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1.NOVEL COMPOUNDS THAT ARE USEFUL FOR IMPROVING PHARMACOKINETICS 审中-公开
Title translation: 新型化合物可用于改善药代动力学公开(公告)号:WO2007103670A2
公开(公告)日:2007-09-13
申请号:PCT/US2007/062906
申请日:2007-02-27
Applicant: ABBOTT LABORATORIES , KEMPF, Dale J. , FLENTGE, Charles A. , RANDOLPH, John T. , HUANG, Peggy , KLEIN, Larry L.
Inventor: KEMPF, Dale J. , FLENTGE, Charles A. , RANDOLPH, John T. , HUANG, Peggy , KLEIN, Larry L.
IPC: A61K31/427 , A61K31/426 , C07D417/02 , C07D277/38
CPC classification number: C07D277/30 , A61K31/426 , A61K31/427 , A61K45/06 , C07C53/18 , C07D213/30 , C07D231/12 , C07D233/64 , C07D263/32 , C07D277/24 , C07D277/38 , C07D277/587 , C07D333/16 , C07D417/04
Abstract: Novel compounds of formula I, or a pharmaceutically acceptable salt thereof inhibit cytochrome P450 monooxygenase.
Abstract translation: 式I的新化合物或其药学上可接受的盐抑制细胞色素P450单加氧酶。 p>
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公开(公告)号:WO2010144646A3
公开(公告)日:2010-12-16
申请号:PCT/US2010/038077
申请日:2010-06-10
Applicant: ABBOTT LABORATORIES , DEGOEY, David A. , KATI, Warren M. , HUTCHINS, Charles W. , DONNER, Pamela L. , KRUEGER, Allan C. , RANDOLPH, John T. , MOTTER, Christopher E. , NELSON, Lissa T. , PATEL, Sachin V. , MATULENKO, Mark A. , KEDDY, Ryan G. , JINKERSON, Tammie K. , SOLTWEDEL, Todd N. , HUTCHINSON, Douglas K. , FLENTGE, Charles A. , WAGNER, Rolf , MARING, Clarence J. , TUFANO, Michael D. , BETEBENNER, David A. , ROCKWAY, Todd W. , LIU, Dachun , PRATT, John K. , LAVIN, Michael J. , SARRIS, Kathy , WOLLER, Kevin R. , WAGAW, Seble H. , CALIFANO, Jean C. , LI, Wenke , CASPI, Daniel, D. , BELLIZZI, Mary, E.
Inventor: DEGOEY, David A. , KATI, Warren M. , HUTCHINS, Charles W. , DONNER, Pamela L. , KRUEGER, Allan C. , RANDOLPH, John T. , MOTTER, Christopher E. , NELSON, Lissa T. , PATEL, Sachin V. , MATULENKO, Mark A. , KEDDY, Ryan G. , JINKERSON, Tammie K. , SOLTWEDEL, Todd N. , HUTCHINSON, Douglas K. , FLENTGE, Charles A. , WAGNER, Rolf , MARING, Clarence J. , TUFANO, Michael D. , BETEBENNER, David A. , ROCKWAY, Todd W. , LIU, Dachun , PRATT, John K. , LAVIN, Michael J. , SARRIS, Kathy , WOLLER, Kevin R. , WAGAW, Seble H. , CALIFANO, Jean C. , LI, Wenke , CASPI, Daniel, D. , BELLIZZI, Mary, E.
IPC: C07D403/14 , C07D401/14 , C07D417/14 , A61K31/4025 , A61K31/4178 , A61K31/4184 , A61K31/4196 , A61K31/4439 , A61P31/14
Abstract: Compounds effective in inhibiting replication of Hepatitis C virus ("HCV") are described. This invention also relates to processes of making such compounds, compositions comprising such compounds, and methods of using such compounds to treat HCV infection.
