-
公开(公告)号:BG66151B1
公开(公告)日:2011-08-31
申请号:BG10730302
申请日:2002-11-21
Applicant: ABBOTT LAB
Inventor: SCHRIMPF MICHAEL , TIETJE KARIN , TOUPENCE RICHARD , JI JIANGUO , BASHA ANWER , BUNNELLE WILLIAM , DAANEN JEROME , PACE JENNIFER , SIPPY KEVIN
IPC: C07D231/14 , C07D231/54 , A61K31/454 , A61K31/4545 , A61P25/00 , A61P25/04 , A61P25/14 , A61P25/16 , A61P25/18 , A61P25/24 , A61P25/28 , A61P25/34 , C07D231/00 , C07D471/04 , C07D487/04
Abstract: Изобретениетосеотнасядодиазабициклопроизводнос формула (I)@илинеговифармацевтичноприемливисоли, спосоченитев описаниетозначенияназаместителите. Съединениетос формула (I) сеизползвазаселективенконтролнаневропреноснотоосвобождаванеприбозайники затретираненазависимитеотневропреноснотоосвобождаванеразстройства.
-
公开(公告)号:CZ302072B6
公开(公告)日:2010-09-29
申请号:CZ2008677
申请日:2001-04-27
Applicant: ABBOTT LAB
Inventor: SCHRIMPF MICHAEL R , TIETJE KARIN R , TOUPENCE RICHARD B , JI JIANGUO , BASHA ANWER , BUNNELLE WILLIAM H , DAANEN JEROME F , PACE JENNIFER M , SIPPY KEVIN B
IPC: C07D231/54 , C07D471/04 , A61K31/395 , A61K31/407 , A61K31/454 , A61K31/4545 , A61P1/00 , A61P13/00 , A61P15/10 , A61P25/00 , A61P25/04 , A61P25/06 , A61P25/08 , A61P25/14 , A61P25/16 , A61P25/18 , A61P25/20 , A61P25/22 , A61P25/24 , A61P25/28 , A61P25/34 , C07D487/04
Abstract: Diazabicyklické slouceniny obecného vzorce III, kde obecné symboly mají specifický význam, farmaceutické prípravky techto sloucenin a použití uvedených prípravku k regulaci synaptické transmise u savcu.
-
53.
公开(公告)号:NZ545789A
公开(公告)日:2010-03-26
申请号:NZ54578904
申请日:2004-09-17
Applicant: ABBOTT LAB
Inventor: BASHA ANWER , BUNNELLE WILLIAM H , DART MICHAEL J , GALLAGHER MEGAN E , JI JIANGUO , PACE JENNIFER M , RYTHER KEITH B , TIETJE KARIN R , MORTELL KATHLEEN H , NERSESIAN DIANA L , SCHRIMPF MICHAEL R , LI TAO
IPC: C07D471/04 , A61K31/435 , A61P25/00 , C07D471/08 , C07D487/04 , C07D487/08
Abstract: Disclosed are diazabicycloalkane derivatives of formula (I), wherein the substituents are defined as per the specification. The compounds are useful in treating conditions or disorders prevented by or ameliorated by alpha-7 nAChR ligands. Also disclosed are pharmaceutical compositions comprising compounds of formula (I) and the use such compounds and compositions for the preparation of medicaments for the treatment of such disorders.
-
公开(公告)号:CZ301324B6
公开(公告)日:2010-01-13
申请号:CZ20023765
申请日:2001-04-27
Applicant: ABBOTT LAB
Inventor: SCHRIMPF MICHAEL R , TIETJE KARIN R , TOUPENCE RICHARD B , JI JIANGUO , BASHA ANWER , BUNNELLE WILLIAM H , DAANEN JEROME F , PACE JENNIFER M , SIPPY KEVIN B
IPC: C07D231/54 , C07D471/04 , A61K31/397 , A61K31/407 , A61K31/437 , A61K31/4439 , A61K31/454 , A61K31/4545 , A61K31/4709 , A61P25/00 , A61P25/04 , A61P25/14 , A61P25/16 , A61P25/18 , A61P25/24 , A61P25/28 , A61P25/34 , C07D487/04
Abstract: Diazabicyklické deriváty obecného vzorce IV, farmaceutické prípravky techto sloucenin a použití pro výrobu léciva na selektivní regulaci uvolnování neurotransmiteru u savce.
