PE20050306A1 - Compuestos imidazol condensado, 2-piridilo sustituido como inhibidores del factor de crecimiento transformante (tgf) - Google Patents
Compuestos imidazol condensado, 2-piridilo sustituido como inhibidores del factor de crecimiento transformante (tgf)Info
- Publication number
- PE20050306A1 PE20050306A1 PE2004000223A PE2004000223A PE20050306A1 PE 20050306 A1 PE20050306 A1 PE 20050306A1 PE 2004000223 A PE2004000223 A PE 2004000223A PE 2004000223 A PE2004000223 A PE 2004000223A PE 20050306 A1 PE20050306 A1 PE 20050306A1
- Authority
- PE
- Peru
- Prior art keywords
- imidazol
- tgf
- inhibitors
- growth factor
- compounds
- Prior art date
Links
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 title abstract 6
- 102000009618 Transforming Growth Factors Human genes 0.000 title abstract 4
- 108010009583 Transforming Growth Factors Proteins 0.000 title abstract 4
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000003112 inhibitor Substances 0.000 title abstract 2
- -1 2-PYRIDYL Chemical group 0.000 title 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 title 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000003176 fibrotic effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 230000019491 signal transduction Effects 0.000 abstract 1
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
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
- 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
- A61P9/08—Vasodilators for multiple indications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Urology & Nephrology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Steroid Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE LAS FORMULAS (Ia) O (Ib), EN DONDE R1 ES UN ANILLO MONO, BI O POLICICLICO(C3-C20) SATURADO, INSATURADO O AROMATICO, OPCIONALMENTE SUSTITUIDO, QUE CONTIENE AL MENOS UN HETEROATOMO DE N, O Y S; CADA R3 ES H, HALO, HALOALQUILO(C1-C6), ALQUILO(C1-C6), ALQUENILO O ALQUILO(C2-C6), HETEROCICLILO(C5-C10), PERHALOALQUILO(C1-C6), ENTRE OTROS; S ES DE 1 A 5; R4 Y R6 TOMADOS JUNTO CON LOS ATOMOS A LOS QUE ESTAN UNIDOS FORMAN UN NUCLEO HETEROAROMATICO CONDENSADO. SON COMPUESTOS PREFERIDOS: 6-[2-(6-METILPIRIDIN-2-IL)IMIDAZOL[1,2-a]PIRIDIN-3-IL]QUINOLINA, 2-BENZO[1,3]DIOXOL-5-IL-3-(6-METILPIRIDINIL-2-IL)-1H-IMIDAZOL[1,2-a]IMIDAZOL, 1-METIL-6-[6-(6-METILPIRIDIN-2-IL)IMIDAZOL[2,1-b]TIAZOL-5-IL]-1H-BENZOTRIAZOL, 3-BENZOTIAZOL-6-IL-2-(6-METILPIRIDIN-2-IL)IMIDAZOL[1,2-a]PIRIMIDIN-7-ILAMINA, ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. ESTOS COMPUESTOS SON INHIBIDORES DE LA RUTA SENALIZADORA DEL FACTOR DE CRECIMIENTO TRANSFORMANTE (TGF)-BETA Y SON UTILES EN EL TRATAMIENTO DEL CANCER Y ENFERMEDADES FIBROTICAS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45168303P | 2003-03-04 | 2003-03-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20050306A1 true PE20050306A1 (es) | 2005-05-16 |
Family
ID=32962623
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2004000223A PE20050306A1 (es) | 2003-03-04 | 2004-03-01 | Compuestos imidazol condensado, 2-piridilo sustituido como inhibidores del factor de crecimiento transformante (tgf) |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US7417041B2 (es) |
| EP (1) | EP1601676A2 (es) |
| JP (1) | JP2006519249A (es) |
| AR (1) | AR043449A1 (es) |
| BR (1) | BRPI0407999A (es) |
| CA (1) | CA2517933C (es) |
