-
公开(公告)号:US07662815B2
公开(公告)日:2010-02-16
申请号:US11985987
申请日:2007-11-19
IPC分类号: A61K31/4704 , A61K31/4725 , A61K31/5377
CPC分类号: C07C217/80 , C07C217/60 , C07C233/43 , C07C233/80 , C07C255/54 , C07D215/26
摘要: The invention provides novel β2 adrenergic receptor agonist compounds. The invention also provides pharmaceutical compositions comprising such compounds, methods of using such compounds to treat diseases associated with β2 adrenergic receptor activity, and processes and intermediates useful for preparing such compounds.
摘要翻译: 本发明提供新颖的β2肾上腺素能受体激动剂化合物。 本发明还提供包含这些化合物的药物组合物,使用这些化合物治疗与β2肾上腺素能受体活性有关的疾病的方法,以及可用于制备这些化合物的方法和中间体。
-
公开(公告)号:US07317023B2
公开(公告)日:2008-01-08
申请号:US11185295
申请日:2005-07-20
IPC分类号: A61K31/4704 , A61K31/16 , A61K31/137 , C07D21/00 , C07C217/76
CPC分类号: C07C217/80 , C07C217/60 , C07C233/43 , C07C233/80 , C07C255/54 , C07D215/26
摘要: The invention provides novel β2 adrenergic receptor agonist compounds. The invention also provides pharmaceutical compositions comprising such compounds, methods of using such compounds to treat diseases associated with β2 adrenergic receptor activity, and processes and intermediates useful for preparing such compounds.
摘要翻译: 本发明提供了新的β2肾上腺素能受体激动剂化合物。 本发明还提供包含这些化合物的药物组合物,使用这些化合物治疗与β2肾上腺素能受体活性相关的疾病的方法,以及可用于制备这些化合物的方法和中间体。
-
公开(公告)号:US20140343138A1
公开(公告)日:2014-11-20
申请号:US14180479
申请日:2014-02-14
IPC分类号: C07C233/56 , C07C271/22 , C07D317/40
CPC分类号: A61K31/197 , A61K31/16 , A61K31/164 , A61K31/165 , A61K31/166 , A61K31/167 , A61K31/24 , A61K31/27 , A61K31/365 , A61K45/06 , C07C231/02 , C07C233/56 , C07C243/26 , C07C243/28 , C07C243/30 , C07C271/22 , C07D207/263 , C07D317/40 , C07D319/06
摘要: In one aspect, the invention relates to compounds having the formula: where R1-R6, a, b, and Z are as defined in the specification, or a pharmaceutically acceptable salt thereof. These compounds have neprilysin inhibition activity. In another aspect, the invention relates to pharmaceutical compositions comprising such compounds; methods of using such compounds; and processes and intermediates for preparing such compounds.
摘要翻译: 一方面,本发明涉及具有下式的化合物:其中R 1 -R 6,a,b和Z如说明书中所定义,或其药学上可接受的盐。 这些化合物具有去血清抑制活性。 另一方面,本发明涉及包含这些化合物的药物组合物; 使用这些化合物的方法; 以及制备这些化合物的方法和中间体。
-
公开(公告)号:US20090306134A1
公开(公告)日:2009-12-10
申请号:US12286528
申请日:2008-09-30
申请人: James Aggen , John H. Griffin , Mathai Mammen , Daniel Marquess , Edmund J. Moran , David Oare
发明人: James Aggen , John H. Griffin , Mathai Mammen , Daniel Marquess , Edmund J. Moran , David Oare
IPC分类号: A61K31/4545 , A61K31/54 , A61K31/5377 , A61K31/495 , A61K31/445 , C07D413/12 , C07D403/06 , C07D401/06 , C07D211/00
CPC分类号: A61K31/40 , C07C211/32 , C07C2603/32 , C07D207/08 , C07D209/48 , C07D211/46 , C07D401/06 , C07D401/12 , C07D401/14 , C07D403/12 , C07D405/06 , C07D405/12 , C07D409/12 , C07D417/12 , C07D519/00 , G01N33/566
摘要: Disclosed are multibinding compounds which are muscarinic receptor antagonists. The multibinding compounds of this invention containing from 2 to 10 ligands covalently attached to one or more linkers. Each ligand is, independently of each other, a muscarinic receptor antagonist or an allosteric modulator provided that at least one of said ligand is a muscarinic receptor antagonist. The multibinding compounds of this invention are useful in the treatment and prevention of diseases such as chronic obstructive pulmonary disease, chronic bronchitis, irritable bowel syndrome, urinary incontinence, and the like.
