JP2002526501A5 - - Google Patents

Download PDF

Info

Publication number
JP2002526501A5
JP2002526501A5 JP2000574113A JP2000574113A JP2002526501A5 JP 2002526501 A5 JP2002526501 A5 JP 2002526501A5 JP 2000574113 A JP2000574113 A JP 2000574113A JP 2000574113 A JP2000574113 A JP 2000574113A JP 2002526501 A5 JP2002526501 A5 JP 2002526501A5
Authority
JP
Japan
Prior art keywords
pharmaceutical composition
compound
disease
ring
treating
Prior art date
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.)
Pending
Application number
JP2000574113A
Other languages
English (en)
Japanese (ja)
Other versions
JP2002526501A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US1999/021567 external-priority patent/WO2000017204A1/en
Publication of JP2002526501A publication Critical patent/JP2002526501A/ja
Publication of JP2002526501A5 publication Critical patent/JP2002526501A5/ja
Pending legal-status Critical Current

Links

JP2000574113A 1998-09-18 1999-09-16 p38のインヒビター Pending JP2002526501A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US10101398P 1998-09-18 1998-09-18
US60/101,013 1998-09-18
PCT/US1999/021567 WO2000017204A1 (en) 1998-09-18 1999-09-16 INHIBITORS OF p38

Publications (2)

Publication Number Publication Date
JP2002526501A JP2002526501A (ja) 2002-08-20
JP2002526501A5 true JP2002526501A5 (enExample) 2006-11-24

Family

ID=22282668

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000574113A Pending JP2002526501A (ja) 1998-09-18 1999-09-16 p38のインヒビター

Country Status (13)

Country Link
US (2) US6635644B2 (enExample)
EP (1) EP1114051B1 (enExample)
JP (1) JP2002526501A (enExample)
AR (1) AR023659A1 (enExample)
AT (1) ATE236167T1 (enExample)
AU (1) AU761599B2 (enExample)
CA (1) CA2339253C (enExample)
DE (1) DE69906554T2 (enExample)
DK (1) DK1114051T3 (enExample)
ES (1) ES2192864T3 (enExample)
MY (1) MY117696A (enExample)
PT (1) PT1114051E (enExample)
WO (1) WO2000017204A1 (enExample)

