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公开(公告)号:PT1734041E
公开(公告)日:2011-01-25
申请号:PT06015189
申请日:2002-07-25
Applicant: PORTOLA PHARM INC
Inventor: HUANG WOLIN , SCARBOROUGH ROBERT M , JANTZEN HANS-MICHAEL , SEDLOCK DAVID M , MARLOWE CHARLES K , KANE-MAGUIRE KIM A
IPC: C07D239/96 , C07D409/14 , A61K31/16 , A61K31/175 , A61K31/381 , A61K31/4035 , A61K31/4196 , A61K31/4725 , A61K31/519 , A61K31/54 , A61K31/64 , A61P7/02 , A61P9/00 , A61P9/04 , A61P9/10 , A61P9/14 , A61P43/00 , C07D209/48 , C07D213/70 , C07D239/22 , C07D239/50 , C07D333/34 , C07D401/04 , C07D401/12 , C07D405/12 , C07D409/12 , C07D417/12 , C07D487/04 , C07D495/04 , C07D521/00
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公开(公告)号:CL2009002040A1
公开(公告)日:2010-09-10
申请号:CL2009002040
申请日:2009-11-05
Applicant: PORTOLA PHARM INC
Inventor: SHARP EMMA , QUEGAN LOUISA JANE , PANDEY ANJALI , WANG JUAN , NIEDER MATTHEW , HUANG WOLIN
IPC: A61K31/517 , A61P9/00 , C07D409/12
Abstract: Sales de [4-(6-fluoro-7-metilamino-2,4-dioxo-1,4-dihidro-2h-quinazolin-3-il)-fenil]-5-cloro-tiofen-2-il-sulfonilurea; formas cristalinas de dichas sales; método de preparación; composición farmacéutica, útil para prevenir o tratar trombosis y condiciones patológicas relacionadas con trombosis.
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公开(公告)号:ZA200907493B
公开(公告)日:2010-07-28
申请号:ZA200907493
申请日:2009-10-26
Applicant: PORTOLA PHARM INC
Inventor: SHARP EMMA , QUEGAN LOUISA JANE , PANDEY ANJALI , WANG JUAN , NIEDER MATTHEW , HUANG WOLIN
IPC: A61K20100101 , C07D20100101
Abstract: The present invention provides novel sulfonylurea salts of a salt of formula (I) and polymorph forms thereof. The compounds in their various forms are effective platelet ADP receptor inhibitors and may be used in various pharmaceutical compositions, and are particularly effective for the prevention and/or treatment of cardiovascular diseases, particularly those diseases related to thrombosis. The invention also provides a method for preparing such compounds and forms and for preventing or treating thrombosis and thrombosis related conditions in a mammal comprising the step of administering a therapeutically effective amount of a salt of formula (I) or a pharmaceutically acceptable form thereof.
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公开(公告)号:MX2009011836A
公开(公告)日:2010-05-20
申请号:MX2009011836
申请日:2008-05-02
Applicant: PORTOLA PHARM INC
Inventor: PANDEY ANJALI , SHARP EMMA , QUEGAN LOUISA JANE , WANG JUAN , NIEDER MATTHEW , HUANG WOLIN
IPC: C07D409/12 , A61K31/517
Abstract: La presente invención proporciona sales de sulfonilurea novedosas de una sal de la fórmula (I) y formas polimorfas de la misma. Los compuestos en sus diferentes formas son efectivos inhibidores del receptor de plaquetas ADP y pueden ser utilizadas en varias composiciones farmacéuticas, y son particularmente efectivas para la prevención y/o tratamiento de enfermedades cardiovasculares, particularmente esas enfermedades relacionadas con la trombosis. La presente invención también proporciona un método para preparar dichos compuestos y formas y para prevenir o tratar la trombosis y los padecimientos relacionados con la trombosis en un mamífero que comprenden el paso de administrar una cantidad terapéuticamente efectiva de una sal de la fórmula (I) o una forma farmacéuticamente aceptable de la misma.
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公开(公告)号:CA2742601A1
公开(公告)日:2010-05-14
申请号:CA2742601
申请日:2009-11-04
Applicant: PORTOLA PHARM INC
Inventor: SHARP EMMA , QUEGAN LOUISA JANE , PANDEY ANJALI , WANG JUAN , NIEDER MATTHEW , HUANG WOLIN
IPC: C07D409/12 , A61K31/517 , A61P7/02
Abstract: The present invention provides novel sulfonylurea salts of a salt of formula (I) \ and polymorph forms thereof. The compounds in their various forms are effective platelet ADP receptor inhibitors and may be used in various pharmaceutical compositions, and are particularly effective for the prevention and/or treatment of cardiovascular diseases, particularly those diseases related to thrombosis. The invention also provides a method for preparing such compounds and forms and for preventing or treating thrombosis and thrombosis related conditions in a mammal comprising the step of administering a therapeutically effective amount of a salt of formula (I) or a pharmaceutically acceptable form thereof.
