PE20030119A1 - Derivados de 4-piperazinil indol con afinidad por el receptor 5-ht6 - Google Patents
Derivados de 4-piperazinil indol con afinidad por el receptor 5-ht6Info
- Publication number
- PE20030119A1 PE20030119A1 PE2002000503A PE2002000503A PE20030119A1 PE 20030119 A1 PE20030119 A1 PE 20030119A1 PE 2002000503 A PE2002000503 A PE 2002000503A PE 2002000503 A PE2002000503 A PE 2002000503A PE 20030119 A1 PE20030119 A1 PE 20030119A1
- Authority
- PE
- Peru
- Prior art keywords
- piperazin
- indol
- alkyl
- benzenosulfonil
- alcoxyl
- Prior art date
Links
Classifications
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- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/40—Nitrogen atoms, not forming part of a nitro radical, e.g. isatin semicarbazone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive 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
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- General 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)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Psychology (AREA)
- Pain & Pain Management (AREA)
- Child & Adolescent Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
SE REFIERE A DERIVADOS DE 4-PIPERAZINIL INDOL DE FORMULA I DONDE R1 ES H, HALO, HALOALQUILO, ALQUILO C1-C6; R2 ES H, ALQUILO C1-C6, ALCOXILO C1-C6, TIOALQUILO C1-C6; R3 ES SO2Ar; Ar ES ARILO, HETEROARILO OPCIONALMENTE SUSTITUIDO CON ALQUILO, ALCOXILO, TIOALQUILO, HALO, HALOALQUILO, HIDROXIALQUILO, NITRO, ENTRE OTROS; R4 ES H, HALOGENO, ALQUILO C1-C6, ALCOXILO C1-C6, TIOALQUILO C1-C6, TRIFLUOROMETILO, CIANO, ACILO; R5 ES H, BENCILO, ALQUILO C1-C6. SON COMPUESTOS PREFERIDOS 1-(NAFTALEN-1-SULFONIL)-4-PIPERAZIN-1-IL-1H-INDOL; 1-(3,5-DICLORO-BENCENOSULFONIL)-4-PIPERAZIN-1-IL-1H-INDOL; 1-BENCENOSULFONIL-4-PIPERAZIN-1-IL-1H-INDOL; 4-PIPERAZIN-1-IL-1-(3-TRIFLUOROMETIL-BENCENOSULFONIL)-1H-INDOL; 1-(4-METOXI-BENCENOSULFONIL)-4-PIPERAZIN-1-IL-1H-INDOL, ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION. LOS COMPUESTOS SON AGONISTAS DEL RECEPTOR 5-HIDROXITRIPTAMINA 5-HT6 Y PUEDEN SER UTILES PARA EL TRATAMIENTO DE ALZHEIMER, HUNTINGTON, PSICOSIS, ESQUIZOFRENIA, DEPRESIONES MANIACAS, TRASTORNOS DE DEFICIT DE ATENCION, ESCLEROSIS LATERAL AMIOTROFICA
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US29883401P | 2001-06-15 | 2001-06-15 | |
US37874802P | 2002-05-08 | 2002-05-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20030119A1 true PE20030119A1 (es) | 2003-02-13 |
Family
ID=26970893
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2002000503A PE20030119A1 (es) | 2001-06-15 | 2002-06-12 | Derivados de 4-piperazinil indol con afinidad por el receptor 5-ht6 |
Country Status (15)
Country | Link |
---|---|
US (1) | US6790848B2 (es) |
EP (1) | EP1401812B1 (es) |
JP (1) | JP2005501019A (es) |
KR (1) | KR20040010709A (es) |
AR (1) | AR036057A1 (es) |
AT (1) | ATE331707T1 (es) |
BR (1) | BR0210411A (es) |
CA (1) | CA2450245A1 (es) |
DE (1) | DE60212841T2 (es) |
ES (1) | ES2268113T3 (es) |
MX (1) | MXPA03011638A (es) |
PA (1) | PA8547901A1 (es) |
PE (1) | PE20030119A1 (es) |
UY (1) | UY27336A1 (es) |
WO (1) | WO2002102774A1 (es) |
Families Citing this family (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MXPA03003397A (es) * | 2000-10-20 | 2004-06-30 | Biovitrum Ab | N1-(bencensulfonil)indoles sustituidos en las posiciones 2-, 3-, 4-, o 5 y su uso en terapia. |