摘要翻译: 公开了作为毒蕈碱受体拮抗剂的多重联结化合物。 含有2-10个配体的本发明的多相结合化合物共价连接到一个或多个接头上。 每个配体彼此独立地是毒蕈碱受体拮抗剂或变构调节剂,只要至少一种所述配体是毒蕈碱受体拮抗剂即可。 本发明的多重联结化合物可用于治疗和预防慢性阻塞性肺疾病,慢性支气管炎,肠易激综合征,尿失禁等疾病。
-
公开(公告)号:US07612037B2
公开(公告)日:2009-11-03
申请号:US11977604
申请日:2007-10-25
申请人: Paul R. Fatheree , Martin S. Linsell , Daniel D. Long , Daniel Marquess , Edmund J. Moran , Matthew B. Nodwell , S. Derek Turner , James Aggen
发明人: Paul R. Fatheree , Martin S. Linsell , Daniel D. Long , Daniel Marquess , Edmund J. Moran , Matthew B. Nodwell , S. Derek Turner , James Aggen
CPC分类号: A61K31/545 , A61K38/00 , C07D277/40 , C07D277/42 , C07D407/12 , C07D407/14 , C07D501/00 , C07D501/46 , C07K9/008
摘要: This invention provides cross-linked glycopeptide-cephalosporin compounds and pharmaceutically acceptable salts thereof which are useful as antibiotics. This invention also provides pharmaceutical compositions containing such compounds; methods for treating bacterial infections in a mammal using such compounds; and processes and intermediates useful for preparing such compounds.
摘要翻译: 本发明提供可用作抗生素的交联糖肽 - 头孢菌素化合物及其药学上可接受的盐。 本发明还提供含有这些化合物的药物组合物; 使用这些化合物治疗哺乳动物细菌感染的方法; 以及可用于制备这些化合物的方法和中间体。
-
公开(公告)号:US06949568B2
公开(公告)日:2005-09-27
申请号:US10642926
申请日:2003-08-18
申请人: Edmund J. Moran , John R. Jacobsen , James Aggen
发明人: Edmund J. Moran , John R. Jacobsen , James Aggen
IPC分类号: A61P43/00 , C07C215/60 , C07C217/84 , C07C229/38 , C07C233/43 , C07D213/75 , C07D215/22 , C07D215/227 , C07D215/26 , C07D231/22 , C07D239/38 , C07D239/42 , C07D239/46 , C07D277/46 , C07D311/80 , C07D319/08 , C07D321/10 , C07D401/12 , C07D409/12 , C07D413/12 , A61K31/47 , C07D215/16
CPC分类号: C07D213/75 , C07C215/60 , C07C217/84 , C07C229/38 , C07C233/43 , C07D215/227 , C07D215/26 , C07D231/22 , C07D239/38 , C07D239/42 , C07D239/47 , C07D277/46 , C07D311/80 , C07D319/08 , C07D321/10 , C07D401/12 , C07D409/12 , C07D413/12
摘要: The invention provides novel β2 adrenergic receptor agonist compounds. The invention also provides pharmaceutical compositions comprising such compounds, methods of using such compounds to treat diseases associated with β2 adrenergic receptor activity, and processes and intermediates useful for preparing such compounds.
