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1.Pharmaceutical composition for treatment of central nervous system disorder 审中-公开
Title translation: 用于治疗中枢神经系统疾病的药物组合物公开(公告)号:JP2013209377A
公开(公告)日:2013-10-10
申请号:JP2013086296
申请日:2013-04-17
Applicant: Abbott Lab , アボット・ラボラトリーズAbbott Laboratories
Inventor: BROWMAN KAITLIN E , ROHDE JEFFREY , JACOBSON PEER B , BRUNE MICHAEL E , RUETER LYNNE E , WANG JIAHONG , LINK JAMES T , ROBERT S BITNER , CHEN YIXIAN , DINGES JURGEN , DRESCHER KARLA , JAE HWAN-SOO , KURUKULASURIYA RAVI , MADAR DAVID J , PATEL JYOTI , PLIUSHCHEV MARINA , SHUAI QI , SORENSEN BRYAN , WICKE KARSTEN , WINN MARTIN , WODKA DARIUSZ , YEH VINCE , YONG HONG
CPC classification number: C07D403/12 , A61K31/44 , A61K31/495 , C07D207/267 , C07D401/12 , C07D401/14
Abstract: PROBLEM TO BE SOLVED: To provide a therapeutic agent for a patient suffering from disorders and deficits of the central nervous system associated with diabetes, associated with aging and neurodegeneration, comprising attention deficit disorder in general, attention deficit hyperactivity disorder (ADHD), Alzheimer's disease (AD), mild cognitive impairment, senile dementia, AIDS dementia, neurodegeneration, and schizophrenia.SOLUTION: A pharmaceutical composition includes an effective amount of a selective inhibitor of the 11-β-hydroxysteroid dehydrogenase type 1 enzyme activity represented by formula.
Abstract translation: 要解决的问题:为患有与衰老和神经变性相关的糖尿病中枢神经系统紊乱和缺陷的患者提供治疗剂,其包括注意力缺陷障碍,注意力缺陷多动障碍(ADHD),阿尔茨海默病 (AD),轻度认知障碍,老年性痴呆,艾滋病痴呆,神经变性和精神分裂症。解决方案:药物组合物包括有效量的由式表示的11-&bgr-羟基类固醇脱氢酶1型酶活性的选择性抑制剂。
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2.Pharmaceutical composition for treating central-nervous-system disorder 有权
Title translation: 用于治疗中枢神经系统疾病的药物组合物公开(公告)号:JP2009046464A
公开(公告)日:2009-03-05
申请号:JP2007241117
申请日:2007-09-18
Applicant: Abbott Lab , アボット・ラボラトリーズAbbott Laboratories
Inventor: BROWMAN KAITLIN E , ROHDE JEFFREY , JACOBSON PEER B , BRUNE MICHAEL E , RUETER LYNNE E , WANG JIAHONG , LINK JAMES T , ROBERT S BITNER , CHEN YIXIAN , DINGES JURGEN , DRESCHER KARLA , JAE HWAN-SOO , KURUKULASURIYA RAVI , MADAR DAVID J , PATEL JYOTI , PLIUSHCHEV MARINA , SHUAI QI , SORENSEN BRYAN , WICKE KARSTEN , WINN MARTIN , WODKA DARIUSZ , YEH VINCE , YONG HONG
IPC: A61K31/165 , A61K31/496 , A61P25/00 , A61P25/18 , A61P25/22 , A61P25/24 , A61P25/28 , A61P43/00 , C07D213/74
CPC classification number: C07D403/12 , A61K31/44 , A61K31/495 , C07D207/267 , C07D401/12 , C07D401/14
