BRPI0511768A - composto, pró-droga, métodos para a produção de um composto, e para a profilaxia ou tratamento de cáncer em um mamìfero, agente farmacêutico, e, uso de um composto - Google Patents
composto, pró-droga, métodos para a produção de um composto, e para a profilaxia ou tratamento de cáncer em um mamìfero, agente farmacêutico, e, uso de um compostoInfo
- Publication number
- BRPI0511768A BRPI0511768A BRPI0511768-2A BRPI0511768A BRPI0511768A BR PI0511768 A BRPI0511768 A BR PI0511768A BR PI0511768 A BRPI0511768 A BR PI0511768A BR PI0511768 A BRPI0511768 A BR PI0511768A
- Authority
- BR
- Brazil
- Prior art keywords
- compound
- optionally substituted
- prodrug
- prophylaxis
- cancer
- Prior art date
Links
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- 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
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- 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
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- 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
- C07D487/12—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 three hetero rings
- C07D487/16—Peri-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Urology & Nephrology (AREA)
- Oncology (AREA)
- Virology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Molecular Biology (AREA)
- Endocrinology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Vascular Medicine (AREA)
- AIDS & HIV (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Communicable Diseases (AREA)
- Reproductive Health (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
COMPOSTO, PRó-DROGA, MéTODOS PARA A PRODUçãO DE UM COMPOSTO, PARA A PROFILAXIA OU TRATAMENTO DE CáNCER EM UM MAMìFERO, AGENTE FARMACêUTICO, E, USO DE UM COMPOSTO A presente invenção diz respeito a um composto representado pela fórmula: em que W é C(R¬ ¹¬) ou N, cada A é um grupo arila opcionalmente substituído ou um grupo heteroarila, X¬ ¹¬ é -NR¬ ³¬-Y~ ¹¬m-, -O-, -S-, -SO-, -SO~ 2~- ou -CHR¬ ³¬- em que R¬ ³¬ é um átomo de hidrogênio ou um grupo hidrocarboneto alifático opcionalmente substituído, ou R¬ ³¬ é opcionalmente ligado a A para formar uma estrutura de anel opcionalmente substituído, R¬ ¹¬ é um átomo de hidrogênio ou um grupo opcionalmente substituído ligado por intermédio de um átomo de carbono, um átomo de nitrogênio ou um átomo de oxigênio, R¬ ²¬ é um átomo de hidrogênio ou grupo opcionalmente substituído ligado por intermédio de um átomo de carbono ou um átomo de enxofre, ou e R¬ ¹¬ e R¬ ²¬, ou R~ ²¬ e R¬ ³¬ são opcionalmente ligados para formar uma estrutura de anel opcionalmente substituído, ou um sal deste e um inibidor da tirosina quinase ou um agente para a profilaxia ou tratamento de câncer, que contenha este composto ou uma pró-droga deste.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004165050 | 2004-06-02 | ||
| JP2005058231 | 2005-03-02 | ||
| PCT/JP2005/010451 WO2005118588A1 (ja) | 2004-06-02 | 2005-06-01 | 縮合複素環化合物 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0511768A true BRPI0511768A (pt) | 2008-01-08 |
Family
ID=35462874
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0511768-2A BRPI0511768A (pt) | 2004-06-02 | 2005-06-01 | composto, pró-droga, métodos para a produção de um composto, e para a profilaxia ou tratamento de cáncer em um mamìfero, agente farmacêutico, e, uso de um composto |
Country Status (18)
| Country | Link |
|---|---|
| US (4) | US7507740B2 (pt) |
| EP (1) | EP1752457B1 (pt) |
| JP (2) | JP4134227B2 (pt) |
| KR (1) | KR101194622B1 (pt) |
| AU (1) | AU2005250285B2 (pt) |
| BR (1) | BRPI0511768A (pt) |
| CA (1) | CA2569016C (pt) |
| CR (1) | CR8827A (pt) |
| GE (1) | GEP20105024B (pt) |