-
公开(公告)号:US06919482B2
公开(公告)日:2005-07-19
申请号:US10769219
申请日:2004-01-30
申请人: Edmund J. Moran , Seok-Ki Choi
发明人: Edmund J. Moran , Seok-Ki Choi
IPC分类号: A61K31/165 , A61K31/382 , A61K31/405 , A61K31/4172 , A61K31/4184 , A61K31/4706 , C07B61/00 , C07C215/60 , C07C217/10 , C07C323/62 , C07D211/42 , C07D211/56 , C07D213/74 , C07D213/80 , C07D263/32 , C07D263/34 , C07D265/32 , C07D277/24 , C07D277/28 , C07D277/34 , C07D295/13 , C07D401/12 , C07D401/14 , C07D413/06 , C07D413/14 , C07D417/12 , C07K1/04 , G01N33/94 , C07C211/43 , A61K31/135 , C07C211/16 , C07D241/02
CPC分类号: C07D295/13 , C07B2200/11 , C07C215/08 , C07C215/16 , C07C215/60 , C07C217/10 , C07C217/16 , C07C217/20 , C07C217/34 , C07C323/62 , C07C2601/14 , C07D211/42 , C07D211/56 , C07D213/74 , C07D213/80 , C07D263/32 , C07D263/34 , C07D265/32 , C07D277/24 , C07D277/28 , C07D277/34 , C07D401/12 , C07D401/14 , C07D413/06 , C07D413/14 , C07D417/12 , C07K1/047 , C40B40/00 , G01N33/9406 , G01N2333/62 , G01N2333/70578 , G01N2333/726 , G01N2500/00
摘要: Disclosed are multibinding compounds which are β2-adrenergic receptor agonists and are useful in the treatment and prevention of respiratory diseases such as asthma, bronchitis. They are also useful in the treatment of nervous system injury and premature labor.
摘要翻译: 公开了作为β2-肾上腺素能受体激动剂的多重联结化合物,并且可用于治疗和预防呼吸系统疾病如哮喘,支气管炎。 它们也可用于治疗神经系统损伤和早产。
-
公开(公告)号:US06593497B1
公开(公告)日:2003-07-15
申请号:US09504761
申请日:2000-02-14
申请人: Seok-Ki Choi , Edmund J. Moran
发明人: Seok-Ki Choi , Edmund J. Moran
IPC分类号: C07C21100
CPC分类号: C07C217/28 , C08G65/329 , C08G65/33396 , C08G2650/06 , C08L2203/02
摘要: The present invention is directed to multibinding compounds which are &bgr;2 adrenergic receptor agonists and are therefore useful in the treatment and prevention of respiratory diseases such asthma, bronchitis, and the like. They are also useful in the treatment of nervous system injury and premature labor.
摘要翻译: 本发明涉及作为β2肾上腺素能受体激动剂的多重结合化合物,因此可用于治疗和预防呼吸系统疾病如哮喘,支气管炎等。 它们也可用于治疗神经系统损伤和早产。
-
公开(公告)号:US06576793B1
公开(公告)日:2003-06-10
申请号:US09637899
申请日:2000-08-14
申请人: Edmund J. Moran , John H. Griffin , Seok-Ki Choi
发明人: Edmund J. Moran , John H. Griffin , Seok-Ki Choi
IPC分类号: C07C23300
CPC分类号: A61K45/06 , A61K31/137 , A61K31/167 , A61K31/403 , A61K31/404 , A61K31/4164 , A61K31/4706 , C07C215/60 , C07C215/68 , C07C233/43 , C40B40/00
摘要: Disclosed are multibinding compounds which are &bgr;2 adrenergic receptor agonists and are useful in the treatment and prevention of respiratory diseases such as asthma and bronchitis. They are also useful in the treatment of nervous system injury and premature labor.
摘要翻译: 公开了作为β2肾上腺素能受体激动剂的多重联结化合物,并且可用于治疗和预防呼吸系统疾病如哮喘和支气管炎。 它们也可用于治疗神经系统损伤和早产。
-
公开(公告)号:US20160074352A1
公开(公告)日:2016-03-17
申请号:US14838842
申请日:2015-08-28
IPC分类号: A61K31/197 , A61K31/24 , C07D317/40 , A61K45/06 , C07C271/22 , A61K31/27 , C07C243/28 , C07C233/56 , A61K31/365
CPC分类号: A61K31/197 , A61K31/16 , A61K31/164 , A61K31/165 , A61K31/166 , A61K31/167 , A61K31/24 , A61K31/27 , A61K31/365 , A61K45/06 , C07C231/02 , C07C233/56 , C07C243/26 , C07C243/28 , C07C243/30 , C07C271/22 , C07D207/263 , C07D317/40 , C07D319/06
摘要: In one aspect, the invention relates to compounds having the formula: where R1-R6, a, b, and Z are as defined in the specification, or a pharmaceutically acceptable salt thereof. These compounds have neprilysin inhibition activity. In another aspect, the invention relates to pharmaceutical compositions comprising such compounds; methods of using such compounds; and processes and intermediates for preparing such compounds.
-
-
-
-
-
-
-
-
-