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公开(公告)号:AU2013205040A1
公开(公告)日:2013-05-16
申请号:AU2013205040
申请日:2013-04-13
Applicant: ABBOTT LAB , ENANTA PHARM INC
Inventor: KU YIYIN , MCDANIEL KEITH F , CHEN HUI-JU , SHANLEY JASON P , KEMPF DALE J , GRAMPOVNIK DAVID J , SUN YING , LIU DONG , YONGHUA GAI , OR YAT SUN , WAGAW SABLE H , ENGSTROM KEN , GRIEME TIM , SHEIKH AHMAD , MEI JIANZHANG
Abstract: MACROCYCLIC HEPATITIS C SERINE PROTEASE Abstract The present invention relates to novel macrocyclic compounds and methods of use thereof. The present invention further relates to pharmaceutical compositions comprising the compounds of the present invention, or pharmaceutical acceptable salts, esters, or prodrugs thereof, in combination with a pharmaceutical carrier or excipient.
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公开(公告)号:ES2395386T3
公开(公告)日:2013-02-12
申请号:ES06849251
申请日:2006-12-20
Applicant: ABBOTT LAB
Inventor: BETEBENNER DAVID A , DEGOEY DAVID A , MARING CLARENCE J , KRUEGER ALLAN C , IWASAKI NOBUHIKO , ROCKWAY TODD W , COOPER CURT S , ANDERSON DAVID D , DONNER PAMELA L , GREEN BRIAN E , KEMPF DALE J , LIU DACHUN , MCDANIEL KEITH F , MADIGAN DAROLD L , MOTTER CHRISTOPHER E , PRATT JOHN K , SHANLEY JASON P , TUFANO MICHAEL D , WAGNER ROLF , ZHANG RONG , MOLLA AKHTERUZZAMAN , MO HONGMEI , PILOT-MATIAS TAMI J , MASSE SHERIE , CARRICK ROBERT J , HE WEPING , LU LIANGJUN , GRAMPOVNIK DAVID J
IPC: C07D495/04 , C07D471/04 , C07D513/04
Abstract: Un compuesto, un tautómero del compuesto, o una sal aceptable desde el punto de vista farmacéutico delcompuesto o tautómero, en donde el compuesto se selecciona del grupo que consiste en:un compuesto que tiene la Fórmula II:en donde:R6 se selecciona del grupo que consiste en hidrógeno y ciano;R8 se selecciona del grupo que consiste en hidrógeno y arilalquilo;R25 se selecciona del grupo que consiste en hidrógeno y alquilo;R37 se selecciona del grupo que consiste en hidrógeno, alquilo, hidroxialquilo, y cicloalquilo;R42 se selecciona del grupo que consiste en arilsulfanilo, heteroarilsulfanilo, y ariloxi; en donde R42 estásustituido en forma opcional con uno o más sustituyentes seleccionados en forma independiente de R46;R46 es uno o más sustituyentes seleccionados del grupo que consiste en hidrógeno, hidroxi, amino,halógeno, dialquilamino, y alcoxicarbonilamino;R70 se selecciona del grupo que consiste en arilo, y heterociclo; en donde R70 está sustituido en formaopcional con R75;R75 es uno o más sustituyentes seleccionados en forma independiente del grupo que consiste enhidrógeno, halógeno, alcoxi, ciano, alquilo, haloalquilo, y arilo.un compuesto que tiene la Fórmula III:
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公开(公告)号:SG179414A1
公开(公告)日:2012-04-27
申请号:SG2012014080
申请日:2009-09-10
Applicant: ABBOTT LAB , ENANTA PHARM INC
Inventor: KU YIYIN , MCDANIEL KEITH F , CHEN HUI-JU , SHANLEY JASON P , KEMPF DALE J , GRAMPOVNIK DAVID J , SUN YING , LIU DONG , GAI YONGHUA , OR YAT SUN , WAGAW SABLE H , ENGSTROM KEN , GRIEME TIM , SHEIKH AHMAD , MEI JIANZHANG
Abstract: The present invention relates to novel macrocyclic compounds and methods of use thereof. The present invention further relates to pharmaceutical compositions comprising the compounds of the present invention, or pharmaceutically acceptable salts, esters, or prodrugs thereof, in combination with a pharmaceutically acceptable carrier or excipient.
