KR20080095877A - 아자사이클릴-치환된 아릴디하이드로이소퀴놀리논, 이의 제조 방법 및 약제로서 이의 용도 - Google Patents
아자사이클릴-치환된 아릴디하이드로이소퀴놀리논, 이의 제조 방법 및 약제로서 이의 용도 Download PDFInfo
- Publication number
- KR20080095877A KR20080095877A KR1020087019922A KR20087019922A KR20080095877A KR 20080095877 A KR20080095877 A KR 20080095877A KR 1020087019922 A KR1020087019922 A KR 1020087019922A KR 20087019922 A KR20087019922 A KR 20087019922A KR 20080095877 A KR20080095877 A KR 20080095877A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- alkoxy
- ring
- compound
- hydroxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
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- 0 C[C@](CCc1cc(C=CN(C2O)c(cc3F)ccc3N(CC3)C[C@@]3*3CCCC3)c2cc1)O Chemical compound C[C@](CCc1cc(C=CN(C2O)c(cc3F)ccc3N(CC3)C[C@@]3*3CCCC3)c2cc1)O 0.000 description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N C1NCCNC1 Chemical compound C1NCCNC1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N C1NCCOC1 Chemical compound C1NCCOC1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
- YPHPAIYMPJAKHT-UHFFFAOYSA-N CC(COc(cc1CCN2c(cc3)cc(F)c3N(CC3)CC3NC)ccc1C2=O)O Chemical compound CC(COc(cc1CCN2c(cc3)cc(F)c3N(CC3)CC3NC)ccc1C2=O)O YPHPAIYMPJAKHT-UHFFFAOYSA-N 0.000 description 1
- DXWMUSBDFDCQHJ-UHUGOGIASA-N CC(COc(cc1CCN2c(cc3)cc(F)c3N(CC3)C[C@@H]3NC)ccc1C2=O)OC Chemical compound CC(COc(cc1CCN2c(cc3)cc(F)c3N(CC3)C[C@@H]3NC)ccc1C2=O)OC DXWMUSBDFDCQHJ-UHUGOGIASA-N 0.000 description 1
- WAUBSNAUAVDBLJ-ITUIMRKVSA-N CCCC(CO)Oc(cc1)cc(C=CN2c(cc3)cc(F)c3N(CC3)C[C@@H]3NC)c1C2=O Chemical compound CCCC(CO)Oc(cc1)cc(C=CN2c(cc3)cc(F)c3N(CC3)C[C@@H]3NC)c1C2=O WAUBSNAUAVDBLJ-ITUIMRKVSA-N 0.000 description 1
- DZGOPQMGDFVESS-UHFFFAOYSA-N CCCCOc(cc1)cc(C=CN2c(cc3)cc(F)c3N(CC3)CC3N(C)C)c1C2=O Chemical compound CCCCOc(cc1)cc(C=CN2c(cc3)cc(F)c3N(CC3)CC3N(C)C)c1C2=O DZGOPQMGDFVESS-UHFFFAOYSA-N 0.000 description 1
- AQOKIDBUMLZUFI-NYRYZVAPSA-N CCC[C@@H]([C@@H](c(cc1)cc(C=CN2c(cc3)cc(F)c3N(CC3)CC3N3CCCC3)c1C2=O)O)O Chemical compound CCC[C@@H]([C@@H](c(cc1)cc(C=CN2c(cc3)cc(F)c3N(CC3)CC3N3CCCC3)c1C2=O)O)O AQOKIDBUMLZUFI-NYRYZVAPSA-N 0.000 description 1
- FKXXRUNEVVLJOT-OZAIVSQSSA-N CN(C)[C@H](CC1)CN1C(C(F)=C1)=CCC1N(CCc1c2ccc(-c(cc3)ccc3F)c1)C2=O Chemical compound CN(C)[C@H](CC1)CN1C(C(F)=C1)=CCC1N(CCc1c2ccc(-c(cc3)ccc3F)c1)C2=O FKXXRUNEVVLJOT-OZAIVSQSSA-N 0.000 description 1
- AZEOUAIFRVGNMX-OAQYLSRUSA-N CN(C)[C@H](CC1)CN1c(cc1)ccc1N(CCc1c2[s]c(C#CC3CC3)c1)C2=O Chemical compound CN(C)[C@H](CC1)CN1c(cc1)ccc1N(CCc1c2[s]c(C#CC3CC3)c1)C2=O AZEOUAIFRVGNMX-OAQYLSRUSA-N 0.000 description 1
- IEOPZUMPHCZMCS-LURJTMIESA-N COC[C@H]1OCCC1 Chemical compound COC[C@H]1OCCC1 IEOPZUMPHCZMCS-LURJTMIESA-N 0.000 description 1
- FTXIRJHSMDMCHM-UHFFFAOYSA-N Cc(cc1)ccc1-c1cc(CCN(c(cc2)ccc2N2CCN(C)CCC2)C2=O)c2[s]1 Chemical compound Cc(cc1)ccc1-c1cc(CCN(c(cc2)ccc2N2CCN(C)CCC2)C2=O)c2[s]1 FTXIRJHSMDMCHM-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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- A—HUMAN NECESSITIES
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- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4355—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