| GT (1) | GT200400032A (es) |
| MX (1) | MXPA05008148A (es) |
| NL (1) | NL1025623C2 (es) |
| PA (1) | PA8595001A1 (es) |
| PE (1) | PE20050306A1 (es) |
| TW (1) | TW200504069A (es) |
| UY (1) | UY28214A1 (es) |
| WO (1) | WO2004078110A2 (es) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA80295C2 (en) | 2002-09-06 | 2007-09-10 | Biogen Inc | Pyrazolopyridines and using the same |
| UA80296C2 (en) * | 2002-09-06 | 2007-09-10 | Biogen Inc | Imidazolopyridines and methods of making and using the same |
| DE60330362D1 (de) * | 2002-09-18 | 2010-01-14 | Pfizer Prod Inc | Neue pyrazol-verbindungen als hemmer des transformierenden wachstumsfaktors (tgf) |
| BR0314372A (pt) * | 2002-09-18 | 2005-07-19 | Pfizer Prod Inc | Compostos imidazol como inibidores do fator de crescimento tranformador (tgf) |
| JP2008516962A (ja) * | 2004-10-15 | 2008-05-22 | バイオジェン・アイデック・エムエイ・インコーポレイテッド | 血管傷害を治療する方法 |
| JPWO2006070943A1 (ja) * | 2004-12-28 | 2008-06-12 | 武田薬品工業株式会社 | 縮合イミダゾール化合物およびその用途 |
| US7709468B2 (en) * | 2005-09-02 | 2010-05-04 | Abbott Laboratories | Imidazo based heterocycles |
| AU2006325706B2 (en) * | 2005-12-16 | 2012-03-29 | Novartis Ag | Control of intraocular pressure using ALK5 modulation agents |
| PT1966214T (pt) * | 2005-12-21 | 2017-02-03 | Janssen Pharmaceutica Nv | Triazolpiridazinas como moduladores de tirosina quinase |
| CN101553224A (zh) * | 2006-10-06 | 2009-10-07 | 艾博特公司 | 新型咪唑并噻唑和咪唑并唑 |
| DK2497470T3 (en) | 2006-11-22 | 2015-12-07 | Incyte Holdings Corp | Imidazotriaziner and imidazopyrimidines as kinase inhibitors |
| US20080249305A1 (en) * | 2007-03-27 | 2008-10-09 | Calderwood David J | Novel imidazole based heterocycles |
| CN103214482B (zh) | 2007-04-03 | 2016-06-29 | 阵列生物制药公司 | 作为受体酪氨酸激酶抑制剂的咪唑并[1,2-a]吡啶化合物 |
| WO2008133192A1 (ja) * | 2007-04-19 | 2008-11-06 | Takeda Pharmaceutical Company Limited | 縮合イミダゾール化合物およびその用途 |
| EP2162132A4 (en) * | 2007-05-21 | 2013-01-16 | Sgx Pharmaceuticals Inc | Heterocyclic kinase modulators |
| WO2008150827A1 (en) * | 2007-05-29 | 2008-12-11 | Smithkline Beecham Corporation | Naphthyridine, derivatives as p13 kinase inhibitors |
| EP2170337A4 (en) * | 2007-06-28 | 2013-12-18 | Abbvie Inc | NEW TRIAZOLOPYRIDAZINE |
| DK2193133T3 (en) | 2007-09-27 | 2015-10-05 | Fundacion Ct Nac Investigaciones Oncologicas Carlos Iii | IMIDAZOLOTHIADIAZOLES USED AS PROTEINKINASE INHIBITORS |
| WO2010012345A1 (en) * | 2008-07-29 | 2010-02-04 | Merck Patent Gmbh | Imidazothiadiazoles derivatives |
| NZ595674A (en) | 2009-04-02 | 2012-12-21 | Ct Nac Investigaciones Oncologicas Cnio | Imidazo[2,1-b][1,3,4]thiadiazole derivatives |
| FR2945289A1 (fr) * | 2009-05-11 | 2010-11-12 | Sanofi Aventis | Derives de 2-cycloamino-5-(pyridin-4-yl)imidazo°2,1-b! °1,3,4!thiadiazole, leur preparation et leur application en therapeutique |
| MX2012004341A (es) | 2009-10-16 | 2012-10-05 | Rib X Pharmaceuticals Inc | Compuestos antimicrobianos y metodos para fabricar y utilizar los mismos. |
| US20120220581A1 (en) | 2009-10-30 | 2012-08-30 | Janssen-Cilag, S.A. | IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS |
| MX2012006994A (es) | 2009-12-18 | 2012-07-03 | Mitsubishi Tanabe Pharma Corp | Agente antiplaquetas novedoso. |
| AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
| EP2723744B1 (en) | 2011-06-27 | 2016-03-23 | Janssen Pharmaceutica, N.V. | 1-ARYL-4-METHYL-[1,2,4]TRIAZOLO[4,3-a]QUINOXALINE DERIVATIVES |
