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公开(公告)号:MX2021013993A
公开(公告)日:2021-12-10
申请号:MX2021013993
申请日:2020-05-14
Applicant: VERTEX PHARMA
Inventor: LOOKER ADAM , ROEPER STEFANIE , FANNING LEV TYLER DEWEY , HURLEY DENNIS JAMES , JONES PETER , SHI YI , COTTRELL KEVIN MICHAEL , MAXWELL JOHN PATRICK , RONKIN STEVEN M , GIROUX SIMON , STAVROPOULOS KATHY , BRODNEY MICHAEL AARON , MEDEK ALES , SHRESTHA MUNA , ZAKY MARIAM , NUHANT PHILIPPE MARCEL , BLIGH CAVAN MCKEON , GAGNON KEVIN JAMES , HOOD SARAH CAROL , RODAY SETU , SAWANT RUPA , TANG QING , BANDARAGE UPUL KEERTHI , DAMAGNEZ VERONIQUE , GREY JR RONALD LEE , HALL AMY BETH , SWETT REBECCA JANE , TAPLEY TIMOTHY LEWIS , XU JINWANG , BOUCHER DIANE , BOYD MICHAEL JOHN , CLARK MICHAEL PHILIP , FIMOGNARI ROBERT FRANCIS , FLEMING GABRIELLE SIMONE , GUIDO SAMANTHA , JOHNSON JR MAC ARTHUR , KESAVAN SARATHY , LAI MEI-HSIU , LIU SIYING , MAXWELL BRAD , OVERHOFF KIRK ALAN , SPOSATO MARISA , THOMSON STEPHEN , GARCIA BARRANTES PEDRO , GIACOMETTI ROBERT
IPC: A61K31/429 , A61K31/4162 , A61P1/16 , A61P11/00 , C07D231/56 , C07D487/04 , C07D498/18 , C07D513/04
Abstract: La descripción proporciona compuestos útiles para tratar la deficiencia de alfa-1 antitripsina (AATD), de acuerdo con la fórmula (I), tautómeros de estos, sales farmacéuticamente aceptables de los compuestos, sales farmacéuticamente aceptables de los tautómeros, derivados deuterados de los compuestos, derivados deuterados de los tautómeros y derivados deuterados de las sales, formas sólidas de esos compuestos y procesos para preparar esos compuestos. (ver Fórmula).
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公开(公告)号:UY38696A
公开(公告)日:2020-11-30
申请号:UY38696
申请日:2020-05-13
Applicant: VERTEX PHARMA
Inventor: JONES PETER , NUHANT PHILIPPE MARCEL , BANDARAGE UPUL KEERTHI , BLIGH CAVAN MCKEON , GAGNON KEVIN JAMES , BOYD MICHAEL JOHN , GIROUX SIMON , GREY JR RONALD LEE , HALL AMY BETH , HOOD SARAH CAROL , HURLEY DENNIS JAMES , JOHNSON JR , KESAVAN SARATHY , LOOKER ADAM , MAXWELL JOHN PATRICK , MEDEK ALES , RODAY SETU , ROEPER STEFANIE , SAWANT RUPA , SHI YI , SWETT REBECCA JANE , TANG QING , TAPLEY TIMOTHY LEWIS , XU JINWANG , BOUCHER DIANE , CLARK MICHAEL PHILIP , DAMAGNEZ VERONIQUE , FANNING LEV TYLER DEWEY , FIMOGNARI ROBERT FRANCIS , FLEMING GABRIELLE SIMONE , GARCIA BARRANTES PEDRO MANUEL , GIACOMETTI ROBERT DANIEL , GUIDO SAMANTHA , LAI MEI-HSIU , LIU SIYING , MAXWELL BRAD , OVERHOFF KIRK ALAN , RONKIN STEVEN M , SHRESTHA MUNA , SPOSATO MARISA , STAVROPOULOS KATHY , THOMSON STEPHEN , ZAKY MARIAM , BRODNEY MICHAEL AARON
IPC: A61P1/16 , A61K31/4162 , A61P11/00 , C07D487/14 , C07D498/18
Abstract: La descripción proporciona compuestos útiles para tratar la deficiencia de alfa-1 antitripsina (AATD), de acuerdo con la fórmula (I), tautómeros de estos, sales farmacéuticamente aceptables de los compuestos, sales farmacéuticamente aceptables de los tautómeros, derivados deuterados de los compuestos, derivados deuterados de los tautómeros y derivados deuterados de las sales, formas sólidas de esos compuestos y procesos para preparar esos compuestos.
