PE20010529A1 - Moduladores de los receptores activados del proliferador de peroxisomas - Google Patents
Moduladores de los receptores activados del proliferador de peroxisomasInfo
- Publication number
- PE20010529A1 PE20010529A1 PE2000000876A PE0008762000A PE20010529A1 PE 20010529 A1 PE20010529 A1 PE 20010529A1 PE 2000000876 A PE2000000876 A PE 2000000876A PE 0008762000 A PE0008762000 A PE 0008762000A PE 20010529 A1 PE20010529 A1 PE 20010529A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- aryl
- etoxy
- methyloxazole
- acid
- Prior art date
Links
- 210000002824 peroxisome Anatomy 0.000 title 1
- -1 BROMOPHENYL Chemical class 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical class [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 1
- WZKSXHQDXQKIQJ-UHFFFAOYSA-N F[C](F)F Chemical class F[C](F)F WZKSXHQDXQKIQJ-UHFFFAOYSA-N 0.000 abstract 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000003614 peroxisome proliferator Substances 0.000 abstract 1
- 229940075993 receptor modulator Drugs 0.000 abstract 1
- 208000011580 syndromic disease Diseases 0.000 abstract 1
- 150000003626 triacylglycerols Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/24—Radicals substituted by oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Abstract
SE REFIERE A DERIVADOS DE BIARIL OXAZOLES DE FORMULA I, DONDE n ES 2-4; V ES O, S; W ES O, S, SO2; R1 ES H, ALQUILO C1-C4, FENILO, TRIFLUOROMETILO; R2 ES H, ALQUILO C1-C6, ARIL-ALQUILO C1-C6, ENTRE OTROS; R3 ES H, ALQUILO C1-C6, ARIL-ALQUILO C1-C6, ENTRE OTROS; R4 ES H, ALQUILO C1-C4, ARILO, BENCILO; R5 ES H, ARILO, HETEROARILO; R6 ES H, ALQUILO C1-C4, AMINOALQUILO. SON COMPUESTOS PREFERIDOS ACIDO 2-{4-[2-(2-BIFENIL-4-IL-5-METILOXAZOL-4-IL)ETOXI]NAFTALEN-1-ILOXI}-2-METILPROPIONICO, ACIDO 2-{4-[2-(2-BIFENIL-4-IL-5-METILOXAZOL-4-IL)ETOXI]-5,6,7,8-TETRAHIDRONAFTALEN-1-ILOXI}-2-METIL-PROPIONICO, ACIDO 2-{3-[2-(2-ARILFENILOXAZOL-5-SUSTITUIDO-4-IL)ETOXI]2-FENOXI}ETANOICO, ACIDO 2-(4-{2-[2-(4-TIOFEN-2-IL-FENIL)-5-METILOXAZOL-4-IL]ETOXI}FENOXI)-2-METILPROPIONICO, ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION DE 2-(BROMOFENIL)-4-(2-HIDROXIETIL)OXAZOL-5 SUSTITUIDO. EL COMPUESTO I ES UN MODULADOR DEL RECEPTOR þ ACTIVADO DEL PROLIFERADOR DE PEROXISOMAS, REDUCE LOS TRIGLICERIDOS Y PUEDE SER UTIL PARA EL TRATAMIENTO DE LA DIABETES MELLITUS, SINDROME X
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15116299P | 1999-08-27 | 1999-08-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20010529A1 true PE20010529A1 (es) | 2001-05-18 |
Family
ID=22537578
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2000000876A PE20010529A1 (es) | 1999-08-27 | 2000-08-25 | Moduladores de los receptores activados del proliferador de peroxisomas |
Country Status (13)
| Country | Link |
|---|---|
| US (3) | US6417212B1 (es) |
| EP (1) | EP1206457B1 (es) |
| JP (1) | JP2003508389A (es) |
| AR (1) | AR025386A1 (es) |
| AT (1) | ATE252091T1 (es) |
| AU (1) | AU7073400A (es) |
| CA (1) | CA2382966A1 (es) |
| DE (1) | DE60005973T2 (es) |
| DK (1) | DK1206457T3 (es) |
| ES (1) | ES2204684T3 (es) |
| PE (1) | PE20010529A1 (es) |
| PT (1) | PT1206457E (es) |
| WO (1) | WO2001016120A1 (es) |
Families Citing this family (100)
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|---|---|---|---|---|