Abstract: PROBLEM TO BE SOLVED: To provide a pharmaceutical composition for treating patients with diabetes-, aging- and neurodegeneration-related central-nervous-system disorders and deletions including ordinary attention-deficit disorders, attention-deficit hyperactivity disorders (ADHD), Alzheimer's disease (AD), mild cognitive damage, senile dementia, AIDS dementia, neurodegeneration and schizophrenia. SOLUTION: The pharmaceutical composition for treating glucocorticoid-related central-nervous-system disorders contains a selective inhibitor for 11-β-hydroxysteroid dehydrogenase 1-type enzyme activity. COPYRIGHT: (C)2009,JPO&INPIT
Abstract translation: 待解决的问题:提供一种用于治疗患有糖尿病,老化和神经变性相关的中枢神经系统疾病和缺失的药物组合物,包括普通注意力缺陷障碍,注意力缺陷多动障碍(ADHD) 阿尔茨海默病(AD),轻度认知损伤,老年痴呆,艾滋病痴呆,神经变性和精神分裂症。 解决方案:用于治疗糖皮质激素相关中枢神经系统疾病的药物组合物含有11-β-羟基类固醇脱氢酶1型酶活性的选择性抑制剂。 版权所有(C)2009,JPO&INPIT
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3.CELL ADHESION-INHIBITING ANTIINFLAMMATORY AND IMMUNE-SUPPRESSIVE COMPOUNDS 审中-公开
Title translation: 细胞粘附抑制抗炎和免疫抑制化合物公开(公告)号:WO0039081A3
公开(公告)日:2001-05-25
申请号:PCT/US9931162
申请日:1999-12-29
Applicant: ABBOTT LAB
Inventor: LINK JAMES , LIU GANG , PEI ZHONGHUA , VON GELDERN TOM , WINN MARTIN , XIN ZHILI , BOYD STEVEN A , JAE HWAN-SOO , LYNCH JOHN K , ZHU GUI-DONG , FREEMAN JENNIFER C , GUNAWARDANA INDRANI W , STAEGER MICHAEL A
IPC: C07D295/12 , A61K31/16 , A61K31/164 , A61K31/165 , A61K31/167 , A61K31/40 , A61K31/4015 , A61K31/404 , A61K31/407 , A61K31/417 , A61K31/438 , A61K31/44 , A61K31/443 , A61K31/445 , A61K31/4465 , A61K31/4468 , A61K31/45 , A61K31/453 , A61K31/454 , A61K31/472 , A61K31/495 , A61K31/496 , A61K31/506 , A61K31/5375 , A61K31/5377 , A61K31/54 , A61K31/541 , A61P29/00 , A61P37/02 , C07C323/00 , C07C323/62 , C07C323/63 , C07D207/08 , C07D207/09 , C07D207/12 , C07D207/14 , C07D207/20 , C07D207/22 , C07D207/26 , C07D207/263 , C07D207/27 , C07D207/273 , C07D207/34 , C07D207/36 , C07D209/08 , C07D209/12 , C07D209/14 , C07D209/18 , C07D211/22 , C07D211/26 , C07D211/42 , C07D211/44 , C07D211/46 , C07D211/54 , C07D211/60 , C07D211/62 , C07D211/66 , C07D211/74 , C07D213/74 , C07D213/75 , C07D213/81 , C07D213/82 , C07D215/04 , C07D215/36 , C07D217/06 , C07D233/61 , C07D235/26 , C07D239/42 , C07D241/04 , C07D241/18 , C07D241/24 , C07D243/08 , C07D265/30 , C07D295/13 , C07D295/16 , C07D295/18 , C07D295/185 , C07D295/205 , C07D295/215 , C07D295/26 , C07D295/32 , C07D307/52 , C07D307/68 , C07D317/58 , C07D317/62 , C07D319/18 , C07D319/20 , C07D401/04 , C07D401/06 , C07D401/12 , C07D403/04 , C07D403/12 , C07D405/06 , C07D405/12 , C07D405/14 , C07D411/04 , C07D413/04 , C07D413/12 , C07D413/14 , C07D417/12 , C07D471/10 , C07D487/08 , C07D491/10 , A61K31/10 , A61K31/33 , C07D295/20