Families Citing this family (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2221426T3 (es) 1998-08-20 2004-12-16 Smithkline Beecham Corporation Nuevos compuestos de triazol sustituidos.
MXPA03001256A (es) * 2000-08-11 2004-12-06 Vertex Pharma Inhibidores de p38.
WO2002100405A1 (en) 2001-06-11 2002-12-19 Vertex Pharmaceuticals Incorporated Isoquinoline inhibitors of p38
JP2005519895A (ja) * 2002-01-18 2005-07-07 ファルマシア・コーポレーション P38阻害剤としての置換ピリダジノン
AU2003245989A1 (en) 2002-07-09 2004-01-23 Boehringer Ingelheim Pharma Gmbh And Co. Kg Pharmaceutical compositions of anticholinergics and p38 kinase inhibitors in the treatment of respiratory diseases
EP1539121A4 (en) 2002-08-29 2008-08-13 Scios Inc METHOD OF REQUESTING OSTEOGENESIS
ES2401079T3 (es) 2002-12-20 2013-04-16 Amgen Inc. Moduladores del asma y de la inflamación alérgica
CA2526285A1 (en) 2003-05-15 2004-12-23 Arqule, Inc. Inhibitors of p38 and methods of using the same
WO2005007632A1 (en) * 2003-07-18 2005-01-27 Pharmacia Corporation Substituted pyridazinones as inhibitors of p38
US7244441B2 (en) 2003-09-25 2007-07-17 Scios, Inc. Stents and intra-luminal prostheses containing map kinase inhibitors
JP4608888B2 (ja) * 2004-01-23 2011-01-12 宇部興産株式会社 2−シアノ−2−(4−テトラヒドロピラニル)酢酸エステルの製法
WO2006010082A1 (en) 2004-07-08 2006-01-26 Arqule, Inc. 1,4-disubstituted naphtalenes as inhibitors of p38 map kinase
US20060035893A1 (en) 2004-08-07 2006-02-16 Boehringer Ingelheim International Gmbh Pharmaceutical compositions for treatment of respiratory and gastrointestinal disorders
US20070054916A1 (en) * 2004-10-01 2007-03-08 Amgen Inc. Aryl nitrogen-containing bicyclic compounds and methods of use
CA2584368A1 (en) 2004-10-19 2006-04-27 Arqule, Inc. Synthesis of imidazooxazole and imidazothiazole inhibitors of p38 map kinase
PE20060777A1 (es) 2004-12-24 2006-10-06 Boehringer Ingelheim Int Derivados de indolinona para el tratamiento o la prevencion de enfermedades fibroticas
EP1676574A3 (en) 2004-12-30 2006-07-26 Johnson & Johnson Vision Care, Inc. Methods for promoting survival of transplanted tissues and cells
US20060178388A1 (en) * 2005-02-04 2006-08-10 Wrobleski Stephen T Phenyl-substituted pyrimidine compounds useful as kinase inhibitors
US7759337B2 (en) * 2005-03-03 2010-07-20 Amgen Inc. Phthalazine compounds and methods of use
ATE480524T1 (de) 2005-07-21 2010-09-15 Hoffmann La Roche Pyridazinonderivate als schilddrüsenhormon- rezeptoragonisten
US7482345B2 (en) * 2005-12-05 2009-01-27 Meng-Hsin Chen P38 kinase inhibiting agents
EP3205644A1 (en) 2005-12-29 2017-08-16 Celtaxsys Inc. Diamine derivatives as inhibitors of leukotriene a4 hydrolase
EP2038289A2 (en) * 2006-04-21 2009-03-25 Amgen Inc. Thieno-[2,3-d]pyrimidine and thieno-pyridazine compounds and methods of use
CA2656507C (en) * 2006-07-17 2012-03-20 Amgen Inc. Quinazoline and pyridopyrimidine derivatives as p38 kinase inhibitors
AU2007293065B2 (en) * 2006-09-05 2011-08-18 Amgen Inc. Phthalazine, AZA- and diaza-phthalazine compounds and methods of use
EP2086973B1 (en) * 2006-10-11 2012-01-25 Amgen Inc., Imidazo- and triazolo-pyridine compounds and methods of use therof
CA2681420A1 (en) * 2007-03-20 2008-09-25 Cadila Pharmaceuticals Limited P38 inhibitors
AU2008248073B2 (en) * 2007-05-07 2011-03-24 Amgen Inc. Pyrazolo-pyridinone compounds, process for their preparation, and their pharmaceutical use
US8022085B2 (en) * 2007-05-07 2011-09-20 Amgen Inc. Pyrazolo-pyridinone and pyrazolo-pyrazinone compounds as P38 modulators and methods of use thereof
EP1992344A1 (en) 2007-05-18 2008-11-19 Institut Curie P38 alpha as a therapeutic target in pathologies linked to FGFR3 mutation
US8314131B2 (en) * 2007-09-21 2012-11-20 Amgen Inc. Triazole fused heteroaryl compounds and methods of use thereof
WO2009078992A1 (en) * 2007-12-17 2009-06-25 Amgen Inc. Linear tricyclic compounds as p38 kinase inhibitors
ES2471919T3 (es) 2007-12-19 2014-06-27 Amgen, Inc Derivados de ácido fenilac�tico como moduladores de inflamación
US8367671B2 (en) * 2008-03-21 2013-02-05 Amgen Inc. Pyrazolo[3.4-B]pyrazine compounds as p38 modulators and methods of use as anti-inflamatory agents
WO2010025202A1 (en) 2008-08-29 2010-03-04 Amgen Inc. PYRIDO[3,2-d]PYRIDAZINE-2(1H)-ONE COMPOUNDS AS P38 MODULATORS AND METHODS OF USE THEREOF
WO2010025201A1 (en) 2008-08-29 2010-03-04 Amgen Inc. Pyridazino- pyridinone compounds for the treatment of protein kinase mediated diseases.
US8497269B2 (en) 2008-10-10 2013-07-30 Amgen Inc. Phthalazine compounds as p38 map kinase modulators and methods of use thereof
US8772481B2 (en) 2008-10-10 2014-07-08 Amgen Inc. Aza- and diaza-phthalazine compounds as P38 map kinase modulators and methods of use thereof
SG172160A1 (en) 2008-12-17 2011-07-28 Scripps Research Inst Generation and maintenance of stem cells
GB0902648D0 (en) * 2009-02-17 2009-04-01 Argenta Discovery Ltd Pharmaceutical compounds and compositions
GB0908317D0 (en) * 2009-05-14 2009-06-24 Argenta Discovery Ltd Pharmaceutical compounds and compositions
JP6105594B2 (ja) 2011-09-30 2017-03-29 エンドゥ ファーマシューティカルズ,インコーポレイティド 癌処置用cyp17阻害剤としてのイミダゾール誘導体
JP6130383B2 (ja) 2011-09-30 2017-05-17 エンドゥ ファーマシューティカルズ,インコーポレイティド ピリジン誘導体
US20150104870A1 (en) 2012-04-27 2015-04-16 Keio University Neuronal differentiation promoter
AU2014249168B2 (en) 2013-03-12 2018-07-12 Celltaxis, Llc Methods of inhibiting leukotriene A4 hydrolase
MX2015011678A (es) 2013-03-14 2016-07-08 Celtaxsys Inc Inhibidores de leucotrieno a4 hidrolasa.
EP2968265A4 (en) 2013-03-14 2016-12-28 Celtaxsys Inc INHIBITORS OF THE LEUKOTRIEN A4 HYDROLASE
AU2014240042C1 (en) 2013-03-14 2019-09-05 Celltaxis, Llc Inhibitors of leukotriene A4 hydrolase
DK3368052T3 (da) 2015-10-27 2022-03-14 Childrens Hospital Med Ct Anvendelse af mapk-hæmmere for at nedbringe tabet af hæmatopoietiske stamceller under ex vivo-dyrkning og -genmanipulation
US20190060286A1 (en) 2016-02-29 2019-02-28 University Of Florida Research Foundation, Incorpo Chemotherapeutic Methods
EP3773579A4 (en) 2018-03-26 2022-03-09 Clear Creek Bio, Inc. COMPOSITIONS AND METHODS FOR INHIBITING DIHYDROOROTATE DEHYDROGENASE
EP3801559B1 (en) 2018-05-31 2025-01-01 Celltaxis, LLC Method of reducing pulmonary exacerbations in respiratory disease patients
US12076315B2 (en) 2020-03-20 2024-09-03 Clear Creek Bio, Inc. Stable polymorphic compositions of brequinar sodium and methods of use and manufacture thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6147080A (en) * 1996-12-18 2000-11-14 Vertex Pharmaceuticals Incorporated Inhibitors of p38
MXPA03001256A (es) * 2000-08-11 2004-12-06 Vertex Pharma Inhibidores de p38.

