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公开(公告)号:US08410124B2
公开(公告)日:2013-04-02
申请号:US12288186
申请日:2008-10-17
申请人: Craig E. Masse
发明人: Craig E. Masse
IPC分类号: A61K31/505 , C07D239/02
CPC分类号: C07D239/48
摘要: This disclosure relates to novel di-aryl-pyrimidine (DAPY) compounds and pharmaceutically acceptable salts thereof. This disclosure also provides compositions comprising a compound of this disclosure and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering a non-nucleoside reverse transcriptase inhibitor (NNRTI).
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公开(公告)号:US08178557B2
公开(公告)日:2012-05-15
申请号:US12157303
申请日:2008-06-09
申请人: Michele Potashman , Tae-Seong Kim , Steven Bellon , Shon Booker , Yuan Cheng , Joseph L. Kim , Andrew Tasker , Ning Xi , Shimin Xu , Jean-Christophe Harmange , George Borg , Matthew Weiss , Brian L. Hodous , Russell Graceffa , William H. Buckner , Craig E. Masse , Deborah Choquette , Matthew W. Martin , Julie Germain , Lucian V. DiPietro , Stuart C. Chaffee , Joseph J. Nunes , John L. Buchanan , David C. McGowan , Douglas A. Whittington , Gregory J. Habgood , Vinod F. Patel , Daniel La
发明人: Michele Potashman , Tae-Seong Kim , Steven Bellon , Shon Booker , Yuan Cheng , Joseph L. Kim , Andrew Tasker , Ning Xi , Shimin Xu , Jean-Christophe Harmange , George Borg , Matthew Weiss , Brian L. Hodous , Russell Graceffa , William H. Buckner , Craig E. Masse , Deborah Choquette , Matthew W. Martin , Julie Germain , Lucian V. DiPietro , Stuart C. Chaffee , Joseph J. Nunes , John L. Buchanan , David C. McGowan , Douglas A. Whittington , Gregory J. Habgood , Vinod F. Patel , Daniel La
IPC分类号: A61K31/04
CPC分类号: C07D213/64 , C07D213/81 , C07D215/233 , C07D215/38 , C07D215/48 , C07D215/54 , C07D237/34 , C07D239/34 , C07D239/47 , C07D239/84 , C07D239/94 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12 , C07D471/04 , C07D487/04
摘要: Selected compounds are effective for prophylaxis and treatment of diseases, such as HGF mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
摘要翻译: 所选化合物对于预防和治疗诸如HGF介导的疾病等疾病是有效的。 本发明包括新颖的化合物,类似物,前药和药学上可接受的盐,用于预防和治疗疾病和其它疾病或涉及癌症等的病症的药物组合物和方法。 本发明还涉及制备这些化合物的方法以及在这些方法中有用的中间体。
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公开(公告)号:US09260432B2
公开(公告)日:2016-02-16
申请号:US13394025
申请日:2010-09-01
申请人: Roger D. Tung , Craig E. Masse
发明人: Roger D. Tung , Craig E. Masse
IPC分类号: C07D487/04 , A61K31/519 , A61P13/12 , A61P7/00 , C07D513/04 , A61P1/16
CPC分类号: C07D487/04 , C07B2200/05 , C07D513/04
摘要: This invention relates to novel compounds of the Formula A, B, or C, and pharmaceutically acceptable salts thereof. This invention also provides compositions comprising one or more compounds of this invention and a carrier.
摘要翻译: 本发明涉及式A,B或C的新化合物及其药学上可接受的盐。 本发明还提供包含一种或多种本发明化合物和载体的组合物。
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公开(公告)号:US08575221B2
公开(公告)日:2013-11-05
申请号:US13049481
申请日:2011-03-16
申请人: Craig E. Masse , Roger D. Tung
发明人: Craig E. Masse , Roger D. Tung
CPC分类号: C07B59/001 , C07B2200/05 , C07C49/255
摘要: The invention relates to compounds of Formula I or Ia as disclosed herein: or pharmaceutically acceptable salts thereof or tautomers thereof.
摘要翻译: 本发明涉及本文公开的式I或Ia化合物或其药学上可接受的盐或其互变异构体。
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公开(公告)号:US20110281828A1
公开(公告)日:2011-11-17
申请号:US13189003
申请日:2011-07-22
申请人: Craig E. Masse
发明人: Craig E. Masse
IPC分类号: A61K31/5377 , A61P7/02 , A61P9/10 , C12N9/99 , A61K31/616
CPC分类号: C07D413/14
摘要: This invention relates to novel compounds that are substituted oxazolidinones derivatives and pharmaceutically acceptable salts thereof. More specifically, this invention relates to novel oxazolidinones compounds that are derivatives of rivaroxaban. The invention also provides pyrogen-free compositions comprising one or more compounds of the invention and a carrier, and the use of the disclosed compounds and compositions in methods of treating diseases and condition that are beneficially treated by administering a selective inhibitor of factor Xa, such as rivaroxaban.
