公开(公告)号:US08461159B2
公开(公告)日:2013-06-11
申请号:US13131067
申请日:2009-11-24
申请人: J. Guy Breitenbucher , John M. Keith , Mark S. Tichenor , Alison L. Chambers , William M. Jones , Natalie A. Hawryluk , Amy K. Timmons , Jeffrey E. Merit , Mark J. Seierstad
发明人: J. Guy Breitenbucher , John M. Keith , Mark S. Tichenor , Alison L. Chambers , William M. Jones , Natalie A. Hawryluk , Amy K. Timmons , Jeffrey E. Merit , Mark J. Seierstad
IPC分类号: A61K31/495 , C07D419/00
CPC分类号: C07D498/04 , C07D231/56 , C07D295/195 , C07D403/12 , C07D413/12 , C07D413/14 , C07D471/04 , C07D471/12 , C07D487/04
摘要: Certain heteroaryl-substituted piperidinyl and piperazinyl urea compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity, such as anxiety, pain, inflammation, sleep disorders, eating disorders, insulin resistance, diabetes, osteoporosis, and movement disorders (e.g., multiple sclerosis).
摘要翻译: 描述了某些杂芳基取代的哌啶基和哌嗪基脲化合物,其可用作FAAH抑制剂。 这些化合物可用于治疗由脂肪酸酰胺水解酶(FAAH)活性介导的疾病状态,病症和病症的药物组合物和方法,例如焦虑症,疼痛,炎症,睡眠障碍,进食障碍,胰岛素抵抗,糖尿病 ,骨质疏松症和运动障碍(例如,多发性硬化症)。
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2.
公开(公告)号:US20090062294A1
公开(公告)日:2009-03-05
申请号:US12126389
申请日:2008-05-23
申请人: Richard Apodaca , J. Guy Breitenbucher , Natalie A. Hawryluk , William M. Jones , John M. Keith , Jeffrey E. Merit , Mark S. Tichenor , Amy K. Timmons
发明人: Richard Apodaca , J. Guy Breitenbucher , Natalie A. Hawryluk , William M. Jones , John M. Keith , Jeffrey E. Merit , Mark S. Tichenor , Amy K. Timmons
IPC分类号: A61K31/501 , C07D401/00 , C07D403/00 , C07D403/14 , A61P35/00 , A61P25/00 , A61P1/04 , A61P9/00 , A61P37/00 , A61P31/12 , A61P1/00 , A61K31/445 , A61K31/496
CPC分类号: C07D231/40 , C07D237/20 , C07D241/20 , C07D257/06 , C07D261/14 , C07D261/20 , C07D271/12 , C07D285/14 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D413/14 , C07D417/12 , C07D471/04
摘要: Certain heteroaryl-substituted piperidinyl and piperazinyl urea compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity, such as anxiety, pain, inflammation, sleep disorders, eating disorders, insulin resistance, diabetes, osteoporosis, and movement disorders (e.g., multiple sclerosis).
摘要翻译: 描述了某些杂芳基取代的哌啶基和哌嗪基脲化合物,其可用作FAAH抑制剂。 这些化合物可用于治疗由脂肪酸酰胺水解酶(FAAH)活性介导的疾病状态,病症和病症的药物组合物和方法,例如焦虑症,疼痛,炎症,睡眠障碍,进食障碍,胰岛素抵抗,糖尿病 ,骨质疏松症和运动障碍(例如,多发性硬化症)。
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3.