CPC classification number: C07D207/27 , C07C323/62 , C07C2601/02 , C07C2601/04 , C07C2601/08 , C07D207/09 , C07D207/14 , C07D207/20 , C07D207/22 , C07D207/26 , C07D209/08 , C07D209/18 , C07D211/22 , C07D211/26 , C07D211/42 , C07D211/46 , C07D211/54 , C07D211/60 , C07D211/62 , C07D211/74 , C07D213/74 , C07D213/75 , C07D213/81 , C07D215/36 , C07D217/06 , C07D235/26 , C07D239/42 , C07D241/04 , C07D241/24 , C07D243/08 , C07D265/30 , C07D295/13 , C07D295/185 , C07D295/205 , C07D295/215 , C07D295/26 , C07D295/32 , C07D307/52 , C07D307/68 , C07D317/58 , C07D317/62 , C07D319/18 , C07D319/20 , C07D401/04 , C07D401/06 , C07D401/12 , C07D403/12 , C07D405/12 , C07D405/14 , C07D413/04 , C07D413/14 , C07D471/10 , C07D487/08 , C07D491/10
Abstract: The present invention relates to novel cinnamide compounds that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions containing these compounds, and to methods of inhibiting inflammation or suppressing immune response in a mammal.
Abstract translation: 本发明涉及可用于治疗炎症和免疫疾病的新颖的肉桂酰胺化合物,含有这些化合物的药物组合物,以及抑制哺乳动物炎症或抑制免疫反应的方法。
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公开(公告)号:WO2009026422A2
公开(公告)日:2009-02-26
申请号:PCT/US2008073830
申请日:2008-08-21
Applicant: ABBOTT LAB , BITNER R SCOTT , BROWMAN KAITLIN E , BRUNE MICHAEL E , CHEN YIXIAN , DINGES JURGEN , DRESCHER KARLA , JACOBSON PEER , JAE HWAN-SOO , KURUKULASURIYA RAVI , LINK JAMES T , MADAR DAVID J , PATEL JYOTI R , PLIUSHCHEV MARINA A , ROHDE JEFFREY J , RUETER LYNNE E , SHUAI QI , SORENSEN BRYAN K , WANG JIAHONG , WICKE KARSTEN M , WINN MARTIN , WODKA DARIUSZ , YEH VINCE , YONG HONG
Inventor: BITNER R SCOTT , BROWMAN KAITLIN E , BRUNE MICHAEL E , CHEN YIXIAN , DINGES JURGEN , DRESCHER KARLA , JACOBSON PEER , JAE HWAN-SOO , KURUKULASURIYA RAVI , LINK JAMES T , MADAR DAVID J , PATEL JYOTI R , PLIUSHCHEV MARINA A , ROHDE JEFFREY J , RUETER LYNNE E , SHUAI QI , SORENSEN BRYAN K , WANG JIAHONG , WICKE KARSTEN M , WINN MARTIN , WODKA DARIUSZ , YEH VINCE , YONG HONG
IPC: A61K31/495 , A61K31/44
CPC classification number: C07D403/12 , A61K31/44 , A61K31/495 , C07D207/267 , C07D401/12 , C07D401/14
Abstract: A method for treating a patient suffering from disorders and deficits of the central nervous system associated with diabetes, associated with aging and neurodegeneration, comprising attention deficit disorder in general, attention deficit hyperactivity disorder (ADHD), Alzheimer's disease (AD), mild cognitive impairment, senile dementia, AIDS dementia, neurodegeneration, depression, and schizophrenia, comprising administering to a patient in need of such treatment an effective amount of a selective inhibitor of the 11-ß-hydroxysteroid dehydrogenase Type 1 enzyme activity.
