MA27475A1 - Composes de pyrazolo [3,4-b] pyridine et leur utilisation en tant qu'inhibiteurs de phosphodiesterase - Google Patents
Composes de pyrazolo [3,4-b] pyridine et leur utilisation en tant qu'inhibiteurs de phosphodiesteraseInfo
- Publication number
- MA27475A1 MA27475A1 MA28224A MA28224A MA27475A1 MA 27475 A1 MA27475 A1 MA 27475A1 MA 28224 A MA28224 A MA 28224A MA 28224 A MA28224 A MA 28224A MA 27475 A1 MA27475 A1 MA 27475A1
- Authority
- MA
- Morocco
- Prior art keywords
- sub
- sup
- optionally substituted
- formula
- inhibitors
- 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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Neurology (AREA)
- Otolaryngology (AREA)
- Hospice & Palliative Care (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
L'invention concerne un composé de la formule (I) ou bien un sel de celui-ci, dans laquelle R1 représente alkyle C1-4, fluoroalkyle C1-3, -CH2CH2OH ou -CH2CH2CO2 alkyle C1-2;R2 représente un atome d'hydrogène (H), méthyle ou fluoroalkyle C1;R3 représente cycloalkyle C3-8 facultativement substitué ou cycloalcényle C1-7 facultativement substitué mono-insaturé ou un groupe hétérocyclique facultativement substitué de sous-formule (aa), (bb) ou (cc); dans lesquelles n1 et n2 représentent indépendamment 1 ou 2, et dans lesquelles Y représente O, S, SO2, ou NR10; ou R3 représente un groupe bicyclique (dd) ou (ee); et dans laquelle X représente NR4R5 ou OR5a. Les composés sont des inhibiteurs de phosphodiestérase (PDE), en particulier des inhibiteurs de PDE4. L'invention concerne également l'utilisation d'un composé de la formule (I), ou d'un sel pharmaceutiquement acceptable de celui-ci, dans la fabrication d'un médicament destiné au traitement et/ou à la prophylaxie d'une maladie inflammatoire et/ou allergique chez un mammifère tel que l'homme, par exemple la bronchopneumopathie chronique obstructive (PBCO), l'asthme ou la rhinite allergique.
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0221455A GB0221455D0 (en) | 2002-09-16 | 2002-09-16 | Compounds |
GBGB0230045.7A GB0230045D0 (en) | 2002-12-23 | 2002-12-23 | Compounds |
GB0306595A GB0306595D0 (en) | 2003-03-21 | 2003-03-21 | Compounds |
GB0308017A GB0308017D0 (en) | 2003-04-07 | 2003-04-07 | Compounds |
GB0319708A GB0319708D0 (en) | 2003-08-21 | 2003-08-21 | Compounds |
GB0321074A GB0321074D0 (en) | 2003-09-09 | 2003-09-09 | Compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
MA27475A1 true MA27475A1 (fr) | 2005-08-01 |
Family
ID=31999797
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA28224A MA27475A1 (fr) | 2002-09-16 | 2005-04-15 | Composes de pyrazolo [3,4-b] pyridine et leur utilisation en tant qu'inhibiteurs de phosphodiesterase |
Country Status (23)
Country | Link |
---|---|
US (2) | US20060089375A1 (fr) |
EP (1) | EP1539753B1 (fr) |
JP (1) | JP2006503108A (fr) |
KR (1) | KR20050052501A (fr) |
CN (1) | CN100387598C (fr) |
AT (1) | ATE442367T1 (fr) |
AU (1) | AU2010201417A1 (fr) |
BR (1) | BR0314392A (fr) |
CA (1) | CA2497550A1 (fr) |
CY (1) | CY1109619T1 (fr) |
DE (1) | DE60329193D1 (fr) |
DK (1) | DK1539753T3 (fr) |
ES (1) | ES2331119T3 (fr) |
IL (1) | IL166898A (fr) |
IS (1) | IS7709A (fr) |
MA (1) | MA27475A1 (fr) |
MX (1) | MXPA05002887A (fr) |
NO (1) | NO20050841L (fr) |
NZ (1) | NZ538515A (fr) |
PL (1) | PL375993A1 (fr) |
PT (1) | PT1539753E (fr) |
SI (1) | SI1539753T1 (fr) |
WO (1) | WO2004024728A2 (fr) |
