MX2009008606A - Agente terapeutico para trastorno de excrecion urinaria. - Google Patents
Agente terapeutico para trastorno de excrecion urinaria.Info
- Publication number
- MX2009008606A MX2009008606A MX2009008606A MX2009008606A MX2009008606A MX 2009008606 A MX2009008606 A MX 2009008606A MX 2009008606 A MX2009008606 A MX 2009008606A MX 2009008606 A MX2009008606 A MX 2009008606A MX 2009008606 A MX2009008606 A MX 2009008606A
- Authority
- MX
- Mexico
- Prior art keywords
- urinary
- urinary excretion
- excretion disorder
- compound
- therapeutic agent
- Prior art date
Links
- 230000036325 urinary excretion Effects 0.000 title abstract 3
- 239000003814 drug Substances 0.000 title 1
- 229940124597 therapeutic agent Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 230000027939 micturition Effects 0.000 abstract 2
- 239000012453 solvate Substances 0.000 abstract 2
- 230000002485 urinary effect Effects 0.000 abstract 2
- 206010052901 Terminal dribbling Diseases 0.000 abstract 1
- 206010046640 Urine flow decreased Diseases 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- 230000003111 delayed effect Effects 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 208000024430 slowing of urinary stream Diseases 0.000 abstract 1
Classifications
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/70—Sulfur atoms
- C07D213/71—Sulfur atoms to which a second hetero atom is attached
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/426—1,3-Thiazoles
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4402—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 2, e.g. pheniramine, bisacodyl
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
-
- 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
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- 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
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
-
- 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
- C07D277/32—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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/36—Sulfur atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
Se describe un antagonista de EPl, particularmente un compuesto representado por la fórmula general (I), una sal del mismo, un solvato del compuesto o la sal, o un profármaco del compuesto, la sal o el solvato. El compuesto es efectivo para la prevención o tratamiento de trastorno de excreción urinaria y/o la mejora de una condición asociada con trastorno de excreción urinaria (por ejemplo, desaceleración de la corriente urinaria, división de la corriente urinaria, interrupción de la corriente urinaria, micción retrasada, esfuerzo en la micción, incontinencia terminal), (1) en donde todos los símbolos son como se definen en la descripción.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007035661 | 2007-02-16 | ||
| PCT/JP2008/052486 WO2008099907A1 (ja) | 2007-02-16 | 2008-02-15 | 尿排出障害治療剤 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2009008606A true MX2009008606A (es) | 2009-09-16 |
Family
ID=39690132
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2009008606A MX2009008606A (es) | 2007-02-16 | 2008-02-15 | Agente terapeutico para trastorno de excrecion urinaria. |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US9181187B2 (es) |
| EP (1) | EP2123273B1 (es) |
| JP (1) | JP5439817B2 (es) |
| KR (1) | KR101492552B1 (es) |
| CN (1) | CN101663034B (es) |
| AU (1) | AU2008215431C1 (es) |
| BR (1) | BRPI0807942A2 (es) |
| CA (1) | CA2677769C (es) |
| ES (1) | ES2437323T3 (es) |
| IL (1) | IL200377A (es) |
| MX (1) | MX2009008606A (es) |
| NZ (1) | NZ578988A (es) |
| RU (1) | RU2452479C2 (es) |
