ATE374201T1 - 6-alkoxypyridopyrimidine als inhibitoren der p-38-map-kinase - Google Patents
6-alkoxypyridopyrimidine als inhibitoren der p-38-map-kinaseInfo
- Publication number
- ATE374201T1 ATE374201T1 AT03784102T AT03784102T ATE374201T1 AT E374201 T1 ATE374201 T1 AT E374201T1 AT 03784102 T AT03784102 T AT 03784102T AT 03784102 T AT03784102 T AT 03784102T AT E374201 T1 ATE374201 T1 AT E374201T1
- Authority
- AT
- Austria
- Prior art keywords
- alkoxypyridopyrimidines
- inhibitors
- map kinase
- kinase
- map
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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Landscapes
- Health & Medical Sciences (AREA)
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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- Hematology (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Tropical Medicine & Parasitology (AREA)
- Ophthalmology & Optometry (AREA)
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Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US40149102P | 2002-08-06 | 2002-08-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE374201T1 true ATE374201T1 (de) | 2007-10-15 |
Family
ID=31715709
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT03784102T ATE374201T1 (de) | 2002-08-06 | 2003-07-29 | 6-alkoxypyridopyrimidine als inhibitoren der p-38-map-kinase |
Country Status (15)
Country | Link |
---|---|
US (4) | US6965030B2 (de) |
EP (1) | EP1539755B1 (de) |
JP (1) | JP4252534B2 (de) |
CN (1) | CN100432073C (de) |
AR (1) | AR040787A1 (de) |
AT (1) | ATE374201T1 (de) |
AU (1) | AU2003251661A1 (de) |
BR (1) | BR0313297A (de) |
CA (1) | CA2492112A1 (de) |
DE (1) | DE60316581T2 (de) |
ES (1) | ES2293064T3 (de) |
MX (1) | MXPA05001332A (de) |
PL (1) | PL375403A1 (de) |
RU (1) | RU2324695C2 (de) |
WO (1) | WO2004014907A1 (de) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1774250A (zh) * | 2003-04-16 | 2006-05-17 | 霍夫曼-拉罗奇有限公司 | 作为治疗诸如类风湿性关节炎的炎性疾病的p38激酶抑制剂的(6-(苯氧基)-吡啶并[3,4-d]嘧啶-2-基)-胺衍生物 |
CN1926139A (zh) * | 2004-02-27 | 2007-03-07 | 霍夫曼-拉罗奇有限公司 | 稠合吡唑衍生物 |
DE102004018198A1 (de) * | 2004-04-15 | 2005-11-03 | Merck Patent Gmbh | Sulfonamide |
JP2009506008A (ja) | 2005-08-25 | 2009-02-12 | エフ.ホフマン−ラ ロシュ アーゲー | p38MAPキナーゼ阻害剤及びその使用方法 |
US20090221600A1 (en) * | 2005-09-28 | 2009-09-03 | Ashwani Kumar Verma | Pyrido-pyridimidine derivatives useful as antiinflammatory agents |
CN101478989A (zh) * | 2006-06-28 | 2009-07-08 | Aska制药株式会社 | 炎性肠病的处置剂 |
US7835569B2 (en) * | 2006-10-13 | 2010-11-16 | Apple Inc. | System and method for raw image processing using conversion matrix interpolated from predetermined camera characterization matrices |
AU2008215659B2 (en) | 2007-02-16 | 2012-11-01 | Aska Pharmaceutical Co., Ltd. | Pharmaceutical composition comprising microparticle oily suspension |
ES2324083B1 (es) * | 2007-10-22 | 2010-05-31 | Consejo Superior De Investigaciones Cientificas | Procedimiento para el diagnostico y tratamiento de enfermedades que cursan con alteracion de la quinasa p38, elementos necesarios para llevarlo a cabo y sus aplicaciones. |
US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
EA036592B1 (ru) | 2012-06-13 | 2020-11-26 | Инсайт Холдингс Корпорейшн | Замещенные трициклические соединения как ингибиторы fgfr |
WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
GB201216017D0 (en) * | 2012-09-07 | 2012-10-24 | Cancer Rec Tech Ltd | Inhibitor compounds |
US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
CN103145626B (zh) * | 2013-02-28 | 2015-02-11 | 山东大学 | 一种合成4-氨基-2-甲巯基嘧啶-5-甲醛的方法 |
CN103145632B (zh) * | 2013-03-26 | 2015-07-08 | 浙江普洛得邦制药有限公司 | 一种1h-1,2,4-三氮唑-3-甲酸甲酯的制备方法 |
WO2014172644A2 (en) | 2013-04-19 | 2014-10-23 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
ES2895769T3 (es) | 2015-02-20 | 2022-02-22 | Incyte Corp | Heterociclos bicíclicos como inhibidores de FGFR |
WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
US20190060286A1 (en) | 2016-02-29 | 2019-02-28 | University Of Florida Research Foundation, Incorpo | Chemotherapeutic Methods |
CA3058820A1 (en) * | 2017-04-04 | 2018-10-11 | Strekin Ag | Methods of preventing or treating ophthalmic diseases |
AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
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 |
CN114748622A (zh) | 2017-10-05 | 2022-07-15 | 弗尔康医疗公司 | P38激酶抑制剂降低dux4和下游基因表达以用于治疗fshd |
US11174257B2 (en) | 2018-05-04 | 2021-11-16 | Incyte Corporation | Salts of an FGFR inhibitor |
CA3099287A1 (en) | 2018-05-04 | 2019-11-07 | Incyte Corporation | Solid forms of an fgfr inhibitor and processes for preparing the same |
AU2019384646A1 (en) * | 2018-11-20 | 2021-06-17 | Nflection Therapeutics, Inc. | Naphthyridinone-aniline compounds for treatment of dermal disorders |
US11572344B2 (en) | 2018-11-20 | 2023-02-07 | Nflection Therapeutics, Inc. | Cyanoaryl-aniline compounds for treatment of dermal disorders |
US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
CR20220169A (es) | 2019-10-14 | 2022-10-27 | Incyte Corp | Heterociclos bicíclicos como inhibidores de fgfr |
WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
EP4069696A1 (de) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Tricyclische heterocyclen als fgfr-inhibitoren |
BR112022010664A2 (pt) | 2019-12-04 | 2022-08-16 | Incyte Corp | Derivados de um inibidor de fgfr |
EP4352059A1 (de) | 2021-06-09 | 2024-04-17 | Incyte Corporation | Tricyclische heterocyclen als fgfr-inhibitoren |
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US5037826A (en) * | 1986-10-15 | 1991-08-06 | Schering Corporation | 1-substituted naphthyridine and pyridopyrazine derivatives |
EP0278686A1 (de) | 1987-02-07 | 1988-08-17 | The Wellcome Foundation Limited | Pyridopyrimidine, Verfahren zu ihrer Herstellung und pharmazeutische Zubereitungen davon |
WO1993017682A1 (en) | 1992-03-04 | 1993-09-16 | Abbott Laboratories | Angiotensin ii receptor antagonists |
GEP20012444B (en) | 1994-11-14 | 2001-05-25 | Warner Lambert Company Us | 6-Aryl Pyrido[2,3-d]Pyrimidines and Naphthyridines, Pharmaceutical Composition on Their Basis and Application for Inhibiting Cellular Proliferation |
IL115256A0 (en) * | 1994-11-14 | 1995-12-31 | Warner Lambert Co | 6-Aryl pyrido (2,3-d) pyrimidines and naphthyridines and their use |
US6007425A (en) | 1995-05-02 | 1999-12-28 | Kabushiki Kaisha Ace Denken | Simulation system for place of amusement |