| PT2731949T (pt) | 2011-07-13 | 2018-06-15 | Tiumbio Co Ltd | Imidazóis substituídos com 2-piridilo como inibidores de alk5 e/ou alk4 |
| EP2855665B8 (en) | 2012-05-30 | 2019-09-25 | Cornell University | Generation of functional and durable endothelial cells from human amniotic fluid-derived cells |
| RU2657540C2 (ru) | 2012-06-26 | 2018-06-14 | Янссен Фармацевтика Нв | Комбинации, содержащие ингибиторы pde 2, такие как 1-арил-4-метил-[1,2,4]триазоло[4,3-а]хиноксалиновые соединения, и ингибиторы pde 10, для применения в лечении неврологических или метаболических расстройств |
| ES2607184T3 (es) | 2012-07-09 | 2017-03-29 | Janssen Pharmaceutica, N.V. | Inhibidores de la enzima fosfodiesterasa 10 |
| US20140120116A1 (en) * | 2012-10-26 | 2014-05-01 | The Chinese University Of Hong Kong | Treatment of cancer using smad3 inhibitor |
| EP3003290B1 (en) | 2013-06-05 | 2021-03-10 | AgeX Therapeutics, Inc. | Compositions for use in the treatment of wounds in mammalian species |
| CN109045032A (zh) | 2014-01-01 | 2018-12-21 | 麦迪威森技术有限责任公司 | 氨基吡啶类化合物和使用方法 |
| US11078462B2 (en) | 2014-02-18 | 2021-08-03 | ReCyte Therapeutics, Inc. | Perivascular stromal cells from primate pluripotent stem cells |
| US10240127B2 (en) | 2014-07-03 | 2019-03-26 | ReCyte Therapeutics, Inc. | Exosomes from clonal progenitor cells |
| JP6789941B2 (ja) * | 2014-11-21 | 2020-11-25 | ライジェル ファーマシューティカルズ, インコーポレイテッド | Tgf−ベータ阻害剤としての縮合イミダゾール誘導体 |
| TW201630907A (zh) * | 2014-12-22 | 2016-09-01 | 必治妥美雅史谷比公司 | TGFβR拮抗劑 |
| SG11201707346RA (en) | 2015-03-11 | 2017-10-30 | Melinta Therapeutics Inc | Antimicrobial compounds and methods of making and using the same |
| EP3387112A4 (en) | 2015-12-07 | 2019-08-21 | BioTime, Inc. | METHOD FOR RECONNECTING BROWN FAT CELLS DERIVED FROM VARIOUS PLURIPOTENT STEM CELLS |
| JP2019515041A (ja) | 2016-05-06 | 2019-06-06 | メリンタ セラピューティクス、 インコーポレイテッドMelinta Therapeutics, Inc. | 抗菌剤ならびにそれを作製および使用する方法 |
| SG11202104331YA (en) | 2018-12-11 | 2021-05-28 | Theravance Biopharma R&D Ip Llc | Naphthyridine and quinoline derivatives useful as alk5 inhibitors |
| AU2020385400A1 (en) * | 2019-11-22 | 2022-06-09 | Theravance Biopharma R&D Ip, Llc | Substituted 1,5-naphthyridines or quinolines as ALK5 inhibitors |
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| BE640616A (es) | 1962-12-19 | |||
| US3492397A (en) | 1967-04-07 | 1970-01-27 | Warner Lambert Pharmaceutical | Sustained release dosage in the pellet form and process thereof |
| US4060598A (en) | 1967-06-28 | 1977-11-29 | Boehringer Mannheim G.M.B.H. | Tablets coated with aqueous resin dispersions |
| US3538214A (en) | 1969-04-22 | 1970-11-03 | Merck & Co Inc | Controlled release medicinal tablets |
| US4173626A (en) | 1978-12-11 | 1979-11-06 | Merck & Co., Inc. | Sustained release indomethacin |
| ZW24186A1 (en) | 1985-12-12 | 1987-07-08 | Smithkline Beckman Corp | Inhibition of the 5-lipoxygenase pathway |
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| US4719218A (en) * | 1985-12-12 | 1988-01-12 | Smithkline Beckman Corporation | Pyrrolo[1,2-a]imidazole and pyrrolo[1,2-a]pyridine derivatives and their use as 5-lipoxygenase pathway inhibitor |
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| US6514977B1 (en) | 1997-05-22 | 2003-02-04 | G.D. Searle & Company | Substituted pyrazoles as p38 kinase inhibitors |