| WO (1) | WO2008099907A1 (es) |
| ZA (1) | ZA200905681B (es) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW201107309A (en) * | 2009-07-27 | 2011-03-01 | Kissei Pharmaceutical | Indole derivatives, or the pharmaceutically acceptable salts |
| US20140039004A1 (en) | 2012-07-31 | 2014-02-06 | Ono Pharmaceutical Co., Ltd. | Method of treating of gastroesophageal reflux disease |
| RU2550968C1 (ru) * | 2013-11-29 | 2015-05-20 | Федеральное государственное бюджетное учреждение "Научный центр акушерства, гинекологии и перинатологии имени академика В.И. Кулакова" Министерства здравоохранения Российской Федерации | Комплексный способ лечения пациенток с хроническими рецидивирующими циститами и рефрактерным гиперактивным мочевым пузырем |
| CN114502239B (zh) * | 2019-10-02 | 2024-12-03 | Aska制药株式会社 | 排尿障碍改善剂 |
Family Cites Families (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US530464A (en) | 1894-12-04 | Robert b | ||
| JPS503362B1 (es) | 1970-06-10 | 1975-02-04 | ||
| JPS5231404B1 (es) | 1971-04-28 | 1977-08-15 | ||
| CH545364A (de) | 1972-05-29 | 1973-12-15 | Rueti Ag Vormals C Honegger Ma | Düse zum Erzeugen eines Strahles eines Fluidums |
| US4132847A (en) | 1977-07-22 | 1979-01-02 | Pfizer Inc. | 4-Pyrone prostaglandin antagonists |
| JPS57156460A (en) | 1981-03-20 | 1982-09-27 | Ono Pharmaceut Co Ltd | Stabilized composition of prostaglandin and prostaglandin mimic compound, and its preparation |
| IL74694A0 (en) | 1984-04-02 | 1985-06-30 | Merck & Co Inc | N-alkenyl-3-hydroxybenzo(b)thiophene-2-carboxamide derivatives,their preparation and pharmaceutical compositions containing them |
| US4614617A (en) | 1985-02-25 | 1986-09-30 | G. D. Searle & Co. | Intermediates for 8-chlorodibenz[(b,f)][1,4]oxazepine-10(11H)-carboxylic acid, 2-(sulfinyl- and sulfonyl-containing acyl)hydrazides |
| US4704386A (en) | 1985-08-29 | 1987-11-03 | G. D. Searle & Co. | 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[(phenylsulfinyl-, and phenylsulfonyl)alkanoyl]hydrazides |
| US4808608A (en) | 1986-01-23 | 1989-02-28 | Merck & Co., Inc. | Tetrahydrocarbazole 1-alkanoic acids, pharmaceutical compositions and use |
| US4775680A (en) | 1987-07-21 | 1988-10-04 | Merck & Co., Inc. | Cyclohept[b]indolealkanoic acids, pharmaceutical compositions and use |
| GB9021813D0 (en) | 1990-10-08 | 1990-11-21 | Ici Plc | Tricyclic heterocycles |
| ES2133324T3 (es) | 1991-05-03 | 1999-09-16 | Searle & Co | Compuestos de dibenzoxazepina sustituidos, composiciones farmaceuticas y metodos de uso. |
| US5180720A (en) | 1991-05-03 | 1993-01-19 | G. D. Searle & Co. | 2- and 3-alkoxy or hydroxy-8-substituted-dibenz[b,f]-[1,4]oxazepine-10(11H)-carboxylic acid, substituted hydrazides and methods for treating pain |
| US5182272A (en) | 1991-05-03 | 1993-01-26 | G. D. Searle & Co. | 8-substituted-dibenz[b,f][1,4]oxazepine-10(11)-carboxylic acid, substituted hydrazides, pharmaceutical compositions, and methods for treating pain |
| GB9120640D0 (en) | 1991-09-27 | 1991-11-06 | Ici Plc | Tricyclic heterocycles |
| WO1993007132A1 (en) | 1991-10-01 | 1993-04-15 | G.D. Searle & Co. | 10-acyl-dibenz(b,f)(1,4)-oxazepines and their thiazepines and diazepines analogues useful as prostaglandin antagonists |
| US5212169A (en) | 1991-10-31 | 1993-05-18 | G. D. Searle & Co. | Substituted dibenzoxazepine compounds, pharmaceutical compositions and methods for treating pain |
| WO1993013082A1 (en) | 1991-12-20 | 1993-07-08 | G.D. Searle & Co. | Substituted dibenzoxazepines or dibenzothiazepines and their use as prostaglandin e2 antagonists |
| IL104567A (en) | 1992-02-03 | 1997-03-18 | Fujisawa Pharmaceutical Co | Ethanolamine derivatives, processes for the preparation thereof and pharmaceutical compositions containing the same |
| US5354746A (en) | 1993-06-01 | 1994-10-11 | G. D. Searle & Co. | Squaric acid derivatives of substituted dibenzoxazepine compounds, pharmaceutical compositions and methods of use |
| US5354747A (en) | 1993-06-16 | 1994-10-11 | G. D. Searle & Co. | 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9- and/or 10-substituted dibenzoxazepine and dibenzthiazepine compounds, pharmaceutical compositions and methods of use |
| US5420270A (en) | 1993-10-07 | 1995-05-30 | G. D. Searle & Co. | Aryl substituted dibenzoxazepine compounds, pharmaceutical compositions and methods of use |
| US5441950A (en) | 1994-06-09 | 1995-08-15 | G. D. Searle & Co. | Substituted dibenzoxazepine and dibenzthiazepine carbamate compounds, pharmaceutical compositions and methods of use |
| GB9514160D0 (en) | 1994-07-25 | 1995-09-13 | Zeneca Ltd | Aromatic compounds |
| US5612359A (en) * | 1994-08-26 | 1997-03-18 | Bristol-Myers Squibb Company | Substituted biphenyl isoxazole sulfonamides |
| GB9417532D0 (en) | 1994-08-31 | 1994-10-19 | Zeneca Ltd | Aromatic compounds |
| GB9420557D0 (en) | 1994-10-12 | 1994-11-30 | Zeneca Ltd | Aromatic compounds |
| TW434240B (en) | 1995-06-20 | 2001-05-16 | Zeneca Ltd | Aromatic compounds, preparation thereof and pharmaceutical composition comprising same |
| TW502026B (en) | 1995-06-20 | 2002-09-11 | Zeneca Ltd | Aromatic compounds useful as antagonists of e-type prostaglandins, processes for the preparation thereof, pharmaceutical compositions comprising the compounds, and intermediates |
| EP0752421B1 (en) | 1995-07-07 | 2005-10-12 | AstraZeneca AB | Ortho-substituted aromatic compounds, containing three (het)aryl moieties, their preparation and their use as prostaglandin E2-(PGE2)-antagonists |
| TW523506B (en) | 1996-12-18 | 2003-03-11 | Ono Pharmaceutical Co | Sulfonamide or carbamide derivatives and drugs containing the same as active ingredients |
| ZA984040B (en) | 1997-05-15 | 1998-11-20 | Ono Pharmaceutical Co | Benzenesulfonamide compounds |
| WO1999047497A2 (en) | 1998-03-13 | 1999-09-23 | Merck Frosst Canada & Co. | Carboxylic acids and acylsulfonamides, compositions containing such compounds and methods of treatment |
| ATE423555T1 (de) | 1998-04-06 | 2009-03-15 | Astellas Pharma Inc | Verwendung von beta-3-adrenergen-rezeptoren agonisten in der behandlung von dysurie |
| US6211197B1 (en) | 1998-10-07 | 2001-04-03 | Merck Frosst Canada & Co. | Prostaglandin receptor ligands |
| AU4431400A (en) | 1999-05-12 | 2000-12-05 | Japan As Represented By President Of National Cancer Center | Anticancer agents containing ep1 antagonists as the active ingredient |
| CA2384783A1 (en) | 1999-09-14 | 2001-03-22 | Merck Frosst Canada & Co./Merck Frosst Canada & Cie | Carboxylic acids and acylsulfonamides, compositions containing such compounds and methods of treatment |
| ATE312095T1 (de) | 1999-09-14 | 2005-12-15 | Merck Frosst Canada Inc | Carbonsäuren und acylsulfonamide, diese verbindungen enthaltende zubereitungen und behandlungsmethoden |
| AU2001286557A1 (en) | 2000-08-23 | 2002-03-04 | Merck Frosst Canada And Co. | Method of treating or preventing urinary incontinence using prostanoid ep1 receptor antagonists |
| MXPA03008134A (es) * | 2001-03-12 | 2004-03-10 | Ono Pharmaceutical Co | Compuesto de n-fenilarilsulfonamida, medicamento que contiene el compuesto como ingrediente activo, intermediario para el compuesto y procedimientos para su produccion. |
| SE0100873D0 (sv) | 2001-03-13 | 2001-03-13 | Astrazeneca Ab | Method of treatment |
| WO2002072145A1 (en) | 2001-03-14 | 2002-09-19 | Ono Pharmaceutical Co., Ltd. | Remedies for depression containing ep1 antagonist as the active ingredient |
| EP1447096A1 (en) | 2001-11-19 | 2004-08-18 | Ono Pharmaceutical Co., Ltd. | Remedies for urinary frequency |
| AU2003211574A1 (en) | 2002-03-05 | 2003-09-16 | Ono Pharmaceutical Co., Ltd. | 8-azaprostaglandin derivative compounds and drugs containing the compounds as the active ingredient |
| CN1659131A (zh) | 2002-04-08 | 2005-08-24 | 葛兰素集团有限公司 | 2-((2-烷氧基)-苯基)-环戊-1-烯基)芳香碳-以及杂环羧酸及其衍生物 |
| GB0212785D0 (en) | 2002-05-31 | 2002-07-10 | Glaxo Group Ltd | Compounds |
| EP1551394A1 (en) | 2002-08-14 | 2005-07-13 | Janssen Pharmaceutica N.V. | Treatment of lower urinary tract symptoms associated with overactive bladder in men and women |
| JP2004099493A (ja) | 2002-09-09 | 2004-04-02 | Ono Pharmaceut Co Ltd | 4−[6−[n−イソブチル−n−(4−メチル−2−チアゾリルスルフォニル)アミノ]インダン−5−イルオキシメチル]安息香酸の新規結晶、その製造方法およびそれを有効成分として含有する薬剤 |
| GB0317500D0 (en) | 2003-07-25 | 2003-08-27 | Pfizer Ltd | Treatment of bph |
| KR101083414B1 (ko) | 2003-06-27 | 2011-11-14 | 혼다 기켄 고교 가부시키가이샤 | 다리식 이동 로봇의 제어장치 |
| GB0508460D0 (en) | 2005-04-26 | 2005-06-01 | Glaxo Group Ltd | Compounds |
| JP2008189549A (ja) * | 2005-05-12 | 2008-08-21 | Astellas Pharma Inc | カルボン酸誘導体またはその塩 |
| JP2009057282A (ja) | 2005-12-19 | 2009-03-19 | Astellas Pharma Inc | カルボン酸誘導体又はその塩 |
| GB0606876D0 (en) | 2006-04-05 | 2006-05-17 | Glaxo Group Ltd | Compounds |
| TW200817319A (en) | 2006-08-10 | 2008-04-16 | Astellas Pharma Inc | Sulfonamide compound or salt thereof |
-
2008
- 2008-02-15 MX MX2009008606A patent/MX2009008606A/es active IP Right Grant
- 2008-02-15 RU RU2009134485/15A patent/RU2452479C2/ru not_active IP Right Cessation
- 2008-02-15 KR KR20097018350A patent/KR101492552B1/ko not_active Expired - Fee Related
- 2008-02-15 EP EP08711316.3A patent/EP2123273B1/en not_active Not-in-force
- 2008-02-15 CN CN200880012411.5A patent/CN101663034B/zh not_active Expired - Fee Related
- 2008-02-15 AU AU2008215431A patent/AU2008215431C1/en not_active Ceased
- 2008-02-15 WO PCT/JP2008/052486 patent/WO2008099907A1/ja not_active Ceased
- 2008-02-15 NZ NZ578988A patent/NZ578988A/en not_active IP Right Cessation
- 2008-02-15 US US12/527,340 patent/US9181187B2/en not_active Expired - Fee Related
- 2008-02-15 JP JP2008558140A patent/JP5439817B2/ja not_active Expired - Fee Related
- 2008-02-15 CA CA2677769A patent/CA2677769C/en not_active Expired - Fee Related
- 2008-02-15 ES ES08711316.3T patent/ES2437323T3/es active Active
- 2008-02-15 BR BRPI0807942-0A2A patent/BRPI0807942A2/pt not_active IP Right Cessation
-
2009
- 2009-08-13 IL IL200377A patent/IL200377A/en not_active IP Right Cessation
- 2009-08-14 ZA ZA200905681A patent/ZA200905681B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2677769A1 (en) | 2008-08-21 |
| WO2008099907A1 (ja) | 2008-08-21 |
| JP5439817B2 (ja) | 2014-03-12 |
| IL200377A (en) | 2016-04-21 |
| ES2437323T3 (es) | 2014-01-10 |
| EP2123273A4 (en) | 2010-09-15 |
| US9181187B2 (en) | 2015-11-10 |
| NZ578988A (en) | 2012-03-30 |
| CA2677769C (en) | 2016-01-19 |
| KR20090114433A (ko) | 2009-11-03 |
| EP2123273B1 (en) | 2013-10-23 |
| AU2008215431A1 (en) | 2008-08-21 |
| JPWO2008099907A1 (ja) | 2010-05-27 |
| CN101663034B (zh) | 2014-11-05 |
| AU2008215431C1 (en) | 2013-10-17 |
| RU2452479C2 (ru) | 2012-06-10 |
| ZA200905681B (en) | 2010-04-28 |
| CN101663034A (zh) | 2010-03-03 |
| IL200377A0 (en) | 2010-04-29 |
| KR101492552B1 (ko) | 2015-02-12 |
| RU2009134485A (ru) | 2011-03-27 |
| BRPI0807942A2 (pt) | 2014-07-01 |
| EP2123273A1 (en) | 2009-11-25 |
| US20100076038A1 (en) | 2010-03-25 |
| AU2008215431B2 (en) | 2012-09-06 |
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