JP2000503304A5 - - Google Patents

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Publication number
JP2000503304A5
JP2000503304A5 JP1997525466A JP52546697A JP2000503304A5 JP 2000503304 A5 JP2000503304 A5 JP 2000503304A5 JP 1997525466 A JP1997525466 A JP 1997525466A JP 52546697 A JP52546697 A JP 52546697A JP 2000503304 A5 JP2000503304 A5 JP 2000503304A5
Authority
JP
Japan
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
JP1997525466A
Other languages
English (en)
Japanese (ja)
Other versions
JP2000503304A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US1997/000619 external-priority patent/WO1997025048A1/en
Publication of JP2000503304A publication Critical patent/JP2000503304A/ja
Publication of JP2000503304A5 publication Critical patent/JP2000503304A5/ja
Ceased legal-status Critical Current

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JP9525466A 1996-01-11 1997-01-10 新規シクロアルキル置換イミダゾール Ceased JP2000503304A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US1001096P 1996-01-11 1996-01-11
US60/010,010 1996-01-11
PCT/US1997/000619 WO1997025048A1 (en) 1996-01-11 1997-01-10 Novel cycloalkyl substituted imidazoles

Publications (2)

Publication Number Publication Date
JP2000503304A JP2000503304A (ja) 2000-03-21
JP2000503304A5 true JP2000503304A5 (ref) 2004-11-11

Family

ID=21743297

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9525466A Ceased JP2000503304A (ja) 1996-01-11 1997-01-10 新規シクロアルキル置換イミダゾール

Country Status (24)

Country Link
US (1) US6329526B1 (ref)
EP (1) EP0889726B1 (ref)
JP (1) JP2000503304A (ref)
CN (1) CN1213305A (ref)
AP (1) AP9700912A0 (ref)
AR (1) AR005434A1 (ref)
AT (1) ATE276248T1 (ref)
AU (1) AU715315B2 (ref)
BR (1) BR9708149A (ref)
CZ (1) CZ218198A3 (ref)
DE (1) DE69730704T2 (ref)
ES (1) ES2229335T3 (ref)
HU (1) HUP9901233A2 (ref)
ID (1) ID18759A (ref)
IL (1) IL125224A0 (ref)
MA (1) MA24055A1 (ref)
MX (1) MX9805628A (ref)
NO (1) NO983182L (ref)
NZ (1) NZ330889A (ref)
PL (1) PL327939A1 (ref)
TR (1) TR199801350T2 (ref)
UY (1) UY24434A1 (ref)
WO (1) WO1997025048A1 (ref)
ZA (1) ZA97173B (ref)

