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公开(公告)号:WO2012083053A3
公开(公告)日:2012-08-02
申请号:PCT/US2011065224
申请日:2011-12-15
Applicant: ABBOTT LAB , KRUEGER ALLAN C , KATI WARREN M , MARING CLARENCE J , WAGNER ROLF , HUTCHINS CHARLES W
Inventor: KRUEGER ALLAN C , KATI WARREN M , MARING CLARENCE J , WAGNER ROLF , HUTCHINS CHARLES W
IPC: C07D403/14 , A61K31/4178 , A61P31/00 , C07D403/10 , C07D409/14
CPC classification number: C07D403/14 , C07D409/14
Abstract: The present invention relates to anti-HCV compounds, compositions comprising the same and methods of using the same to treat HCV infection.
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公开(公告)号:WO2010075376A2
公开(公告)日:2010-07-01
申请号:PCT/US2009069177
申请日:2009-12-22
Applicant: ABBOTT LAB , DEGOEY DAVID A , DONNER PAMELA L , KATI WARREN M , HUTCHINS CHARLES W , MATULENKO MARK A , JINKERSON TAMMIE K , KEDDY RYAN G
Inventor: DEGOEY DAVID A , DONNER PAMELA L , KATI WARREN M , HUTCHINS CHARLES W , MATULENKO MARK A , JINKERSON TAMMIE K , KEDDY RYAN G
IPC: C07D471/04 , A61K31/519 , A61P31/14
CPC classification number: C07D471/04
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.PYRROLIDINE-3-CARBOXYLIC ACID DERIVATIVES AND THEIR USE AS ENDOTHELIN ANTAGONISTS 审中-公开
Title translation: 吡咯烷-3-羧酸衍生物及其作为内皮素拮抗剂的用途公开(公告)号:WO9906397A3
公开(公告)日:1999-12-09
申请号:PCT/US9815479
申请日:1998-07-27
Applicant: ABBOTT LAB
Inventor: WINN MARTIN , BOYD STEVEN A , HUTCHINS CHARLES W , JAE HWAN-SOO , TASKER ANDREW S , GELDERN THOMAS W VON , KESTER JEFFREY A , SORENSEN BRYAN K , SZCZEPANKIEWICZ BRUCE G , HENRY KENNETH J , LIU GANG , WITTENBERGER STEVEN J , KING STEVEN A
IPC: C07D491/048 , A61K31/40 , A61K31/41 , A61K31/423 , A61K31/435 , A61K31/4355 , A61K31/495 , A61K31/506 , A61K31/535 , A61K31/55 , A61P1/00 , A61P1/04 , A61P7/02 , A61P9/08 , A61P9/10 , A61P9/12 , A61P9/14 , A61P13/08 , A61P13/12 , A61P21/00 , A61P21/04 , A61P25/06 , A61P35/00 , A61P43/00 , C07D207/16 , C07D207/26 , C07D207/27 , C07D403/04 , C07D405/00 , C07D405/04 , C07D405/14 , C07D413/14 , C07D417/14 , C07D491/056
CPC classification number: C07D207/27 , C07D207/16 , C07D403/04 , C07D405/04 , C07D405/14 , C07D413/14 , C07D417/14
Abstract: A compound of formula (I), or a pharmaceutically acceptable salt thereof, is disclosed, as well as processes for and intermediates in the preparation thereof, and a method of antagonizing endothelin.
Abstract translation: 公开了式(I)化合物或其药学上可接受的盐,以及其制备方法和中间体,以及拮抗内皮素的方法。
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4.
公开(公告)号:WO2012088302A3
公开(公告)日:2012-10-11
申请号:PCT/US2011066557
申请日:2011-12-21
Applicant: ABBOTT LAB , GHAYUR TARIQ , GU JIJIE , LIU JUNJIAN , HUTCHINS CHARLES W
Inventor: GHAYUR TARIQ , GU JIJIE , LIU JUNJIAN , HUTCHINS CHARLES W
IPC: A61K39/395 , C12P21/08
CPC classification number: C07K16/2863 , C07K16/00 , C07K16/2803 , C07K16/2809 , C07K16/2818 , C07K16/468 , C07K2317/31 , C07K2317/52 , C07K2317/55 , C07K2317/60 , C07K2317/64 , C07K2317/92 , C07K2317/94 , C07K2319/00
Abstract: The invention provides compositions, methods, and kits related to half-Ig binding proteins that include a functional antibody binding site and a CH3 domain wherein the CH3 domain includes at least one mutation to inhibit CH3-CH3 dimerization.