Similar Documents

Publication Publication Date Title
JP2002526482A5 (enExample)
JP2002514625A5 (enExample)
JP2009509961A5 (enExample)
HRP20120900T1 (hr) Inhibitori p38 kinaze bazirani na peteroäślanom heterociklu
RU2222534C2 (ru) Замещенные имидазолы, способ их получения, фармацевтическая композиция на их основе, способы лечения цитокин-опосредованных заболеваний
CA2331460A1 (en) Heterocyclic inhibitors of p38
IL301757A (en) Cystic fibrosis transmembrane regulator conductance modulators
JP2002543185A5 (enExample)
JP2019517487A5 (enExample)
JP2005507380A5 (enExample)
CA2491895A1 (en) Inhibitors of c-jun n-terminal kinases (jnk) and other protein kinases
JP2005534684A5 (enExample)
JP2004535447A5 (enExample)
JP2010506854A5 (enExample)
JP2003528084A5 (enExample)
MY146279A (en) Compounds affecting glucokinase
JP2003531103A5 (enExample)
HRP20130155T1 (hr) Fuzionirani heterocikliäśki spojevi korisni kao modulatori kinaze
IL153805A0 (en) Cinnoline compounds
JP2020517707A5 (enExample)
JP2004509120A5 (enExample)
JP2006514960A5 (enExample)
JP2020520957A5 (enExample)
JP2019505529A5 (enExample)
EP1125936A3 (en) Aryl substituted azabenzimidazoles and their use in the treatment of HIV and AIDS related diseases