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US6239279B1 (en) 1998-12-16 2001-05-29 Smithkline Beecham Corporation Synthesis for 4-aryl-5-pyrimidine imidazole substituted derivatives
US6930101B1 (en) 1999-05-17 2005-08-16 The Regents Of The University Of California Thiazolopyrimidines useful as TNFα inhibitors
EP1223924A4 (en) * 1999-09-17 2004-07-14 Smithkline Beecham Corp USE OF CSAIDS AGAINST RHINOVIRUS INFECTION
EP1233951B1 (en) 1999-11-23 2005-06-01 SmithKline Beecham Corporation 3,4-dihydro-(1h)quinazolin-2-one compounds as csbp/p38 kinase inhibitors
US6759410B1 (en) 1999-11-23 2004-07-06 Smithline Beecham Corporation 3,4-dihydro-(1H)-quinazolin-2-ones and their use as CSBP/p38 kinase inhibitors
DE60023025T2 (de) 1999-11-23 2006-07-13 Smithkline Beecham Corp. 3,4-dihydro-(1h)chinazolin-2-on-verbindungen als csbp/p39-kinase-inhibitoren
WO2001041760A2 (en) 1999-12-08 2001-06-14 Pharmacia Corporation Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
US7235551B2 (en) 2000-03-02 2007-06-26 Smithkline Beecham Corporation 1,5-disubstituted-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one compounds and their use in treating csbp/p38 kinase mediated diseases
US6673818B2 (en) 2001-04-20 2004-01-06 Pharmacia Corporation Fluoro-substituted benzenesulfonyl compounds for the treatment of inflammation
US7473695B2 (en) * 2001-10-22 2009-01-06 Mitsubishi Tanabe Pharma Corporation 4-imidazolin-2-one compounds
WO2004004725A2 (en) 2002-07-09 2004-01-15 Boehringer Ingelheim Pharma Gmbh & Co. Kg Pharmaceutical compositions of anticholinergics and p38 kinase inhibitors in the treatment of respiratory diseases
US20050009931A1 (en) * 2003-03-20 2005-01-13 Britten Nancy Jean Dispersible pharmaceutical composition for treatment of mastitis and otic disorders
MXPA05009978A (es) * 2003-03-20 2005-11-04 Pharmacia Corp Formulacion dispersable de un agente antiinflamatorio.
US20050004098A1 (en) * 2003-03-20 2005-01-06 Britten Nancy Jean Dispersible formulation of an anti-inflammatory agent
US20040214753A1 (en) * 2003-03-20 2004-10-28 Britten Nancy Jean Dispersible pharmaceutical composition for treatment of mastitis and otic disorders
US7105467B2 (en) * 2003-07-08 2006-09-12 Pharmacore, Inc. Nickel catalyzed cross-coupling reactions between organomagnesium compounds and anisole derivatives
US7105707B2 (en) * 2003-12-17 2006-09-12 Pharmacore, Inc. Process for preparing alkynyl-substituted aromatic and heterocyclic compounds
US20060035893A1 (en) 2004-08-07 2006-02-16 Boehringer Ingelheim International Gmbh Pharmaceutical compositions for treatment of respiratory and gastrointestinal disorders
WO2006062069A1 (ja) * 2004-12-06 2006-06-15 Santen Pharmaceutical Co., Ltd. p38MAPキナーゼ阻害剤を有効成分とする掻痒治療剤
PE20060777A1 (es) 2004-12-24 2006-10-06 Boehringer Ingelheim Int Derivados de indolinona para el tratamiento o la prevencion de enfermedades fibroticas
JP2007145819A (ja) * 2005-10-28 2007-06-14 Tanabe Seiyaku Co Ltd 医薬組成物
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EP2111861A1 (en) 2008-04-21 2009-10-28 Ranbaxy Laboratories Limited Compositions of phosphodiesterase type IV inhibitors
WO2013100208A1 (ja) 2011-12-28 2013-07-04 京都府公立大学法人 角膜内皮細胞の培養正常化
JP6730701B2 (ja) 2013-11-14 2020-07-29 学校法人同志社 細胞増殖促進または細胞障害抑制による角膜内皮治療薬
US10342786B2 (en) 2017-10-05 2019-07-09 Fulcrum Therapeutics, Inc. P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD
NZ762856A (en) 2017-10-05 2020-07-31 Fulcrum Therapeutics Inc P38 kinase inhibitors reduce dux4 and downstream gene expression for the treatment of fshd
US20240165148A1 (en) 2021-03-15 2024-05-23 Saul Yedgar Hyaluronic acid-conjugated dipalmitoyl phosphatidyl ethanolamine in combination with non-steroidal anti-inflammatory drugs (nsaids) for treating or alleviating inflammatory diseases

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US5739143A (en) * 1995-06-07 1998-04-14 Smithkline Beecham Corporation Imidazole compounds and compositions
AP9700912A0 (en) 1996-01-11 1997-01-31 Smithkline Beecham Corp Novel cycloalkyl substituted imidazoles
CN1213306A (zh) 1996-01-11 1999-04-07 史密丝克莱恩比彻姆公司 新的取代咪唑化合物
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ZA97175B (en) 1996-01-11 1997-11-04 Smithkline Beecham Corp Novel substituted imidazole compounds.
EP0889887A4 (en) 1996-03-25 2003-06-11 Smithkline Beecham Corp TREATMENT OF CENTRAL NERVOUS SYSTEM INJURIES
EP0889888A4 (en) 1996-03-25 2003-01-08 Smithkline Beecham Corp NEW TREATMENT OF LESIONS IN THE CENTRAL NERVOUS SYSTEM
JP2000514088A (ja) 1996-11-20 2000-10-24 メルク エンド カンパニー インコーポレーテッド グルカゴンアンタゴニストとしてのトリアリール置換イミダゾール

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