DK1318992T3 - Imidazolderivater som Raf-kinaseinhibitorer - Google Patents
Imidazolderivater som Raf-kinaseinhibitorerInfo
- Publication number
- DK1318992T3 DK1318992T3 DK01967528T DK01967528T DK1318992T3 DK 1318992 T3 DK1318992 T3 DK 1318992T3 DK 01967528 T DK01967528 T DK 01967528T DK 01967528 T DK01967528 T DK 01967528T DK 1318992 T3 DK1318992 T3 DK 1318992T3
- Authority
- DK
- Denmark
- Prior art keywords
- kinase inhibitors
- raf kinase
- imidazole derivatives
- migraine
- pain
- Prior art date
Links
- 229940043355 kinase inhibitor Drugs 0.000 title abstract 2
- 239000003757 phosphotransferase inhibitor Substances 0.000 title abstract 2
- 102000009929 raf Kinases Human genes 0.000 title abstract 2
- 108010077182 raf Kinases Proteins 0.000 title abstract 2
- 150000002460 imidazoles Chemical class 0.000 title 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 title 1
- 206010007572 Cardiac hypertrophy Diseases 0.000 abstract 1
- 208000006029 Cardiomegaly Diseases 0.000 abstract 1
- 208000019695 Migraine disease Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 208000002193 Pain Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 230000006726 chronic neurodegeneration Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 206010027599 migraine Diseases 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/001—Preparation for luminescence or biological staining
- A61K49/0013—Luminescence
- A61K49/0017—Fluorescence in vivo
- A61K49/0019—Fluorescence in vivo characterised by the fluorescent group, e.g. oligomeric, polymeric or dendritic molecules
- A61K49/0021—Fluorescence in vivo characterised by the fluorescent group, e.g. oligomeric, polymeric or dendritic molecules the fluorescent group being a small organic molecule
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0023197A GB0023197D0 (en) | 2000-09-21 | 2000-09-21 | Compounds |
GB0023193A GB0023193D0 (en) | 2000-09-21 | 2000-09-21 | Compounds |
GB0023208A GB0023208D0 (en) | 2000-09-21 | 2000-09-21 | Compounds |
GB0023196A GB0023196D0 (en) | 2000-09-21 | 2000-09-21 | Compouds |
Publications (1)
Publication Number | Publication Date |
---|---|
DK1318992T3 true DK1318992T3 (da) | 2005-11-21 |
Family
ID=27447885
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK01967528T DK1318992T3 (da) | 2000-09-21 | 2001-09-19 | Imidazolderivater som Raf-kinaseinhibitorer |
Country Status (21)
Country | Link |
---|---|
US (2) | US7199137B2 (da) |
EP (1) | EP1318992B1 (da) |
JP (1) | JP2004509882A (da) |
KR (1) | KR20030030027A (da) |
CN (1) | CN1471523A (da) |
AT (1) | ATE300529T1 (da) |
AU (1) | AU2001287901A1 (da) |
BR (1) | BR0114023A (da) |
CA (1) | CA2423154A1 (da) |
CY (1) | CY1105251T1 (da) |
CZ (1) | CZ2003793A3 (da) |
DE (1) | DE60112312T2 (da) |
DK (1) | DK1318992T3 (da) |
ES (1) | ES2242767T3 (da) |
HU (1) | HUP0301181A2 (da) |
IL (1) | IL154949A0 (da) |
MX (1) | MXPA03002449A (da) |
NO (1) | NO20031270L (da) |
PL (1) | PL361397A1 (da) |
PT (1) | PT1318992E (da) |
WO (1) | WO2002024680A1 (da) |
Families Citing this family (55)
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EP1233769B1 (en) | 1999-11-22 | 2007-12-26 | SmithKline Beecham plc | Imidazole derivatives |
EP1263753B1 (en) * | 2000-03-06 | 2004-05-06 | SmithKline Beecham plc | Imidazol derivatives as raf kinase inhibitors |
US20040053943A1 (en) | 2000-11-20 | 2004-03-18 | Adams Jerry L. | Novel compounds |
GB0112348D0 (en) * | 2001-05-19 | 2001-07-11 | Smithkline Beecham Plc | Compounds |
US20040192689A1 (en) * | 2001-09-05 | 2004-09-30 | Dean David Kenneth | Heterocycle-carboxamide derivatives as raf kinase inhibitors |