Families Citing this family (89)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004024728A2 (fr) * | 2002-09-16 | 2004-03-25 | Glaxo Group Limited | Composes de pyrazolo[3,4-b]pyridine et leur utilisation en tant qu'inhibiteurs de phosphodiesterase |
GB0230045D0 (en) * | 2002-12-23 | 2003-01-29 | Glaxo Group Ltd | Compounds |
US20070179161A1 (en) * | 2003-03-31 | 2007-08-02 | Vernalis (Cambridge) Limited. | Pyrazolopyrimidine compounds and their use in medicine |
AU2004233827B2 (en) | 2003-04-24 | 2009-05-28 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
GB0316290D0 (en) | 2003-07-11 | 2003-08-13 | Glaxo Group Ltd | Novel compounds |
CA2557004A1 (fr) * | 2003-12-19 | 2005-06-30 | Glaxo Group Limited | Composes pyrazolo [3,4-b] pyridine et leur utilisation en tant qu'inhibiteurs de la phosphodiesterase |
WO2005090352A1 (fr) * | 2004-03-16 | 2005-09-29 | Glaxo Group Limited | Compose de pyrazolo[3,4-b]pyridine, et son utilisation en tant qu'inhibiteur de pdea4 |
GB0405933D0 (en) * | 2004-03-16 | 2004-04-21 | Glaxo Group Ltd | Compounds |
JP2007530652A (ja) | 2004-04-02 | 2007-11-01 | グラクソ グループ リミテッド | 化学物質、調製方法、及び、新規結晶形態 |
PE20060272A1 (es) | 2004-05-24 | 2006-05-22 | Glaxo Group Ltd | (2r,3r,4s,5r,2'r,3'r,4's,5's)-2,2'-{trans-1,4-ciclohexanodiilbis-[imino(2-{[2-(1-metil-1h-imidazol-4-il)etil]amino}-9h-purin-6,9-diil)]}bis[5-(2-etil-2h-tetrazol-5-il)tetrahidro-3,4-furanodiol] como agonista a2a |
TWI307630B (en) | 2004-07-01 | 2009-03-21 | Glaxo Group Ltd | Immunoglobulins |
MXPA06014699A (es) * | 2004-07-05 | 2007-03-26 | Astellas Pharma Inc | Derivados de pirazolo-piridina. |
GB0418045D0 (en) | 2004-08-12 | 2004-09-15 | Glaxo Group Ltd | Compounds |
ATE517908T1 (de) | 2005-01-10 | 2011-08-15 | Glaxo Group Ltd | Androstan-17-alpha-carbonat-derivate zur verwendung bei der behandlung allergischer und entzündlicher zustände |
GB0514809D0 (en) | 2005-07-19 | 2005-08-24 | Glaxo Group Ltd | Compounds |
EP1940836A1 (fr) * | 2005-09-29 | 2008-07-09 | Glaxo Group Limited | Compose de pyrazolo[3,4-b]pyridine et utilisation en tant qu'inhibiteur de pde4 |
TW200730498A (en) | 2005-12-20 | 2007-08-16 | Glaxo Group Ltd | Compounds |
ES2462240T3 (es) * | 2006-02-28 | 2014-05-22 | Dart Neuroscience (Cayman) Ltd | Piperazinas terapéuticas como inhibidores de PDE4 |
US8927546B2 (en) | 2006-02-28 | 2015-01-06 | Dart Neuroscience (Cayman) Ltd. | Therapeutic piperazines |
BRPI0708615A2 (pt) * | 2006-03-07 | 2011-06-07 | Array Biopharma Inc | compostos de pirazol heterobicìclicos e métodos de uso |
US8178573B2 (en) | 2006-04-20 | 2012-05-15 | Glaxo Group Limited | Compounds |
GB0611587D0 (en) | 2006-06-12 | 2006-07-19 | Glaxo Group Ltd | Novel compounds |
CL2007001829A1 (es) | 2006-06-23 | 2008-01-25 | Smithkline Beecham Corp | P-toluensulfonato de n-[4-cloro-2-hidroxi-3-(piperazina-1-sulfonil)fenil]-n-(2-cloro-3-fluorofenil)urea;procedimiento de preparacion;composicion farmaceutica;combinacion farmaceutica;y uso en el tratamiento de una enfermedad mediada por la quiimioquina il-8, tales como asma y epoc. |
PT2046787E (pt) | 2006-08-01 | 2011-06-15 | Glaxo Group Ltd | Compostos de pirazolo[3,4-b]piridina e sua utilização como inibidores de pde4 |
AR065804A1 (es) | 2007-03-23 | 2009-07-01 | Smithkline Beecham Corp | Compuesto de indol carboxamida, composicion farmaceutica que lo comprende y uso de dicho compuesto para preparar un medicamento |