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| AU8588798A (en) * | 1997-07-25 | 1999-02-16 | Institut Pasteur | Human peroxisome proliferator activated receptor gamma (ppargamma) gene re gulatory sequences and uses therefor |
| AU2000265105A1 (en) * | 2000-08-02 | 2002-02-13 | Pharmanutrients | Methods and compositions for the prevention and treatment of syndrome x |
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| JP2004509084A (ja) | 2000-08-23 | 2004-03-25 | イーライ・リリー・アンド・カンパニー | オキサゾリル−アリールオキシ酢酸誘導体およびそのpparアゴニストとしての使用 |
| PT1313716E (pt) | 2000-08-23 | 2007-07-11 | Lilly Co Eli | Derivados do ácido oxazolil-arilpropiónico e a sua utilização como agonistas do ppar |
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| GB0029974D0 (en) * | 2000-12-08 | 2001-01-24 | Glaxo Group Ltd | Chemical compounds |
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| US6982251B2 (en) | 2000-12-20 | 2006-01-03 | Schering Corporation | Substituted 2-azetidinones useful as hypocholesterolemic agents |
| EP1911462A3 (en) | 2001-01-26 | 2011-11-30 | Schering Corporation | Compositions comprising a sterol absorption inhibitor |
| US7071181B2 (en) | 2001-01-26 | 2006-07-04 | Schering Corporation | Methods and therapeutic combinations for the treatment of diabetes using sterol absorption inhibitors |
| CZ305202B6 (cs) | 2001-01-26 | 2015-06-10 | Merck Sharp & Dohme Corp. | Farmaceutický prostředek |
| RU2356550C2 (ru) | 2001-01-26 | 2009-05-27 | Шеринг Корпорейшн | Комбинации активатора (активаторов) рецептора, активируемого пролифератором пероксисом (рапп), и ингибитора (ингибиторов) всасывания стерина и лечение заболеваний сосудов |
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| US20110065129A1 (en) | 2001-07-27 | 2011-03-17 | Lowe Derek B | Indane acetic acid derivatives and their use as pharmaceutical agents, intermediates, and method of preparation |
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| KR100901683B1 (ko) | 2001-08-10 | 2009-06-08 | 닛뽕 케미파 가부시키가이샤 | 퍼옥시좀 증식제 응답성 수용체 δ의 활성화제 |
| MXPA04002330A (es) | 2001-09-14 | 2005-04-08 | Japan Tobacco Inc | Compuestos biarilo ligados. |
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| US7053080B2 (en) | 2001-09-21 | 2006-05-30 | Schering Corporation | Methods and therapeutic combinations for the treatment of obesity using sterol absorption inhibitors |
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| GB201621123D0 (en) | 2016-12-12 | 2017-01-25 | 4D Pharma Plc | Compositions comprising bacterial strains |
| TWI787272B (zh) | 2017-05-22 | 2022-12-21 | 英商4D製藥研究有限公司 | 包含細菌菌株之組合物 |
| JP6978514B2 (ja) | 2017-05-24 | 2021-12-08 | フォーディー ファーマ リサーチ リミテッド4D Pharma Research Limited | 細菌株を含む組成物 |
| WO2018229236A2 (en) | 2017-06-14 | 2018-12-20 | 4D Pharma Research Limited | Compositions comprising bacterial strains |
| ES2841902T3 (es) | 2017-06-14 | 2021-07-12 | 4D Pharma Res Ltd | Composiciones que comprenden cepas bacterianas |
| SG11201912105PA (en) | 2017-06-14 | 2020-01-30 | 4D Pharma Res Ltd | Compositions comprising bacterial strains |
| WO2019036024A1 (en) | 2017-08-17 | 2019-02-21 | Bristol-Myers Squibb Company | 2- (1,1'-BIPHENYL) -1H-BENZO [D] IMIDAZOLE DERIVATIVES AND RELATED COMPOUNDS AS AGONISTS OF APELIN AND APJ FOR THE TREATMENT OF CARDIOVASCULAR DISEASES |
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| US5089514A (en) | 1990-06-14 | 1992-02-18 | Pfizer Inc. | 3-coxazolyl [phenyl, chromanyl or benzofuranyl]-2-hydroxypropionic acid derivatives and analogs as hypoglycemic agents |