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3.N-PHENYL-DIOXO-HYDROPYRIMIDINES USEFUL AS HEPATITIS C VIRUS (HCV) INHIBITORS 审中-公开
Title translation: 用作丙型肝炎病毒(HCV)抑制剂的N-苯基二氧化二氢亚胺嘧啶公开(公告)号:WO2009039135A1
公开(公告)日:2009-03-26
申请号:PCT/US2008/076594
申请日:2008-09-17
Applicant: ABBOTT LABORATORIES , DONNER, Pamela L. , RANDOLPH, John T. , KRUEGER, Allan C. , BETEBENNER, David A. , HUTCHINSON, Douglas K. , LIU, Dachun , LIU, Yaya , LONGENECKER, Kenton L. , MARING, Clarence J. , PRATT, John K. , ROCKWAY, Todd W. , STEWART, Kent D. , WAGNER, Rolf , BARNES, David M. , CHEN, Shuang , FRANCZYK II, Thaddeus S. , GAO, Yi , HAIGHT, Anthony R. , HENGEVELD, John E. , HENRY, Rodger F. , KOTECKI, Brian J. , LOU, Xiaochun , ZHANG, Geoff G. Z.
Inventor: DONNER, Pamela L. , RANDOLPH, John T. , KRUEGER, Allan C. , BETEBENNER, David A. , HUTCHINSON, Douglas K. , LIU, Dachun , LIU, Yaya , LONGENECKER, Kenton L. , MARING, Clarence J. , PRATT, John K. , ROCKWAY, Todd W. , STEWART, Kent D. , WAGNER, Rolf , BARNES, David M. , CHEN, Shuang , FRANCZYK II, Thaddeus S. , GAO, Yi , HAIGHT, Anthony R. , HENGEVELD, John E. , HENRY, Rodger F. , KOTECKI, Brian J. , LOU, Xiaochun , ZHANG, Geoff G. Z.
IPC: C07D239/22 , C07D239/54 , C07D401/10 , C07D403/10 , C07D405/10 , C07D409/10 , C07D413/10 , C07D239/553 , A61K31/513 , A61K31/506 , A61P31/14
CPC classification number: C07D239/22 , A61K31/513 , C07D239/54 , C07D239/553 , C07D401/10 , C07D403/10 , C07D405/10 , C07D409/10 , C07D413/10
Abstract: This invention relates to: (a) compounds and salts thereof that, inter alia, inhibit HCV; (b) intermediates useful for the preparation of such compounds and salts; (c) compositions comprising such compounds and salts; (d) methods for preparing such intermediates, compounds, salts, and compositions; (e) methods of use of such compounds, salts, and compositions; and (f) kits comprising such compounds, salts, and compositions. The compounds are usefull in the treatment of hepatitis C and are of the following general structure: Formula (I)
Abstract translation: 本发明涉及:(a)特别是抑制HCV的化合物及其盐; (b)可用于制备这些化合物和盐的中间体; (c)包含这些化合物和盐的组合物; (d)制备这种中间体,化合物,盐和组合物的方法; (e)使用这些化合物,盐和组合物的方法; 和(f)包含这些化合物,盐和组合物的试剂盒。 该化合物在丙型肝炎的治疗中是有用的,具有以下通用结构:式(I)
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公开(公告)号:WO2012051361A1
公开(公告)日:2012-04-19
申请号:PCT/US2011/056045
申请日:2011-10-12
Applicant: ABBOTT LABORATORIES , DEGOEY, David A. , KATI, Warren M. , HUTCHINS, Charles W. , DONNER, Pamela L. , KRUEGER, Allan C. , RANDOLPH, John T. , MOTTER, Christopher E. , NELSON, Lissa T. , PATEL, Sachel V. , MATULENKO, Mark A. , KEDDY, Ryan G. , JINKERSON, Tammie K. , GAO, Yi , LIU, Dachun , PRATT, John K. , ROCKWAY, Todd W. , MARING, Clarence J. , HUTCHINSON, Douglas K. , FLENTGE, Charles A. , WAGNER, Rolf , TUFANO, Michael D. , BETEBENNER, David A. , SARRIS, Kathy , WOLLER, Kevin R. , WAGAW, Sebel H. , CALIFANO, Jean C. , LI, Wenke , CASPI, Daniel D. , BELLIZZI, Mary E. , CARROLL, William A.