WO2009041591A1 (fr) * | 2007-09-28 | 2009-04-02 | Kyowa Hakko Kirin Co., Ltd. | Dérivé de pyridine fusionnée |
EP2070929A1 (fr) * | 2007-12-11 | 2009-06-17 | Bayer Schering Pharma Aktiengesellschaft | Composés d'alkynylaryle et sels correspondants, compositions pharmaceutiques contenant ceux-ci, procédés de préparation de ceux-ci et usage de ceux-ci |
UY31636A1 (es) | 2008-02-06 | 2009-08-03 | Farmacoforos duales-antagonistas muscarinicos de pde4 | |
PE20091552A1 (es) * | 2008-02-06 | 2009-10-25 | Glaxo Group Ltd | Farmacoforos duales - antagonistas muscarinicos de pde4 |
AR070564A1 (es) | 2008-02-06 | 2010-04-21 | Glaxo Group Ltd | Derivados de 1h-pirazolo[3,4-b]piridin-5-ilo,inhibidores de fosfodiesterasas pde4 y antagonistas de receptores muscarinicos de acetilcolina(machr), utiles en el tratamiento y/o profilaxis de enfermedades respiratorias y alergicas,y composiciones farmaceuticas que los comprenden |
EP2285803A4 (fr) | 2008-05-23 | 2011-10-05 | Amira Pharmaceuticals Inc | Inhibiteur de la protéine d activation de 5-lipoxygénase |
JP5502858B2 (ja) | 2008-06-05 | 2014-05-28 | グラクソ グループ リミテッド | Pi3キナーゼの阻害剤として有用な4−カルボキサミドインダゾール誘導体 |
WO2010094643A1 (fr) | 2009-02-17 | 2010-08-26 | Glaxo Group Limited | Dérivés de quinoline et applications associées dans la rhinite et l'urticaire |
JP5656880B2 (ja) | 2009-03-09 | 2015-01-21 | グラクソ グループ リミテッドGlaxo Group Limited | Pi3キナーゼの阻害剤としての4−オキサジアゾール−2−イル−インダゾール |
WO2010102968A1 (fr) | 2009-03-10 | 2010-09-16 | Glaxo Group Limited | Dérivés d'indole comme inhibiteurs de ikk2 |
WO2010106016A1 (fr) | 2009-03-17 | 2010-09-23 | Glaxo Group Limited | Dérivés de pyrimidine utilisés comme inhibiteurs de ltk |
WO2010107952A2 (fr) | 2009-03-19 | 2010-09-23 | Merck Sharp & Dohme Corp. | Inhibition médiée par arn interférence de l'expression génique de facteur de croissance de tissu conjonctif (ctgf) en utilisant un acide nucléique interférant court (ansi) |
CN102439151A (zh) | 2009-03-19 | 2012-05-02 | 默沙东公司 | 使用短干扰核酸(siNA)的RNA干扰介导的BTB和CNC同系物1,碱性亮氨酸拉链转录因子1(Bach1)基因表达的抑制 |
WO2010107957A2 (fr) | 2009-03-19 | 2010-09-23 | Merck Sharp & Dohme Corp. | Inhibition induite par arn interférence d'une expression génique (gata3) d'une protéine de liaison gata au moyen d'un acide nucléique interférent court |
EP2408458A1 (fr) | 2009-03-19 | 2012-01-25 | Merck Sharp&Dohme Corp. | INHIBITION INDUITE PAR ARN INTERFÉRENCE DE L'EXPRESSION DU GÈNE TRANSDUCTEUR DE SIGNAL ET ACTIVITATEUR DE TRANSCRIPTION 6 (STAT6) AU MOYEN D'UN ACIDE NUCLÉIQUE INTERFÉRENT COURT (ANsi) |
WO2010111464A1 (fr) | 2009-03-27 | 2010-09-30 | Merck Sharp & Dohme Corp. | Inhibition par interférence arn de l'expression du gène kinase 1 de régulation du signal d'apoptose (ask1) au moyen d'un acide nucléique interférent court (ansi) |
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WO2010111490A2 (fr) | 2009-03-27 | 2010-09-30 | Merck Sharp & Dohme Corp. | Inhibition à médiation par l'interférence arn de l'expression du gène de la lymphopoïétine stromale thymique (tslp) faisant appel à de courts acides nucléiques interférents (ansi) |
JP2012521765A (ja) | 2009-03-27 | 2012-09-20 | メルク・シャープ・エンド・ドーム・コーポレイション | 低分子干渉核酸(siNA)を用いた細胞内接着分子1(ICAM−1)遺伝子発現のRNA干渉媒介性阻害 |
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EP2421834A1 (fr) | 2009-04-24 | 2012-02-29 | Glaxo Group Limited | Pyrazole et triazole carboxamides en tant qu'inhibiteurs du canal crac |
