JP5290185B2 - 置換3−イソブチル−9,10−ジメトキシ−1,3,4,6,7,11b−ヘキサヒドロ−2H−ピリド[2,1−a]イソキノリン−2−オール化合物およびそれに関連する方法 - Google Patents
置換3−イソブチル−9,10−ジメトキシ−1,3,4,6,7,11b−ヘキサヒドロ−2H−ピリド[2,1−a]イソキノリン−2−オール化合物およびそれに関連する方法 Download PDFInfo
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- JP5290185B2 JP5290185B2 JP2009536493A JP2009536493A JP5290185B2 JP 5290185 B2 JP5290185 B2 JP 5290185B2 JP 2009536493 A JP2009536493 A JP 2009536493A JP 2009536493 A JP2009536493 A JP 2009536493A JP 5290185 B2 JP5290185 B2 JP 5290185B2
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- isobutyl
- dimethoxy
- pyrido
- hexahydro
- isoquinolin
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- 0 CC(C)CC1C(*C(*I)=*)CC2c3cc(OC)c(*)cc3CC*2C1 Chemical compound CC(C)CC1C(*C(*I)=*)CC2c3cc(OC)c(*)cc3CC*2C1 0.000 description 4
- VEBDPENYIIXRJY-UHFFFAOYSA-N CC(C)CC(C[I](CCc1c2)C(C3)c1cc(OC)c2OC)C3[U]C(Cl)=N Chemical compound CC(C)CC(C[I](CCc1c2)C(C3)c1cc(OC)c2OC)C3[U]C(Cl)=N VEBDPENYIIXRJY-UHFFFAOYSA-N 0.000 description 1
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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
-
- 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
- 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
-
- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86494406P | 2006-11-08 | 2006-11-08 | |
| US60/864,944 | 2006-11-08 | ||
| PCT/US2007/084176 WO2008058261A1 (en) | 2006-11-08 | 2007-11-08 | Substituted 3-isobutyl-9, 10-dimethoxy-1,3,4,6,7,11b-hexahydro-2h-pyrido[2,1-a] isoquinolin-2-ol compounds and methods relating thereto |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010509366A JP2010509366A (ja) | 2010-03-25 |
| JP2010509366A5 JP2010509366A5 (enExample) | 2011-11-24 |
| JP5290185B2 true JP5290185B2 (ja) | 2013-09-18 |
Family
ID=39110526
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009536493A Active JP5290185B2 (ja) | 2006-11-08 | 2007-11-08 | 置換3−イソブチル−9,10−ジメトキシ−1,3,4,6,7,11b−ヘキサヒドロ−2H−ピリド[2,1−a]イソキノリン−2−オール化合物およびそれに関連する方法 |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US8039627B2 (enExample) |
| EP (1) | EP2081929B1 (enExample) |
| JP (1) | JP5290185B2 (enExample) |
| KR (1) | KR101500766B1 (enExample) |
| CN (1) | CN101553487B (enExample) |
| AU (1) | AU2007317242B2 (enExample) |
| BR (1) | BRPI0718247B1 (enExample) |
| CA (1) | CA2668689C (enExample) |
| DK (1) | DK2081929T3 (enExample) |
| EA (1) | EA018378B1 (enExample) |
| ES (1) | ES2402220T3 (enExample) |
| IL (1) | IL198250A0 (enExample) |
| MX (1) | MX2009004910A (enExample) |
| PL (1) | PL2081929T3 (enExample) |
| PT (1) | PT2081929E (enExample) |
| WO (1) | WO2008058261A1 (enExample) |
Families Citing this family (71)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0718247B1 (pt) | 2006-11-08 | 2021-09-21 | Neurocrine Biosciences, Inc. | Composto usado como inibidor do transportador de monoamina vesicular 2, composição farmacêutica compreendendo o dito composto e uso da dita composição farmacêutica no tratamento de transtornos hipercinéticos |
| LT3061760T (lt) | 2008-09-18 | 2018-02-26 | Auspex Pharmaceuticals, Inc. | Deuterinti benzochinolizino dariniai kaip vezikuliarinio monoamino transporterio 2 slopikliai |
