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公开(公告)号:AU2011343647A1
公开(公告)日:2013-05-02
申请号:AU2011343647
申请日:2011-12-16
Applicant: VERTEX PHARMA
Inventor: CHARIFSON PAUL S , CLARK MICHAEL P , BANDARAGE UPUL K , DENG HONGBO , DAVIES IOANA , DUFFY JOHN P , FARMER LUC J , GAO HUAI , GU WENXIN , KENNEDY JOSEPH M , LEDEBOER MARK W , LEDFORD BRIAN , MALTAIS FRANCOIS , PEROLA EMANUELE , WANNAMAKER MARION W , WANG TIANSHENG , SALITURO FRANCESCO G
IPC: C07D471/04 , A61K31/4439 , A61K31/497 , A61K31/506 , A61K31/53
Abstract: Methods of inhibiting the replication of influenza viruses in a biological sample or patient, of reducing the amount of influenza viruses in a biological sample or patient, and of treating influenza in a patient, comprises administering to said biological sample or patient an effective amount of a compound represented by Structural Formula (I): or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (I) are as described herein. A compound is represented by Structural Formula (I) or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (I) are as described herein. A pharmaceutical composition comprises an effective amount of such a compound or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle.
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公开(公告)号:AU2011343646A1
公开(公告)日:2013-05-02
申请号:AU2011343646
申请日:2011-12-16
Applicant: VERTEX PHARMA
Inventor: CHARIFSON PAUL S , CLARK MICHAEL P , DAVIES IOANA , GAO HUAI , KENNEDY JOSEPH M , LEDEBOER MARK W , MALTAIS FRANCOIS , PEROLA EMANUELE
IPC: C07D471/04 , A61K31/16
Abstract: Methods of inhibiting the replication of influenza viruses in a biological sample or patient, of reducing the amount of influenza viruses in a biological sample or patient, and of treating influenza in a patient, comprises administering to said biological sample or patient an effective amount of a compound represented by Structural Formula (I): or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (I) are as described herein. A compound is represented by Structural Formula (I) or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (I) are as described herein. A pharmaceutical composition comprises an effective amount of such a compound or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle.
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33.
公开(公告)号:CA2566461C
公开(公告)日:2012-07-10
申请号:CA2566461
申请日:2005-05-13
Applicant: VERTEX PHARMA
Inventor: MARTINEZ-BOTELLA GABRIEL , HALE MICHAEL R , MALTAIS FRANCOIS , TANG QING , STRAUB JUDITH
IPC: C07D401/04 , A61K31/4439 , A61P9/00 , A61P25/00 , A61P37/00 , C07F9/58 , C07F9/6558
Abstract: The present invention provides a compound of formula I: (see formula I) or a pharmaceutically acceptable salt thereof. The compound or salt may be used to inhibit ERK1 or ERK2 protein kinase activity in a biological sample in vitro or treat or lessen the severity of melanoma, breast cancer, colon cancer, pancreatic cancer, kidney carcinoma, lung cancer, ovarian cancer or prostate cancer in a patient in need thereof.
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公开(公告)号:CA2822059A1
公开(公告)日:2012-06-21
申请号:CA2822059
申请日:2011-12-16
Applicant: VERTEX PHARMA
Inventor: CHARIFSON PAUL S , CLARK MICHAEL P , DAVIES IOANA , GAO HUAI , KENNEDY JOSEPH M , LEDEBOER MARK W , MALTAIS FRANCOIS , PEROLA EMANUELE
IPC: C07D471/04 , A61K31/16
Abstract: Methods of inhibiting the replication of influenza viruses in a biological sample or patient, of reducing the amount of influenza viruses in a biological sample or patient, and of treating influenza in a patient, comprises administering to said biological sample or patient an effective amount of a compound represented by Structural Formula (I): or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (I) are as described herein. A compound is represented by Structural Formula (I) or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (I) are as described herein. A pharmaceutical composition comprises an effective amount of such a compound or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle.
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公开(公告)号:CA2822057A1
公开(公告)日:2012-06-21
申请号:CA2822057
申请日:2011-12-16
Applicant: VERTEX PHARMA
Inventor: CHARIFSON PAUL S , CLARK MICHAEL P , BANDARAGE UPUL K , DAVIES IOANA , DUFFY JOHN P , GAO HUAI , FENG JUN , LIANG JIANGLIN , KENNEDY JOSEPH M , LEDEBOER MARK W , LEDFORD BRIAN , MALTAIS FRANCOIS , PEROLA EMANUELE
IPC: C07D471/04 , A61K31/16
Abstract: Methods of inhibiting the replication of influenza viruses in a biological sample or patient, of reducing the amount of influenza viruses in a biological sample or patient, and of treating influenza in a patient, comprises administering to said biological sample or patient an effective amount of a compound represented by Structural Formula (I): or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (I) are as described herein. A compound is represented by Structural Formula (I) or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (I) are as described herein. A pharmaceutical composition comprises an effective amount of such a compound or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle.