Abstract translation: 用于治疗患有与糖尿病相关的中枢神经系统与衰老和神经变性有关的障碍和缺陷的患者的方法,其包括一般的注意力缺陷障碍,注意力缺陷多动障碍(ADHD),阿尔茨海默病(AD),轻度认知障碍 老年痴呆症,艾滋病痴呆症,神经变性,抑郁症和精神分裂症的方法,包括向需要这种治疗的患者施用有效量的11-β-羟基类固醇脱氢酶1型酶活性的选择性抑制剂。
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5.PYRROLIDINE-3-CARBOXYLIC ACID DERIVATIVES AND THEIR USE AS ENDOTHELIN ANTAGONISTS 审中-公开
Title translation: 吡咯烷-3-羧酸衍生物及其作为内皮素拮抗剂的用途公开(公告)号:WO9906397A3
公开(公告)日:1999-12-09
申请号:PCT/US9815479
申请日:1998-07-27
Applicant: ABBOTT LAB
Inventor: WINN MARTIN , BOYD STEVEN A , HUTCHINS CHARLES W , JAE HWAN-SOO , TASKER ANDREW S , GELDERN THOMAS W VON , KESTER JEFFREY A , SORENSEN BRYAN K , SZCZEPANKIEWICZ BRUCE G , HENRY KENNETH J , LIU GANG , WITTENBERGER STEVEN J , KING STEVEN A
IPC: C07D491/048 , A61K31/40 , A61K31/41 , A61K31/423 , A61K31/435 , A61K31/4355 , A61K31/495 , A61K31/506 , A61K31/535 , A61K31/55 , A61P1/00 , A61P1/04 , A61P7/02 , A61P9/08 , A61P9/10 , A61P9/12 , A61P9/14 , A61P13/08 , A61P13/12 , A61P21/00 , A61P21/04 , A61P25/06 , A61P35/00 , A61P43/00 , C07D207/16 , C07D207/26 , C07D207/27 , C07D403/04 , C07D405/00 , C07D405/04 , C07D405/14 , C07D413/14 , C07D417/14 , C07D491/056
CPC classification number: C07D207/27 , C07D207/16 , C07D403/04 , C07D405/04 , C07D405/14 , C07D413/14 , C07D417/14
Abstract: A compound of formula (I), or a pharmaceutically acceptable salt thereof, is disclosed, as well as processes for and intermediates in the preparation thereof, and a method of antagonizing endothelin.
Abstract translation: 公开了式(I)化合物或其药学上可接受的盐,以及其制备方法和中间体,以及拮抗内皮素的方法。
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公开(公告)号:AU781355B2
公开(公告)日:2005-05-19
申请号:AU2984101
申请日:2001-03-23
Applicant: ABBOTT LAB
Inventor: WINN MARTIN , BOYD STEVEN A , HUTCHINS CHARLES W , JAE HWAN-SOO , TASKER ANDREW , GELDERN THOMAS W VON , KESTER JEFFREY A , SORENSEN BRYAN K , SZCZEPANKIEWICZ BRUCE G , HENRY KENNETH J JR , LIU GANG , WITTENBERGER STEVEN J , KING STEVEN A
IPC: A61K31/40 , C07D207/16 , C07D401/04 , C07D405/04 , C07D405/14 , C07F9/572 , C07F9/59
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公开(公告)号:DE69527072T2
公开(公告)日:2003-02-13
申请号:DE69527072
申请日:1995-08-04
Applicant: ABBOTT LAB
Inventor: WINN MARTIN , BOYD A , HUTCHINS W , JAE HWAN-SOO , TASKER S , VONGELDERN W , KESTER A , SORENSEN K
IPC: A61K31/40 , A61K31/402 , A61K31/4025 , A61K31/403 , A61K31/41 , A61K31/415 , A61K31/422 , A61K31/435 , A61K31/44 , A61K31/4439 , A61K31/445 , A61K31/454 , A61K31/47 , A61K31/505 , A61K31/506 , A61K31/535 , A61K31/5377 , A61P9/00 , A61P9/04 , A61P9/08 , A61P9/10 , A61P9/12 , A61P29/00 , A61P35/00 , A61P43/00 , C07D20060101 , C07D207/14 , C07D207/16 , C07D401/04 , C07D403/04 , C07D405/04 , C07D405/10 , C07D405/14 , C07D413/04 , C07D419/04 , C07D471/04 , C07F9/572 , C07F9/59
Abstract: Processes for preparing endothelin antagonists of formula (I) and pharmaceutically acceptable salts thereof and processes for preparing intermediates thereof.
