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公开(公告)号:MX9703488A
公开(公告)日:1998-07-31
申请号:MX9703488
申请日:1997-05-09
Applicant: COR THERAPEUTICS INC
Inventor: GIESE NEILL A , LOKKER NATHALIE , LAIBELMAN ALAN M , SCARBOROUGH ROBERT M
IPC: A61K31/415 , C07D231/38 , A61K31/4155 , A61K31/44 , A61K31/4427 , A61K31/443 , A61K31/4433 , A61K31/4439 , A61K31/455 , A61P43/00 , C07D231/40 , C07D401/06 , C07D405/04 , C07D409/06 , A61K31/45
Abstract: Se describe un método para inhibir selectivamente una cinasa, el cual comprende poner en contacto una composicion que contiene una cinasa con un compuesto de formula (I), en donde: R1 es alquilo inferior, hidrocarbilo inferior, arilalquilo inferior, hheteroarilalquilo inferior, aromático hheterocíclico de 5 o 6 miembros, poliaromático, carbonilo poliaromático, polihheteroaromático o carbonilo polihheteroaromático; R2 es alquilo inferior, hidrocarbilo inferior, arilalquilo inferior, hheteroarilalquilo inferior, aromático hheterociclico de 5 o 6 miembros, hidrocarbilo inferior, carbonilo aromático hheterocíclico de 5 o 6 miembros, poliaromático o polihheteroaromático; R3 es H o alquilo inferior; R5 es H, alquilo inferior, hidrocarbilo inferior, arilalquilo inferior, hheteroarilalquilo inferior, o aromático hheterocíclico de 5 a 6 miembros, halogeno, o ciano; y R6 es H o hidrocarboilo inferior.
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公开(公告)号:CA2271935A1
公开(公告)日:1998-05-28
申请号:CA2271935
申请日:1997-11-21
Applicant: COR THERAPEUTICS INC
Inventor: PHILLIPS DAVID R , JENKINS ALISON L
IPC: A61K38/39 , C07K14/705 , C07K14/78
Abstract: The present invention describes a direct interaction between myosin and the cytoplasmic domain of membrane proteins, particularly the phosphorylated cytoplasmic domains of the .beta.-subunit of integrins. The invention provides methods of identifying agents which block integrin binding to myosin, methods of using agents which block integrin binding to myosin to modulate biological and pathological processes, and provides agents that block integrin mediated binding to myosin and thereby modulate related cellular or cellular component movement.
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公开(公告)号:AR002425A1
公开(公告)日:1998-03-11
申请号:AR10308496
申请日:1996-06-07
Applicant: COR THERAPEUTICS INC
IPC: A61K38/00 , A61P7/02 , C07C279/24 , C07C281/06 , C07C309/30 , C07C335/38 , C07K5/06 , C07K5/068 , C07K5/072 , C07K5/08 , C07K7/06 , A61K38/55
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公开(公告)号:AU677930B2
公开(公告)日:1997-05-08
申请号:AU4564696
申请日:1996-02-20
Applicant: COR THERAPEUTICS INC
Inventor: WOLF DAVID
IPC: A61K38/43 , A61K38/00 , A61P7/02 , C07K14/00 , C07K14/475 , C07K14/745 , C07K14/81 , C12N5/10 , C12N9/64 , C12N15/09 , C12P21/02 , A61K38/36
Abstract: Analogs of Factor Xa (Factor Xai) which are inactive as proteases in the prothrombinase reaction are useful in treatment of diseases characterized by thrombosis. These antithrombotic agents can be conveniently prepared using recombinant techniques.
