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公开(公告)号:AU2003223602A1
公开(公告)日:2003-10-27
申请号:AU2003223602
申请日:2003-04-11
Applicant: VERTEX PHARMA
Inventor: PITLIK JANOS , COTTRELL KEVIN M , FARMER LUC J , PERNI ROBERT B , COURTNEY LAWRENCE F , DRIE JOHN H VAN , MURCKO MARK A
IPC: C12N9/99 , A61K38/00 , A61K38/04 , A61P1/16 , A61P31/12 , A61P31/14 , A61P37/02 , A61P43/00 , C07D209/42 , C07D401/12 , C07D403/12 , C07D405/12 , C07D405/14 , C07D417/12 , C07D471/04 , C07K5/04 , C07K5/06 , C07K5/10 , C07K7/02 , C07F5/02 , C07K5/08 , A61K31/404
Abstract: The present invention relates to compounds that inhibit serine protease activity, particularly the activity of hepatitis C virus NS3-NS4A protease. As such, they act by interfering with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The invention further relates to compositions comprising these compounds either for ex vivo use or for administration to a patient suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a patient by administering a composition comprising a compound of this invention. The invention further relates to processes for preparing these compounds.
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公开(公告)号:CY1110176T1
公开(公告)日:2015-01-14
申请号:CY091100274
申请日:2009-03-10
Applicant: VERTEX PHARMA
Inventor: TUNG ROGER D , CHANDORKAR GURUDATT , PERNI ROBERT B
IPC: A61K45/00 , A61K31/7056 , A61K38/21 , A61K45/06
Abstract: Ηπαρούσαεφεύρεσηαφοράτηνσυν-χορήγησηενόςαναστολέαπρωτεάσης NS3/4A ιούΗπατίτιδας C καιενόςαναστολέαμονο-οξυγενάσηςκυτοχρώματοςΡ450. Οσυνδυασμόςδρααλληλεπιδρώνταςμετονκύκλοζωήςτουιούηπατίτιδας C καιεπομένωςείναιχρήσιμοςωςμιααντι-ιϊκήθεραπεία. Έτσι, οσυνδυασμόςμπορείναχρησιμοποιείταιγιατηνθεραπείαή πρόληψημολύνσεωνηπατίτιδας C σεασθενείς. Ηεφεύρεσηεπίσηςαφοράσυνθέσειςπουπεριλαμβάνουντονσυνδυασμόαναστολέων. Ηεφεύρεσηεπίσηςαφοράκιτκαιφαρμακευτικέςσυσκευασίεςπουπεριλαμβάνουνέναναναστολέαπρωτεάσης NS3/4A ιούηπατίτιδας C καιένααναστολέαμονο-οξυγενάσηςκυτοχρώματοςΡ450. Ηεφεύρεσηεπίσηςαφοράμεθόδουςπαρασκευήςαυτώντωνσυνθέσεων, συνδυασμών, κιτκαισυσκευασιών.
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公开(公告)号:AU2012202822A1
公开(公告)日:2012-06-07
申请号:AU2012202822
申请日:2012-05-15
Applicant: VERTEX PHARMA
Inventor: COTTRELL KEVIN M , DEININGER DAVID D , FARMER LUC J , PITLIK JANOS , PERNI ROBERT B , COURT JOHN J
Abstract: The present invention relates to compounds of formula (I), or a pharmaceutically acceptable salt or mixtures thereof that inhibit serine protease activity, particularly the activity of hepatitis C virus NS3-NS4A protease. As such, they act by interfering with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The invention further relates to compositions comprising these compounds either for ex vivo use or for administration to a patient suffering from HCV infection and to processes for preparing the compounds. The invention also relates to methods of treating an HCV infection in a patient by administering a composition comprising a compound of this invention. The invention further relates to processes for preparing these compounds.
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公开(公告)号:AU2011203054A1
公开(公告)日:2011-08-11
申请号:AU2011203054
申请日:2011-06-23
Applicant: VERTEX PHARMA
Inventor: FARMER LUC J , PERNI ROBERT B , RAO BHISETTI GOVINDA , WILSON KEITH P
IPC: C07D403/12 , A61K31/401 , A61K31/4155 , A61K31/425 , A61K31/4965 , C07D417/12
Abstract: Abstract The present invention relates to compounds of formula (I) or a pharmaceutically acceptable salt, or mixtures thereof, that inhibit serine protease activity, particularly the activity of hepatitis C virus NS3-NS4A protease. As such, they act by interfering with the life cycle of the hepatitis C virus and are useful as antiviral agents. The invention further relates to pharmaceutically acceptable compositions comprising said compounds either for ex vivo use of for administration to a patient suffering from HCV infection and processes for preparing the compounds. The invention also relates to methods of treating HCV infection in a patient by administering a pharmaceutical composition comprising a compound of this invention. R1, RR, 2 0 0
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公开(公告)号:NZ546663A
公开(公告)日:2010-01-29
申请号:NZ54666304
申请日:2004-10-08
Applicant: VERTEX PHARMA
Inventor: COTTRELL KEVIN M , PERNI ROBERT B , PITLIK JANOS
Abstract: Disclosed is a compound of formula I or a pharmaceutically acceptable salt or mixture thereof wherein the substituents are disclosed within the specification. Also disclosed is the use of the above compound in the production of a composition for inhibiting the activity of a serine protease such as HCV NS3 protease.
