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公开(公告)号:AT317382T
公开(公告)日:2006-02-15
申请号:AT01971244
申请日:2001-09-20
Applicant: ABBOTT LAB
Inventor: MCCLELLAN WILLIAM , OOST THORSTEN , BRUNCKO MILAN , WANG XILU , AUGERI DAVID J , BAUMEISTER STEVEN A , DICKMAN DANIEL A , DING HONG , DINGES JURGEN , FESIK STEPHEN W , HAJDUK PHILIP J , KUNZER AARON R , NETTESHEIM DAVID G , PETROS ANDREW M , ROSENBERG SAUL H , SHEN WANG , THOMAS SHEELA A , WENDT MICHAEL D
IPC: A61K31/18 , A61K31/428 , A61K31/63 , A61K31/635 , A61P9/10 , A61P25/16 , A61P25/28 , A61P29/00 , A61P31/12 , A61P31/18 , A61P35/00 , A61P37/02 , C07C311/46 , C07C311/51 , C07C317/28 , C07C323/12 , C07C323/17 , C07C323/25 , C07C323/30 , C07C323/37 , C07C323/43 , C07C323/44 , C07C323/48 , C07C323/58 , C07C323/60 , C07D203/10 , C07D205/04 , C07D205/12 , C07D207/09 , C07D207/24 , C07D207/40 , C07D207/404 , C07D209/08 , C07D209/52 , C07D209/54 , C07D209/96 , C07D211/14 , C07D211/44 , C07D211/70 , C07D211/74 , C07D213/56 , C07D213/61 , C07D213/64 , C07D213/69 , C07D213/70 , C07D213/71 , C07D215/14 , C07D215/22 , C07D215/227 , C07D215/38 , C07D215/48 , C07D217/04 , C07D221/20 , C07D231/12 , C07D233/60 , C07D235/08 , C07D235/26 , C07D241/08 , C07D241/16 , C07D249/04 , C07D263/32 , C07D263/56 , C07D263/58 , C07D277/62 , C07D277/64 , C07D295/13 , C07D295/155 , C07D295/16 , C07D295/185 , C07D295/20 , C07D295/205 , C07D295/215 , C07D295/26 , C07D307/14 , C07D317/54 , C07D333/28 , C07D333/68 , C07D333/70 , C07D401/06 , C07D401/12 , C07D405/04 , C07D405/06 , C07D417/12 , C07D451/02 , C07D491/107
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公开(公告)号:ES2215296T3
公开(公告)日:2004-10-01
申请号:ES98918461
申请日:1998-04-17
Applicant: ABBOTT LAB
Inventor: FESIK STEPHEN W , HAJDUK PHILIP J , OLEJNICZAK EDWARD T
IPC: G01R33/32 , A61K45/00 , C07K14/705 , C12N9/00 , C12Q1/68 , G01N24/08 , G01N33/15 , G01N33/50 , G01N33/53 , G01N33/68 , G01R33/44
Abstract: The present invention provides a process for identifying compounds which bind to a specific target molecule. The process comprises the steps of: a) generating a first T2- or diffusion-filtered proton spectrum of one or a mixture of chemical compounds; b) exposing one or a mixture of chemical compounds to the target molecule; c) generating a second T2- or diffusion-filtered proton spectrum of one or a mixture of chemical compounds that has been exposed the target molecule in step (b); and d) comparing said first and second T2- or diffusion-filtered proton spectra to determine differences between said first and said second spectra, the differences identifying the presence of one or more compounds that are ligands which have bound to the target molecule.
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公开(公告)号:PT975954E
公开(公告)日:2004-06-30
申请号:PT98918461
申请日:1998-04-17
Applicant: ABBOTT LAB
Inventor: FESIK STEPHEN W , HAJDUK PHILIP J , ONEJNICZAK EDWARD T
IPC: G01R33/32 , A61K45/00 , C07K14/705 , C12N9/00 , C12Q1/68 , G01N24/08 , G01N33/15 , G01N33/50 , G01N33/53 , G01N33/68 , G01R33/44
Abstract: The present invention provides a process for identifying compounds which bind to a specific target molecule. The process comprises the steps of: a) generating a first T2- or diffusion-filtered proton spectrum of one or a mixture of chemical compounds; b) exposing one or a mixture of chemical compounds to the target molecule; c) generating a second T2- or diffusion-filtered proton spectrum of one or a mixture of chemical compounds that has been exposed the target molecule in step (b); and d) comparing said first and second T2- or diffusion-filtered proton spectra to determine differences between said first and said second spectra, the differences identifying the presence of one or more compounds that are ligands which have bound to the target molecule.
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14.