Abstract translation: 本发明提供了与包含功能性抗体结合位点和CH3结构域的半-Ig结合蛋白有关的组合物,方法和试剂盒,其中CH3结构域包含至少一个抑制CH3-CH3二聚化的突变。
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公开(公告)号:WO2012083061A3
公开(公告)日:2012-08-02
申请号:PCT/US2011065247
申请日:2011-12-15
Applicant: ABBOTT LAB , KRUEGER ALLAN C , KATI WARREN M , MARING CLARENCE J , WAGNER ROLF , HUTCHINS CHARLES W
Inventor: KRUEGER ALLAN C , KATI WARREN M , MARING CLARENCE J , WAGNER ROLF , HUTCHINS CHARLES W
IPC: C07D403/14 , A61K31/4178 , A61P31/14 , C07D403/10 , C07D403/12
CPC classification number: C07D403/14 , C07D401/14 , C07D413/14 , C07D417/14
Abstract: The present invention relates to anti-HCV compounds, compositions comprising the same and methods of using the same to treat HCV infection.
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公开(公告)号:WO2012083048A3
公开(公告)日:2012-08-02
申请号:PCT/US2011065215
申请日:2011-12-15
Applicant: ABBOTT LAB , KRUEGER ALLAN C , KATI WARREN M , MARING CLARENCE J , WAGNER ROLF , HUTCHINS CHARLES W
Inventor: KRUEGER ALLAN C , KATI WARREN M , MARING CLARENCE J , WAGNER ROLF , HUTCHINS CHARLES W
IPC: C07D401/14 , A61K31/4439 , A61P31/00 , C07D401/12
CPC classification number: C07K5/06052 , A61K31/4439 , C07D401/12 , C07D401/14 , C07D403/14
Abstract: The present invention relates to anti-HCV compounds, compositions comprising the same and methods of using the same to treat HCV infection.
Abstract translation: 本发明涉及抗HCV化合物,包含其的组合物以及使用该化合物治疗HCV感染的方法。
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公开(公告)号:WO0181316A3
公开(公告)日:2002-05-23
申请号:PCT/US0113678
申请日:2001-04-25
Applicant: ABBOTT LAB
Inventor: WANG WEI-BO , CURTIN MICHAEL L , FAKHOURY STEPHEN A , GWALTNEY STEPHEN L II , HASVOLD LISA A , HUTCHINS CHARLES W , LI QUI , LIN NAN-HORNG , JENNINGS NELSON LISSA TAKA , O'CONNOR STEPHEN J , SHAM HING L , SULLIVAN GERALD M , WANG GARY T , WANG XILU
IPC: C07D233/22 , A61K31/381 , A61K31/415 , A61K31/4164 , A61K31/4178 , A61K31/4245 , A61K31/426 , A61K31/4406 , A61K31/4412 , A61K31/443 , A61K31/4436 , A61K31/4439 , A61K31/444 , A61K31/454 , A61K31/4545 , A61K31/4709 , A61K31/496 , A61P17/06 , A61P27/02 , A61P27/06 , A61P29/00 , A61P35/00 , A61P35/02 , A61P37/06 , A61P43/00 , C07D213/30 , C07D213/36 , C07D213/38 , C07D213/40 , C07D213/42 , C07D213/57 , C07D213/61 , C07D213/64 , C07D213/80 , C07D213/82 , C07D213/84 , C07D213/85 , C07D231/12 , C07D233/26 , C07D233/54 , C07D249/04 , C07D249/08 , C07D277/20 , C07D277/24 , C07D277/28 , C07D277/30 , C07D333/16 , C07D333/24 , C07D401/06 , C07D401/10 , C07D401/12 , C07D401/14 , C07D405/10 , C07D405/12 , C07D409/10 , C07D413/10 , C07D413/12 , C07D417/06 , C07D417/10 , C07D417/12 , A61K31/33 , C07D213/74 , C07D409/12
CPC classification number: C07D213/30 , C07D213/36 , C07D231/12 , C07D233/64 , C07D249/04 , C07D249/08 , C07D277/24 , C07D277/28 , C07D277/30 , C07D333/16 , C07D333/24 , C07D401/06 , C07D401/10 , C07D401/12 , C07D401/14 , C07D409/10 , C07D413/12 , C07D417/06
Abstract: Compounds of formula (I) or pharmaceutically acceptable salts thereof, inhibit farnesyltransferase. Methods for making the compounds, pharmaceutical compositions containing the compounds, and methods of treatment using the compounds are disclosed.