| WO1993021166A1 (en) * | 1992-04-10 | 1993-10-28 | Smithkline Beecham Plc | Heterocyclic compounds and their use in the treatment of type ii-diabetes |
| PL174610B1 (pl) | 1992-07-03 | 1998-08-31 | Smithkline Beecham Plc | Nowe związki heterocykliczne |
| GB9225386D0 (en) | 1992-12-04 | 1993-01-27 | Smithkline Beecham Plc | Novel compounds |
| GB9326171D0 (en) | 1993-12-22 | 1994-02-23 | Smithkline Beecham Plc | Novel compounds |
| WO1996004261A1 (en) | 1994-07-29 | 1996-02-15 | Smithkline Beecham Plc | Benzoxazoles and pryridine derivatives useful in the treatment of the type ii diabetes |
| US5902726A (en) | 1994-12-23 | 1999-05-11 | Glaxo Wellcome Inc. | Activators of the nuclear orphan receptor peroxisome proliferator-activated receptor gamma |
| US7115728B1 (en) | 1995-01-30 | 2006-10-03 | Ligand Pharmaceutical Incorporated | Human peroxisome proliferator activated receptor γ |
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| US6022897A (en) * | 1995-04-25 | 2000-02-08 | The Salk Institute For Biological Studies | Selective modulators of peroxisome proliferator activated receptor-gamma, and methods for the use thereof |
| JPH08325264A (ja) | 1995-05-31 | 1996-12-10 | Sumitomo Metal Ind Ltd | 新規2−芳香環置換−3−フェニルプロピオン酸またはアクリル酸誘導体 |
| JPH08325250A (ja) | 1995-05-31 | 1996-12-10 | Sumitomo Metal Ind Ltd | 新規置換フェノール誘導体 |
| US5939442A (en) * | 1995-06-07 | 1999-08-17 | The Salk Institute For Biological Studies | Modulations of peroxisome proliferator activated receptor-γ, and methods for the use thereof |
| KR19990045756A (ko) * | 1995-09-18 | 1999-06-25 | 윌리암 엘. 레스페스 | Rxr 작용제를 이용하는 niddm 치료 방법 |
| GB9600464D0 (en) * | 1996-01-09 | 1996-03-13 | Smithkline Beecham Plc | Novel method |
| ES2202582T3 (es) * | 1996-02-02 | 2004-04-01 | MERCK & CO., INC. | Agentes antidiabeticos. |
| GB9604242D0 (en) * | 1996-02-28 | 1996-05-01 | Glaxo Wellcome Inc | Chemical compounds |
| FR2749583B1 (fr) * | 1996-06-07 | 1998-08-21 | Lipha | Nouveaux derives de thiazolidine -2,4- dione substitues, leurs procedes d'obtention et les compositions pharmaceutiques en renfermant |
| WO1998005331A2 (en) * | 1996-08-02 | 1998-02-12 | Ligand Pharmaceuticals Incorporated | Prevention or treatment of type 2 diabetes or cardiovascular disease with ppar modulators |
| CN1233241A (zh) | 1996-08-19 | 1999-10-27 | 日本烟草产业株式会社 | 丙酸衍生物及其用途 |
| EP1005344A4 (en) * | 1996-12-31 | 2003-03-19 | Salk Inst For Biological Studi | TREATMENT OF LIPOSARCOMES USING A COMBINATION OF THIAZOLIDINEDIONES AND SELECTIVE AGONISTS OF RETINO X RECEPTORS |
| US5814647A (en) * | 1997-03-04 | 1998-09-29 | Board Of Regents, The University Of Texas System | Use of troglitazone and related compounds for the treatment of the climacteric symptoms |
| AU6773598A (en) * | 1997-03-26 | 1998-10-20 | Institut Pasteur | Treatment of gastrointestinal disease with ppar modulators |
| US6166192A (en) * | 1997-05-30 | 2000-12-26 | Dana-Farber Cancer Institute | PGC-1, a novel brown fat PPARγ coactivator |
| US5925657A (en) * | 1997-06-18 | 1999-07-20 | The General Hospital Corporation | Use of PPARγ agonists for inhibition of inflammatory cytokine production |
| AU8588798A (en) * | 1997-07-25 | 1999-02-16 | Institut Pasteur | Human peroxisome proliferator activated receptor gamma (ppargamma) gene re gulatory sequences and uses therefor |