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公开(公告)号:AU2018236800B2
公开(公告)日:2020-04-09
申请号:AU2018236800
申请日:2018-09-27
Applicant: VERTEX PHARMA
Inventor: MAXWELL JOHN PATRICK , CHARIFSON PAUL S , TANG QING , RONKIN STEVEN M , JACKSON KATRINA LEE , PIERCE ALBERT CHARLES , LAUFFER DAVID J , LI PAN , GIROUX SIMON , XU JINWANG , COTTRELL KEVIN M , MORRIS MARK A , WAAL NATHAN D , COURT JOHN J , GU WENXIN , DENG HONGBO
IPC: C07D403/12 , A61K31/517 , A61P35/00 , C07D405/12 , C07D413/04 , C07D417/12 , C07D491/052
Abstract: The present invention relates to compounds (I) which are useful as inhibitors of DNA-PK. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders related to undesirable DNA-PK activity. (I)
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公开(公告)号:CA3088792A1
公开(公告)日:2019-07-25
申请号:CA3088792
申请日:2019-01-16
Applicant: VERTEX PHARMA
Inventor: MAXWELL JOHN PATRICK , JACKSON KATRINA LEE , TANG QING , MORRIS MARK A , RONKIN STEVEN M , XU JINWANG , COTTRELL KEVIN M , CHARIFSON PAUL S
IPC: C07D403/12 , A61P35/00 , C07D239/74 , C07D239/86 , C07D239/88 , C07D239/94 , C07D401/12 , C07D417/12 , C07D491/048
Abstract: The present invention relates to compounds useful as inhibitors of DNA-PK. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various diseases, conditions, or disorders.
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公开(公告)号:AU2004261545B2
公开(公告)日:2010-06-24
申请号:AU2004261545
申请日:2004-01-29
Applicant: VERTEX PHARMA
Inventor: DEININGER DAVID D , DRUMM JOSEPH , LIAO YUSHENG , WANG TIANSHENG , STAMOS DEAN , GRILLOT ANNE-LAURE , CHARIFSON PAUL S , PEROLA EMAUELE , LETIRAN ARNAUD , RONKIN STEVEN M
IPC: C07D403/14 , A61P31/04 , C07D401/14 , C07D403/04 , C07D405/04 , C07D405/14 , C07D413/14 , C07D417/14 , C07D471/04 , C07D487/04 , C07D491/04
Abstract: The present invention relates to compounds which inhibit bacterial gyrase and/or Topo IV and pharmaceutically acceptable compositions comprising said compounds. These compounds, and compositions thereof, are useful in treating bacterial infection. Accordingly, the present invention also relates to methods for treating bacterial infections in mammals.
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公开(公告)号:PL1789419T3
公开(公告)日:2009-11-30
申请号:PL04810009
申请日:2004-10-21
Applicant: VERTEX PHARMA
Inventor: CHARIFSON PAUL S , DEININGER DAVID D , GRILLOT ANNE-LAURE , LIAO YUSHENG , RONKIN STEVEN M , STAMOS DEAN , PEROLA EMANUELE , WANG TIANSHENG , LE TIRAN ARNAUD , DRUMM JOSEPH
IPC: C07D491/04 , A61K31/4184 , A61K31/4439 , A61K31/506 , A61P31/00 , A61P31/04 , C07D401/14 , C07D403/04 , C07D403/14 , C07D405/04 , C07D405/14 , C07D413/14 , C07D417/14 , C07D471/04 , C07D487/04
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公开(公告)号:HRP20090491T1
公开(公告)日:2009-11-30
申请号:HRP20090491
申请日:2009-09-15
Applicant: VERTEX PHARMA
Inventor: CHARIFSON PAUL S , DEININGER DAVID D , GRILLOT ANNE-LAURE , LIAO YUSHENG , RONKIN STEVEN M , STAMOS DEAN , PEROLA EMANUELE , WANG TIANSHENG , TIRAN ARNAUD LE , DRUMM JOSEPH
IPC: C07D491/04 , A61K31/4184 , A61K31/4439 , A61K31/506 , A61P31/00 , A61P31/04 , C07D401/14 , C07D403/04 , C07D403/14 , C07D405/04 , C07D405/14 , C07D413/14 , C07D417/14 , C07D471/04 , C07D487/04
Abstract: The present invention relates to compounds that inhibit bacterial gyrase and/or Topo IV and pharmaceutically acceptable compositions comprising said compounds. These compounds, and compositions thereof, are useful in treating bacterial infection. Accordingly, the present invention also relates to methods for treating bacterial infections in mammals.