EP2421835A1 (fr) | 2009-04-24 | 2012-02-29 | Glaxo Group Limited | Carboxamides n-pyrazolyl en tant qu'inhibiteurs du canal crac |
AU2010243613B2 (en) | 2009-04-30 | 2015-05-07 | Glaxo Group Limited | Oxazole substituted indazoles as PI3-kinase inhibitors |
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EP3020393B1 (fr) | 2009-12-16 | 2020-10-07 | 3M Innovative Properties Company | Formulations et procédés de commande de distribution granulométrique mdi |
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GB201007203D0 (en) | 2010-04-29 | 2010-06-16 | Glaxo Group Ltd | Novel compounds |
WO2011143106A1 (fr) * | 2010-05-10 | 2011-11-17 | Gilead Sciences, Inc. | Composés pyrazolopyridiniques bifonctionnels |
EP2397482A1 (fr) | 2010-06-15 | 2011-12-21 | Almirall, S.A. | Dérivés d'imidazolone d'hétéroaryle en tant qu'inhibiteurs de JAK |
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WO2012035055A1 (fr) | 2010-09-17 | 2012-03-22 | Glaxo Group Limited | Nouveaux composés |
EP2630126B1 (fr) | 2010-10-21 | 2015-01-07 | Glaxo Group Limited | Composés pyrazole agissant contre des états allergiques, immunitaires et inflammatoires |
EP2630127A1 (fr) | 2010-10-21 | 2013-08-28 | Glaxo Group Limited | Composés de pyrazole agissant contre des troubles allergiques, inflammatoires et immunitaires |
GB201018124D0 (en) | 2010-10-27 | 2010-12-08 | Glaxo Group Ltd | Polymorphs and salts |
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MX2023002539A (es) | 2020-09-10 | 2023-03-14 | Vanda Pharmaceuticals Inc | Metodos para tratar enfermedades o afecciones mediadas por fosfodiesterasa iv (pde iv). |
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Publication number | Priority date | Publication date | Assignee | Title |
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US598973A (en) * | 1898-02-15 | Water-heater and smoke-consumer | ||
US598838A (en) * | 1898-02-08 | William b | ||
US3833594A (en) * | 1971-08-05 | 1974-09-03 | Squibb & Sons Inc | Amino derivatives of pyrazolopyridine carboxylic acids and esters |
US3856799A (en) * | 1971-08-05 | 1974-12-24 | Squibb & Sons Inc | Intermediates for production of amino derivatives of pyrazolopyridine carboxylic acids and esters |
BE787249A (fr) * | 1971-08-05 | 1973-02-05 | Squibb & Sons Inc | Derives amino d'acides pyrazolopyridine carboxyliques, leurs esters et les sels de ces composes, ainsi que leurs procedes de preparation |
US3925388A (en) * | 1971-08-05 | 1975-12-09 | Squibb & Sons Inc | 4-Piperazino-{8 3,4-b{9 pyridine-5-carboxylic acids and esters |
US4012373A (en) * | 1972-09-22 | 1977-03-15 | E. R. Squibb & Sons, Inc. | Pyrazolo[3',4'-2,3]pyrido[4,5-e]b-benzo-1,5-diazepinones |
US3979399A (en) * | 1972-11-15 | 1976-09-07 | E. R. Squibb & Sons, Inc. | Amino derivatives of pyrazolopyridine carboxamides |
US3840546A (en) * | 1972-11-15 | 1974-10-08 | Squibb & Sons Inc | Amino derivatives of pyrazolopyridine carboxamides |
US3833598A (en) * | 1972-12-29 | 1974-09-03 | Squibb & Sons Inc | Amino derivatives of pyrazolopyridine-6-carboxylic acids and esters |
US4115394A (en) * | 1974-05-06 | 1978-09-19 | E. R. Squibb & Sons, Inc. | Amino derivatives of 6-phenylpyrazolo[3,4-b]pyridines |
US5593997A (en) * | 1995-05-23 | 1997-01-14 | Pfizer Inc. | 4-aminopyrazolo(3-,4-D)pyrimidine and 4-aminopyrazolo-(3,4-D)pyridine tyrosine kinase inhibitors |