| WO2011153157A2 (en) * | 2010-06-01 | 2011-12-08 | Auspex Pharmaceutical, Inc. | Benzoquinolone inhibitors of vmat2 |
| WO2012000308A1 (zh) * | 2010-06-29 | 2012-01-05 | 中国药科大学 | 丁苯那嗪的拆分方法 |
| US8351329B2 (en) * | 2010-09-14 | 2013-01-08 | Cisco Technology, Inc. | Universal load-balancing tunnel encapsulation |
| CN102285984B (zh) * | 2010-11-25 | 2012-10-10 | 江苏威凯尔医药科技有限公司 | (2R,3R,11bR)-二氢丁苯那嗪及相关化合物的制备方法 |
| WO2012081031A1 (en) * | 2010-12-15 | 2012-06-21 | Enaltec Labs Pvt. Ltd. | Process for preparing tetrabenazine |
| US9550780B2 (en) | 2012-09-18 | 2017-01-24 | Auspex Pharmaceuticals, Inc. | Formulations pharmacokinetics of deuterated benzoquinoline inhibitors of vesicular monoamine transporter 2 |
| NZ705372A (en) | 2012-09-18 | 2018-07-27 | Auspex Pharmaceuticals Inc | Formulations pharmacokinetics of deuterated benzoquinoline inhibitors of vesicular monoamine transporter 2 |
| MX2015009719A (es) | 2013-01-31 | 2016-08-08 | Auspex Pharmaceuticals Inc | Inhibidores benzoquinolona de vmat2. |
| EP3049087A4 (en) * | 2013-09-27 | 2017-05-24 | Auspex Pharmaceuticals, Inc. | Benzoquinolone inhibitors of vmat2 |
| KR102391134B1 (ko) * | 2013-12-03 | 2022-04-28 | 오스펙스 파마슈티칼스, 인코포레이티드 | 벤조퀴놀린 화합물을 제조하는 방법 |
| MX2016009817A (es) | 2014-01-27 | 2017-02-28 | Auspex Pharmaceuticals Inc | Inhibidores de benzoquinolina del transportador vesicular de monoaminas 2. |
| EA201691582A1 (ru) | 2014-02-07 | 2017-01-30 | Оспекс Фармасьютикалз, Инк. | Новые фармацевтические препараты |
| US9782398B2 (en) * | 2014-02-07 | 2017-10-10 | Neurocrine Biosciences, Inc. | Pharmaceutical compositions comprising an antipsychotic drug and a VMAT2 inhibitor and uses thereof |
| PE20161573A1 (es) | 2014-02-13 | 2017-01-19 | Incyte Corp | Ciclopropilamina como inhibidor de la lsd1 |
| CN112741835A (zh) * | 2014-05-06 | 2021-05-04 | 纽罗克里生物科学有限公司 | 用于运动机能亢进性运动障碍的治疗的vmat2抑制剂 |
| WO2016127133A1 (en) * | 2015-02-06 | 2016-08-11 | Neurocrine Biosciences, Inc. | [9,10-dimethoxy-3-(2-methylpropyl)-1h,2h,3h,4h,6h,7h,11bh-pyrido-[2,1-a]isoquinolin-2-yl]methanol and compounds, compositions and methods relating thereto |
| DK3265085T3 (da) | 2015-03-06 | 2022-10-03 | Auspex Pharmaceuticals Inc | Fremgangsmåder til behandling af forstyrrelser med abnorme ufrivillige bevægelser |
| MY191796A (en) | 2015-04-03 | 2022-07-15 | Incyte Corp | Heterocyclic compounds as lsd1 inhibitors |
| MY189806A (en) * | 2015-06-23 | 2022-03-08 | Neurocrine Biosciences Inc | Vmat2 inhibitors for treating neurological diseases or disorders |
| KR102710120B1 (ko) | 2015-08-12 | 2024-09-27 | 인사이트 홀딩스 코포레이션 | Lsd1 저해제의 염 |
| TW201720443A (zh) | 2015-10-09 | 2017-06-16 | 梯瓦製藥國際有限責任公司 | 用以治療帕金森氏症之經氘化左旋多巴、碳度巴、以及奧匹卡朋的組合 |
| MA56137B1 (fr) * | 2015-10-30 | 2024-03-29 | Neurocrine Biosciences Inc | Sels de dihydrochlorure de valbénazine et leurs polymorphes |
| CA3009169A1 (en) * | 2015-12-23 | 2017-06-29 | Neurocrine Biosciences, Inc. | Synthetic methods for preparation of (s)-(2r,3r,11br)-3-isobutyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-pyrido[2,1-a]isoquinolin-2-yl 2-amino-3-methylbutanoate di(4-methylbenzenesulfonate) |