摘要翻译: 本发明涉及取代的恶唑烷酮衍生物的新化合物及其药学上可接受的盐。 更具体地,本发明涉及作为利伐沙班的衍生物的新的恶唑烷酮化合物。 本发明还提供了包含一种或多种本发明化合物和载体的无热原组合物,以及所公开的化合物和组合物在治疗通过施用选择性因子Xa抑制剂有益治疗的疾病和病症的方法中的用途, 作为利伐沙班。
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公开(公告)号:US20110237635A1
公开(公告)日:2011-09-29
申请号:US13038533
申请日:2011-03-02
申请人: Roger Tung , Craig E. Masse
发明人: Roger Tung , Craig E. Masse
IPC分类号: A61K31/4184 , C07D235/14 , A61P9/06 , A61P9/12 , A61P29/00 , A61P9/10 , A61P9/04 , A61P9/00
CPC分类号: C07D235/14 , A61K31/4184
摘要: This invention relates to novel tetrahydronaphthalene derivatives, and pharmaceutically acceptable salts thereof according to the following formulae, in one embodiment: as described herein.This invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering a selective T-type calcium channel blocker.
摘要翻译: 本发明涉及新的四氢萘衍生物及其药学上可接受的盐,在一个实施方案中:如本文所述。 本发明还提供包含本发明化合物的组合物和这些组合物在治疗通过施用选择性T型钙通道阻断剂有益治疗的疾病和病症的方法中的用途。
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公开(公告)号:US07973047B2
公开(公告)日:2011-07-05
申请号:US12779858
申请日:2010-05-13
申请人: Wenge Zhong , Stephen Hitchcock , Brian K. Albrecht , Michael D. Bartberger , James Brown , Ryan Brown , Stuart C. Chaffee , Yuan Cheng , Michael Croghan , Russell Graceffa , Scott Harried , Dean Hickman , Daniel Horne , Randall Hungate , Ted Judd , Matthew Kaller , Charles Kreiman , Daniel La , Patricia Lopez , Craig E. Masse , Thomas Nixey , Vinod F. Patel , Lewis Pennington , Matthew Weiss , Qiufen Xue , Bryant Yang , Holger Monenschein , Thomas Nguyen
发明人: Wenge Zhong , Stephen Hitchcock , Brian K. Albrecht , Michael D. Bartberger , James Brown , Ryan Brown , Stuart C. Chaffee , Yuan Cheng , Michael Croghan , Russell Graceffa , Scott Harried , Dean Hickman , Daniel Horne , Randall Hungate , Ted Judd , Matthew Kaller , Charles Kreiman , Daniel La , Patricia Lopez , Craig E. Masse , Thomas Nixey , Vinod F. Patel , Lewis Pennington , Matthew Weiss , Qiufen Xue , Bryant Yang , Holger Monenschein , Thomas Nguyen
IPC分类号: A61K31/438 , C07D471/00
CPC分类号: C07D405/12 , C07D311/68 , C07D413/12 , C07D491/052
摘要: The present invention comprises a new class of compounds useful for the modulation of Beta-secretase enzyme activity and for the treatment of Beta-secretase mediated diseases, including Alzheimer's disease (AD) and related conditions. In one embodiment, the compounds have a general Formula I wherein A, B, W, R3, R4, R5, i and j are defined herein. The invention also comprises pharmaceutical compositions including one or more compounds of Formula I, methods of use for these compounds, including treatment of AD and related diseases, by administering the compound(s) of Formula I, or compositions including them, to a subject. The invention also comprises further embodiments of Formulas II and III, intermediates and processes useful for the preparation of compounds of the invention.
摘要翻译: 本发明包括可用于调节β-分泌酶酶活性和用于治疗β-分泌酶介导的疾病(包括阿尔茨海默病(AD))和相关病症的新一类化合物。 在一个实施方案中,化合物具有通式I,其中A,B,W,R 3,R 4,R 5,i和j在本文中定义。 本发明还包括药物组合物,其包括一种或多种式I化合物,这些化合物的使用方法,包括治疗AD和相关疾病,通过给受试者施用式I化合物或包含它们的组合物。 本发明还包括式II和III的其它实施方案,可用于制备本发明化合物的中间体和方法。
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公开(公告)号:US20100305173A1
公开(公告)日:2010-12-02
申请号:US12771551
申请日:2010-04-30
申请人: Scott L. Harbeson , Roger D. Tung , Julie F. Liu , Craig E. Masse
发明人: Scott L. Harbeson , Roger D. Tung , Julie F. Liu , Craig E. Masse
IPC分类号: A61K31/428 , C07D493/04 , A61K31/34 , A61K31/427 , A61P31/18 , A61P33/06 , A61K31/36
CPC分类号: C07D493/04
摘要: This invention relates to novel hydroxyethylamino sulfonamides, their derivatives, pharmaceutically acceptable salts thereof. This invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering a compound with the ability to act as an HIV (human immunodeficiency virus) protease inhibitor.