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| GB0007405D0 (en) | 2000-03-27 | 2000-05-17 | Smithkline Beecham Corp | Compounds |
| PE20020506A1 (es) | 2000-08-22 | 2002-07-09 | Glaxo Group Ltd | Derivados de pirazol fusionados como inhibidores de la proteina cinasa |
| AU2002225730A1 (en) | 2000-11-16 | 2002-05-27 | Smith Kline Beecham Corporation | Compounds |
| GB0027987D0 (en) | 2000-11-16 | 2001-01-03 | Smithkline Beecham Plc | Compounds |
| GB0100762D0 (en) | 2001-01-11 | 2001-02-21 | Smithkline Beecham Plc | Novel use |
| US20040097502A1 (en) | 2001-02-02 | 2004-05-20 | Gellibert Francoise Jeanne | Pyrazoles as tgf inhibitors |
| GB0102672D0 (en) | 2001-02-02 | 2001-03-21 | Glaxo Group Ltd | Compounds |
| ES2237671T3 (es) | 2001-02-02 | 2005-08-01 | Smithkline Beecham Corporation | Derivados de pirazol contra la sobreexpresion de tgf. |
| DE60207390T2 (de) | 2001-03-09 | 2006-07-20 | Pfizer Products Inc., Groton | Entzündungshemmende benzimidazolverbindungen |
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| BR0314372A (pt) | 2002-09-18 | 2005-07-19 | Pfizer Prod Inc | Compostos imidazol como inibidores do fator de crescimento tranformador (tgf) |
| DE60330362D1 (de) * | 2002-09-18 | 2010-01-14 | Pfizer Prod Inc | Neue pyrazol-verbindungen als hemmer des transformierenden wachstumsfaktors (tgf) |
| EP1542685A1 (en) * | 2002-09-18 | 2005-06-22 | Pfizer Products Inc. | Triazole derivatives as transforming growth factor (tgf) inhibitors |
-
2004
- 2004-01-30 PA PA20048595001A patent/PA8595001A1/es unknown
- 2004-02-20 US US10/783,251 patent/US7417041B2/en not_active Expired - Fee Related
- 2004-02-23 BR BRPI0407999-0A patent/BRPI0407999A/pt not_active IP Right Cessation
- 2004-02-23 EP EP04713609A patent/EP1601676A2/en not_active Withdrawn
- 2004-02-23 WO PCT/IB2004/000532 patent/WO2004078110A2/en not_active Ceased
- 2004-02-23 MX MXPA05008148A patent/MXPA05008148A/es active IP Right Grant
- 2004-02-23 CA CA002517933A patent/CA2517933C/en not_active Expired - Fee Related
- 2004-02-23 JP JP2006506271A patent/JP2006519249A/ja active Pending
- 2004-03-01 PE PE2004000223A patent/PE20050306A1/es not_active Application Discontinuation
- 2004-03-02 GT GT200400032A patent/GT200400032A/es unknown
- 2004-03-02 AR ARP040100654A patent/AR043449A1/es not_active Application Discontinuation
- 2004-03-02 UY UY28214A patent/UY28214A1/es not_active Application Discontinuation
- 2004-03-03 TW TW093105533A patent/TW200504069A/zh unknown
- 2004-03-03 NL NL1025623A patent/NL1025623C2/nl not_active IP Right Cessation
-
2008
- 2008-07-23 US US12/178,160 patent/US20080275235A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| WO2004078110A3 (en) | 2004-11-11 |
| NL1025623A1 (nl) | 2004-09-07 |
| TW200504069A (en) | 2005-02-01 |
| CA2517933A1 (en) | 2004-09-16 |
| NL1025623C2 (nl) | 2005-03-14 |
| JP2006519249A (ja) | 2006-08-24 |
| PA8595001A1 (es) | 2004-09-28 |
| WO2004078110A2 (en) | 2004-09-16 |
| GT200400032A (es) | 2004-10-21 |
| US20040176390A1 (en) | 2004-09-09 |
| EP1601676A2 (en) | 2005-12-07 |
| US7417041B2 (en) | 2008-08-26 |
| UY28214A1 (es) | 2004-09-30 |
| CA2517933C (en) | 2009-05-12 |
| AR043449A1 (es) | 2005-07-27 |
| US20080275235A1 (en) | 2008-11-06 |
| BRPI0407999A (pt) | 2006-03-07 |
| MXPA05008148A (es) | 2005-09-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |