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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:CA2824516C
公开(公告)日:2019-02-26
申请号:CA2824516
申请日:2012-01-13
Applicant: VERTEX PHARMA
Inventor: LE TIRAN ARNAUD , GRILLOT ANNE-LAURE , CHARIFSON PAUL , BENNANI YOUSSEF LAAFIRET , O'DOWD HARDWIN , PEROLA EMANUELE
IPC: C07D405/14 , A61K31/506 , A61P31/04 , C07F9/6558
Abstract: The present invention relates to a compound of formula (I): or a pharmaceutically acceptable salt thereof wherein X and R are as defined herein. The compounds of formula (I) are useful as gyrase and/or topoisomerase IV inhibitors for treating bacterial infections. The compounds of formula (I) either possess a broad range of anti¬ bacterial activity and advantageous toxicological properties or are prodrugs of compounds having said activity.
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公开(公告)号:ES2545516T3
公开(公告)日:2015-09-11
申请号:ES12702920
申请日:2012-01-13
Applicant: VERTEX PHARMA
Inventor: LE TIRAN ARNAUD , GRILLOT ANNE-LAURE , CHARIFSON PAUL S , BENNANI YOUSSEF LAAFIRET , O'DOWD HARDWIN , PEROLA EMANUELE
IPC: C07D405/14 , A61K31/506 , A61P31/04 , C07F9/6558
Abstract: Un compuesto de fórmula **Fórmula** donde R es hidrógeno o flúor; X es hidrógeno, -PO(OH)2, -PO(OH)O-M+, -PO(O-)2*2M+ o -PO(O-)2*D2+; M+ es un catión monovalente farmacéuticamente aceptable; y D2+ es un catión divalente farmacéuticamente aceptable; o una de sus sales farmacéuticamente aceptables.
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公开(公告)号:CL2013002025A1
公开(公告)日:2013-12-27
申请号:CL2013002025
申请日:2013-07-12
Applicant: VERTEX PHARMA
Inventor: LE TIRAN ARNAUD , GRILLOT ANNE-LAURE , CHARIFSON PAUL , BENNANI YOUSSEF LAAFIRET , O DOWD HARDWIN , PEROLA EMANUELE
IPC: C07D405/14 , A61K31/506 , A61P31/04
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公开(公告)号:AU2012205415A1
公开(公告)日:2013-08-01
申请号:AU2012205415
申请日:2012-01-13
Applicant: VERTEX PHARMA
Inventor: LE TIRAN ARNAUD , GRILLOT ANNE-LAURE , CHARIFSON PAUL S , BENNANI YOUSSEF LAAFIRET , O'DOWD HARDWIN , PEROLA EMANUELE
IPC: C07D405/14 , A61K31/506 , A61P31/04 , C07F9/6558
Abstract: The present invention relates to a compound of formula (I): or a pharmaceutically acceptable salt thereof wherein X and R are as defined herein. The compounds of formula (I) are useful as gyrase and/or topoisomerase IV inhibitors for treating bacterial infections. The compounds of formula (I) either possess a broad range of anti¬ bacterial activity and advantageous toxicological properties or are prodrugs of compounds having said activity.
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公开(公告)号:AR084863A1
公开(公告)日:2013-07-10
申请号:ARP120100137
申请日:2012-01-16
Applicant: VERTEX PHARMA
Inventor: PEROLA EMANUELE , LE TIRAN ARNAUD , GRILLOT ANNE , LAURE-CHARIFSON PAUL , BENNANI YOUSSEF L , ODOWD HARDWIN
IPC: C07D405/14 , A61K31/506 , A61P31/04 , C07F9/6558
Abstract: Reivindicación 1: Un compuesto de la fórmula caracterizado porque tiene la fórmula (1) donde R es hidrógeno o flúor; X es hidrógeno, -PO(OH)2, -PO(OH)O-M+, -PO(O-)2·2M+, o -PO(O-)2·D2+; M+ es un catión monovalente farmacéuticamente aceptable; y D2+ es un catión divalente farmacéuticamente aceptable; o una sal farmacéuticamente aceptable del mismo.
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公开(公告)号:NZ588700A
公开(公告)日:2012-07-27
申请号:NZ58870009
申请日:2009-04-14
Applicant: VERTEX PHARMA
Inventor: WANG TIANSHENG , ARONOV ALEXANDER , CORNEBISE MARK , MALTAIS FRANCOIS , LEDOBOER MARK , LE TIRAN ARNAUD , MARONE VALERIE , MESSERSMITH DAVID , COTTRELL KEVIN , COME JON H
IPC: C07D417/04 , A61K31/428 , A61K31/4365 , A61P37/00 , C07D513/04
Abstract: Provided are inhibitors of phosphatidylinositol 3-kinases with formula (I) as depicted, with defined substituents. The compounds are useful for lessening the severity of a disease or condition selected from an autoimmune disease or an inflammatory disease of the brain or spinal cord.
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公开(公告)号:CA2752596A1
公开(公告)日:2010-08-26
申请号:CA2752596
申请日:2010-02-16
Applicant: VERTEX PHARMA
Inventor: ARONOV ALEX , BANDARAGE UPUL KEERTHI , COTTRELL KEVIN , DAVIES ROBERT , KRUEGER ELAINE , LEDEBOER MARK , LEDFORD BRIAN , LE TIRAN ARNAUD , LIAO YUSHENG , MESSERSMITH DAVID , WANG TIANSHENG , XU JINWANG
IPC: C07D513/04 , A61K31/4365 , A61P25/00
Abstract: The present invention relates to compounds (I) useful as inhibitors of PBK, particularly of PI3K?. 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.
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公开(公告)号:DK1592686T3
公开(公告)日:2009-10-19
申请号:DK04775744
申请日:2004-01-29
Applicant: VERTEX PHARMA
Inventor: CHARIFSON PAUL S , DEININGER DAVID D , LIAO YUSHENG , RONKIN STEVEN M , STAMOS DEAN , PEROLA EMAUELE , WANG TIANSHENG , DRUMM JOSEPH , GRILLOT ANNE-LAURE , LE TIRAN ARNAUD
IPC: C07D403/14 , A61K31/4184 , A61P31/04 , C07D401/14 , C07D403/04 , C07D403/10 , 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:DE602004021644D1
公开(公告)日:2009-07-30
申请号:DE602004021644
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
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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