公开(公告)号:AU772620B2
公开(公告)日:2004-05-06
申请号:AU2925002
申请日:2002-03-28
Applicant: ABBOTT LAB
Inventor: FESIK STEPHEN W , HAJDUK PHILIP J , OLEJNICZAK EDWARD T
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公开(公告)号:CA2423103A1
公开(公告)日:2002-03-28
申请号:CA2423103
申请日:2001-09-20
Applicant: ABBOTT LAB
Inventor: THOMAS SHEELA A , PETROS ANDREW M , DING HONG , BAUMEISTER STEVEN A , AUGERI DAVID J , DICKMAN DANIEL A , MCCLELLAN WILLIAM , SHEN WANG , FESIK STEPHEN W , WENDT MICHAEL D , WANG XILU , BRUNCKO MILAN , NETTESHEIM DAVID G , KUNZER AARON R , DINGES JURGEN , ROSENBERG SAUL H , HAJDUK PHILIP J , OOST THORSTEN
IPC: A61K31/18 , A61K31/428 , A61K31/63 , A61K31/635 , A61P9/10 , A61P25/16 , A61P25/28 , A61P29/00 , A61P31/12 , A61P31/18 , A61P35/00 , A61P37/02 , C07C311/46 , C07C311/51 , C07C317/28 , C07C323/12 , C07C323/17 , C07C323/25 , C07C323/30 , C07C323/37 , C07C323/43 , C07C323/44 , C07C323/48 , C07C323/58 , C07C323/60 , C07D203/10 , C07D205/04 , C07D205/12 , C07D207/09 , C07D207/24 , C07D207/40 , C07D207/404 , C07D209/08 , C07D209/52 , C07D209/54 , C07D209/96 , C07D211/14 , C07D211/44 , C07D211/70 , C07D211/74 , C07D213/56 , C07D213/61 , C07D213/64 , C07D213/69 , C07D213/70 , C07D213/71 , C07D215/14 , C07D215/22 , C07D215/227 , C07D215/38 , C07D215/48 , C07D217/04 , C07D221/20 , C07D231/12 , C07D233/60 , C07D235/08 , C07D235/26 , C07D241/08 , C07D241/16 , C07D249/04 , C07D263/32 , C07D263/56 , C07D263/58 , C07D277/62 , C07D277/64 , C07D295/13 , C07D295/155 , C07D295/16 , C07D295/185 , C07D295/20 , C07D295/205 , C07D295/215 , C07D295/26 , C07D307/14 , C07D317/54 , C07D333/28 , C07D333/68 , C07D333/70 , C07D401/06 , C07D401/12 , C07D405/04 , C07D405/06 , C07D417/12 , C07D451/02 , C07D491/107 , C07D295/14 , C07D317/58
Abstract: N-Benzoyl arylsulfonamides having the formula (I) are BCL-Xl inhibitors and are useful for promoting apoptosis. Also disclosed are BCL-Xl inhibiting compositions and methods of promoting apoptosis in a mammal.
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公开(公告)号:PT870197E
公开(公告)日:2001-11-30
申请号:PT96939709
申请日:1996-11-13
Applicant: ABBOTT LAB
Inventor: FESIK STEPHEN W , ONEJNICZAK EDWARD T , HAJDUK PHILIP J
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公开(公告)号:PT866967E
公开(公告)日:2000-04-28
申请号:PT96940448
申请日:1996-11-13
Applicant: ABBOTT LAB
Inventor: FESIK STEPHEN W , HAJDUK PHILIP J
IPC: G01R33/465 , C12Q1/00 , G01N20060101 , G01N24/08 , G01N33/15 , G01N33/50 , G01N33/53 , G01N33/542 , G01N33/566 , G01N33/58 , G01N33/68
Abstract: A method for designing and forming a ligand which binds to a specific target molecule comprises the steps of: (a) identifying a first ligand moiety that binds to the target molecule using two-dimensional N/ H NMR correlation spectroscopy; (b) identifying subsequent ligand moieties that bind to the target molecule using two-dimensional N/ H NMR correlation spectroscopy; (c) forming a complex of the first and subsequent ligand moieties to the target molecule; (d) determining the three-dimensional structure of the complex and, thus, the spatial orientation of the first and subsequent ligand moieties on the target molecule; and (e) linking the first and subsequent ligand moieties to form a new ligand to maintain the spatial orientation of the ligand moieties.
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公开(公告)号:CA2655561C
公开(公告)日:2014-10-21
申请号:CA2655561
申请日:2007-06-20
Applicant: ABBOTT LAB
Inventor: PENNING THOMAS D , THOMAS SHEELA A , HAJDUK PHILIP J , SAUER DARYL R , SARRIS KATHY , GIRANDA VINCENT L
IPC: C07D487/04 , A61K31/519
Abstract: The present invention relates to pyrazolo[1,5-a]quinazolin-5(4H)-ones of formula (I), (see formula I) their preparation, and their use as inhibitors of the enzyme poly(ADP-ribose)polymerase for the preparation of drugs."
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公开(公告)号:CA2365385C
公开(公告)日:2009-11-03
申请号:CA2365385
申请日:2000-03-21
Applicant: ABBOTT LAB
Inventor: FESIK STEPHEN W , HAJDUK PHILIP J
IPC: G01N24/08 , G01N24/12 , B08B9/04 , C07K1/13 , E21B37/04 , G01N33/483 , G01N33/50 , G01N33/53 , G01N33/542 , G01N33/566 , G01N33/58 , G01N33/68 , G01N33/94 , G01R33/46 , G01R33/465
Abstract: Methods of detecting binding of a putative ligand to a 13C-enriched target molecule, methods of screening for compounds which bind to a 13C-enriched target molecule, methods for calculating the dissociation constant of a ligand compound which binds to a 13C-enriched target molecule, and methods employed in the determination of the specific amino acids in a 13C-enriched target molecule affected by the binding of a ligand, as well as compounds identified by these screening methods, are provided herewith.
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公开(公告)号:CA2655561A1
公开(公告)日:2007-12-27
申请号:CA2655561
申请日:2007-06-20
Applicant: ABBOTT LAB
Inventor: GIRANDA VINCENT L , SARRIS KATHY , HAJDUK PHILIP J , THOMAS SHEELA A , SAUER DARYL R , PENNING THOMAS D
IPC: C07D487/04 , A61K31/519
Abstract: The present invention relates to 1H-benzimidazole-4-carboxamides of formu la (I), their preparation, and their use as inhibitors of the enzyme poly(AD P-ribose)polymerase for the preparation of drugs.
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