-
公开(公告)号:CA2407094C
公开(公告)日:2009-11-17
申请号:CA2407094
申请日:2001-04-27
Applicant: ABBOTT LAB
Inventor: BASHA ANWER , SIPPY KEVIN B , SCHRIMPF MICHAEL R , BUNNELLE WILLIAM H , DAANEN JEROME F , TOUPENCE RICHARD B , JI JIANGUO , PACE JENNIFER M , TIETJE KARIN R
IPC: C07D231/54 , C07D487/08 , A61K31/395 , A61K31/454 , A61K31/4545 , A61P25/00 , A61P25/04 , A61P25/14 , A61P25/16 , A61P25/18 , A61P25/24 , A61P25/28 , A61P25/34 , C07D209/00 , C07D221/00 , C07D241/00 , C07D471/04 , C07D471/08 , C07D487/04 , C07D519/00
Abstract: Compounds of formula (I), pharmaceutical compositions of these compounds, and use of said compositions to control synaptic transmission in mammals (nicotinic acetylcholine receptor ligands).
-
公开(公告)号:SK286806B6
公开(公告)日:2009-05-07
申请号:SK5542001
申请日:1999-10-27
Applicant: ABBOTT LAB
Inventor: BLACK LAWRENCE A , BASHA ANWER , KORT MICHAEL E , LIU HUAQING , MCCARTY CATHERINE M , PATEL MEENA V , ROHDE JEFFREY J , COGHLAN MICHAEL J , STEWART ANDREW O
IPC: C07D237/00 , A61K31/00 , A61K31/50 , A61K31/501 , A61P19/00 , A61P19/02 , A61P25/04 , A61P29/00 , A61P31/00 , A61P35/00 , C07D237/14 , C07D237/16 , C07D237/18 , C07D237/22 , C07D401/00 , C07D401/04 , C07D401/06 , C07D401/12 , C07D403/00 , C07D403/04 , C07D403/10 , C07D403/12 , C07D405/00 , C07D405/04 , C07D405/12 , C07D409/00 , C07D409/04 , C07D409/06 , C07D409/12 , C07D413/00 , C07D413/04 , C07D413/12 , C07D417/00 , C07D417/06
Abstract: The present invention describes pyridazinone compounds of formula (I) which are cyclooxygenase inhibitors, and in particular, are selective inhibitors of cyclooxygenase-2 (Cox-2), Cox-2 is the inducible isoform associated with inflammation, as opposed to the constitutive isoform, cyclooxygenase-1 (Cox-1) which is an important "housekeeping" enzyme in many tissues, including the gastrointestinal (GI) tract and the kidneys. The selectively of these compounds for Cox-2 minimizes the unwanted GI and renal side-effects seen with currently marketed non-steroidal anti-inflammatory drugs.
-
公开(公告)号:MY137020A
公开(公告)日:2008-12-31
申请号:MYPI20011984
申请日:2001-04-26
Applicant: ABBOTT LAB
Inventor: SCHRIMPF MICHAEL R , TIETJE KARIN R , TOUPENCE RICHARD B , JI JIANGUO , BASHA ANWER , BUNNELLE WILLIAM H , DAANEN JEROME F , PACE JENNIFER MARY , SIPPY KEVIN B
IPC: C07D231/54 , A61K31/454 , A61K31/4545 , A61P25/00 , A61P25/04 , A61P25/14 , A61P25/16 , A61P25/18 , A61P25/24 , A61P25/28 , A61P25/34 , C07D471/04 , C07D487/04
Abstract: COMPOUNDS OF FORMULA I(I)@PHARMACEUTICAL COMPOSITIONS OF THESE COMPOUNDS, AND USE OF SAID COMPOSITIONS TO CONTROL SYNAPTIC TRANSMISSION IN MAMMALS.