GB0121488D0 (en) | 2001-09-05 | 2001-10-24 | Smithkline Beecham Plc | Compounds |
WO2003022832A1 (en) * | 2001-09-05 | 2003-03-20 | Smithkline Beecham P.L.C. | Pyridylfurans and pyrroles as raf kinase inhibitors |
GB0121490D0 (en) | 2001-09-05 | 2001-10-24 | Smithkline Beecham Plc | Ciompounds |
AR039241A1 (es) * | 2002-04-04 | 2005-02-16 | Biogen Inc | Heteroarilos trisustituidos y metodos para su produccion y uso de los mismos |
EP1492568A1 (en) * | 2002-04-08 | 2005-01-05 | SmithKline Beecham Corporation | Cancer treatment method comprising administration of an erb-family inhibitor and a raf and/or ras inhibitor |
AU2003264018A1 (en) | 2002-08-09 | 2004-02-25 | Astrazeneca Ab | Compounds having an activity at metabotropic glutamate receptors |
JP2006506340A (ja) * | 2002-08-09 | 2006-02-23 | アストラゼネカ アクチボラグ | 代謝調節型グルタミン酸受容体5のモジュレーターとしてのオキサジアゾール |
IL166510A0 (en) | 2002-08-09 | 2006-01-15 | Nps Pharma Inc | 1,2,4"oxadiazole as modulators of metabotropic glutamate receptor-5 |
CN101899006B (zh) | 2002-08-19 | 2013-11-06 | 劳洛斯治疗公司 | 2,4,5-三取代的咪唑及其作为抗菌剂的用途 |
UA80295C2 (en) * | 2002-09-06 | 2007-09-10 | Biogen Inc | Pyrazolopyridines and using the same |
US20090264494A1 (en) * | 2002-10-18 | 2009-10-22 | Board Of Regents, The University Of Texas System | Use of neuroprotective 3-substituted indolone compositions |
US20050250837A1 (en) * | 2002-10-18 | 2005-11-10 | D Mello Santosh R | Use of C-Raf inhibitors for the treatment of neurodegenerative diseases |
US20070099250A1 (en) * | 2003-04-14 | 2007-05-03 | Ping Hu | Methods for treating proliferative diseases and for monitoring the effectiveness of treatment of proliferative diseases |
JP2007507540A (ja) * | 2003-10-02 | 2007-03-29 | アイアールエム・リミテッド・ライアビリティ・カンパニー | タンパク質キナーゼ阻害剤としての化合物および組成物 |
CA2545942C (en) * | 2003-11-14 | 2012-07-10 | Lorus Therapeutics Inc. | Aryl imidazoles and their use as anti-cancer agents |
TW200639163A (en) | 2005-02-04 | 2006-11-16 | Genentech Inc | RAF inhibitor compounds and methods |
US8148392B2 (en) | 2005-05-25 | 2012-04-03 | Lorus Therapeutics Inc. | 2-indolyl imidazo [4,5-d] phenanthroline derivatives and their use in the treatment of cancer |
CA2622295C (en) * | 2005-09-12 | 2019-01-15 | The Regents Of The University Of Michigan | Recurrent gene fusions in prostate cancer |
US9957569B2 (en) * | 2005-09-12 | 2018-05-01 | The Regents Of The University Of Michigan | Recurrent gene fusions in prostate cancer |
US20090018142A9 (en) * | 2006-05-02 | 2009-01-15 | Zhengping Zhuang | Use of phosphatases to treat tumors overexpressing N-CoR |
CN101652484B (zh) * | 2006-11-08 | 2013-03-20 | 密歇根大学董事会 | ***癌标志物spink1及其应用 |
CN101662939B (zh) | 2007-02-06 | 2015-11-25 | 利克斯特生物技术公司 | 氧杂双环庚烷和氧杂双环庚烯,它们的制备及用途 |
EP2162445B1 (en) | 2007-06-05 | 2013-11-27 | Takeda Pharmaceutical Company Limited | Heterobicyclic compounds as kinase inhibitors |
CA2692793C (en) | 2007-07-06 | 2014-05-20 | The Regents Of The University Of Michigan | Mipol1-etv1 gene rearrangements |
US20100190777A1 (en) | 2007-07-17 | 2010-07-29 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
US8324395B2 (en) | 2007-08-23 | 2012-12-04 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
WO2009028629A1 (ja) | 2007-08-29 | 2009-03-05 | Takeda Pharmaceutical Company Limited | 複素環化合物およびその用途 |
MX2010003417A (es) * | 2007-10-01 | 2010-09-10 | Lixte Biotechnology Inc | Inhibidores de histona desacetilasa. |
US8227473B2 (en) | 2008-08-01 | 2012-07-24 | Lixte Biotechnology, Inc. | Oxabicycloheptanes and oxabicycloheptenes, their preparation and use |