公开(公告)号:US20110237596A1
公开(公告)日:2011-09-29
申请号:US13131067
申请日:2009-11-24
申请人: J. Guy Breitenbucher , John M. Keith , Mark S. Tichenor , Alison L. Chambers , William M. Jones , Natalie A. Hawryluk , Amy K. Timmons , Jeffrey E. Merit , Mark J. Seierstad
发明人: J. Guy Breitenbucher , John M. Keith , Mark S. Tichenor , Alison L. Chambers , William M. Jones , Natalie A. Hawryluk , Amy K. Timmons , Jeffrey E. Merit , Mark J. Seierstad
IPC分类号: A61K31/5025 , C07D413/14 , A61K31/497 , A61K31/4709 , A61P25/24 , C07D471/04 , A61K31/4353 , C07D487/04 , A61P25/22 , A61P29/00 , A61P3/00 , A61P31/18 , A61K31/501 , A61P25/00 , A61P25/28 , A61P25/16 , A61P25/30 , A61P27/02 , A61P37/00 , A61P15/00 , A61P1/00 , A61P1/12 , A61P1/04 , A61P19/02 , A61P9/12 , A61P35/00 , A61P37/08 , A61P3/10
CPC分类号: C07D498/04 , C07D231/56 , C07D295/195 , C07D403/12 , C07D413/12 , C07D413/14 , C07D471/04 , C07D471/12 , C07D487/04
摘要: Certain heteroaryl-substituted piperidinyl and piperazinyl urea compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity, such as anxiety, pain, inflammation, sleep disorders, eating disorders, insulin resistance, diabetes, osteoporosis, and movement disorders (e.g., multiple sclerosis).
摘要翻译: 描述了某些杂芳基取代的哌啶基和哌嗪基脲化合物,其可用作FAAH抑制剂。 这些化合物可用于治疗由脂肪酸酰胺水解酶(FAAH)活性介导的疾病状态,病症和病症的药物组合物和方法,例如焦虑症,疼痛,炎症,睡眠障碍,进食障碍,胰岛素抵抗,糖尿病 ,骨质疏松症和运动障碍(例如,多发性硬化症)。
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公开(公告)号:US20110230490A1
公开(公告)日:2011-09-22
申请号:US13131061
申请日:2009-11-24
申请人: J. Guy Breitenbucher , John M. Keith , Mark S. Tichenor , Alison L. Chambers , William M. Jones , Natalie A. Hawryluk , Amy K Timmons , Jeffrey E. Merit , Mark J. Seierstad
发明人: J. Guy Breitenbucher , John M. Keith , Mark S. Tichenor , Alison L. Chambers , William M. Jones , Natalie A. Hawryluk , Amy K Timmons , Jeffrey E. Merit , Mark J. Seierstad
IPC分类号: A61K31/5025 , C07D405/14 , A61K31/4545 , A61P29/00 , A61P25/04 , A61P25/22 , A61P25/24 , A61P9/10 , A61P25/08 , A61P25/30 , A61P1/08 , A61P15/00 , A61P37/06 , A61P19/02 , C07D401/12 , A61K31/506 , C07D413/12 , A61K31/454 , C07D487/04 , A61K31/4709 , C07D401/14 , C07D471/04 , A61K31/437
CPC分类号: C07D498/04 , A61K31/437 , A61K31/454 , A61K31/4545 , A61K31/4709 , A61K31/5025 , A61K31/506 , A61K45/06 , C07D401/12 , C07D401/14 , C07D405/14 , C07D413/12 , C07D471/04 , C07D487/04
摘要: Certain heteroaryl-substituted piperidinyl and piperazinyl urea compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity, such as anxiety, pain, inflammation, sleep disorders, eating disorders, insulin resistance, diabetes, osteoporosis, and movement disorders (e.g., multiple sclerosis).
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公开(公告)号:US08598356B2
公开(公告)日:2013-12-03
申请号:US13131061
申请日:2009-11-24
申请人: J. Guy Breitenbucher , John M. Keith , Mark S. Tichenor , Alison L. Chambers , William M. Jones , Natalie A. Hawryluk , Amy K. Timmons , Jeffrey E. Merit , Mark J. Seierstad
发明人: J. Guy Breitenbucher , John M. Keith , Mark S. Tichenor , Alison L. Chambers , William M. Jones , Natalie A. Hawryluk , Amy K. Timmons , Jeffrey E. Merit , Mark J. Seierstad
IPC分类号: C07D211/68 , A61K31/445
CPC分类号: C07D498/04 , A61K31/437 , A61K31/454 , A61K31/4545 , A61K31/4709 , A61K31/5025 , A61K31/506 , A61K45/06 , C07D401/12 , C07D401/14 , C07D405/14 , C07D413/12 , C07D471/04 , C07D487/04
摘要: Certain heteroaryl-substituted piperidinyl and piperazinyl urea compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity, such as anxiety, pain, inflammation, sleep disorders, eating disorders, insulin resistance, diabetes, osteoporosis, and movement disorders (e.g., multiple sclerosis).
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