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公开(公告)号:CR20110123A
公开(公告)日:2011-07-11
申请号:CR20110123
申请日:2011-03-07
Applicant: ENANTA PHARM INC , ABBOTT LAB
Inventor: KU YIYIN , MCDANIEL KEITH F , CHEN HUI-JU , SHANLEY JASON P , KEMPF DALE J , GRAMPOVNIK DAVID J , SUN YING , LIU DONG , GAI YONGHUA , OR YAT SUN , WAGAW SABLE H , ENGSTROM KEN , GRIEME TIM , SHEIKH AHMAD , MEI JIANZHANG
Abstract: La presente invención se relaciona con nuevos compuestos macrocíclicos y con métodos de uso de los mismos. La presente invención también se relaciona con composiciones farmacéuticas que comprenden los compuestos de la presente invención, o las sales, ésteres o prodrogas farmacéuticamente aceptables, en combinación con un vehículo o excipiente farmacéuticamente aceptable.
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公开(公告)号:HK1121765A1
公开(公告)日:2009-04-30
申请号:HK09101934
申请日:2009-03-02
Applicant: ABBOTT LAB
Inventor: BETEBENNER DAVID A , DEGOEY DAVID A , MARING CLARENCE J , KRUEGER ALLAN C , IWASAKI NOBUHIKO , ROCKWAY TODD W , COOPER CURT S , ANDERSON DAVID D , DONNER PAMELA L , GREEN BRIAN E , KEMPF DALE J , LIU DACHUN , MCDANIEL KEITH F , MADIGAN DAROLD L , MOTTER CHRISTOPHER E , PRATT JOHN K , SHANLEY JASON P , TUFANO MICHAEL D , WAGNER ROLF , ZHANG RONG , MOLLA AKHTERUZZAMAN , MO HONGMEI , PILOT-MATIAS TAMI J , MASSE SHERIE VL , CARRICK ROBERT J , HE WEPING , LU LIANGJUN , GRAMPOVNIK DAVID J
IPC: C07D20060101
Abstract: Compounds effective in inhibiting replication of Hepatitis C virus (“HCV”) or other viruses are disclosed. This invention is also directed to compositions comprising such compounds, co-formulation or co-administration of such compounds with other anti-viral or therapeutic agents, processes and intermediates for the syntheses of such compounds, and methods of using such compounds for the treatment of HCV or other viral infections.
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公开(公告)号:BRPI0512970A
公开(公告)日:2008-04-22
申请号:BRPI0512970
申请日:2005-06-29
Applicant: ABBOTT LAB
Inventor: DEGOEY DAVID A , FLOSI WILLIAM J , GRAMPOVNIK DAVID J , KLEIN LARRY L , KEMPF DALE J , WANG XIU C
IPC: C07F9/09 , A61K31/661 , A61P35/00
Abstract: A compound of the formula I, II or III is disclosed as a prodrug of an HIV protease inhibitor. Methods and compositions of inhibiting HIV protease activity and treating HIV infection are also disclosed.