| US10479787B2 (en) | 2016-04-22 | 2019-11-19 | Lupin Limited | Process for preparation of tetrabenazine and deutetrabenazine |
| EP3473623B1 (en) * | 2016-06-29 | 2020-07-15 | Crystal Pharmaceutical (Suzhou) Co., Ltd. | Crystal forms of nbi-98854, preparation method therefor and use thereof |
| EP3523300A1 (en) * | 2016-10-06 | 2019-08-14 | Assia Chemical Industries Ltd. | Solid state forms of valbenazine |
| TW201827051A (zh) | 2016-12-02 | 2018-08-01 | 美商神經性分泌生物科學公司 | 戊苯那嗪(valbenazine)於治療精神分裂症或情感性精神分裂症之用途 |
| WO2018130345A1 (en) | 2017-01-10 | 2018-07-19 | Sandoz Ag | Crystalline valbenazine free base |
| MY203491A (en) * | 2017-01-27 | 2024-06-30 | Neurocrine Biosciences Inc | Methods for the administration of certain vmat2 inhibitors |
| US10954235B2 (en) | 2017-02-27 | 2021-03-23 | Sandoz Ag | Crystalline forms of valbenazine salts |
| WO2018164996A1 (en) | 2017-03-06 | 2018-09-13 | Neurocrine Biosciences, Inc. | Dosing regimen for valbenazine |
| KR20200003791A (ko) | 2017-03-15 | 2020-01-10 | 오스펙스 파마슈티칼스, 인코포레이티드 | 듀테트라베나진의 유사체, 이의 제조 및 용도 |
| GB201705304D0 (en) | 2017-04-01 | 2017-05-17 | Adeptio Pharmaceuticals Ltd | Pharmaceutical compositions |
| GB201705303D0 (en) * | 2017-04-01 | 2017-05-17 | Adeptio Pharmaceuticals Ltd | Pharmaceutical compositions |
| RU2768738C2 (ru) * | 2017-04-01 | 2022-03-24 | Адептио Фармасьютикалз Лимитед | ПРИМЕНЕНИЕ (-)-α-ДИГИДРОТЕТРАБЕНАЗИНА ИЛИ ЕГО КОМБИНАЦИИ С (+)-α-ДИГИДРОТЕТРАБЕНАЗИНОМ В ЛЕЧЕНИИ ГИПЕРКИНЕТИЧЕСКОГО ДВИГАТЕЛЬНОГО РАССТРОЙСТВА, А ТАКЖЕ СООТВЕТСТВУЮЩИЕ СПОСОБЫ |
| GB201705302D0 (en) | 2017-04-01 | 2017-05-17 | Adeptio Pharmaceuticals Ltd | Pharmaceutical compositions |
| GB201705306D0 (en) | 2017-04-01 | 2017-05-17 | Adeptio Pharmaceuticals Ltd | Pharmaceutical compositions |
| JOP20190239A1 (ar) * | 2017-04-19 | 2019-10-09 | Neurocrine Biosciences Inc | مركبات مثبطة لـ vmat2 وتركيبات منها |
| WO2018200605A1 (en) | 2017-04-26 | 2018-11-01 | Neurocrine Biosciences, Inc. | Use of valbenazine for treating levodopa-induced dyskinesia |
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| KR20250110361A (ko) * | 2017-10-10 | 2025-07-18 | 뉴로크린 바이오사이언시즈 인코퍼레이티드 | 특정 vmat2 억제제의 투여 방법 |
| KR20250070134A (ko) | 2017-10-10 | 2025-05-20 | 뉴로크린 바이오사이언시즈 인코퍼레이티드 | 특정 vmat2 억제제의 투여 방법 |
| US11306082B2 (en) | 2017-11-08 | 2022-04-19 | Foresee Pharmaceuticals Co., Ltd. | Esters of dihydrotetrabenazine |
| US11384077B2 (en) | 2017-11-22 | 2022-07-12 | Assia Chemical Industries Ltd. | Solid state form of Valbenazine |
| CA3086611C (en) | 2017-12-26 | 2023-07-25 | Crystal Pharmaceutical (Suzhou) Co., Ltd. | A crystalline form of valbenazine ditosylate, processes for preparation thereof and use thereof |
| CN110092785A (zh) * | 2018-01-31 | 2019-08-06 | 广东东阳光药业有限公司 | 一种丁苯那嗪的动态拆分方法 |
| GB201808464D0 (en) | 2018-05-23 | 2018-07-11 | Adeptio Pharmaceuticals Ltd | Pharmaceutical compounds for use in treating huntington's disease |
| MX2020013004A (es) | 2018-06-14 | 2021-02-17 | Neurocrine Biosciences Inc | Compuestos inhibidores del transportador de monoamina 2 (vmat2), composiciones, y metodos relacionados con los mismos. |
| MX2021001017A (es) | 2018-08-15 | 2021-04-19 | Neurocrine Biosciences Inc | Metodos para la administracion de ciertos inhibidores de transportador vesicular de monoamina de proteinas transportadoras-2 (vmat2). |
| US10968200B2 (en) | 2018-08-31 | 2021-04-06 | Incyte Corporation | Salts of an LSD1 inhibitor and processes for preparing the same |
| EP3860599B1 (en) | 2018-10-04 | 2024-05-15 | Adeptio Pharmaceuticals Limited | (+)-alpha-dihydrotetrabenazine dosage regimen for treating movement disorders |
| CA3065236A1 (en) | 2018-12-27 | 2020-06-27 | Apotex Inc. | Novel crystalline form of valbenazine dibesylate |
| WO2020213014A1 (en) | 2019-04-19 | 2020-10-22 | Mylan Laboratories Limited | An improved process for the preparation of valbenazine and its salts |
| US10689380B1 (en) | 2019-07-30 | 2020-06-23 | Farmhispania S.A. | Crystalline forms of valbenazine ditosylate |
| EP4015517A4 (en) * | 2019-08-12 | 2023-10-18 | Geneora Pharma (Shijiazhuang) Co., Ltd. | VMAT2 INHIBITOR AND PRODUCTION METHOD THEREOF AND USE THEREOF |
| US10940141B1 (en) | 2019-08-23 | 2021-03-09 | Neurocrine Biosciences, Inc. | Methods for the administration of certain VMAT2 inhibitors |
| WO2021050977A1 (en) | 2019-09-13 | 2021-03-18 | Neurocrine Biosciences, Inc. | Processes for the synthesis of valbenazine |
| CN110698397A (zh) * | 2019-10-28 | 2020-01-17 | 南京红杉生物科技有限公司 | 丁苯那嗪中间体及其合成方法、应用和合成用中间产物 |
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| IL307826A (en) | 2021-04-26 | 2023-12-01 | Neurocrine Biosciences Inc | Processes for the synthesis of valbanazine |
| AU2022302155A1 (en) | 2021-06-30 | 2024-02-08 | Neurocrine Biosciences, Inc. | Valbenazine for use in the treatment of dyskinesia due to cerebral palsy |
| WO2023278987A1 (en) | 2021-06-30 | 2023-01-05 | Neurocrine Biosciences, Inc. | Valbenazine for use in the add-on treatment of schizophrenia |
| CA3245030A1 (en) | 2022-03-07 | 2023-09-14 | Neurocrine Biosciences Inc | VALBENAZINE, A VMAT2 INHIBITOR, AS A FREE BASE OF A TOSYLATE OR DITOSYLATE SALT, INTENDED FOR USE IN THE TREATMENT OF CHOREA ASSOCIATED WITH HUNTINGTON'S DISEASE |
| EP4590676A1 (en) | 2022-09-21 | 2025-07-30 | Neurocrine Biosciences, Inc. | Hexahydro-2h-pyrido[2,1-a]isoquinoline vmat2 inhibitors and methods of use |
| WO2025038959A1 (en) | 2023-08-17 | 2025-02-20 | Neurocrine Biosciences, Inc. | Methods for the administration of certain vmat2 inhibitors |
| TW202521119A (zh) | 2023-08-17 | 2025-06-01 | 美商紐羅克里生物科學有限公司 | 用於投與特定vmat2抑制劑之方法 |
| WO2025096823A1 (en) | 2023-11-01 | 2025-05-08 | Neurocrine Biosciences, Inc. | Improvement, maintenance or reduction of decline of motor function associated with huntington disease using valbenazine |
| WO2025188830A1 (en) | 2024-03-06 | 2025-09-12 | Neurocrine Biosciences, Inc. | Methods for the administration of certain vmat2 inhibitors |