Abstract translation: 式(I)化合物或其药学上可接受的盐抑制法呢基转移酶。 公开了制备该化合物的方法,含该化合物的药物组合物和使用该化合物的治疗方法。
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公开(公告)号:WO2012024650A3
公开(公告)日:2012-05-31
申请号:PCT/US2011048518
申请日:2011-08-19
Applicant: ABBOTT LAB , LACY SUSAN E , BARBON JEFFREY A , CHHAYA MEHA , FUNG EMMA , HUTCHINS CHARLES W , LANG DIANE M , BARLOW EVE H , LEDDY MARY , CHARI RAVI
Inventor: LACY SUSAN E , BARBON JEFFREY A , CHHAYA MEHA , FUNG EMMA , HUTCHINS CHARLES W , LANG DIANE M , BARLOW EVE H , LEDDY MARY , CHARI RAVI
IPC: C07K16/22
CPC classification number: C07K16/22 , A61K2039/505 , C07K2317/24 , C07K2317/31 , C07K2317/50 , C07K2317/51 , C07K2317/515 , C07K2317/54 , C07K2317/55 , C07K2317/565 , C07K2317/569 , C07K2317/60 , C07K2317/622 , C07K2317/624 , C07K2317/626 , C07K2317/64 , C07K2317/73 , C07K2317/76 , C07K2317/92 , C07K2317/94 , G01N33/566
Abstract: The present disclosure encompasses NGF binding proteins, specifically to antibodies that are chimeric, CDR grafted and caninized antibodies, and methods of making and uses thereof. The antibodies, or antibody portions, of the disclosure are useful for detecting NGF and for inhibiting NGF activity, e.g., in a mammal subject suffering from a disorder in which NGF activity is detrimental.
Abstract translation: 本公开内容涵盖NGF结合蛋白,特别是嵌合抗体,CDR移植和可插入抗体的抗体及其制备及其用途的方法。 本公开的抗体或抗体部分可用于检测NGF和抑制NGF活性,例如在患有NGF活性有害的病症的哺乳动物受试者中。
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公开(公告)号:WO2010144646A2
公开(公告)日:2010-12-16
申请号:PCT/US2010038077
申请日:2010-06-10
Applicant: ABBOTT LAB , 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
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
IPC: C07D403/14
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.
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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公开(公告)号:WO2010006059A8
公开(公告)日:2010-09-02
申请号:PCT/US2009049953
申请日:2009-07-08
Applicant: ABBOTT LAB , GU JIJIE , HUTCHINS CHARLES W , ZHU RONG-RONG , SHEN JIANWEI , HARRIS MARIA C , BELANGER EILEEN , MURTAZA ANWAR , TARCSA EDIT , STINE WILLIAM B , HSIEH CHUNG-MING
Inventor: GU JIJIE , HUTCHINS CHARLES W , ZHU RONG-RONG , SHEN JIANWEI , HARRIS MARIA C , BELANGER EILEEN , MURTAZA ANWAR , TARCSA EDIT , STINE WILLIAM B , HSIEH CHUNG-MING
IPC: A61K39/395
CPC classification number: C07K16/18 , A61K31/405 , A61K31/573 , A61K39/39533 , A61K2039/505 , C07K16/26 , C07K2317/21 , C07K2317/24 , C07K2317/55 , C07K2317/56 , C07K2317/565 , C07K2317/622 , C07K2317/76
Abstract: The present invention encompasses prostaglandin E2 (PGE2) binding proteins. The invention relates to antibodies that are wild-type, chimeric, CDR grafted and humanized. Preferred antibodies have high affinity for prostaglandin E2 and neutralize prostaglandin E2 activity in vitro and in vivo. An antibody of the invention can be a full-length antibody, or an antigen-binding portion thereof. Methods of making and methods of using the antibodies of the invention are also provided. The antibodies, or antigen-binding portions, of the invention are useful for detecting prostaglandin E2 and for inhibiting prostaglandin E2 activity, e.g., in a human subject suffering from a disorder in which prostaglandin E2 activity is detrimental.
Abstract translation: 本发明包括前列腺素E2(PGE2)结合蛋白。 本发明涉及野生型,嵌合,CDR移植和人源化的抗体。 优选的抗体对前列腺素E2具有高亲和力并且在体外和体内中和前列腺素E2的活性。 本发明的抗体可以是全长抗体或其抗原结合部分。 还提供了制备方法和使用本发明抗体的方法。 本发明的抗体或抗原结合部分可用于检测前列腺素E2和用于抑制前列腺素E2活性,例如,在患有前列腺素E2活性是有害的病症的人类受试者中。
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