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公开(公告)号:NZ578744A
公开(公告)日:2012-02-24
申请号:NZ57874408
申请日:2008-01-30
Applicant: VERTEX PHARMA
Inventor: JIMENEZ JUAN-MIGUEL , BEMIS GUY , MALTAIS FRANCOIS , WANG TIANSHENG , KNEGTEL RONALD , DAVIS CHRIS , FRAYSSE DAMIEN , BOYALL DEAN , SETTIMO LUCA , YOUNG STEPHEN , MORTIMORE MICHAEL
IPC: A61K31/444 , C07D213/73 , A61P25/00 , A61P35/00 , C07D401/14 , C07D409/06 , C07D417/06 , C07D487/04
Abstract: Disclosed are (2-aminopyridin-3-yl)(heteroaryl)methanone derivatives as represented by the general formula, wherein B is a monocyclic heteroaromatic ring, a 6,6 bicyclic heteroaromatic ring, or a 6,5 bicyclic heteroaromatic ring wherein B is optionally and independently substituted with R12' and independently optionally and independently substituted with one or more R12 groups in addition to R3; Z is O or S; R1 is hydrogen, halogen, cyano, nitro, or -T1-Q1; R2 is hydrogen, halogen, cyano, nitro or optionally and independently substituted alkyl; R3 is halogen, cyano, nitro, or -T2-Q2; and wherein the remaining substituents are as defined herein. Further disclosed is a composition which comprises a compound of pharmaceutically acceptable salt thereof as defined above, and a pharmaceutically acceptable carrier, adjuvant, or vehicle for treating or preventing a protein kinase-mediated condition and particularly a GSK 3 mediated condition such as diabetes, Alzheimer's disease, Huntington's disease, Parkinson's disease, AIDS-associated dementia, bipolar disorder, amyotrophic lateral sclerosis, multiple sclerosis, schizophrenia, leukocytopenia, cardiomyocyte hypertrophy, stroke, and rheumatoid arthritis.
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公开(公告)号:MX2010011370A
公开(公告)日:2010-12-15
申请号:MX2010011370
申请日:2009-04-14
Applicant: VERTEX PHARMA
Inventor: MESSERSMITH DAVID , CORNEBISE MARK , TIRAN ARNAUD LE , ARONOV ALEXANDER , WANG TIANSHENG , MARONE VALERIE , COTTRELL KEVIN , MALTAIS FRANCOIS , LEDOBOER MARK , COME JON H , BOTELA GABRIEL MARTINEZ
IPC: C07D417/04 , A61K31/428 , A61K31/4365 , A61P37/00 , C07D513/04
Abstract: La presente invención se refiere a compuestos útiles como inhibidores de PI3K, particularmente de PI3K ggr. La invención también proporciona composiciones farmacéuticamente aceptables que comprenden los compuestos y métodos para usar las composiciones en el tratamiento de varias enfermedades, afecciones, o trastornos.
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公开(公告)号:AU2006202623B2
公开(公告)日:2009-05-14
申请号:AU2006202623
申请日:2006-06-20
Applicant: VERTEX PHARMA
Inventor: HALE MICHAEL , CAO JINGRONG , STRAUB JUDY , ARONOV ALEX , GREEN JEREMY , MALTAIS FRANCOIS , TANG QING
IPC: C07D403/04 , A61K31/506 , A61P35/00 , C07D401/14 , C07D403/14 , C07D405/14 , C07D413/14
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公开(公告)号:CA2369504C
公开(公告)日:2009-01-06
申请号:CA2369504
申请日:2001-02-05
Applicant: VERTEX PHARMA
Inventor: BEMIS GUY , CAO JINGRONG , MULLICAN MICHAEL , XIE XIAOLING , GREEN JEREMY , STRAUB JUDITH , MASHALL ROBERT , JANETKA JAMES , MALTAIS FRANCOIS , BAKER CHRISTOPHER , HALE MICHAEL , TANG QING
IPC: A61B17/00 , C07D403/04 , A61F2/02 , A61K31/4155 , A61K31/4178 , A61K31/433 , A61K31/437 , A61K31/4439 , A61K31/454 , A61K31/4709 , A61K31/4725 , A61K31/496 , A61K31/497 , A61K31/506 , A61K31/5377 , A61K31/551 , A61K45/00 , A61L27/00 , A61L27/28 , A61L31/08 , A61P1/00 , A61P1/16 , A61P1/18 , A61P3/10 , A61P5/00 , A61P7/02 , A61P9/00 , A61P9/04 , A61P9/10 , A61P11/00 , A61P13/00 , A61P13/10 , A61P13/12 , A61P15/00 , A61P17/00 , A61P17/06 , A61P19/00 , A61P21/00 , A61P25/00 , A61P25/28 , A61P29/00 , A61P31/00 , A61P31/12 , A61P35/00 , A61P35/02 , A61P37/00 , A61P37/02 , A61P37/04 , A61P37/06 , A61P37/08 , A61P43/00 , C07D231/38 , C07D401/14 , C07D403/14 , C07D405/14 , C07D413/14 , C07D417/14 , C07D471/04
Abstract: Described herein are compounds that are useful as protein kinase inhibitors having the formula: (I) where R1-4, Q, and T are described in the specification. Th e compounds are useful for treating disease states in mammals that are alleviated by a prote in kinase inhibitor, particularly diseases such as cancer, inflammatory disorders, restenosis, an d cardiovascular disease.
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公开(公告)号:UA84929C2
公开(公告)日:2008-12-10
申请号:UAA200613207
申请日:2005-05-13
Applicant: VERTEX PHARMA
Inventor: MARTINEZ-BOTELLA GABRIEL , HALE MICHAEL R , MALTAIS FRANCOIS , TANG QING , STRAUB JUDITH
IPC: C07D403/04 , A61K31/506 , A61P35/00
Abstract: Этоизобретениекасаетсясоединений, которыеиспользуютсякакингибиторыпротеинкиназ.Изобретениепредлагаеттакжефармацевтическиприемлемыекомпозиции, которыесодержатуказанныесоединения, испособыприменениятакихкомпозицийв леченииразныхболезней, состоянийилирасстройств.
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