| WO2025199234A1 (en) | 2024-03-20 | 2025-09-25 | Neurocrine Biosciences, Inc. | Vmat2 inhibitors and methods of use |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2843591A (en) | 1958-07-15 | Method for preparing same | ||
| US3209005A (en) | 1965-09-28 | Hexahydro-llbh-benzo[a] quinolizines and processes therefor | ||
| US2852518A (en) | 1957-05-23 | 1958-09-16 | Parke Davis & Co | Di-substituted quinoline compounds |
| WO1991016920A1 (en) | 1990-05-07 | 1991-11-14 | Vical, Inc. | Lipid prodrugs of salicylate and nonsteroidal anti-inflammatory drugs |
| US6610841B1 (en) | 1997-12-18 | 2003-08-26 | Gilead Sciences, Inc. | Nucleotide-based prodrugs |
| US7045543B2 (en) | 2001-11-05 | 2006-05-16 | Enzrel Inc. | Covalent conjugates of biologically-active compounds with amino acids and amino acid derivatives for targeting to physiologically-protected sites |
| GB2410947B (en) | 2004-02-11 | 2008-09-17 | Cambridge Lab Ltd | Pharmaceutical compounds |
| WO2006053067A2 (en) | 2004-11-09 | 2006-05-18 | Prestwick Pharmaceuticals, Inc. | Combination of amantadine and a tetrabenazine compound for treating hyperkinetic disorders |
| WO2007005283A2 (en) | 2005-06-29 | 2007-01-11 | Trustees Of Columbia University In The City Of New York | Use of dtbz for imaging endocrine pancreas and beta cell mass in type 1 diabetes |
| GB0514501D0 (en) | 2005-07-14 | 2005-08-24 | Cambridge Lab Ireland Ltd | Pharmaceutical compounds |
| GB0516168D0 (en) | 2005-08-05 | 2005-09-14 | Cambridge Lab Ireland Ltd | Pharmaceutical compounds |
| ATE415968T1 (de) | 2005-08-06 | 2008-12-15 | Cambridge Lab Ireland Ltd | 3,11b-cis-dihydrotetrabanezin zur behandlung von schizophrenie und anderen psychosen |
| BRPI0718247B1 (pt) | 2006-11-08 | 2021-09-21 | Neurocrine Biosciences, Inc. | Composto usado como inibidor do transportador de monoamina vesicular 2, composição farmacêutica compreendendo o dito composto e uso da dita composição farmacêutica no tratamento de transtornos hipercinéticos |
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Also Published As
| Publication number | Publication date |
|---|---|
| KR101500766B1 (ko) | 2015-03-16 |
| CN101553487A (zh) | 2009-10-07 |
| US20080167337A1 (en) | 2008-07-10 |
| AU2007317242A1 (en) | 2008-05-15 |
| BRPI0718247A2 (pt) | 2014-01-07 |
| EA200970461A1 (ru) | 2009-12-30 |
| CA2668689C (en) | 2015-12-29 |
| IL198250A0 (en) | 2009-12-24 |
| US8039627B2 (en) | 2011-10-18 |
| PT2081929E (pt) | 2013-04-15 |
| AU2007317242B2 (en) | 2013-08-01 |
| EP2081929B1 (en) | 2013-01-09 |
| CA2668689A1 (en) | 2008-05-15 |
| EA018378B1 (ru) | 2013-07-30 |
| KR20090079257A (ko) | 2009-07-21 |
| PL2081929T3 (pl) | 2013-06-28 |
| EP2081929A1 (en) | 2009-07-29 |
| WO2008058261A1 (en) | 2008-05-15 |
| US20120077839A1 (en) | 2012-03-29 |
| CN101553487B (zh) | 2012-06-13 |
| ES2402220T8 (es) | 2021-12-23 |
| ES2402220T3 (es) | 2013-04-29 |
| JP2010509366A (ja) | 2010-03-25 |
| DK2081929T3 (da) | 2013-04-15 |
| MX2009004910A (es) | 2009-07-24 |
| KR101500766B9 (ko) | 2024-09-25 |
| BRPI0718247B1 (pt) | 2021-09-21 |
| US8357697B2 (en) | 2013-01-22 |
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