Inventor: DEGOEY, David A. , KATI, Warren M. , HUTCHINS, Charles W. , DONNER, Pamela L. , KRUEGER, Allan C. , RANDOLPH, John T. , MOTTER, Christopher E. , NELSON, Lissa T. , PATEL, Sachel V. , MATULENKO, Mark A. , KEDDY, Ryan G. , JINKERSON, Tammie K. , GAO, Yi , LIU, Dachun , PRATT, John K. , ROCKWAY, Todd W. , MARING, Clarence J. , HUTCHINSON, Douglas K. , FLENTGE, Charles A. , WAGNER, Rolf , TUFANO, Michael D. , BETEBENNER, David A. , SARRIS, Kathy , WOLLER, Kevin R. , WAGAW, Sebel H. , CALIFANO, Jean C. , LI, Wenke , CASPI, Daniel D. , BELLIZZI, Mary E. , CARROLL, William A.
IPC: C07D403/14
CPC classification number: A61K31/454 , A61K31/4178 , A61K31/4184 , A61K31/422 , A61K31/435 , A61K31/4355 , A61K31/438 , A61K31/4418 , A61K31/4439 , A61K31/4545 , A61K31/496 , A61K31/506 , A61K31/5377 , A61K31/695 , A61K45/06 , C07D401/14 , C07D403/14 , C07D405/14 , C07D413/14 , C07D417/14 , C07D453/00 , C07D491/113 , C07F7/02 , Y02P20/582
Abstract: Compounds effective in inhibiting replication of Hepatitis C virus (HCV) are described. This invention also relates to processes of making such compounds, compositions comprising such compounds, and methods of using such compounds to treat HCV infection.
Abstract translation: 描述了有效抑制丙型肝炎病毒(HCV)复制的化合物。 本发明还涉及制备这种化合物的方法,包含这些化合物的组合物,以及使用这些化合物治疗HCV感染的方法。
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5.
公开(公告)号:WO2009039127A1
公开(公告)日:2009-03-26
申请号:PCT/US2008/076576
申请日:2008-09-17
Applicant: ABBOTT LABORATORIES , WAGNER, Rolf , TUFANO, Michael D. , STEWART, Kent D. , ROCKWAY, Todd W. , RANDOLPH, John T. , PRATT, John K. , MOTTER, Christopher E. , MARING, Clarence J. , LONGENECKER, Kenton L. , LIU, Yaya , LIU, Dachun , KRUEGER, Allan C. , KATI, Warren M. , HUTCHINSON, Douglas K. , HUANG, Peggy P. , FLENTGE, Charles A. , DONNER, Pamela L. , DEGOEY, David A. , BETEBENNER, David A. , BARNES, David M. , CHEN, Shuang , FRANCZYK II, Thaddeus S. , GAO, Yi , HAIGHT, Anthony R. , HENGEVELD, John E. , HENRY, Rodger F. , KOTECKI, Brian J. , LOU, Xiaochun , SARRIS, Kathy , ZHANG, Geoff G. Z.