摘要翻译: 本发明涉及新的羟乙基氨基磺酰胺,其衍生物,其药学上可接受的盐。 本发明还提供了包含本发明化合物的组合物和这些组合物在治疗通过施用具有作为HIV(人类免疫缺陷病毒)蛋白酶抑制剂的能力的化合物有益治疗的疾病和病症的方法中的用途。
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公开(公告)号:US20100249079A1
公开(公告)日:2010-09-30
申请号:US12644758
申请日:2009-12-22
IPC分类号: A61K31/4709 , C07D401/12 , A61K31/616 , A61K31/4365 , A61P9/00 , A61P9/10 , A61P29/00 , A61P11/06 , A61P3/10
CPC分类号: C07D215/20 , A61K31/10 , A61K31/4365 , A61K31/4709 , A61K31/60 , C07D401/12
摘要: This invention relates to novel compounds which are derivatives of the phosphodiesterase inhibitor, cilostazol and pharmaceutically acceptable salts thereof. This invention also provides pyrogen-free compositions comprising one or more compounds of the invention and the use of the disclosed compounds and compositions in methods of treating diseases and conditions that are treated by administration of a phosphodiesterase inhibitor, such as cilostazol. The invention also relates to the use of the disclosed compounds and compositions as reagents in analytical studies involving cilostazol.
摘要翻译: 本发明涉及作为磷酸二酯酶抑制剂西洛他唑及其药学上可接受的盐的衍生物的新化合物。 本发明还提供了包含一种或多种本发明化合物的无热原组合物,以及所公开的化合物和组合物在治疗通过施用磷酸二酯酶抑制剂如西洛他唑治疗的疾病和病症的方法中的用途。 本发明还涉及所公开的化合物和组合物在涉及西洛他唑的分析研究中作为试剂的用途。
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公开(公告)号:US20100222338A1
公开(公告)日:2010-09-02
申请号:US12779858
申请日:2010-05-13
申请人: Wenge Zhong , Stephen Hitchcock , Brian K. Albrecht , Michael D. Bartberger , James Brown , Ryan Brown , Stuart C. Chaffee , Yuan Cheng , Michael Croghan , Russell Graceffa , Scott Harried , Dean Hickman , Daniel Horne , Randall Hungate , Ted Judd , Matthew Kaller , Charles Kreiman , Daniel La , Patricia Lopez , Craig E. Masse , Thomas Nixey , Vinod F. Patel , Lewis Pennington , Matthew Weiss , Qiufen Xue , Bryant Yang , Holger Monenschein , Thomas Nguyen
发明人: Wenge Zhong , Stephen Hitchcock , Brian K. Albrecht , Michael D. Bartberger , James Brown , Ryan Brown , Stuart C. Chaffee , Yuan Cheng , Michael Croghan , Russell Graceffa , Scott Harried , Dean Hickman , Daniel Horne , Randall Hungate , Ted Judd , Matthew Kaller , Charles Kreiman , Daniel La , Patricia Lopez , Craig E. Masse , Thomas Nixey , Vinod F. Patel , Lewis Pennington , Matthew Weiss , Qiufen Xue , Bryant Yang , Holger Monenschein , Thomas Nguyen
IPC分类号: A61K31/165 , C07D307/78 , C07D409/02 , C07D311/04 , C07C255/49 , C07C237/00 , C07D491/052 , C07D215/00 , C07D405/02 , C07D413/02 , A61K31/343 , A61K31/4025 , A61K31/352 , A61K31/47 , A61K31/5377 , A61P25/28 , A61P25/00 , A61P25/16
CPC分类号: C07D405/12 , C07D311/68 , C07D413/12 , C07D491/052
摘要: The present invention comprises a new class of compounds useful for the modulation of Beta-secretase enzyme activity and for the treatment of Beta-secretase mediated diseases, including Alzheimer's disease (AD) and related conditions. In one embodiment, the compounds have a general Formula I wherein A, B, W, R3, R4, R5, i and j are defined herein. The invention also comprises pharmaceutical compositions including one or more compounds of Formula I, methods of use for these compounds, including treatment of AD and related diseases, by administering the compound(s) of Formula I, or compositions including them, to a subject. The invention also comprises further embodiments of Formulas II and III, intermediates and processes useful for the preparation of compounds of the invention.
摘要翻译: 本发明包括可用于调节β-分泌酶酶活性和用于治疗β-分泌酶介导的疾病(包括阿尔茨海默病(AD))和相关病症的新一类化合物。 在一个实施方案中,化合物具有通式I,其中A,B,W,R 3,R 4,R 5,i和j在本文中定义。 本发明还包括药物组合物,其包括一种或多种式I化合物,这些化合物的使用方法,包括治疗AD和相关疾病,通过给受试者施用式I化合物或包含它们的组合物。 本发明还包括式II和III的其它实施方案,可用于制备本发明化合物的中间体和方法。
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