EP1956004B1 (en) | 2002-03-27 | 2012-06-13 | Glaxo Group Limited | Quinoline derivatives and their use as 5-HT6 ligands |
DK1587788T3 (da) * | 2002-09-17 | 2007-09-24 | Hoffmann La Roche | 2,7-substituerede indoler og anvendelsen deraf som 5-HT6-modulatorer |
EP1601358B1 (en) * | 2003-03-03 | 2007-12-19 | F. Hoffmann-La Roche Ag | 2,5-substituted tetrahydroisoquinolines for use as 5-ht6 modulators |
WO2004080407A2 (en) * | 2003-03-07 | 2004-09-23 | Predix Pharmaceuticals Holdings, Inc. | New serotonin modulating compounds and uses therefor |
ES2313002T3 (es) * | 2003-05-09 | 2009-03-01 | Laboratorios Del Dr. Esteve, S.A. | Uso de derivados de sulfonamida para la fabricacion de un medicamento para la profilaxis y/o tratamiento de la ingestion de alimentos. |
ES2219181B1 (es) * | 2003-05-09 | 2005-12-16 | Laboratorios Del Dr. Esteve, S.A. | Uso de derivados de sulfonamidas para la fabricacion de un medicamento para la profilaxis y/o tratamiento de las disfunciones alimentarias. |
ATE313532T1 (de) | 2003-07-22 | 2006-01-15 | Arena Pharm Inc | Diaryl- und arylheteroarylharnstoffderivate als modulatoren des 5-ht2a-serotoninrezeptors, die sich zur prophylaxe und behandlung von damit im zusammenhang stehenden erkrankungen eignen |
JP4964593B2 (ja) * | 2003-09-25 | 2012-07-04 | セノメド バイオサイエンシーズ,エルエルシー | 神経学的病状の治療用のテトラヒドロインドロン誘導体 |
SE0302760D0 (sv) * | 2003-10-20 | 2003-10-20 | Biovitrum Ab | New compounds |
ES2302174T3 (es) * | 2004-01-16 | 2008-07-01 | F. Hoffmann-La Roche Ag | Derivados 1-bencil-5-piperacin-1-il-3,4-dihidro-1h-quinazolin-2-ona y derivados respectivos de 1h-benzo(1,2,6)tiadiacin-2,2-dioxido y 1,4-dihidro-benzo(d)(1,3)oxacin-2-ona como moduladores del receptor 5-hidroxitriptamina(5-ht) para tratamiento enfermed. sistema nervioso central. |
US7713954B2 (en) * | 2004-09-30 | 2010-05-11 | Roche Palo Alto Llc | Compositions and methods for treating cognitive disorders |
ES2359725T3 (es) | 2004-09-30 | 2011-05-26 | F. Hoffmann-La Roche Ag | Composiciones y métodos para el tratamiento de trastornos cognitivos. |
US9216966B2 (en) | 2004-10-04 | 2015-12-22 | John Manfredi | Compounds for Alzheimer's disease |
US7678823B2 (en) * | 2004-10-04 | 2010-03-16 | Myriad Pharmaceticals, Inc. | Compounds for alzheimer's disease |
US7534796B2 (en) | 2005-02-18 | 2009-05-19 | Wyeth | Imidazo[4,5-b]pyridine antagonists of gonadotropin releasing hormone receptor |
US7538113B2 (en) | 2005-02-18 | 2009-05-26 | Wyeth | 4-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor |
US7582634B2 (en) | 2005-02-18 | 2009-09-01 | Wyeth | 7-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor |
US7531542B2 (en) | 2005-05-18 | 2009-05-12 | Wyeth | Benzooxazole and benzothiazole antagonists of gonadotropin releasing hormone receptor |
US7582636B2 (en) | 2005-05-26 | 2009-09-01 | Wyeth | Piperazinylimidazopyridine and piperazinyltriazolopyridine antagonists of Gonadotropin Releasing Hormone receptor |
JP2010519171A (ja) * | 2006-02-17 | 2010-06-03 | メモリー・ファーマシューティカルズ・コーポレイション | 5−ht6受容体親和性を有する化合物 |
KR20080110886A (ko) * | 2006-04-04 | 2008-12-19 | 미리어드 제네틱스, 인크. | 질병 및 장애용 화합물 |
RU2449990C2 (ru) | 2006-07-03 | 2012-05-10 | Биовитрум Аб (Пабл) | Индолы в качестве модуляторов 5-ht6 |
AU2007316736A1 (en) | 2006-11-09 | 2008-05-15 | F. Hoffmann-La Roche Ag | Indole and benzofuran 2-carboxamide derivatives |
JP2010528037A (ja) * | 2007-05-24 | 2010-08-19 | メモリー・ファーマシューティカルズ・コーポレイション | 5−ht6受容体親和性を有する4’置換化合物 |