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公开(公告)号:ES2325026T3
公开(公告)日:2009-08-24
申请号:ES04810009
申请日:2004-10-21
Applicant: VERTEX PHARMA
Inventor: CHARIFSON PAUL S , DEININGER DAVID D , GRILLOT ANNE-LAURE , LIAO YUSHENG , RONKIN STEVEN M , STAMOS DEAN
IPC: C07D491/04 , A61K31/4184 , A61K31/4439 , A61K31/506 , A61P31/00 , A61P31/04 , C07D401/14 , C07D403/04 , C07D403/14 , C07D405/04 , C07D405/14 , C07D413/14 , C07D417/14 , C07D471/04 , C07D487/04
Abstract: Un compuesto de fórmula VII: ** ver fórmula** o una sal farmacéuticamente aceptable del mismo, en donde: V se selecciona de nitrógeno, CH o CF; R 3 es hidrógeno o alifático C1-4, en donde: cuando R 3 es alifático C 1-4, R 3 está sustituido con 0-3 grupos que se seleccionan independientemente de OH, R 5 u OR 5 ; en donde: R 5 es alifático C1-3, en donde: dos grupos R 5 alifáticos opcionalmente pueden tomarse junto con el carbono al que están unidos para formar un anillo cicloalquilo C 3-4; siempre que si R 3 es hidrógeno, entonces V no es nitrógeno ni CH; R 4 es un grupo alifático C 1-3; y el Anillo C es un anillo heteroarilo de 6 miembros que tiene 1-2 nitrógenos, en donde: el Anillo C está sustituido con 1-3 grupos que se seleccionan de R 6 ; en donde: cada R 6 se selecciona independientemente de OR 7 o es halógeno; y R 7 es alifático C1-4; o el Anillo C es un anillo 2-pirimidina insustituido.
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公开(公告)号:DK1789419T3
公开(公告)日:2009-08-10
申请号:DK04810009
申请日:2004-10-21
Applicant: VERTEX PHARMA
Inventor: CHARIFSON PAUL S , DEININGER DAVID D , LIAO YUSHENG , RONKIN STEVEN M , STAMOS DEAN , PEROLA EMANUELE , WANG TIANSHENG , DRUMM JOSEPH , GRILLOT ANNE-LAURE , LE TIRAN ARNAUD
IPC: C07D491/04 , A61K31/4184 , A61K31/4439 , A61K31/506 , A61P31/00 , A61P31/04 , C07D401/14 , C07D403/04 , C07D403/14 , C07D405/04 , C07D405/14 , C07D413/14 , C07D417/14 , C07D471/04 , C07D487/04
Abstract: The present invention relates to compounds that inhibit bacterial gyrase and/or Topo IV and pharmaceutically acceptable compositions comprising said compounds. These compounds, and compositions thereof, are useful in treating bacterial infection. Accordingly, the present invention also relates to methods for treating bacterial infections in mammals.
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公开(公告)号:ZA200701629B
公开(公告)日:2008-09-25
申请号:ZA200701629
申请日:2004-10-21
Applicant: VERTEX PHARMA
Inventor: CHARIFSON PAUL S , DEININGER DAVID D , GRILLOT ANNE-LAURE , RONKIN STEVEN M , DEAN STAMOS , EMANUELE PEROLA , TIANSHENG WANG , ARNAUD LE TIRAN , JOSEPH DRUMM , LIAO YUSHENG
IPC: A61K20090101 , A61K31/4439 , A61K31/506 , A61P20090101 , A61P31/04 , C07D20090101 , C07D401/14 , C07D403/04 , C07D403/14 , C07D405/04 , C07D405/14 , C07D413/14 , C07D417/14 , C07D471/04 , C07D487/04 , C07D491/04
Abstract: The present invention relates to compounds that inhibit bacterial gyrase and/or Topo IV and pharmaceutically acceptable compositions comprising said compounds. These compounds, and compositions thereof, are useful in treating bacterial infection. Accordingly, the present invention also relates to methods for treating bacterial infections in mammals.
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