-
公开(公告)号:BG65261B1
公开(公告)日:2007-10-31
申请号:BG10552301
申请日:2001-05-19
Applicant: ABBOTT LAB
Inventor: BLACK LAWRENCE , BASHA ANWER , KOLASA TEODOZYJ , KORT MICHAEL , LIU HUAQING , MCCARTY CATHERINE , PATEL MEENA , ROHDE JEFFREY , COGHLAN MICHAEL , STEWART ANDREW
IPC: C07D237/14 , A61K31/50 , A61K31/501 , A61P19/02 , A61P25/04 , A61P29/00 , A61P35/00 , C07D237/16 , C07D237/18 , C07D237/22 , C07D401/04 , C07D401/06 , C07D401/12 , C07D403/04 , C07D403/10 , C07D403/12 , C07D405/04 , C07D405/12 , C07D409/04 , C07D409/06 , C07D409/12 , C07D413/04 , C07D413/12 , C07D417/06
Abstract: The present invention describes pyridazoline compounds of formula which are cyclooxygenase (COX) inhibitors, and in particular, are selective inhibitors of cyclooxygenase-2 (COX-2). COX 2 is the inducible isoform associated with inflammation, as opposed to the constitutive isoform, cyclooxygenase-1 (COC-1) which is an important "housekeeping" enzyme in many tissues, including the gastrointestinal(GI) tract and the kidneys. The selectivity of these compounds for COX-2 minimizes the unwanted GI and renal side-effects seen with currently marked non-steroidal anti-inflammatory drugs (NSAIDs).
-
公开(公告)号:SA1077B1
公开(公告)日:2006-08-06
申请号:SA98190764
申请日:1998-11-16
Applicant: ABBOTT LAB
Inventor: BASHA ANWER , ROHDE JEFFREY J , KORT MICHAE L E , BLACK LAWRENCE A , LIU HUAQING , KOLASA TEODOZYJ , MCCARTY CATHERINE M , PATEL MINA V
IPC: C07D237/14 , C07D237/18 , C07D401/06 , C07D401/12 , C07D403/06 , C07D403/12 , C07D405/06 , C07D409/06 , C07D409/12 , C07D417/06
Abstract: الملخص: يصفالاختراعالراهنمركباتبيريدازينون pyridazinone وهيعبارةعنمثبطاتأنزيمالأكسجةالحلقية (سيكلوأكسجيناز) cyclooxygenase inhibitors (cox)،وبصفةخاصةهيعبارةعنمثبطاتانتقائية selective inhibitors لإنزيمالأكسجةالحلقية-٢ (2/cyclooxygenase-2 (COX؛و COX-2 هونظيرالشكلالقابلللحث inducible isoform المقترنبالالتهاب inflammation وهومعاكسلنظيرالشكلالأساسي constitutive isoform؛الذيهوعبارةعنأنزيمالأكسجةالحلقية- ١ (1-cyclooxygenase-l (COX وهوانزيمتهيين &"housekeeping&" enzyme) فيالعديدمنالأنسجة tissues؛بمافيذلكالقناةالهضمية gastrointestinal (GI) tract والكليتين kidneys. وتقللانتقائيةهذهالمركباتنحو -COX2 التأثيراتالجانبيةغيرالمرغوبةفيالقناةالهضميةوالكليتينالملاحظةعنداستخدامالعقاقيرالمضادةللالتهابغيرالستيرويدية -non-steroidal anti (inflammatory drugs (NSAIDs المسوقةحاليا
-
公开(公告)号:ES2249919T3
公开(公告)日:2006-04-01
申请号:ES99953259
申请日:1999-10-27
Applicant: ABBOTT LAB
Inventor: BLACK LAWRENCE A , BASHA ANWER , KOLASA TEODOZYJ , KORT MICHAEL E , LIU HUAQING , MCCARTY CATHERINE M
IPC: A61K31/50 , A61K31/501 , A61P19/02 , A61P25/04 , A61P29/00 , A61P35/00 , C07D237/14 , C07D237/16 , C07D237/18 , C07D237/22 , C07D401/04 , C07D401/06 , C07D401/12 , C07D403/04 , C07D403/10 , C07D403/12 , C07D405/04 , C07D405/12 , C07D409/04 , C07D409/06 , C07D409/12 , C07D413/04 , C07D413/12 , C07D417/06
Abstract: Un compuesto seleccionado entre el grupo compuesto por 2-(4-Fluorofenil)-4-(4-hidroxi-2-metil-1-butoxi)-5-[4-(metilsulfonil)fenil]-3(2H)-piridazinona; o una sal o éster farmacéuticamente aceptable de los mismos.
-
-
-
-
-
-
-
-
-