MX2010001576A (es) * | 2007-08-15 | 2010-09-14 | Memory Pharm Corp | Compuestos 3´sustituidos que tienen afinidad con el receptor 5-hidroxitriptamina 6 (5-ht6). |
WO2009062134A1 (en) * | 2007-11-09 | 2009-05-14 | Cenomed Biosciences, Llc | Treatment of post-traumatic stress disorder with tetrahydroindolone arylpiperazine compounds |
EP2254564A1 (en) | 2007-12-12 | 2010-12-01 | Glaxo Group Limited | Combinations comprising 3-phenylsulfonyl-8-piperazinyl-1yl-quinoline |
US20110021538A1 (en) | 2008-04-02 | 2011-01-27 | Arena Pharmaceuticals, Inc. | Processes for the preparation of pyrazole derivatives useful as modulators of the 5-ht2a serotonin receptor |
US20090264443A1 (en) * | 2008-04-18 | 2009-10-22 | David Helton | Treatment of organophosphate exposure with tetrahydroindolone arylpiperazine compounds |
US20100016297A1 (en) * | 2008-06-24 | 2010-01-21 | Memory Pharmaceuticals Corporation | Alkyl-substituted 3' compounds having 5-ht6 receptor affinity |
US20100022581A1 (en) * | 2008-07-02 | 2010-01-28 | Memory Pharmaceuticals Corporation | Pyrrolidine-substituted azaindole compounds having 5-ht6 receptor affinity |
US20100029629A1 (en) * | 2008-07-25 | 2010-02-04 | Memory Pharmaceuticals Corporation | Acyclic compounds having 5-ht6 receptor affinity |
US20100056531A1 (en) * | 2008-08-22 | 2010-03-04 | Memory Pharmaceuticals Corporation | Alkyl-substituted 3' compounds having 5-ht6 receptor affinity |
US9126946B2 (en) | 2008-10-28 | 2015-09-08 | Arena Pharmaceuticals, Inc. | Processes useful for the preparation of 1-[3-(4-bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenyl]-3-(2,4-difluoro-phenyl)urea and crystalline forms related thereto |
UA100192C2 (en) * | 2008-11-11 | 2012-11-26 | УАЙТ ЭлЭлСи | 1-(arylsulfonyl)-4-(piperazin-1-yl)-1h-benzimidazoles as 5-hydroxytryptamine-6 ligands |
US8367676B2 (en) | 2009-06-30 | 2013-02-05 | Astrazeneca Ab | 2-carboxamide-7-piperazinyl-benzofuran derivatives 774 |
WO2011088836A1 (en) | 2010-01-25 | 2011-07-28 | H. Lundbeck A/S | NOVEL 4-(ARYL-4-SULFONYL)-6,6a,7,8,9,10-HEXAHYDRO-4H-4,8,10a-TRIAZA-ACEPHENANTHRYLENE AND 3-ARYLSULFONYL-6,6a,7,8,9,10-HEXAHYDRO-3H-3,8,10a-TRIAZA-CYCLOPENTA[C]FLUORENE DERIVATIVES AS SEROTONIN 5-HT6 LIGANDS |
US20120157494A1 (en) * | 2010-12-16 | 2012-06-21 | Harris Iii Ralph New | Isoindolyl compounds |
KR20130132932A (ko) | 2010-12-20 | 2013-12-05 | 아스트라제네카 아베 | 2-카르복스아미드-4-피페라지닐-벤조푸란 유도체 |
US9663498B2 (en) | 2013-12-20 | 2017-05-30 | Sunshine Lake Pharma Co., Ltd. | Aromatic heterocyclic compounds and their application in pharmaceuticals |
AU2015286049B2 (en) * | 2014-07-08 | 2018-03-01 | Sunshine Lake Pharma Co., Ltd. | Aromatic heterocyclic derivatives and pharmaceutical applications thereof |
KR20180022792A (ko) | 2015-06-12 | 2018-03-06 | 엑소반트 사이언시즈 게엠베하 | 렘 수면 행동 장애의 예방 및 치료에 유용한 디아릴 및 아릴헤테로아릴 우레아 유도체 |
KR20180064373A (ko) | 2015-07-15 | 2018-06-14 | 엑소반트 사이언시즈 게엠베하 | 신경퇴행성 질환과 관련된 환각의 예방 및 치료에 유용한 5-ht2a 세로토닌 수용체의 조절자로서의 다이아릴 및 아릴헤테로아릴 우레아 유도체 |
WO2017052394A1 (en) | 2015-09-23 | 2017-03-30 | Uniwersytet Jagielloński | Imidazopyridine compounds and their use as 5-ht6 receptor ligands |
EP3911651B1 (en) | 2019-01-17 | 2024-01-10 | ViiV Healthcare UK (No.4) Limited | Process for preparing fostemsavir |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60190761A (ja) | 1984-03-09 | 1985-09-28 | Sagami Chem Res Center | 4−アミノインド−ルの製造方法 |