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公开(公告)号:MX2009009176A
公开(公告)日:2009-09-28
申请号:MX2009009176
申请日:2008-02-20
Applicant: VERTEX PHARMA
Inventor: FARMER LUC , PERNI ROBERT B , MAXWELL JOHN , BETHIEL RANDY SCOTT , JACOBS DYLAN , COTTRELL KEVIN , HALAS SUMMER
IPC: C07D487/10 , A61K31/00 , A61P31/12 , C07D498/10
Abstract: La presente invención se refiere a compuestos que inhiben la actividad de serina-proteasas, particularmente la actividad de la proteasa NS3-NS4A del virus de hepatitis C. como tales, actúan al interferir con el ciclo de vida del virus de hepatitis C y también son útiles como agentes antivirales. La invención se refiere adicionalmente a composiciones que comprenden estos compuestos ya sea para el uso ex vivo o para la administración de un paciente que padece de infección de HCV. La invención también se refiere a métodos para tratar una infección de HCV en el paciente al administrar una composición que comprende un compuesto de esta invención.
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公开(公告)号:DE602004018363D1
公开(公告)日:2009-01-22
申请号:DE602004018363
申请日:2004-10-27
Applicant: VERTEX PHARMA
Inventor: TUNG ROGER D , CHANDORKAR GURUDATT , PERNI ROBERT B
IPC: A61K45/00 , A61K31/7056 , A61K38/21 , A61K45/06
Abstract: The present invention relates to co-administering a Hepatitis C virus NS3/4A protease inhibitor and a cytochrome P450 monooxygenase inhibitor. The combination acts by interfering with the life cycle of the hepatitis C virus and is therefore useful as an antiviral therapy. As such, the combination may be used for treating or preventing Hepatitis C infections in patients. The invention also relates to compositions comprising the combination of inhibitors. The invention also relates to kits and pharmaceutical packs comprising a Hepatitis C virus NS3/4A protease inhibitor and a cytochrome P450 monooxygenase inhibitor. The invention also relates to processes for preparing these compositions, combinations, kits, and packs.
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公开(公告)号:MX2008011868A
公开(公告)日:2008-12-15
申请号:MX2008011868
申请日:2007-03-14
Applicant: VERTEX PHARMA
Inventor: PERNI ROBERT B , MALTAIS FRANCOIS , TANOURY GERALD J , CHEN MINZHANG , JUNG YOUNG CHUN , FORSLUND RAYMOND E , BENNANI YOUSSEF , ZLOKARNIK GREGOR
IPC: C07C231/20 , A61K31/403 , A61K31/422 , A61K31/498 , A61P31/12 , C07C237/04 , C07D209/52 , C07D403/12 , C07D403/14 , C07D498/10
Abstract: Se describe un compuesto específico de (-cetoamido estérico deuterado de la Fórmula (I), en donde D denota un átomo de deuterio sobre un átomo de carbono específico, estérico.
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公开(公告)号:AT416789T
公开(公告)日:2008-12-15
申请号:AT04810032
申请日:2004-10-27
Applicant: VERTEX PHARMA
Inventor: TUNG ROGER D , CHANDORKAR GURUDATT , PERNI ROBERT B
IPC: A61K45/00 , A61K31/7056 , A61K38/21 , A61K45/06
Abstract: The present invention relates to co-administering a Hepatitis C virus NS3/4A protease inhibitor and a cytochrome P450 monooxygenase inhibitor. The combination acts by interfering with the life cycle of the hepatitis C virus and is therefore useful as an antiviral therapy. As such, the combination may be used for treating or preventing Hepatitis C infections in patients. The invention also relates to compositions comprising the combination of inhibitors. The invention also relates to kits and pharmaceutical packs comprising a Hepatitis C virus NS3/4A protease inhibitor and a cytochrome P450 monooxygenase inhibitor. The invention also relates to processes for preparing these compositions, combinations, kits, and packs.
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公开(公告)号:ZA200801114B
公开(公告)日:2008-11-26
申请号:ZA200801114
申请日:2008-02-01
Applicant: VERTEX PHARMA
Inventor: STEVE LYONS , PERNI ROBERT B
IPC: A61K20090101 , A61P20090101 , C07D20090101
Abstract: This invention relates to a mixture of diastereomeric compounds of Formula I: or a pharmaceutically acceptable salt or mixtures thereof, wherein C* represents a diastereomeric carbon atom.
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