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公开(公告)号:HK1100037A1
公开(公告)日:2007-08-31
申请号:HK07103390
申请日:2007-03-29
Applicant: ABBOTT LAB DEPT
Inventor: FLENTGE CHARLES A , CHEN HUI-JU , DEGOEY DAVID A , FLOSI WILLIAM J , GRAMPOVNIK DAVID J , HUANG PEGGY P , KEMPF DALE J , KLEIN LARRY L , KRUEGER ALLAN C , MADIGAN DAROLD L , RANDOLPH JOHN T , SUN MINGHUA , YEUNG MING C , ZHAO CHEN
IPC: A61K31/175 , A61K31/18 , A61K31/195 , A61K31/277 , A61K31/4168 , A61K31/65 , A61K45/06 , C07C311/17 , C07D20100101 , C07D213/30 , C07D213/40 , C07D213/78 , C07D233/32 , C07D233/72 , C07D277/28 , C07D277/46 , C07D277/48 , C07D307/20 , C07D307/42 , C07D401/06 , C07D403/06 , C07D403/10 , C07D405/06 , C07D405/10 , C07D409/06 , C07D417/06 , C07D417/14 , C07D471/04 , C07D493/04
Abstract: A compound of the formula is disclosed as an HIV protease inhibitor. Methods and compositions for inhibiting an HIV infection are also disclosed.
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公开(公告)号:CA2633752A1
公开(公告)日:2007-07-19
申请号:CA2633752
申请日:2006-12-20
Applicant: ABBOTT LAB
Inventor: MARING CLARENCE J , LU LIANGJUN , GRAMPOVNIK DAVID J , CARRICK ROBERT J , HE WEPING , KRUEGER ALLAN C , BETEBENNER DAVID A , TUFANO MICHAEL D , PILOT-MATIAS TAMI J , MASSE SHERIE VL , WAGNER ROLF , MCDANIEL KEITH F , IWASAKI NOBUHIKO , DEGOEY DAVID A , LIU DACHUN , ROCKWAY TODD W , MO HONGMEI , COOPER CURT S , DONNER PAMELA L , ANDERSON DAVID D , MOLLA AKHTERUZZAMAN , MOTTER CHRISTOPHER E , ZHANG RONG , GREEN BRIAN E , MADIGAN DAROLD L , PRATT JOHN K , KEMPF DALE J , SHANLEY JASON P
IPC: C07D495/04 , C07D471/04 , C07D513/04
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公开(公告)号:HK1094579A1
公开(公告)日:2007-04-04
申请号:HK07101712
申请日:2007-02-13
Applicant: ABBOTT LAB
Inventor: RANDOLPH JOHN T , CHEN HUI-JU , DEGOEY DAVID A , FLENTGE CHARLES A , FLOSI WILLIAM J , GRAMPOVNIK DAVID J , HUANG PEGGY P , HUTCHINSON DOUGLAS K , KEMPF DALE J , KLEIN LARRY L , YEUNG MING C
IPC: A61K20060101 , A61P20060101 , C07C20060101 , C07D20060101
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公开(公告)号:CA2792483A1
公开(公告)日:2005-07-07
申请号:CA2792483
申请日:2004-11-10
Applicant: ABBOTT LAB
Inventor: FLENTGE CHARLES A , CHEN HUI-JU , DEGOEY DAVID A , FLOSI WILLIAM J , GRAMPOVNIK DAVID J , HUANG PEGGY P , KEMPF DALE J , KLEIN LARRY L , KRUEGER ALLAN C , MADIGAN DAROLD L , RANDOLPH JOHN T , SUN MINGHUA , YEUNG MING C , ZHAO CHEN
IPC: C07D277/20 , A61K31/175 , A61K31/18 , A61K31/195 , A61K31/27 , A61K31/277 , A61K31/341 , A61K31/4168 , A61K31/426 , A61K31/44 , A61K31/65 , A61K45/06 , A61P31/18 , C07C311/00 , C07C311/17 , C07D213/00 , C07D213/30 , C07D213/40 , C07D213/78 , C07D233/32 , C07D233/72 , C07D277/28 , C07D277/46 , C07D277/48 , C07D307/20 , C07D307/42 , C07D401/06 , C07D403/06 , C07D403/10 , C07D405/06 , C07D405/10 , C07D409/06 , C07D417/06 , C07D417/14 , C07D471/04 , C07D493/04
Abstract: A compound of the formula is disclosed as an HIV protease inhibitor. Methods and compositions for inhibiting an HIV infection are also disclosed.
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