WO2010147612A1 (en) | 2009-06-18 | 2010-12-23 | Lixte Biotechnology, Inc. | Methods of modulating cell regulation by inhibiting p53 |
WO2010014220A1 (en) | 2008-08-01 | 2010-02-04 | Lixte Biotechnology, Inc. | Neuroprotective agents for the prevention and treatment of neurodegenerative diseases |
WO2010064611A1 (ja) | 2008-12-01 | 2010-06-10 | 武田薬品工業株式会社 | 複素環化合物およびその用途 |
JO3101B1 (ar) | 2008-12-02 | 2017-09-20 | Takeda Pharmaceuticals Co | مشتقات بنزوثيازول كعوامل مضادة للسرطان |
AU2010295689B2 (en) | 2009-09-17 | 2014-02-13 | The Regents Of The University Of Michigan | Recurrent gene fusions in prostate cancer |
US20130040983A1 (en) * | 2010-01-08 | 2013-02-14 | Jean-Michel Vernier | Raf kinase inhibitors |
US8945556B2 (en) | 2010-11-19 | 2015-02-03 | The Regents Of The University Of Michigan | RAF gene fusions |
US8962650B2 (en) | 2011-04-18 | 2015-02-24 | Eisai R&D Management Co., Ltd. | Therapeutic agent for tumor |
WO2012145503A1 (en) | 2011-04-21 | 2012-10-26 | Novartis Ag | Pharmaceutical combinations |
CN103159736B (zh) * | 2011-12-10 | 2015-05-13 | 通化济达医药有限公司 | 取代的吡唑激酶抑制剂 |
CN103159735B (zh) * | 2011-12-10 | 2015-12-09 | 通化济达医药有限公司 | 取代的咪唑激酶抑制剂 |
WO2013109142A1 (en) | 2012-01-16 | 2013-07-25 | Stichting Het Nederlands Kanker Instituut | Combined pdk and mapk/erk pathway inhibition in neoplasia |
US20150232452A1 (en) * | 2012-09-19 | 2015-08-20 | Ruga Corporation | Novel raf kinase inhibitors |
AU2014235962A1 (en) | 2013-03-20 | 2015-09-10 | Aptose Biosciences Inc. | 2-substituted imidazo[4,5-d]phenanthroline derivatives and their use in the treatment of cancer |
KR20160004299A (ko) | 2013-04-09 | 2016-01-12 | 릭스트 바이오테크놀로지, 인코포레이티드 | 옥사바이시클로헵탄류 및 옥사바이시클로헵텐류의 제형 |
EP3046557A1 (en) | 2013-09-20 | 2016-07-27 | Stichting Het Nederlands Kanker Instituut | Rock in combination with mapk-pathway |
WO2015041534A1 (en) | 2013-09-20 | 2015-03-26 | Stichting Het Nederlands Kanker Instituut | P90rsk in combination with raf/erk/mek |
DK3052102T3 (da) | 2013-10-04 | 2020-03-09 | Aptose Biosciences Inc | Sammensætninger til behandling af cancere |
WO2019089511A1 (en) | 2017-10-30 | 2019-05-09 | Aptose Biosciences Inc. | Aryl imidazoles for the treatment of cancer |
CN108484587A (zh) * | 2018-06-03 | 2018-09-04 | 刘思良 | 一种Raf激酶抑制剂及其在癌症治疗中的应用 |
WO2022249192A1 (en) * | 2021-05-27 | 2022-12-01 | Ramot At Tel-Aviv University Ltd. | Broad-spectrum metastasis suppressing compounds and therapeutic uses thereof in human tumors |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5236917A (en) * | 1989-05-04 | 1993-08-17 | Sterling Winthrop Inc. | Saccharin derivatives useful as proteolytic enzyme inhibitors and compositions and method of use thereof |
WO1995003297A1 (en) | 1993-07-21 | 1995-02-02 | Smithkline Beecham Corporation | Imidazoles for treating cytokine mediated disease |
US5620999A (en) | 1994-07-28 | 1997-04-15 | Weier; Richard M. | Benzenesulfonamide subtituted imidazolyl compounds for the treatment of inflammation |
US5514505A (en) * | 1995-05-15 | 1996-05-07 | Xerox Corporation | Method for obtaining improved image contrast in migration imaging members |
EP0833664A1 (en) | 1995-06-12 | 1998-04-08 | G.D. SEARLE & CO. | Combination of a cyclooxygenase-2 inhibitor and a leukotriene b 4? receptor antagonist for the treatment of inflammations |
US5717100A (en) * | 1995-10-06 | 1998-02-10 | Merck & Co., Inc. | Substituted imidazoles having anti-cancer and cytokine inhibitory activity |
GB2306108A (en) | 1995-10-13 | 1997-04-30 | Merck & Co Inc | Treatment of Raf-mediated cancers with imidazole derivatives |