Inventor: WAGNER, Rolf , TUFANO, Michael D. , STEWART, Kent D. , ROCKWAY, Todd W. , RANDOLPH, John T. , PRATT, John K. , MOTTER, Christopher E. , MARING, Clarence J. , LONGENECKER, Kenton L. , LIU, Yaya , LIU, Dachun , KRUEGER, Allan C. , KATI, Warren M. , HUTCHINSON, Douglas K. , HUANG, Peggy P. , FLENTGE, Charles A. , DONNER, Pamela L. , DEGOEY, David A. , BETEBENNER, David A. , BARNES, David M. , CHEN, Shuang , FRANCZYK II, Thaddeus S. , GAO, Yi , HAIGHT, Anthony R. , HENGEVELD, John E. , HENRY, Rodger F. , KOTECKI, Brian J. , LOU, Xiaochun , SARRIS, Kathy , ZHANG, Geoff G. Z.
IPC: C07D239/22 , C07D239/54 , C07D401/10 , C07D403/10 , C07D409/10 , C07D413/10 , C07D417/10 , A61P31/12 , A61K31/513
CPC classification number: A61K31/513 , A61K31/5377 , C07D239/22 , C07D239/54 , C07D401/10 , C07D403/10 , C07D405/10 , C07D409/10 , C07D413/10 , C07D417/10 , C07D417/14
Abstract: Present application relates to the compounds of formula I useful to treat hepatitis C (HCV) infections. In the structure of the disclosed compounds is the uracil or thymine derivative linked via a phenylene into either fused 2-ring cyclic system (R6) or alternatively via additional two-atom linker (L) to a 5-6 membered monocycle (R6). Application further discloses polymorphs and pseudopolymorphs of two specific compounds: N-(6(3-t-butyl-5-(2>4-dioxo-3,4-dihydropyrimidin-1 (2H)- y!)2-methoxy-phenyl)naphthalen-2-yl)methanesulfonamide and (E)-N-(4(3-t- butyl-5-(2,4-dioxo-3)4-dihydropyrimidin-1 (2H)-yl)2-methoxy-styryl- phenyl)methanesulfonamide.
Abstract translation: 本申请涉及可用于治疗丙型肝炎(HCV)感染的式I化合物。 所公开的化合物的结构是通过亚苯基连接成稠合的2-环环系(R6)或者另外通过另外的两个原子连接基(L)与5-6元单环(R6)连接的尿嘧啶或胸腺嘧啶衍生物。 应用进一步公开了两种特定化合物的多晶型物和假多晶型物:N-(6(3-叔丁基-5-(2,4-二氧代-3,4-二氢嘧啶-1(2H) - 基)-2-甲氧基 - 苯基 )萘-2-基)甲磺酰胺和(E)-N-(4(3-叔丁基-5-(2,4-二氧代-3)4-二氢嘧啶-1(2H) - 基)2-甲氧基 - 苯乙烯基 - 苯基)甲磺酰胺。
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6.
公开(公告)号:EP1993820A2
公开(公告)日:2008-11-26
申请号:EP07757576.9
申请日:2007-02-27
Applicant: ABBOTT LABORATORIES
Inventor: KEMPF, Dale J. , FLENTGE, Charles A. , RANDOLPH, John T. , HUANG, Peggy , KLEIN, Larry L.
CPC classification number: C07D277/30 , A61K31/426 , A61K31/427 , A61K45/06 , C07C53/18 , C07D213/30 , C07D231/12 , C07D233/64 , C07D263/32 , C07D277/24 , C07D277/38 , C07D277/587 , C07D333/16 , C07D417/04
Abstract: Novel compounds of formula I, or a pharmaceutically acceptable salt thereof inhibit cytochrome P450 monooxygenase.