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公开(公告)号:HRP20010776A2
公开(公告)日:2002-12-31
申请号:HRP20010776
申请日:2001-10-23
Applicant: ABBOTT LAB
Inventor: LINK JAMES , LIU GANG , PEI ZHONGHUA , GELDERN THOMAS W VON , WINN MARTIN , XIN ZHILI , WANG SHELDON , BOYD STEVEN A , ZHU GUI-DONG , FREEMAN JENNIFER C , GUNAWARDANA INDRANI W , STAEGER MICHAEL A , JAE HWAN-SOO , LYNCH JOHN K
IPC: C07D243/08 , A61K20060101 , A61K31/10 , A61K31/165 , A61K31/33 , A61K31/40 , A61K31/4015 , A61K31/41 , A61K31/417 , A61K31/438 , A61K31/44 , A61K31/4427 , A61K31/445 , A61K31/4468 , A61K31/451 , A61K31/453 , A61K31/454 , A61K31/4545 , A61K31/472 , A61K31/496 , A61K31/4965 , A61K31/506 , A61K31/5375 , A61K31/5377 , A61K31/54 , A61K31/541 , A61K31/55 , A61K31/551 , A61P20060101 , A61P29/00 , A61P37/06 , C07C20060101 , C07C323/60 , C07C323/62 , C07D20060101 , C07D205/04 , C07D207/09 , C07D207/12 , C07D207/14 , C07D207/16 , C07D207/26 , C07D207/27 , C07D207/273 , C07D209/08 , C07D209/12 , C07D211/20 , C07D211/22 , C07D211/46 , C07D211/60 , C07D211/62 , C07D211/64 , C07D211/66 , C07D211/70 , C07D213/40 , C07D213/74 , C07D213/81 , C07D215/24 , C07D217/02 , C07D217/04 , C07D217/06 , C07D233/61 , C07D239/42 , C07D241/04 , C07D241/24 , C07D257/04 , C07D279/12 , C07D295/18 , C07D295/185 , C07D295/20 , C07D295/205 , C07D295/22 , C07D295/26 , C07D307/24 , C07D307/52 , C07D307/68 , C07D317/58 , C07D317/66 , C07D319/18 , C07D401/04 , C07D401/12 , C07D405/12 , C07D417/12 , C07D471/20 , C07D487/04 , C07D491/113 , C07D521/00
Abstract: The present invention relates to cinnamide compounds of formula (I), in which at least one of R1 to R5 is a "cis-cinnamide" (a) or a "trans-cinnamide" (b) and the other variables are as defined in the claims, that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions containing these compounds and to methods of inhibiting inflammation or suppressing immune response in a mammal.
