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公开(公告)号:US07189712B2
公开(公告)日:2007-03-13
申请号:US10530810
申请日:2003-10-10
申请人: Matthew Lee Brown , Mui Cheung , Scott Howard Dickerson , Cassandra Gauthier , Philip Anthony Harris , Robert Neil Hunter , Gregory Pacofsky , Michael Robert Peel , Jeffrey Alan Stafford
发明人: Matthew Lee Brown , Mui Cheung , Scott Howard Dickerson , Cassandra Gauthier , Philip Anthony Harris , Robert Neil Hunter , Gregory Pacofsky , Michael Robert Peel , Jeffrey Alan Stafford
IPC分类号: A61K31/541 , A61K31/5355 , A61K31/496 , A61K31/4525 , A61K31/443 , A61K31/421 , C07D417/10 , C07D413/10
CPC分类号: C07D263/48 , C07D413/04 , C07D413/10 , C07D413/12 , C07D413/14 , C07D417/04 , C07D417/10 , C07D417/12
摘要: Oxazole derivatives, which are useful as VEGFR2, CDK2, and CDK4 inhibitors are described herein. The described invention also includes methods of making such oxazole derivatives as well as methods of using the same in the treatment of hyperproliferative diseases.
摘要翻译: 本文描述了可用作VEGFR2,CDK2和CDK4抑制剂的恶唑衍生物。 所述的发明还包括制备这种恶唑衍生物的方法以及使用它们在治疗过度增殖性疾病中的方法。
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公开(公告)号:US5665754A
公开(公告)日:1997-09-09
申请号:US123837
申请日:1993-09-20
IPC分类号: C07D403/06 , A61K31/40 , A61K31/4025 , A61K31/415 , A61P25/00 , A61P29/00 , A61P43/00 , C07D207/08 , C07D207/10 , C07D207/14 , C07D207/16 , C07D405/06 , C07D207/09
CPC分类号: C07D207/08 , C07D207/10 , C07D207/14 , C07D207/16
摘要: Novel pyrrolidine compounds which are useful for inhibiting the function of Type IV phosphodiesterase (PDE-IV) as well as methods for making the same are disclosed. Applications in treating inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS) disorders, are also disclosed.
摘要翻译: 公开了可用于抑制IV型磷酸二酯酶(PDE-IV)的功能的新型吡咯烷化合物及其制备方法。 还公开了治疗炎性疾病和涉及细胞因子水平升高的其它疾病以及中枢神经系统(CNS)病症的应用。
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公开(公告)号:US20120277258A1
公开(公告)日:2012-11-01
申请号:US13545029
申请日:2012-07-10
申请人: Amogh Boloor , Mui Cheung , Philip Anthony Harris , Kevin Hinkle , Christopher P. Laudeman , Jeffrey Alan Stafford , James Marvin Veal
发明人: Amogh Boloor , Mui Cheung , Philip Anthony Harris , Kevin Hinkle , Christopher P. Laudeman , Jeffrey Alan Stafford , James Marvin Veal
IPC分类号: A61K31/506 , A61P35/00
CPC分类号: C07D239/30 , C07D231/56 , C07D235/08 , C07D403/12 , C07D413/14
摘要: Pyrimidine derivatives, which are useful as VEGFR2 inhibitors are described herein. The described invention also includes methods of making such pyrimidine derivatives as well as methods of using the same in the treatment of hyperproliferative diseases.
摘要翻译: 本文描述了可用作VEGFR2抑制剂的嘧啶衍生物。 所述的发明还包括制备此类嘧啶衍生物的方法以及使用该嘧啶衍生物的方法来治疗过度增殖性疾病。
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公开(公告)号:US07795428B2
公开(公告)日:2010-09-14
申请号:US11835295
申请日:2007-08-07
申请人: Jun Feng , Stephen L. Gwaltney , Jeffrey Alan Stafford , Zhiyuan Zhang , Bruce Elder , Paul Isbester , Grant Palmer , Jonathan S. Salsbury , Luckner Ulysse
发明人: Jun Feng , Stephen L. Gwaltney , Jeffrey Alan Stafford , Zhiyuan Zhang , Bruce Elder , Paul Isbester , Grant Palmer , Jonathan S. Salsbury , Luckner Ulysse
IPC分类号: C07D401/04 , A61K31/506 , A61P3/10 , A61P19/02 , A61P35/00
CPC分类号: C07D403/04 , C07D239/545 , C07D401/04 , C07D401/14 , C07D403/12 , C07D409/14
摘要: Compounds are provided for use with DPP-IV of the formula: Also provided are pharmaceutical compositions, kits and articles of manufacture comprising such compounds; methods and intermediates useful for making the compounds; and methods of using said compounds.
摘要翻译: 化合物被提供用于下式的DPP-IV:还提供包含这些化合物的药物组合物,试剂盒和制品; 用于制备化合物的方法和中间体; 以及使用所述化合物的方法。
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公开(公告)号:US20050288515A1
公开(公告)日:2005-12-29
申请号:US10530810
申请日:2003-10-10
申请人: Matthew Brown , Mui Cheung , Scott, Howard Dickerson , Cassandra Gauthier , Philip, Anthony Harris , Robert, Neil Hunter , Gregory Pacofsky , Michael, Robert Peel , Jeffrey, Alan Stafford
发明人: Matthew Brown , Mui Cheung , Scott, Howard Dickerson , Cassandra Gauthier , Philip, Anthony Harris , Robert, Neil Hunter , Gregory Pacofsky , Michael, Robert Peel , Jeffrey, Alan Stafford
IPC分类号: A61K20060101 , A61K31/421 , A61K31/422 , C07D263/30 , C07D263/48 , C07D413/02 , C07D413/12 , C07D413/14 , C07D417/04 , C07D417/10 , C07D417/12
CPC分类号: C07D263/48 , C07D413/04 , C07D413/10 , C07D413/12 , C07D413/14 , C07D417/04 , C07D417/10 , C07D417/12
摘要: Oxazole derivatives, which are useful as VEGFR2, CDK2, and CDK4 inhibitors are described herein. The described invention also includes methods of making such oxazole derivatives as well as methods of using the same in the treatment of hyperproliferative diseases.
摘要翻译: 本文描述了可用作VEGFR2,CDK2和CDK4抑制剂的恶唑衍生物。 所述的发明还包括制备这种恶唑衍生物的方法以及使用它们在治疗过度增殖性疾病中的方法。
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