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7.N-PHENYL-DIOXO-HYDROPYRIMIDINES USEFUL AS HEPATITIS C VIRUS (HCV) INHIBITORS 有权
Title translation: 丙型肝炎病毒抑制剂(HCV)合适的N- PHENYLDIOXOHYDROPYRIMIDINE公开(公告)号:EP2203430B1
公开(公告)日:2011-06-15
申请号:EP08831558.5
申请日:2008-09-17
Applicant: Abbott Laboratories
Inventor: DONNER, Pamela L. , RANDOLPH, John T. , KRUEGER, Allan C. , BETEBENNER, David A. , HUTCHINSON, Douglas K. , LIU, Dachun , LIU, Yaya , LONGENECKER, Kenton L. , MARING, Clarence J. , PRATT, John K. , ROCKWAY, Todd W. , STEWART, Kent D. , WAGNER, Rolf , BARNES, David M. , CHEN, Shuang , FRANCZYK II, Thaddeus S. , GAO, Yi , HAIGHT, Anthony R. , HENGEVELD, John E. , HENRY, Rodger F. , KOTECKI, Brian J. , LOU, Xiaochun , ZHANG, Geoff G. Z.
IPC: C07D239/22 , C07D239/54 , C07D401/10 , C07D403/10 , C07D405/10 , C07D409/10 , C07D413/10 , C07D239/553 , A61K31/513 , A61K31/506 , A61P31/14
CPC classification number: C07D239/22 , A61K31/513 , C07D239/54 , C07D239/553 , C07D401/10 , C07D403/10 , C07D405/10 , C07D409/10 , C07D413/10
Abstract: This invention relates to: (a) compounds and salts thereof that, inter alia, inhibit HCV; (b) intermediates useful for the preparation of such compounds and salts; (c) compositions comprising such compounds and salts; (d) methods for preparing such intermediates, compounds, salts, and compositions; (e) methods of use of such compounds, salts, and compositions; and (f) kits comprising such compounds, salts, and compositions. The compounds are usefull in the treatment of hepatitis C and are of the following general structure: Formula (I)
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8.
公开(公告)号:EP2222646A1
公开(公告)日:2010-09-01
申请号:EP08831873.8
申请日:2008-09-17
Applicant: Abbott Laboratories
Inventor: WAGNER, Rolf , TUFANO, Michael D. , STEWART, Kent D. , ROCKWAY, Todd W. , RANDOLPH, John T. , PRATT, John K. , MOTTER, Christopher E. , MARING, Clarence J. , LONGENECKER, Kenton L. , LIU, Yaya , LIU, Dachun , KRUEGER, Allan C. , KATI, Warren M. , HUTCHINSON, Douglas K. , HUANG, Peggy P. , FLENTGE, Charles A. , DONNER,Pamela L. , DEGOEY, David A. , BETEBENNER, David A. , BARNES, David M. , CHEN, Shuang , FRANCZYK II, Thaddeus S. , GAO, Yi , HAIGHT, Anthony R. , HENGEVELD, John E. , HENRY, Rodger F. , KOTECKI, Brian J. , LOU, Xiaochun , SARRIS, Kathy , ZHANG, Geoff G. Z.
IPC: C07D239/22 , C07D239/54 , C07D401/10 , C07D403/10 , C07D409/10 , C07D413/10 , C07D417/10 , A61P31/12 , A61K31/513
CPC classification number: A61K31/513 , A61K31/5377 , C07D239/22 , C07D239/54 , C07D401/10 , C07D403/10 , C07D405/10 , C07D409/10 , C07D413/10 , C07D417/10 , C07D417/14
Abstract: Present application relates to the compounds of formula I useful to treat hepatitis C (HCV) infections. In the structure of the disclosed compounds is the uracil or thymine derivative linked via a phenylene into either fused 2-ring cyclic system (R6) or alternatively via additional two-atom linker (L) to a 5-6 membered monocycle (R6). Application further discloses polymorphs and pseudopolymorphs of two specific compounds: N-(6(3-t-butyl-5-(2>4-dioxo-3,4-dihydropyrimidin-1 (2H)- y!)2-methoxy-phenyl)naphthalen-2-yl)methanesulfonamide and (E)-N-(4(3-t- butyl-5-(2,4-dioxo-3)4-dihydropyrimidin-1 (2H)-yl)2-methoxy-styryl- phenyl)methanesulfonamide.