US5620981A (en) * | 1995-05-03 | 1997-04-15 | Warner-Lambert Company | Pyrido [2,3-D]pyrimidines for inhibiting protein tyrosine kinase mediated cellular proliferation |
IL117923A (en) | 1995-05-03 | 2000-06-01 | Warner Lambert Co | Anti-cancer pharmaceutical compositions containing polysubstituted pyrido¬2,3-d¾pyrimidine derivatives and certain such novel compounds |
US5945422A (en) * | 1997-02-05 | 1999-08-31 | Warner-Lambert Company | N-oxides of amino containing pyrido 2,3-D! pyrimidines |
US6498163B1 (en) * | 1997-02-05 | 2002-12-24 | Warner-Lambert Company | Pyrido[2,3-D]pyrimidines and 4-aminopyrimidines as inhibitors of cellular proliferation |
JP2001509805A (ja) * | 1997-02-05 | 2001-07-24 | ワーナー−ランバート・コンパニー | 細胞増殖阻害剤としてのピリド〔2,3−d〕ピリミジンおよび4−アミノピリミジン |
US6150359A (en) * | 1997-08-20 | 2000-11-21 | Warner-Lambert Company | Naphthyridinones for inhibiting protein tyrosine kinase and cell cycle kinase mediated cellular proliferation |
AU745579B2 (en) * | 1997-10-20 | 2002-03-21 | F. Hoffmann-La Roche Ag | Bicyclic kinase inhibitors |
ES2310039T3 (es) | 1998-05-26 | 2008-12-16 | Warner-Lambert Company Llc | Pirimidinas biciclicas y 3,4-dihidropirimidinas biciclicas como inhibidores de la proliferacion celular. |
BR0015243A (pt) * | 1999-10-21 | 2002-07-16 | Hoffmann La Roche | Heterociclos de nitrogênio bicìclico substituìdos por heteroalquilamino como inibidores da proteìna cinase p38 |
ES2277858T3 (es) * | 1999-10-21 | 2007-08-01 | F. Hoffmann-La Roche Ag | Heterociclos de nitrogeno biciclicos alquilamino sustituidos como inhibidores de proteina kinasa p38. |
US6518276B2 (en) * | 2000-08-31 | 2003-02-11 | Syntex (U.S.A.) Llc | 7-oxo-pyridopyrimidines (II) |
US6506749B2 (en) * | 2000-08-31 | 2003-01-14 | Syntex (U.S.A.) Llc | 7-oxo-pyridopyrimidines (I) |
WO2002058695A1 (en) * | 2000-12-20 | 2002-08-01 | Merck & Co., Inc. | (halo-benzo carbonyl)heterocyclo fused phenyl p38 kinase inhibiting agents |
CA2434834C (en) * | 2001-02-12 | 2010-09-14 | F. Hoffmann-La Roche Ag | 6-substituted pyrido-pyrimidines |
CN102295643B (zh) * | 2002-01-22 | 2013-12-04 | 沃尼尔·朗伯有限责任公司 | 2-(吡啶-2-基氨基)-吡啶并[2,3-d]嘧啶-7-酮 |
US7069390B2 (en) | 2003-09-04 | 2006-06-27 | International Business Machines Corporation | Implementation of a pseudo-LRU algorithm in a partitioned cache |
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AU2003251661A1 (en) | 2004-02-25 |
US7196097B2 (en) | 2007-03-27 |
MXPA05001332A (es) | 2005-04-28 |
CN1675207A (zh) | 2005-09-28 |
US7105525B2 (en) | 2006-09-12 |
BR0313297A (pt) | 2005-06-21 |
US20040038999A1 (en) | 2004-02-26 |
JP4252534B2 (ja) | 2009-04-08 |
RU2005106202A (ru) | 2006-05-10 |
JP2006507236A (ja) | 2006-03-02 |
US20050203300A1 (en) | 2005-09-15 |
US6965030B2 (en) | 2005-11-15 |
CA2492112A1 (en) | 2004-02-19 |
ES2293064T3 (es) | 2008-03-16 |
DE60316581D1 (de) | 2007-11-08 |
DE60316581T2 (de) | 2008-07-03 |
PL375403A1 (en) | 2005-11-28 |
WO2004014907A1 (en) | 2004-02-19 |
US20070167484A1 (en) | 2007-07-19 |
AR040787A1 (es) | 2005-04-20 |
US20060276646A1 (en) | 2006-12-07 |
EP1539755B1 (de) | 2007-09-26 |
CN100432073C (zh) | 2008-11-12 |
RU2324695C2 (ru) | 2008-05-20 |
US7320987B2 (en) | 2008-01-22 |
EP1539755A1 (de) | 2005-06-15 |
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