| IL (1) | IL179414A (pt) |
| MA (1) | MA28973B1 (pt) |
| ME (1) | MEP8409A (pt) |
| MX (1) | MXPA06013996A (pt) |
| NO (1) | NO20066015L (pt) |
| NZ (1) | NZ551938A (pt) |
| RU (1) | RU2389731C2 (pt) |
| TW (1) | TWI392679B (pt) |
| WO (1) | WO2005118588A1 (pt) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200740820A (en) * | 2005-07-05 | 2007-11-01 | Takeda Pharmaceuticals Co | Fused heterocyclic derivatives and use thereof |
| US7932257B2 (en) * | 2005-07-22 | 2011-04-26 | Sunesis Pharmaceuticals, Inc. | Substituted pyrazolo[4,3-d]pyrimidines as aurora kinase inhibitors |
| TW200730527A (en) * | 2005-12-02 | 2007-08-16 | Takeda Pharmaceuticals Co | Fused heterocyclic compound |
| US20080161320A1 (en) * | 2006-09-11 | 2008-07-03 | Xiong Cai | Fused bicyclic pyrimidines as ptk inhibitors containing a zinc binding moiety |
| US7517882B2 (en) * | 2006-09-18 | 2009-04-14 | Polaris Group | Protein kinase inhibitors |
| EA200970353A1 (ru) | 2006-10-06 | 2009-10-30 | Такеда Фармасьютикал Компани Лимитед | Комбинированное лекарственное средство |
| US20100004238A1 (en) | 2006-12-12 | 2010-01-07 | Takeda Pharmaceutical Company Limited | Fused heterocyclic compound |
| US7825127B2 (en) * | 2006-12-28 | 2010-11-02 | Takeda Pharmaceutical Company, Limited | Method for treating cancer |
| US7776857B2 (en) * | 2007-04-05 | 2010-08-17 | Amgen Inc. | Aurora kinase modulators and method of use |
| JP5603770B2 (ja) * | 2007-05-31 | 2014-10-08 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ccr2受容体拮抗薬およびその使用 |
| RU2010101416A (ru) | 2007-06-19 | 2011-07-27 | Такеда Фармасьютикал Компани Лимитед (Jp) | Профилактическое/лекарственное средство от рака |
| EP2255830A1 (en) * | 2008-03-03 | 2010-12-01 | Takeda Pharmaceutical Company Limited | Concomitant drug |
| EP2253633A4 (en) * | 2008-03-12 | 2012-02-29 | Takeda Pharmaceutical | CONDENSED HETEROCYCLIC COMPOUND |
| CA2716856C (en) * | 2008-03-20 | 2013-02-19 | Amgen Inc. | Aurora kinase modulators and method of use |
| US9126935B2 (en) | 2008-08-14 | 2015-09-08 | Amgen Inc. | Aurora kinase modulators and methods of use |
| TW201016703A (en) * | 2008-09-26 | 2010-05-01 | Takeda Pharmaceutical | Prevention and treatment of cancer with LKB1 non-expression (deletion or mutation) |
| TW201016704A (en) * | 2008-09-26 | 2010-05-01 | Takeda Pharmaceutical | Prevention and treatment of cancer with RAS gene mutation |
| WO2010036910A1 (en) * | 2008-09-26 | 2010-04-01 | Yoshikazu Ohta | Heart protection by administering an amp-activated protein kinase activator |
| CN102256963B (zh) | 2008-12-19 | 2014-06-11 | 贝林格尔.英格海姆国际有限公司 | 作为ccr2受体拮抗剂用于治疗炎症、哮喘和copd的环状嘧啶-4-甲酰胺 |
| CN102369205B (zh) | 2009-01-30 | 2014-10-29 | 武田药品工业株式会社 | 稠环化合物和其用途 |
| US8614208B2 (en) * | 2009-08-26 | 2013-12-24 | Takeda Pharmaceutical Company Limited | Fused heterocyclic ring derivative and use thereof |
| WO2011040212A1 (en) | 2009-10-01 | 2011-04-07 | Takeda Pharmaceutical Company Limited | Therapeutic agent for brain tumor |
| ES2674275T3 (es) | 2009-12-17 | 2018-06-28 | Centrexion Therapeutics Corporation | Antagonistas del receptor CCR2 y usos de los mismos |
| JP5646736B2 (ja) | 2010-05-12 | 2014-12-24 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規ccr2受容体アンタゴニスト、これらの製造方法、及び薬物としてのこれらの使用 |
| WO2011141474A1 (en) | 2010-05-12 | 2011-11-17 | Boehringer Ingelheim International Gmbh | Novel ccr2 receptor antagonists, method for producing the same, and use thereof as medicaments |
| WO2011144501A1 (en) | 2010-05-17 | 2011-11-24 | Boehringer Ingelheim International Gmbh | Ccr2 antagonists and uses thereof |
| WO2011147772A1 (en) | 2010-05-25 | 2011-12-01 | Boehringer Ingelheim International Gmbh | Ccr2 receptor antagonists |