WO1997036587A1 (en) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | A method of treating cancer |
JP3418624B2 (ja) * | 1996-06-10 | 2003-06-23 | メルク エンド カンパニー インコーポレーテッド | サイトカイン阻害活性を有する置換イミダゾール類 |
DE69728986T2 (de) | 1996-06-21 | 2005-04-07 | Allergan, Inc., Irvine | Substituierte tetrahydronaphthalin- und dihydronaphthalin-derivate mit einer retinoiden und/oder retinoid antagonist-ähnlichen biologischen aktivität |
CA2267186C (en) | 1996-10-15 | 2002-05-14 | G.D. Searle & Co. | Method of using cyclooxygenase-2 inhibitors in the treatment and prevention of neoplasia |
PE10599A1 (es) | 1996-10-30 | 1999-02-10 | Schering Corp | Derivados de piperazina como antagonistas de neuroquinina |
CA2302417A1 (en) | 1997-10-27 | 1999-05-06 | Takeda Chemical Industries, Ltd. | Adenosine a3 receptor antagonists |
PL340541A1 (en) | 1997-11-14 | 2001-02-12 | Sankyo Co | Pyridipyrrole derivative |
ATE355856T1 (de) | 1998-07-30 | 2007-03-15 | Point Biomedical Corp | Neuer wirkstoffträger für die gefriertrocknung von wässrigen suspensionen von mikropartikeln |
-
2001
- 2001-09-19 WO PCT/GB2001/004195 patent/WO2002024680A1/en active IP Right Grant
- 2001-09-19 US US10/380,891 patent/US7199137B2/en not_active Expired - Fee Related
- 2001-09-19 MX MXPA03002449A patent/MXPA03002449A/es unknown
- 2001-09-19 HU HU0301181A patent/HUP0301181A2/hu unknown
- 2001-09-19 BR BR0114023-0A patent/BR0114023A/pt not_active Application Discontinuation
- 2001-09-19 JP JP2002529090A patent/JP2004509882A/ja active Pending
- 2001-09-19 ES ES01967528T patent/ES2242767T3/es not_active Expired - Lifetime
- 2001-09-19 AU AU2001287901A patent/AU2001287901A1/en not_active Abandoned
- 2001-09-19 CZ CZ2003793A patent/CZ2003793A3/cs unknown
- 2001-09-19 AT AT01967528T patent/ATE300529T1/de not_active IP Right Cessation
- 2001-09-19 IL IL15494901A patent/IL154949A0/xx unknown
- 2001-09-19 EP EP01967528A patent/EP1318992B1/en not_active Expired - Lifetime
- 2001-09-19 PL PL01361397A patent/PL361397A1/xx not_active Application Discontinuation
- 2001-09-19 DE DE60112312T patent/DE60112312T2/de not_active Expired - Fee Related
- 2001-09-19 KR KR10-2003-7004109A patent/KR20030030027A/ko not_active Application Discontinuation
- 2001-09-19 DK DK01967528T patent/DK1318992T3/da active
- 2001-09-19 CA CA002423154A patent/CA2423154A1/en not_active Abandoned
- 2001-09-19 CN CNA018182135A patent/CN1471523A/zh active Pending
- 2001-09-19 PT PT01967528T patent/PT1318992E/pt unknown
-
2003
- 2003-03-19 NO NO20031270A patent/NO20031270L/no not_active Application Discontinuation
-
2005
- 2005-09-06 CY CY20051101069T patent/CY1105251T1/el unknown
-
2007
- 2007-01-22 US US11/625,406 patent/US20070135433A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
US20070135433A1 (en) | 2007-06-14 |
DE60112312T2 (de) | 2005-12-29 |
JP2004509882A (ja) | 2004-04-02 |
CY1105251T1 (el) | 2010-03-03 |
PT1318992E (pt) | 2005-11-30 |
IL154949A0 (en) | 2003-10-31 |
US7199137B2 (en) | 2007-04-03 |
CN1471523A (zh) | 2004-01-28 |
CA2423154A1 (en) | 2002-03-28 |
NO20031270L (no) | 2003-05-19 |
US20040038964A1 (en) | 2004-02-26 |
EP1318992B1 (en) | 2005-07-27 |
WO2002024680A1 (en) | 2002-03-28 |
AU2001287901A1 (en) | 2002-04-02 |
HUP0301181A2 (en) | 2007-02-28 |
BR0114023A (pt) | 2004-02-03 |
EP1318992A1 (en) | 2003-06-18 |
ATE300529T1 (de) | 2005-08-15 |
CZ2003793A3 (cs) | 2004-04-14 |
PL361397A1 (en) | 2004-10-04 |
KR20030030027A (ko) | 2003-04-16 |
MXPA03002449A (es) | 2003-06-19 |
ES2242767T3 (es) | 2005-11-16 |
DE60112312D1 (de) | 2005-09-01 |
NO20031270D0 (no) | 2003-03-19 |
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