US6326379B1 (en) * | 1998-09-16 | 2001-12-04 | Bristol-Myers Squibb Co. | Fused pyridine inhibitors of cGMP phosphodiesterase |
JP2002020386A (ja) * | 2000-07-07 | 2002-01-23 | Ono Pharmaceut Co Ltd | ピラゾロピリジン誘導体 |
US20050043319A1 (en) * | 2001-08-14 | 2005-02-24 | Exonhit Therapeutics Sa | Molecular target of neurotoxicity |
WO2004024728A2 (fr) * | 2002-09-16 | 2004-03-25 | Glaxo Group Limited | Composes de pyrazolo[3,4-b]pyridine et leur utilisation en tant qu'inhibiteurs de phosphodiesterase |
GB0230045D0 (en) * | 2002-12-23 | 2003-01-29 | Glaxo Group Ltd | Compounds |
CA2557004A1 (fr) * | 2003-12-19 | 2005-06-30 | Glaxo Group Limited | Composes pyrazolo [3,4-b] pyridine et leur utilisation en tant qu'inhibiteurs de la phosphodiesterase |
-
2003
- 2003-09-12 WO PCT/EP2003/011814 patent/WO2004024728A2/fr active Application Filing
- 2003-09-12 EP EP03778283A patent/EP1539753B1/fr not_active Expired - Lifetime
- 2003-09-12 CA CA002497550A patent/CA2497550A1/fr not_active Abandoned
- 2003-09-12 SI SI200331680T patent/SI1539753T1/sl unknown
- 2003-09-12 NZ NZ538515A patent/NZ538515A/en unknown
- 2003-09-12 DE DE60329193T patent/DE60329193D1/de not_active Expired - Lifetime
- 2003-09-12 ES ES03778283T patent/ES2331119T3/es not_active Expired - Lifetime
- 2003-09-12 PT PT03778283T patent/PT1539753E/pt unknown
- 2003-09-12 CN CNB038250438A patent/CN100387598C/zh not_active Expired - Fee Related
- 2003-09-12 AT AT03778283T patent/ATE442367T1/de active
- 2003-09-12 KR KR1020057004514A patent/KR20050052501A/ko not_active Application Discontinuation
- 2003-09-12 MX MXPA05002887A patent/MXPA05002887A/es active IP Right Grant
- 2003-09-12 US US10/527,866 patent/US20060089375A1/en not_active Abandoned
- 2003-09-12 PL PL03375993A patent/PL375993A1/xx not_active Application Discontinuation
- 2003-09-12 JP JP2004571743A patent/JP2006503108A/ja active Pending
- 2003-09-12 BR BR0314392-9A patent/BR0314392A/pt not_active IP Right Cessation
- 2003-09-12 DK DK03778283T patent/DK1539753T3/da active
-
2005
- 2005-02-15 IL IL166898A patent/IL166898A/en not_active IP Right Cessation
- 2005-02-16 NO NO20050841A patent/NO20050841L/no unknown
- 2005-02-24 IS IS7709A patent/IS7709A/is unknown
- 2005-04-15 MA MA28224A patent/MA27475A1/fr unknown
-
2008
- 2008-01-14 US US12/013,529 patent/US20080175914A1/en not_active Abandoned
-
2009
- 2009-11-24 CY CY20091101212T patent/CY1109619T1/el unknown
-
2010
- 2010-04-08 AU AU2010201417A patent/AU2010201417A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
US20080175914A1 (en) | 2008-07-24 |
BR0314392A (pt) | 2005-07-12 |
NZ538515A (en) | 2007-04-27 |
PL375993A1 (en) | 2005-12-12 |
US20060089375A1 (en) | 2006-04-27 |
SI1539753T1 (sl) | 2009-12-31 |
CA2497550A1 (fr) | 2004-03-25 |
JP2006503108A (ja) | 2006-01-26 |
ES2331119T3 (es) | 2009-12-22 |
WO2004024728A2 (fr) | 2004-03-25 |
AU2010201417A1 (en) | 2010-04-29 |
EP1539753A2 (fr) | 2005-06-15 |
CN1694882A (zh) | 2005-11-09 |
EP1539753B1 (fr) | 2009-09-09 |
MXPA05002887A (es) | 2005-05-27 |
NO20050841L (no) | 2005-06-15 |
WO2004024728A3 (fr) | 2004-10-21 |
IS7709A (is) | 2005-02-24 |
DE60329193D1 (de) | 2009-10-22 |
CN100387598C (zh) | 2008-05-14 |
CY1109619T1 (el) | 2014-08-13 |
AU2003285300A1 (en) | 2004-04-30 |
ATE442367T1 (de) | 2009-09-15 |
KR20050052501A (ko) | 2005-06-02 |
PT1539753E (pt) | 2009-12-10 |
IL166898A (en) | 2010-06-30 |
DK1539753T3 (da) | 2010-01-04 |
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