| WO1999020275A1 (en) * | 1997-10-17 | 1999-04-29 | Aventis Pharmaceuticals Products Inc. | Therapeutic uses of quinoline derivatives |
| WO1999019313A1 (en) * | 1997-10-27 | 1999-04-22 | Dr. Reddy's Research Foundation | Novel tricyclic compounds and their use in medicine; process for their preparation and pharmaceutical compositions containing them |
| WO1999029317A1 (en) * | 1997-12-12 | 1999-06-17 | Purdue Research Foundation | Methods and compositions for treating diabetes |
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| WO1999038850A1 (en) * | 1998-01-29 | 1999-08-05 | Dr. Reddy's Research Foundation | Novel alkanoic acids and their use in medicine, process for their preparation and pharmaceutical compositions containing them |
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| AU3333399A (en) * | 1998-04-06 | 1999-10-25 | Janssen Pharmaceutica N.V. | Nucleotide sequence expressing human fatty acid transport protein and corresponding aminoacid sequence. use for the regulation of fatty acids metabolism |
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| PL345627A1 (en) * | 1998-07-21 | 2002-01-02 | Smithkline Beecham Plc | Use of glucose uptake enhancer for reducing apoptosis |
| GB9817118D0 (en) * | 1998-08-07 | 1998-10-07 | Glaxo Group Ltd | Pharmaceutical compounds |
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2000
- 2000-08-23 DE DE60005973T patent/DE60005973T2/de not_active Expired - Lifetime
- 2000-08-23 CA CA002382966A patent/CA2382966A1/en not_active Abandoned
- 2000-08-23 AU AU70734/00A patent/AU7073400A/en not_active Abandoned
- 2000-08-23 ES ES00959401T patent/ES2204684T3/es not_active Expired - Lifetime
- 2000-08-23 AT AT00959401T patent/ATE252091T1/de not_active IP Right Cessation
- 2000-08-23 WO PCT/US2000/023358 patent/WO2001016120A1/en not_active Ceased
- 2000-08-23 US US09/644,457 patent/US6417212B1/en not_active Expired - Fee Related
- 2000-08-23 JP JP2001519687A patent/JP2003508389A/ja not_active Withdrawn
- 2000-08-23 EP EP00959401A patent/EP1206457B1/en not_active Expired - Lifetime
- 2000-08-23 DK DK00959401T patent/DK1206457T3/da active
- 2000-08-23 PT PT00959401T patent/PT1206457E/pt unknown
- 2000-08-25 PE PE2000000876A patent/PE20010529A1/es not_active Application Discontinuation
- 2000-08-25 AR ARP000104410A patent/AR025386A1/es unknown
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2002
- 2002-04-11 US US10/121,373 patent/US6610696B2/en not_active Expired - Fee Related
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2003
- 2003-05-07 US US10/434,425 patent/US6825222B2/en not_active Expired - Fee Related
Also Published As
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|---|---|
| AR025386A1 (es) | 2002-11-27 |
| US6417212B1 (en) | 2002-07-09 |
| US6825222B2 (en) | 2004-11-30 |
| DE60005973D1 (de) | 2003-11-20 |
| EP1206457A1 (en) | 2002-05-22 |
| US20030045558A1 (en) | 2003-03-06 |
| DK1206457T3 (da) | 2004-02-16 |
| DE60005973T2 (de) | 2004-05-13 |
| EP1206457B1 (en) | 2003-10-15 |
| ES2204684T3 (es) | 2004-05-01 |
| WO2001016120A9 (en) | 2002-07-11 |
| US20040019090A1 (en) | 2004-01-29 |
| CA2382966A1 (en) | 2001-03-08 |
| US6610696B2 (en) | 2003-08-26 |
| JP2003508389A (ja) | 2003-03-04 |
| ATE252091T1 (de) | 2003-11-15 |
| AU7073400A (en) | 2001-03-26 |
| WO2001016120A1 (en) | 2001-03-08 |
| PT1206457E (pt) | 2004-03-31 |
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