| US8962656B2 (en) | 2010-06-01 | 2015-02-24 | Boehringer Ingelheim International Gmbh | CCR2 antagonists |
| CA2760174A1 (en) * | 2011-12-01 | 2013-06-01 | Pharmascience Inc. | Protein kinase inhibitors and uses thereof |
| AP2013007253A0 (en) * | 2011-04-21 | 2013-11-30 | Origenis Gmbh | Pyrazolo [4,3-D] pyrimidines useful as kinase inhibitors |
| EP2731941B1 (en) | 2011-07-15 | 2019-05-08 | Boehringer Ingelheim International GmbH | Novel and selective ccr2 antagonists |
| GB201311891D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel compound |
| GB201311888D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
| RS58361B1 (sr) * | 2013-07-31 | 2019-03-29 | Merck Patent Gmbh | Piridini, pirimidini i pirazini, kao inhibitori btk i njihova upotreba |
| US10040780B2 (en) | 2014-03-03 | 2018-08-07 | The Regents Of The University Of California | Mcl-1 antagonists |
| US20180228907A1 (en) | 2014-04-14 | 2018-08-16 | Arvinas, Inc. | Cereblon ligands and bifunctional compounds comprising the same |
| WO2015162515A1 (en) | 2014-04-25 | 2015-10-29 | Pfizer Inc. | Heteroaromatic compounds and their use as dopamine d1 ligands |
| PL3137470T3 (pl) | 2014-05-01 | 2021-10-11 | Novartis Ag | Związki i kompozycje jako agonisty receptora toll-like 7 |
| ES2908150T3 (es) | 2014-05-01 | 2022-04-27 | Novartis Ag | Compuestos y composiciones como agonistas del receptor de tipo Toll 7 |
| PT3317270T (pt) | 2015-07-02 | 2020-08-24 | Centrexion Therapeutics Corp | (4-((3r,4r)-3-metoxitetrahidro-pirano-4-ilamino)piperidina-1-il)(5-metil-6-(((2r,6s)-6-(p-tolil)tetrahidro-2h-pirano-2-il)metilamino)pirimidina-4-il)citrato de metanona |
| EP3368092B9 (en) | 2015-10-29 | 2020-07-29 | Novartis AG | Antibody conjugates comprising toll-like receptor agonist |
| EP3591845B1 (en) * | 2018-07-05 | 2023-08-09 | Universite De Bretagne Sud | Sorting device and method for elementary check node processing for message-passing decoding of non-binary codes |
| WO2020118183A1 (en) * | 2018-12-06 | 2020-06-11 | Kapoor Tarun M | 2,4-diaminopyrimidine bicycles for treating cancer |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPS554116B2 (pt) * | 1971-08-20 | 1980-01-29 | ||
| DK0705263T3 (da) * | 1993-06-21 | 1997-05-05 | Merrell Pharma Inc | Carbocycliske nukleoside midler anvendelige som selektive inhibitorer af proinflammatoriske cytokiner |
| IL112249A (en) * | 1994-01-25 | 2001-11-25 | Warner Lambert Co | Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds |
| IL112248A0 (en) | 1994-01-25 | 1995-03-30 | Warner Lambert Co | Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them |
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| SI9620103A (sl) | 1995-07-06 | 1998-10-31 | Novartis Ag | Pirolopirimidini in postopki za njihovo pripravo |
| AR004010A1 (es) * | 1995-10-11 | 1998-09-30 | Glaxo Group Ltd | Compuestos heterociclicos |
| EA001595B1 (ru) * | 1996-04-12 | 2001-06-25 | Варнер-Ламберт Компани | Необратимые ингибиторы тирозинкиназ |
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| WO1998023613A1 (en) * | 1996-11-27 | 1998-06-04 | Pfizer Inc. | Fused bicyclic pyrimidine derivatives |
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| WO2000005234A1 (en) * | 1998-07-22 | 2000-02-03 | Suntory Limited | NF-λB INHIBITORS CONTAINING INDAN DERIVATIVES AS THE ACTIVE INGREDIENT |
| CZ27399A3 (cs) * | 1999-01-26 | 2000-08-16 | Ústav Experimentální Botaniky Av Čr | Substituované dusíkaté heterocyklické deriváty, způsob jejich přípravy, tyto deriváty pro použití jako léčiva, farmaceutická kompozice a kombinovaný farmaceutický přípravek tyto deriváty obsahující a použití těchto derivátů pro výrobu léčiv |
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| JP2006020985A (ja) | 2004-07-05 | 2006-01-26 | Kiyoshi Owada | 微小孔を用いた入浴剤用炭酸ガス拡散装置 |
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| AU2006313456B2 (en) * | 2005-05-20 | 2011-06-23 | Methylgene Inc. | Inhibitors of VEGF receptor and HGF receptor signaling |
| TW200730527A (en) * | 2005-12-02 | 2007-08-16 | Takeda Pharmaceuticals Co | Fused heterocyclic compound |
| EA200970353A1 (ru) * | 2006-10-06 | 2009-10-30 | Такеда Фармасьютикал Компани Лимитед | Комбинированное лекарственное средство |
| RU2010101416A (ru) * | 2007-06-19 | 2011-07-27 | Такеда Фармасьютикал Компани Лимитед (Jp) | Профилактическое/лекарственное средство от рака |
| EP2253633A4 (en) * | 2008-03-12 | 2012-02-29 | Takeda Pharmaceutical | CONDENSED HETEROCYCLIC COMPOUND |
-
2005
- 2005-06-01 CA CA2569016A patent/CA2569016C/en not_active Expired - Fee Related
- 2005-06-01 AU AU2005250285A patent/AU2005250285B2/en not_active Ceased
- 2005-06-01 JP JP2006514152A patent/JP4134227B2/ja not_active Expired - Fee Related
- 2005-06-01 MX MXPA06013996A patent/MXPA06013996A/es active IP Right Grant
- 2005-06-01 US US10/592,812 patent/US7507740B2/en not_active Expired - Fee Related
- 2005-06-01 BR BRPI0511768-2A patent/BRPI0511768A/pt not_active IP Right Cessation
- 2005-06-01 ME MEP-84/09A patent/MEP8409A/xx unknown
- 2005-06-01 GE GEAP20059789A patent/GEP20105024B/en unknown
- 2005-06-01 RU RU2006147267/04A patent/RU2389731C2/ru not_active IP Right Cessation
- 2005-06-01 NZ NZ551938A patent/NZ551938A/en not_active IP Right Cessation
- 2005-06-01 WO PCT/JP2005/010451 patent/WO2005118588A1/ja not_active Ceased
- 2005-06-01 KR KR1020067027872A patent/KR101194622B1/ko not_active Expired - Fee Related
- 2005-06-01 EP EP05748463.6A patent/EP1752457B1/en not_active Expired - Lifetime
- 2005-06-02 TW TW094118122A patent/TWI392679B/zh not_active IP Right Cessation
-
2006
- 2006-11-20 IL IL179414A patent/IL179414A/en not_active IP Right Cessation
- 2006-12-15 MA MA29533A patent/MA28973B1/fr unknown
- 2006-12-22 CR CR8827A patent/CR8827A/es unknown
- 2006-12-27 NO NO20066015A patent/NO20066015L/no not_active Application Discontinuation
-
2008
- 2008-03-26 JP JP2008080528A patent/JP4937172B2/ja not_active Expired - Fee Related
- 2008-07-14 US US12/172,684 patent/US20090018335A1/en not_active Abandoned
- 2008-07-14 US US12/172,631 patent/US8178543B2/en not_active Expired - Fee Related
- 2008-07-14 US US12/172,775 patent/US20090203717A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| IL179414A0 (en) | 2007-05-15 |
| JP4134227B2 (ja) | 2008-08-20 |
| AU2005250285B2 (en) | 2011-08-18 |
| US20070244132A1 (en) | 2007-10-18 |
| US20090203717A1 (en) | 2009-08-13 |
| WO2005118588A1 (ja) | 2005-12-15 |
| MXPA06013996A (es) | 2007-02-08 |
| US20090018335A1 (en) | 2009-01-15 |
| EP1752457A1 (en) | 2007-02-14 |
| JP4937172B2 (ja) | 2012-05-23 |
| EP1752457A4 (en) | 2010-05-26 |
| AU2005250285A1 (en) | 2005-12-15 |
| NZ551938A (en) | 2010-07-30 |
| RU2389731C2 (ru) | 2010-05-20 |
| GEP20105024B (en) | 2010-06-25 |
| CR8827A (es) | 2007-04-20 |
| EP1752457B1 (en) | 2014-03-19 |
| TWI392679B (zh) | 2013-04-11 |
| JPWO2005118588A1 (ja) | 2008-04-03 |
| KR101194622B1 (ko) | 2012-10-29 |
| JP2008247907A (ja) | 2008-10-16 |
| TW200611907A (en) | 2006-04-16 |
| CA2569016A1 (en) | 2005-12-15 |
| KR20070026695A (ko) | 2007-03-08 |
| US20090029973A1 (en) | 2009-01-29 |
| US7507740B2 (en) | 2009-03-24 |
| US8178543B2 (en) | 2012-05-15 |
| NO20066015L (no) | 2007-02-13 |
| RU2006147267A (ru) | 2008-07-20 |
| IL179414A (en) | 2013-11-28 |
| MEP8409A (en) | 2011-12-20 |
| MA28973B1 (fr) | 2007-11-01 |
| CA2569016C (en) | 2012-11-27 |
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