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公开(公告)号:US20120035150A1
公开(公告)日:2012-02-09
申请号:US13184058
申请日:2011-07-15
IPC分类号: A61K31/4709 , C07D401/14 , A61K31/506 , A61P9/00 , A61P25/00 , A61P9/10 , A61P37/00 , A61P29/00 , A61P11/06 , A61P11/00 , A61P17/06 , A61P19/02 , A61P1/00 , A61P1/04 , A61P25/28 , A61P27/02 , A61P21/04 , A61P31/14 , A61P37/08 , A61P37/06 , A61P19/04 , A61P3/10 , A61P17/00 , A61P3/00 , A61P3/04 , A61P3/08 , A61P35/00 , A61P35/02 , A61P35/04 , A61P27/16 , C07D409/14
CPC分类号: A61K31/47 , C07D215/54 , C07D401/12 , C07D401/14 , C07D409/14 , C07D417/14
摘要: The invention relates to MIF inhibitors; compositions comprising an effective amount of a MIF inhibitor; and methods for treating or preventing diseases associated with MIF.
摘要翻译: 本发明涉及MIF抑制剂; 包含有效量的MIF抑制剂的组合物; 以及用于治疗或预防与MIF相关的疾病的方法。
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公开(公告)号:US09050334B2
公开(公告)日:2015-06-09
申请号:US13184058
申请日:2011-07-15
IPC分类号: C07D215/38 , A61K31/47 , C07D215/54 , C07D401/12 , C07D401/14 , C07D409/14 , C07D417/14
CPC分类号: A61K31/47 , C07D215/54 , C07D401/12 , C07D401/14 , C07D409/14 , C07D417/14
摘要: The invention relates to MIF inhibitors; compositions comprising an effective amount of a MIF inhibitor; and methods for treating or preventing diseases associated with MIF.
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公开(公告)号:US20100234435A1
公开(公告)日:2010-09-16
申请号:US12779379
申请日:2010-05-13
申请人: Samit K. Bhattacharya , Matthew F. Brown , Peter H. Dorff , Susan D. LaGreca , John W. Mickelson , Joseph A. Cornicelli , David L. Brown , Jennings Rex , John K. Walker , Rita Huff , Joseph W. Strohbach , Robert J. Maguire
发明人: Samit K. Bhattacharya , Matthew F. Brown , Peter H. Dorff , Susan D. LaGreca , John W. Mickelson , Joseph A. Cornicelli , David L. Brown , Jennings Rex , John K. Walker , Rita Huff , Joseph W. Strohbach , Robert J. Maguire
IPC分类号: A61K31/4245 , C07D271/06 , A61P19/02 , C07D405/14 , C07D401/04
CPC分类号: C07D271/06
摘要: The invention relates to compounds of formula I and to pharmaceutically acceptable salts, prodrugs, solvates or hydrates thereof. This invention also relates to a method of using such compounds in the treatment of hyperproliferative diseases and autoimmune diseases in mammals, especially humans, and to pharmaceutical compositions containing such compounds.
摘要翻译: 本发明涉及式I化合物及其药学上可接受的盐,前药,溶剂合物或水合物。 本发明还涉及使用这些化合物治疗哺乳动物,特别是人类的过度增殖性疾病和自身免疫性疾病的方法,以及含有这些化合物的药物组合物。
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公开(公告)号:US20090227641A1
公开(公告)日:2009-09-10
申请号:US12266997
申请日:2008-11-07
申请人: Samit K. Bhattacharya , Matthew F. Brown , Peter H. Dorff , Susan D. LaGreca , John W. Mickelson , Joseph A. Cornicelli , David L. Brown , Rex Jennings , John K. Walker , Rita Huff , Joseph W. Strohbach , Robert J. Maguire
发明人: Samit K. Bhattacharya , Matthew F. Brown , Peter H. Dorff , Susan D. LaGreca , John W. Mickelson , Joseph A. Cornicelli , David L. Brown , Rex Jennings , John K. Walker , Rita Huff , Joseph W. Strohbach , Robert J. Maguire
IPC分类号: A61K31/4245 , C07D271/06 , A61P19/02 , A61P35/00
CPC分类号: C07D271/06
摘要: The invention relates to compounds of formula I and to pharmaceutically acceptable salts, prodrugs, solvates or hydrates thereof. This invention also relates to a method of using such compounds in the treatment of hyperproliferative diseases and autoimmune diseases in mammals, especially humans, and to pharmaceutical compositions containing such compounds.
摘要翻译: 本发明涉及式I化合物及其药学上可接受的盐,前药,溶剂合物或水合物。 本发明还涉及使用这些化合物治疗哺乳动物,特别是人类的过度增殖性疾病和自身免疫性疾病的方法,以及含有这些化合物的药物组合物。
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公开(公告)号:US06897318B2
公开(公告)日:2005-05-24
申请号:US10254445
申请日:2002-09-25
申请人: Kimberly K. Allen , Dennis K. Anderson , John E. Baldus , Jerry D. Clark , Albert D. Edeny , Patrick H. Lau , Daniel R. Dukesherer , Lisa McDermott , Michael K. Mao , Gopi Yalamanchili , Jodi L. Moe , Partha Mudipalli , Win Naing , Shaun R. Selness , Christine Seymour , Shekhar Viswanath , John K. Walker
发明人: Kimberly K. Allen , Dennis K. Anderson , John E. Baldus , Jerry D. Clark , Albert D. Edeny , Patrick H. Lau , Daniel R. Dukesherer , Lisa McDermott , Michael K. Mao , Gopi Yalamanchili , Jodi L. Moe , Partha Mudipalli , Win Naing , Shaun R. Selness , Christine Seymour , Shekhar Viswanath , John K. Walker
IPC分类号: C07D403/14 , A61K31/506 , A61P1/04 , A61P1/16 , A61P3/10 , A61P9/00 , A61P9/04 , A61P9/10 , A61P13/12 , A61P15/00 , A61P17/00 , A61P17/02 , A61P17/06 , A61P19/02 , A61P19/10 , A61P25/00 , A61P25/04 , A61P25/14 , A61P25/28 , A61P27/02 , A61P27/06 , A61P29/00 , A61P31/04 , A61P31/16 , A61P31/18 , A61P31/22 , A61P33/06 , A61P35/00 , A61P37/06 , C07D401/14 , C07D401/04
CPC分类号: C07D401/14
摘要: This invention is directed generally to a process for making substituted pyrazoles, tautomers of the substituted pyrazoles, and salts of the substituted pyrazoles and tautomers. The substituted pyrazoles correspond in structure to Formula (I): wherein R3A, R3B, R3C, Y1, Y2, Y3, Y4, and Y5 are as defined in the specification.
摘要翻译: 本发明一般涉及制备取代的吡唑,取代的吡唑的互变异构体和取代的吡唑和互变异构体的盐的方法。 取代的吡唑在结构上对应于式(I):其中R 3A,R 3B,R 3C,Y 1, Y 2,Y 2,Y 3,Y 4和Y 5如说明书中所定义。
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公开(公告)号:US07902195B2
公开(公告)日:2011-03-08
申请号:US11737966
申请日:2007-04-20
申请人: Robert O Hughes , Andrew Simon Bell , David Graham Brown , Dafydd Owen , Michael John Palmer , Christopher Phillips , David L. Brown , Yvette M. Fobian , John N. Freskos , Steven E. Heasley , E. Jon Jacobsen , Todd Maddux , Brent Mischke , John M. Molyneaux , Joseph B. Moon , D. Joseph Rogier, Jr. , Michael B. Tollefson , John K. Walker
发明人: Robert O Hughes , Andrew Simon Bell , David Graham Brown , Dafydd Owen , Michael John Palmer , Christopher Phillips , David L. Brown , Yvette M. Fobian , John N. Freskos , Steven E. Heasley , E. Jon Jacobsen , Todd Maddux , Brent Mischke , John M. Molyneaux , Joseph B. Moon , D. Joseph Rogier, Jr. , Michael B. Tollefson , John K. Walker
IPC分类号: A61K31/4985
CPC分类号: C07D471/04
摘要: Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula I: wherein R2, R6A, R6B and R8 are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, synthetic methods, and intermediates are also disclosed.
摘要翻译: 公开了化合物的化合物和药学上可接受的盐,其中所述化合物具有式I的结构:其中R2,R6A,R6B和R8如说明书中所定义。 还公开了相应的药物组合物,治疗方法,合成方法和中间体。
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公开(公告)号:US07057049B2
公开(公告)日:2006-06-06
申请号:US10406150
申请日:2003-04-01
申请人: Kimberley C. Allen , Dennis K. Anderson , John E. Baldus , Todd Boehlow , Jerry D. Clark , Dan R. Dukesherer , Albert D. Edney , Tom Fevig , Sastry Kunda , Jon P. Lawson , Patrick H. Lau , Lisa L. McDermott , Michael K. Mao , Jodi L. Moe , Partha Mudipalli , Win Naing , Shaun R. Selness , Christine B. Seymour , Tobin C. Schilke , Shekhar Viswanath , John K. Walker , Gopichand Yalamanchili
发明人: Kimberley C. Allen , Dennis K. Anderson , John E. Baldus , Todd Boehlow , Jerry D. Clark , Dan R. Dukesherer , Albert D. Edney , Tom Fevig , Sastry Kunda , Jon P. Lawson , Patrick H. Lau , Lisa L. McDermott , Michael K. Mao , Jodi L. Moe , Partha Mudipalli , Win Naing , Shaun R. Selness , Christine B. Seymour , Tobin C. Schilke , Shekhar Viswanath , John K. Walker , Gopichand Yalamanchili
IPC分类号: C07D231/12 , C07D211/06 , C07D211/16
CPC分类号: C07D401/06 , C07D401/14
摘要: This invention is directed generally to a process for making substituted pyrazoles, tautomers of the substituted pyrazoles, and salts of the substituted pyrazoles and tautomers. The substituted pyrazoles correspond in structure to Formula (I): wherein R3A, R3B, R3C, Y1, Y2, Y3, Y4, and Y5 are as defined in the specification.
摘要翻译: 本发明一般涉及制备取代的吡唑,取代的吡唑的互变异构体和取代的吡唑和互变异构体的盐的方法。 取代的吡唑在结构上对应于式(I):其中R 3A,R 3B,R 3C,Y 1, Y 2,Y 2,Y 3,Y 4和Y 5如说明书中所定义。
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