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公开(公告)号:NZ502395A
公开(公告)日:2002-08-28
申请号:NZ50239598
申请日:1998-07-27
Applicant: ABBOTT LAB
Inventor: KING STEVEN A , WITTENBERGER STEVEN J , WINN MARTIN , BOYD STEVEN A , HUTCHINS CHARLES W , JAE HWAN-SOO , TASKER ANDREW S , GELDERN THOMAS W VON , KESTER JEFFREY A , SORENSEN BRYAN K , SZCZEPANKIEWICZ BRUCE G , HENRY KENNETH J , LIU GANG
IPC: C07D491/048 , A61K31/40 , A61K31/41 , A61K31/423 , A61K31/435 , A61K31/4355 , A61K31/495 , A61K31/506 , A61K31/535 , A61K31/55 , A61P1/00 , A61P1/04 , A61P7/02 , A61P9/08 , A61P9/10 , A61P9/12 , A61P9/14 , A61P13/08 , A61P13/12 , A61P21/00 , A61P21/04 , A61P25/06 , A61P35/00 , A61P43/00 , C07D207/16 , C07D207/26 , C07D207/27 , C07D403/04 , C07D405/00 , C07D405/04 , C07D405/14 , C07D413/14 , C07D417/14 , C07D491/056
Abstract: [2S,3R,4S]-2-(2,2-Dimethylpentyl)-4-(7-methoxy-1,3-benzodioxol-5-yl)-1 -(N,N-di-(n-butyl)-aminocarbonylmethyl)-pyrrolidine-3-carboxylic acid and [2S,3R,4S]-2-(4-methoxyphenyl)-4-(1,3-benzodioxol-5-yl)-1-[(N-butyl-N- (4-dimethylaminobutyl)-amino)carbonylmethyl]-pyrrolidine-3-carboxylic acid, a pharmaceutically acceptable salt thereof and the pharmaceutical composition thereof are useful for antagonizing the endothelin activity.
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公开(公告)号:HU0200222A2
公开(公告)日:2002-06-29
申请号:HU0200222
申请日:1999-12-29
Applicant: ABBOTT LAB
Inventor: BOYD STEVEN A , FREEMAN JENNIFER C , VON GELDERN TOM , GUNAWARDANA INDRANI W , JAE HWAN-SOO , LINK JAMES , LIU GANG , LYNCH JOHN K , PEI ZHONGHUA , STAEGER MICHAEL A , WINN MARTIN , XIN ZHILI , ZHU GUI-DONG
IPC: C07D295/12 , A61K31/16 , A61K31/164 , A61K31/165 , A61K31/167 , A61K31/40 , A61K31/4015 , A61K31/404 , A61K31/407 , A61K31/417 , A61K31/438 , A61K31/44 , A61K31/443 , A61K31/445 , A61K31/4465 , A61K31/4468 , A61K31/45 , A61K31/453 , A61K31/454 , A61K31/472 , A61K31/495 , A61K31/496 , A61K31/506 , A61K31/5375 , A61K31/5377 , A61K31/54 , A61K31/541 , A61P29/00 , A61P37/02 , C07C323/00 , C07C323/62 , C07C323/63 , C07D207/08 , C07D207/09 , C07D207/12 , C07D207/14 , C07D207/20 , C07D207/22 , C07D207/26 , C07D207/263 , C07D207/27 , C07D207/273 , C07D207/34 , C07D207/36 , C07D209/08 , C07D209/12 , C07D209/14 , C07D209/18 , C07D211/22 , C07D211/26 , C07D211/42 , C07D211/44 , C07D211/46 , C07D211/54 , C07D211/60 , C07D211/62 , C07D211/66 , C07D211/74 , C07D213/74 , C07D213/75 , C07D213/81 , C07D213/82 , C07D215/04 , C07D215/36 , C07D217/06 , C07D233/61 , C07D235/26 , C07D239/42 , C07D241/04 , C07D241/18 , C07D241/24 , C07D243/08 , C07D265/30 , C07D295/13 , C07D295/16 , C07D295/18 , C07D295/185 , C07D295/205 , C07D295/215 , C07D295/26 , C07D295/32 , C07D307/52 , C07D307/68 , C07D317/58 , C07D317/62 , C07D319/18 , C07D319/20 , C07D401/04 , C07D401/06 , C07D401/12 , C07D403/04 , C07D403/12 , C07D405/06 , C07D405/12 , C07D405/14 , C07D411/04 , C07D413/04 , C07D413/12 , C07D413/14 , C07D417/12 , C07D471/10 , C07D487/08 , C07D491/10
Abstract: The present invention relates to novel cinnamide compounds that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions comprising these compounds, and to methods of inhibiting inflammation or suppressing immune response in a mammal.
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