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公开(公告)号:AU665752B2
公开(公告)日:1996-01-18
申请号:AU1456892
申请日:1992-02-19
Applicant: UNIV CALIFORNIA , COR THERAPEUTICS INC
Inventor: COUGHLIN SHAUN R , SCARBOROUGH ROBERT M
IPC: A61K38/00 , A61K39/00 , A61K39/395 , A61K49/00 , A61P7/02 , A61P9/08 , A61P9/10 , A61P43/00 , C07K7/02 , C07K7/06 , C07K14/705 , C07K16/00 , C07K16/28 , C12N1/15 , C12N1/19 , C12N1/21 , C12N5/10 , C12N9/74 , C12N15/09 , C12N15/12 , C12P21/02 , C12P21/08 , C12R1/19 , G01N33/53 , C07K7/00 , A61K37/02 , C07K5/02 , C07K5/06 , C07K5/08 , C07K5/10 , C07K7/08 , C07K13/00
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公开(公告)号:NZ241666A
公开(公告)日:1995-07-26
申请号:NZ24166692
申请日:1992-02-19
Applicant: UNIV CALIFORNIA , COR THERAPEUTICS INC
Inventor: COUGHLIN SHAUN R , SCARBOROUGH ROBERT M
IPC: A61K38/00 , A61K39/00 , A61K39/395 , A61K49/00 , A61P7/02 , A61P9/08 , A61P9/10 , A61P43/00 , C07K7/02 , C07K7/06 , C07K14/705 , C07K16/00 , C07K16/28 , C12N1/15 , C12N1/19 , C12N1/21 , C12N5/10 , C12N9/74 , C12N15/09 , C12N15/12 , C12P21/02 , C12P21/08 , C12R1/19 , G01N33/53 , A61K37/02 , C07K5/10 , C07K7/08 , C07K15/28 , G01N33/50
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公开(公告)号:NZ241480A
公开(公告)日:1993-09-27
申请号:NZ24148092
申请日:1992-01-31
Applicant: COR THERAPEUTICS INC , ESCORBEDO JAIME A , WILLIAMS LEWIS T
Inventor: WOLF DAVID , TOMLINSON JAMES E , FRETTO LARRY J , GIESE NEILL A , ESCORBEDO JAIME A
IPC: A61K39/395 , A61K38/00 , C07K7/04 , C07K14/00 , C07K14/705 , C07K14/71 , C07K16/00 , C07K16/28 , C12N5/10 , C12N15/02 , C12N15/09 , C12N15/12 , C12P21/02 , C12P21/08 , C12R1/91 , G01N33/53 , G01N33/566 , C12N15/63 , C07K15/06 , C07K15/28 , C07H21/04 , G01N33/50
Abstract: Defined constructs of modified human platelet-derived growth factor receptor polypeptides are provided. Extracellular region domain structures are identified and modifications and combinatorial rearrangements of the receptor segments are provided. Both cell bound and soluble forms of modified segments are made available, as are methods for assays using them, allowing for screening of ligand analogues.
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公开(公告)号:AU636159B2
公开(公告)日:1993-04-22
申请号:AU6036990
申请日:1990-06-15
Applicant: COR THERAPEUTICS, INC.
Inventor: ROBERT M. SCARBOROUGH , DAVID LAWRENCE WOLF , ISRAEL F. CHARO
IPC: A61K38/00 , A61K35/58 , A61K38/02 , A61K38/12 , A61K38/17 , A61K38/36 , A61K38/57 , A61P7/02 , C07K1/14 , C07K1/20 , C07K7/00 , C07K7/06 , C07K7/64 , C07K14/00 , C07K14/435 , C07K14/46 , C07K14/745 , C07K14/75 , C07K14/755 , C07K14/78 , C12N1/21 , C12N15/09 , C12N15/12 , C12P21/00 , C12P21/02 , C12Q1/56 , C12R1/19 , G01N33/86
Abstract: An assay for screening snake venom for the presence or absence of platelet aggregation inhibitors (PAIs) based on specific receptor binding is described. Using this assay, the identification and characterization of PAIs in a wide range of snake venom samples was accomplished. The isolated and purified PAI from several of these active snake venoms is described and characterized. In addition, PAIs lacking the Arg-Gly-Asp (RGD) adhesion sequence but containing K*-(G/Sar)-D wherein K* is a modified lysyl residue of the formula R 2 N(CH2)4CHNHCO- wherein each R is independently H, alkyl(1-6C) or at most one R is R -C=NR wherein R is H, alkyl(1-6C), phenyl or benzyl, or is NR 2 in which each R is independently H or alkyl(1-6C) and R is H, alkyl(1-6C), phenyl or benzyl, or R -C=NR is a radical selected from the group consisting of: where m is an integer of 2-3, and each R is independently H or alkyl(1-6C); and wherein one or two (CH2) may be replaced by O or S provided said O or S is not adjacent to another heteroatom are prepared and shown to specifically inhibit the binding of fibrinogen or von Willebrand Factor to GP IIb-IIIa.
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公开(公告)号:AU1456892A
公开(公告)日:1992-09-15
申请号:AU1456892
申请日:1992-02-19
Applicant: COR THERAPEUTICS INC , UNIV CALIFORNIA
Inventor: COUGHLIN SHAUN R , SCARBOROUGH ROBERT M JR
IPC: A61K38/00 , A61K39/00 , A61K39/395 , A61K49/00 , A61P7/02 , A61P9/08 , A61P9/10 , A61P43/00 , C07K7/02 , C07K7/06 , C07K14/705 , C07K16/00 , C07K16/28 , C12N1/15 , C12N1/19 , C12N1/21 , C12N5/10 , C12N9/74 , C12N15/09 , C12N15/12 , C12P21/02 , C12P21/08 , C12R1/19 , G01N33/53 , C07K7/00 , C07K13/00 , C12N15/63
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