US5696122A (en) * | 1993-09-03 | 1997-12-09 | Smithkline Beecham P.L.C. | Indole and indoline derivatives as 5HT1D receptor antagonists |
WO1996003400A1 (en) | 1994-07-26 | 1996-02-08 | Pfizer Inc. | 4-indole derivatives as serotonin agonists and antagonists |
DZ2376A1 (fr) | 1996-12-19 | 2002-12-28 | Smithkline Beecham Plc | Dérivés de sulfonamides nouveaux procédé pour leurpréparation et compositions pharmaceutiques les c ontenant. |
US6194410B1 (en) | 1998-03-11 | 2001-02-27 | Hoffman-La Roche Inc. | Pyrazolopyrimidine and pyrazolines and process for preparation thereof |
US6251893B1 (en) | 1998-06-15 | 2001-06-26 | Nps Allelix Corp. | Bicyclic piperidine and piperazine compounds having 5-HT6 receptor affinity |
DE19934433A1 (de) * | 1999-07-22 | 2001-01-25 | Merck Patent Gmbh | N-(Indolcarbonyl-)piperazinderivate |
WO2001032660A1 (en) | 1999-11-05 | 2001-05-10 | Nps Allelix Corp. | Compounds having 5-ht6 receptor antagonist activity |
SE0002754D0 (sv) * | 2000-07-21 | 2000-07-21 | Pharmacia & Upjohn Ab | New pharmaceutical combination formulation and method of treatment with the combination |
MXPA03003397A (es) * | 2000-10-20 | 2004-06-30 | Biovitrum Ab | N1-(bencensulfonil)indoles sustituidos en las posiciones 2-, 3-, 4-, o 5 y su uso en terapia. |
BR0115102B1 (pt) * | 2000-11-02 | 2013-11-26 | Compostos 1-aril- ou 1-alquilsulfonil-heterociclilbenzazóis e composição compreendendo os mesmos | |
ES2271124T3 (es) * | 2000-11-24 | 2007-04-16 | Smithkline Beecham Plc | Compuestos indolil-sulfonilicos utiles en el tratamiento de trastornos del snc. |
-
2002
- 2002-06-06 CA CA002450245A patent/CA2450245A1/en not_active Abandoned
- 2002-06-06 AT AT02780760T patent/ATE331707T1/de not_active IP Right Cessation
- 2002-06-06 EP EP02780760A patent/EP1401812B1/en not_active Expired - Lifetime
- 2002-06-06 JP JP2003505317A patent/JP2005501019A/ja active Pending
- 2002-06-06 KR KR10-2003-7016359A patent/KR20040010709A/ko not_active Ceased
- 2002-06-06 WO PCT/EP2002/006201 patent/WO2002102774A1/en active IP Right Grant
- 2002-06-06 BR BR0210411-3A patent/BR0210411A/pt not_active Application Discontinuation
- 2002-06-06 ES ES02780760T patent/ES2268113T3/es not_active Expired - Lifetime
- 2002-06-06 DE DE60212841T patent/DE60212841T2/de not_active Expired - Fee Related
- 2002-06-06 MX MXPA03011638A patent/MXPA03011638A/es unknown
- 2002-06-12 PA PA20028547901A patent/PA8547901A1/es unknown
- 2002-06-12 PE PE2002000503A patent/PE20030119A1/es not_active Application Discontinuation
- 2002-06-14 AR ARP020102239A patent/AR036057A1/es unknown
- 2002-06-14 US US10/172,360 patent/US6790848B2/en not_active Expired - Fee Related
- 2002-06-14 UY UY27336A patent/UY27336A1/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
JP2005501019A (ja) | 2005-01-13 |
BR0210411A (pt) | 2004-08-17 |
US6790848B2 (en) | 2004-09-14 |
ATE331707T1 (de) | 2006-07-15 |
US20030045527A1 (en) | 2003-03-06 |
DE60212841D1 (de) | 2006-08-10 |
MXPA03011638A (es) | 2004-04-02 |
CA2450245A1 (en) | 2002-12-27 |
UY27336A1 (es) | 2002-12-31 |
ES2268113T3 (es) | 2007-03-16 |
KR20040010709A (ko) | 2004-01-31 |
EP1401812A1 (en) | 2004-03-31 |
WO2002102774A1 (en) | 2002-12-27 |
PA8547901A1 (es) | 2003-12-10 |
AR036057A1 (es) | 2004-08-04 |
DE60212841T2 (de) | 2007-06-21 |
EP1401812B1 (en) | 2006-06-28 |
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