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1.Derivatives of 1-(oxoaminoacetyl) pentylcarbamate as cathepsin K inhibitors for the treatment of bone loss 失效
标题翻译: 1-(氧代氨基乙酰基)戊基氨基甲酸酯作为组织蛋白酶K抑制剂用于治疗骨丢失的衍生物公开(公告)号:US07402606B2
公开(公告)日:2008-07-22
申请号:US10510469
申请日:2003-04-01
申请人: David Gene Barrett , John G. Catalano , David Norman Deaton , Aaron Bayne Miller , John A. Ray , Vicente Samano
发明人: David Gene Barrett , John G. Catalano , David Norman Deaton , Aaron Bayne Miller , John A. Ray , Vicente Samano
IPC分类号: A61K31/341 , A61K31/4015 , A61K31/4025 , A61K31/404 , A61K31/4155 , A61K31/416 , A61K31/4192 , A61K31/4196 , A61K31/4245 , A61K31/42 , A61K31/433 , A61K31/4439 , A61K31/4709 , A61K31/497 , A61K31/5377
CPC分类号: C07D207/27 , C07D207/12 , C07D207/273 , C07D207/48 , C07D307/20 , C07D307/33 , C07D401/06 , C07D403/06 , C07D403/12 , C07D405/06 , C07D405/12 , C07D409/06 , C07D409/12 , C07D413/06 , C07D413/12 , C07D413/14 , C07D417/06 , C07D417/12 , C07D417/14
摘要: Heterocycle substituted ketoamide derivatives of Formula (I), wherein the substitutes A, D, A and R are defined as in claim in, which are useful as cathepsin K inhibitors are described herein. The described invention also includes methods of making such heterocycle substituted ketoamide derivatives as well as method of using the same in the manufacture of medicaments for the treatment of disorders, including osteoporosis, associated with an imbalance between bone resorption and formation which can ultimately lead to fracture.
摘要翻译: 式(I)的杂环取代的酮酰胺衍生物,其中取代基A,D,A和R如权利要求1中所定义,其可用作组织蛋白酶K抑制剂。 所描述的发明还包括制备这种杂环取代的酮酰胺衍生物的方法以及在制备用于治疗与骨吸收和形成之间不平衡的疾病(包括骨质疏松症)相关的药物的药物的方法,其可最终导致骨折 。
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公开(公告)号:US20050107616A1
公开(公告)日:2005-05-19
申请号:US10485656
申请日:2002-07-23
申请人: David Gene Barrett , David Deaton , Robert Mcfadyen , Aaron Miller , John Ray , Francis Tavares , Huiqiang Zhou
发明人: David Gene Barrett , David Deaton , Robert Mcfadyen , Aaron Miller , John Ray , Francis Tavares , Huiqiang Zhou
IPC分类号: C07D233/60 , A61K31/415 , A61K31/4155 , A61K31/4164 , A61K31/4178 , A61K31/4184 , A61K31/42 , A61K31/4245 , A61K31/427 , A61K31/428 , A61K31/4439 , A61P19/08 , A61P19/10 , A61P43/00 , C07D207/46 , C07D213/55 , C07D231/12 , C07D231/40 , C07D233/54 , C07D233/64 , C07D271/10 , C07D285/12 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/12 , C07D409/12 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14 , C07D521/00
CPC分类号: C07D233/64 , C04B35/632 , C07D231/12 , C07D231/40 , C07D233/56 , C07D249/08 , C07D271/10 , C07D285/12 , C07D401/12 , C07D401/14 , C07D403/12 , C07D409/12 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14
摘要: Biaryl ketoamide derivatives, which are useful as cathepsin K inhibitors are described herein. The described invention also includes methods of making such biaryl ketoamide derivatives as well as methods of using the same in the treatment of disorders, including osteoporosis, associated with enhanced bone turnover which can ultimately lead to fracture.
摘要翻译: 可用作组织蛋白酶K抑制剂的双芳酮酮酰胺衍生物在本文中描述。 所描述的发明还包括制备这种联芳基酮酰胺衍生物的方法以及用于治疗与骨质疏松增加相关的障碍(包括骨质疏松症)的方法,其可能最终导致骨折。
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公开(公告)号:US08207344B2
公开(公告)日:2012-06-26
申请号:US12834054
申请日:2010-07-12
申请人: David Gene Barrett , Ana Belen Bueno Melendo , Jeffry Bernard Franciskovich , Bin Liu , Kumiko Takeuchi
发明人: David Gene Barrett , Ana Belen Bueno Melendo , Jeffry Bernard Franciskovich , Bin Liu , Kumiko Takeuchi
IPC分类号: C07D401/00 , C07D211/08 , A61K31/445
CPC分类号: C07D401/12 , C07D401/14
摘要: GPR119 agonist compounds of the formula: and pharmaceutical compositions for the treatment of diabetes and obesity.
摘要翻译: GPR119激动剂化合物,以及用于治疗糖尿病和肥胖症的药物组合物。
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公开(公告)号:US20110015199A1
公开(公告)日:2011-01-20
申请号:US12834054
申请日:2010-07-12
申请人: David Gene Barrett , Ana Belen Bueno Melendo , Jeffry Bernard Franciskovich , Bin Liu , Kumiko Takeuchi
发明人: David Gene Barrett , Ana Belen Bueno Melendo , Jeffry Bernard Franciskovich , Bin Liu , Kumiko Takeuchi
IPC分类号: A61K31/4545 , C07D401/12 , C07D401/14 , A61K31/4985 , A61P3/04 , A61P3/10
CPC分类号: C07D401/12 , C07D401/14
摘要: GPR119 agonist compounds of the formula: and pharmaceutical compositions for the treatment of diabetes and obesity.
摘要翻译: GPR119激动剂化合物,以及用于治疗糖尿病和肥胖症的药物组合物。
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5.
公开(公告)号:US07576108B2
公开(公告)日:2009-08-18
申请号:US10541047
申请日:2003-12-16
申请人: Andreas Gerhard Weichert , David Gene Barrett , Stefan Heuser , Rainer Riedl , Mark Joseph Tebbe , Andrea Zaliani
发明人: Andreas Gerhard Weichert , David Gene Barrett , Stefan Heuser , Rainer Riedl , Mark Joseph Tebbe , Andrea Zaliani
IPC分类号: A61K31/433 , A61K31/426 , A61K31/421 , C07D285/135 , C07D277/46 , C07D263/48
CPC分类号: C07D285/135 , C07D261/14 , C07D277/46 , C07D277/56 , C07D417/12 , C07D417/14
摘要: According to the present invention there is provided a compounds of formula (I): and pharmaceutically acceptable salts thereof.
摘要翻译: 根据本发明,提供式(I)的化合物及其药学上可接受的盐。
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