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9.N-PHENYL-DIOXO-HYDROPYRIMIDINES USEFUL AS HEPATITIS C VIRUS (HCV) INHIBITORS 有权
Title translation: 丙型肝炎病毒抑制剂(HCV)合适的N- PHENYLDIOXOHYDROPYRIMIDINE公开(公告)号:EP2203430A1
公开(公告)日:2010-07-07
申请号:EP08831558.5
申请日:2008-09-17
Applicant: Abbott Laboratories
Inventor: DONNER, Pamela L. , RANDOLPH, John T. , KRUEGER, Allan C. , BETEBENNER, David A. , HUTCHINSON, Douglas K. , LIU, Dachun , LIU, Yaya , LONGENECKER, Kenton L. , MARING, Clarence J. , PRATT, John K. , ROCKWAY, Todd W. , STEWART, Kent D. , WAGNER, Rolf , BARNES, David M. , CHEN, Shuang , FRANCZYK II, Thaddeus S. , GAO, Yi , HAIGHT, Anthony R. , HENGEVELD, John E. , HENRY, Rodger F. , KOTECKI, Brian J. , LOU, Xiaochun , ZHANG, Geoff G. Z.
IPC: C07D239/22 , C07D239/54 , C07D401/10 , C07D403/10 , C07D405/10 , C07D409/10 , C07D413/10 , C07D239/553 , A61K31/513 , A61K31/506 , A61P31/14
CPC classification number: C07D239/22 , A61K31/513 , C07D239/54 , C07D239/553 , C07D401/10 , C07D403/10 , C07D405/10 , C07D409/10 , C07D413/10
Abstract: This invention relates to: (a) compounds and salts thereof that, inter alia, inhibit HCV; (b) intermediates useful for the preparation of such compounds and salts; (c) compositions comprising such compounds and salts; (d) methods for preparing such intermediates, compounds, salts, and compositions; (e) methods of use of such compounds, salts, and compositions; and (f) kits comprising such compounds, salts, and compositions. The compounds are usefull in the treatment of hepatitis C and are of the following general structure: Formula (I)
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公开(公告)号:EP2337781A2
公开(公告)日:2011-06-29
申请号:EP10724656.3
申请日:2010-06-10
Applicant: Abbott Laboratories
Inventor: RANDOLPH, John T. , DEGOEY, David A. , KATI, Warren M. , HUTCHINS, Charles W. , DONNER, Pamela L. , KRUEGER, Allan C. , MOTTER, Christopher E. , NELSON, Lissa T. , PATEL, Sachin V. , MATULENKO, Mark A. , KEDDY, Ryan G. , JINKERSON, Tammie K. , SOLTWEDEL, Todd N. , HUTCHINSON, Douglas K. , FLENTGE, Charles A. , WAGNER, Rolf , MARING, Clarence J. , TUFANO, Michael D. , BETEBENNER, David A. , ROCKWAY, Todd W. , LIU, Dachun , PRATT, John K. , LAVIN, Michael J. , SARRIS, Kathy , WOLLER, Kevin R. , WAGAW, Seble H. , CALIFANO, Jean C. , LI, Wenke , CASPI, Daniel.D. , BELLIZZI, Mary, E.
IPC: C07D403/14 , C07D401/14 , C07D417/14 , A61K31/4025 , A61K31/4178 , A61K31/4184 , A61K31/4196 , A61K31/4439 , A61P31/14
CPC classification number: C07F9/65583 , C07C33/26 , C07C201/06 , C07C205/19 , C07D207/08 , C07D207/09 , C07D207/16 , C07D401/14 , C07D403/14 , C07D405/14 , C07D413/14 , C07D417/14 , C07D453/00 , C07D471/04 , C07D491/113 , C07K5/06
Abstract: Compounds effective in inhibiting replication of Hepatitis C virus ("HCV") are described. This invention also relates to processes of making such compounds, compositions comprising such compounds, and methods of using such compounds to treat HCV infection.
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