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21.PYRROLO[2,3-D]PYRIMIDINYL, PYRROLO[2,3-B]PYRAZINYL AND PYR-ROLO[2,3-D]PYRIDINYL ACRYLAMIDES 审中-公开
Title translation: 吡咯并[2,3-D]吡啶二酮,吡咯并[2,3-b]吡嗪并吡咯并[2,3-D]吡啶-2-基丙烯酰胺公开(公告)号:US20150158864A1
公开(公告)日:2015-06-11
申请号:US14559294
申请日:2014-12-03
Applicant: Pfizer Inc.
Inventor: Atli Thorarensen , Matthew Frank Brown , Agustin Casimiro-Garcia , Ye Che , Jotham Wadsworth Coe , Mark Edward Flanagan , Adam Matthew Gilbert , Matthew Merrill Hayward , Jonathan David Langille , Justin Ian Montgomery , Jean-Baptiste Telliez , Rayomand Jal Unwalla
IPC: C07D471/04 , C07D487/10 , C07D498/04 , C07D487/04 , C07D471/08
CPC classification number: C07D471/04 , C07D471/08 , C07D487/04 , C07D487/10 , C07D498/04
Abstract: The present invention provides pharmaceutically active pyrrolo[2,3-d]pyrimidinyl and pyrrolo[2,3-d]pyridinyl acrylamides and analogues thereof. Such compounds are useful for inhibiting Janus Kinase (JAK). This invention also is directed to compositions comprising methods for making such compounds, and methods for treating and preventing conditions mediated by JAK.
Abstract translation: 本发明提供药学活性吡咯并[2,3-d]嘧啶基和吡咯并[2,3-d]吡啶基丙烯酰胺及其类似物。 这些化合物可用于抑制Janus Kinase(JAK)。 本发明还涉及包含制备这种化合物的方法的组合物,以及用于治疗和预防由JAK介导的病症的方法。
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公开(公告)号:US09018384B2
公开(公告)日:2015-04-28
申请号:US14447788
申请日:2014-07-31
Applicant: Pfizer Inc.
Inventor: Matthew Frank Brown , Ye Che , Anthony Marfat , Michael Joesph Melnick , Justin Ian Montgomery , Usa Reilly
IPC: A61K31/44 , C07D401/00 , C07D213/64 , C07D401/04 , C07D401/08 , C07D401/10 , C07D401/12 , C07D405/04 , C07D405/10 , C07D409/04 , C07D413/10 , C07D413/12 , C07D417/04 , C07D417/10 , C07D417/12 , C07D211/86 , C07D403/04 , C07D401/14
CPC classification number: A61K31/4412 , A61K31/4439 , C07D211/86 , C07D213/64 , C07D401/04 , C07D401/08 , C07D401/10 , C07D401/12 , C07D401/14 , C07D403/04 , C07D405/04 , C07D405/10 , C07D409/04 , C07D413/10 , C07D413/12 , C07D417/04 , C07D417/10 , C07D417/12 , Y02A50/473
Abstract: The present invention is directed to a new class of hydroxamic acid derivatives, their use as LpxC inhibitors, and more specifically their use to treat bacterial infections.
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23.N-Link Hydroxamic Acid Derivatives Useful As Antibacterial Agents 有权
Title translation: 用作抗菌剂的N-链氨基恶唑酸衍生物公开(公告)号:US20140343031A1
公开(公告)日:2014-11-20
申请号:US14447788
申请日:2014-07-31
Applicant: Pfizer Inc.
Inventor: Matthew Frank Brown , Ye Che , Anthony Marfat , Michael Joesph Melnick , Justin Ian Montgomery , Usa Reilly
IPC: C07D213/64 , C07D401/12 , C07D401/14 , C07D401/04 , C07D413/10 , C07D401/10 , C07D405/04
CPC classification number: A61K31/4412 , A61K31/4439 , C07D211/86 , C07D213/64 , C07D401/04 , C07D401/08 , C07D401/10 , C07D401/12 , C07D401/14 , C07D403/04 , C07D405/04 , C07D405/10 , C07D409/04 , C07D413/10 , C07D413/12 , C07D417/04 , C07D417/10 , C07D417/12 , Y02A50/473
Abstract: The present invention is directed to a new class of hydroxamic acid derivatives, their use as LpxC inhibitors, and more specifically their use to treat bacterial infections.
Abstract translation: 本发明涉及一类新的异羟肟酸衍生物,它们用作LpxC抑制剂,更具体地说是它们用于治疗细菌感染的用途。
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