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公开(公告)号:PL1668002T3
公开(公告)日:2010-02-26
申请号:PL04789522
申请日:2004-09-29
Applicant: PORTOLA PHARM INC
Inventor: SCARBOROUGH ROBERT M , HUANG WOLIN , PANDEY ANJALI , BAUER SHAWN M , ZHANG XIAOMING , JIA ZHAOZHONG J
IPC: C07D409/12 , A61K20060101 , A61K31/517 , A61P7/02 , C07D409/14
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公开(公告)号:CA2960692A1
公开(公告)日:2009-12-03
申请号:CA2960692
申请日:2009-04-16
Applicant: PORTOLA PHARM INC
Inventor: BAUER SHAWN M , JIA ZHAOZHONG J , SONG YONGHONG , XU QING , MEHROTRA MUKUND , ROSE JACK W , HUANG WOLIN , VENKATARAMANI CHANDRASEKAR , PANDEY ANJALI
IPC: C07D239/48 , A61K31/505 , A61K31/506 , C07D401/12 , C07D403/12 , C07D405/12 , C07D417/12
Abstract: The present specification is directed to compounds of formula I-II and pharmaceutically acceptable tautomers, salts, or stereoisomers thereof which are inhibitors of syk and/or JAK kinase. The present specification is also directed to intermediates used in making such compounds, the preparation of such a compound, methods for inhibition of syk and/or JAK kinase activity, methods for inhibition of the platelet aggregation, and methods to prevent or treat a number of conditions mediated at least in part by syk and/or JAK kinase activity, such as undesired thrombosis and Non Hodgkin's Lymphoma. The present specification is also directed to pharmaceutical compositions containing such a compound and which are formulated for topical administration.
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公开(公告)号:AT448222T
公开(公告)日:2009-11-15
申请号:AT04789522
申请日:2004-09-29
Applicant: PORTOLA PHARM INC
Inventor: SCARBOROUGH ROBERT , HUANG WOLIN , PANDEY ANJALI , BAUER SHAWN , ZHANG XIAOMING , JIA ZHAOZHONG
IPC: C07D409/12 , A61K20060101 , A61K31/517 , A61P7/02 , C07D409/14
Abstract: 2,4-Dioxo-3-quinazolinylaryl sulfonylurea compounds having the formula: wherein R is a member selected from the group consisting of H and C 1-6 alkyl; R 1 is a member selected from the group consisting of H, C 1-6 alkyl, C 1-6 haloalkyl, C 3-5 cycloalkyl and C 3-5 cycloalkyl-alkyl; R 2 is a member selected from the group consisting of H, halogen, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 haloalkyl, C 1-6 alkoxy, cyano and -C(O)R 2a , wherein R 2a is a member selected from the group consisting of C 1-6 alkoxy and (C 1-6 alkyl) 0-2 amino; L is a 1 to 3 carbon linking group selected from the group consisting of -CH 2 -, -CH(CH 3 )-, -CH 2 CH 2 -, -CH 2 CH(CH 3 )- and -CH 2 CH 2 CH 2 -; L 1 is a linking group selected from the group consisting of a bond and -CH 2 -; L 2 is a linking group selected from the group consisting of a bond, -NH- and -CH 2 -; and Ar 1 is an aromatic ring selected from the group consisting of benzene, pyridine and pyrimidine; are provided. The compounds are useful for the inhibition of ADP-platelet aggregation, particularly in the treatment of thrombosis and thrombosis related conditions or disorders.
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公开(公告)号:CA2686221A1
公开(公告)日:2008-11-13
申请号:CA2686221
申请日:2008-05-02
Applicant: PORTOLA PHARM INC
Inventor: HUANG WOLIN , NIEDER MATTHEW , QUEGAN LOUISA JANE , SHARP EMMA , WANG JUAN , PANDEY ANJALI
IPC: C07D409/12 , A61K31/517
Abstract: The present invention provides novel sulfonylurea salts of a salt of form ula (I) and polymorph forms thereof. The compounds in their various forms ar e effective platelet ADP receptor inhibitors and may be used in various phar maceutical compositions, and are particularly effective for the prevention a nd/or treatment of cardiovascular diseases, particularly those diseases rela ted to thrombosis. The invention also provides a method for preparing such c ompounds and forms and for preventing or treating thrombosis and thrombosis related conditions in a mammal comprising the step of administering a therap eutically effective amount of a salt of formula (I) or a pharmaceutically ac ceptable form thereof.
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公开(公告)号:AU2008247457A1
公开(公告)日:2008-11-13
申请号:AU2008247457
申请日:2008-05-02
Applicant: PORTOLA PHARM INC
Inventor: SHARP EMMA , NIEDER MATTHEW , WANG JUAN , PANDEY ANJALI , HUANG WOLIN , QUEGAN LOISA JANE
IPC: A61K31/517 , C07D409/12
Abstract: The present invention provides novel sulfonylurea salts of a salt of formula (I) and polymorph forms thereof. The compounds in their various forms are effective platelet ADP receptor inhibitors and may be used in various pharmaceutical compositions, and are particularly effective for the prevention and/or treatment of cardiovascular diseases, particularly those diseases related to thrombosis. The invention also provides a method for preparing such compounds and forms and for preventing or treating thrombosis and thrombosis related conditions in a mammal comprising the step of administering a therapeutically effective amount of a salt of formula (I) or a pharmaceutically acceptable form thereof.
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