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- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- 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
-
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- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
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- C07D498/10—Spiro-condensed systems
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- 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
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- Chemical & Material Sciences (AREA)
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- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Diabetes (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
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- Hematology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006007045 | 2006-02-15 | ||
| DE102006007045.3 | 2006-02-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20080095877A true KR20080095877A (ko) | 2008-10-29 |
Family
ID=38191074
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020087019922A Withdrawn KR20080095877A (ko) | 2006-02-15 | 2007-02-13 | 아자사이클릴-치환된 아릴디하이드로이소퀴놀리논, 이의 제조 방법 및 약제로서 이의 용도 |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US8822495B2 (enExample) |
| EP (1) | EP1987020B1 (enExample) |
| JP (1) | JP5175228B2 (enExample) |
| KR (1) | KR20080095877A (enExample) |
| CN (1) | CN101384583A (enExample) |
| AR (1) | AR059458A1 (enExample) |
| AU (1) | AU2007214709A1 (enExample) |
| BR (1) | BRPI0707872A2 (enExample) |
| CA (1) | CA2636873A1 (enExample) |
| CR (1) | CR10160A (enExample) |
| EC (1) | ECSP088680A (enExample) |
| IL (1) | IL193340A0 (enExample) |
| MA (1) | MA30221B1 (enExample) |
| NI (1) | NI200800217A (enExample) |
| NZ (1) | NZ570503A (enExample) |
| RU (1) | RU2008136898A (enExample) |
| TN (1) | TNSN08326A1 (enExample) |
| TW (1) | TW200800908A (enExample) |
| UY (1) | UY30166A1 (enExample) |
| WO (1) | WO2007093364A1 (enExample) |
| ZA (1) | ZA200805939B (enExample) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2589695A1 (en) | 2004-12-17 | 2006-06-22 | Eli Lilly And Company | Thiazolopyridinone derivates as mch receptor antagonists |
| US7728031B2 (en) | 2006-02-24 | 2010-06-01 | Abbott Laboratories | Octahydro-pyrrolo[3,4-b]pyrrole derivatives |
| CN101460503A (zh) | 2006-06-08 | 2009-06-17 | 伊莱利利公司 | 新的mch受体拮抗剂 |
| WO2007146758A2 (en) * | 2006-06-08 | 2007-12-21 | Eli Lilly And Company | Novel mch receptor antagonists |
| EA026578B1 (ru) | 2007-01-22 | 2017-04-28 | ДЖиТиЭкс, ИНК. | Вещества, связывающие ядерные рецепторы |
| US9623021B2 (en) | 2007-01-22 | 2017-04-18 | Gtx, Inc. | Nuclear receptor binding agents |
| US9604931B2 (en) | 2007-01-22 | 2017-03-28 | Gtx, Inc. | Nuclear receptor binding agents |
| US8853392B2 (en) | 2007-06-03 | 2014-10-07 | Vanderbilt University | Benzamide mGluR5 positive allosteric modulators and methods of making and using same |
| RU2486187C2 (ru) | 2007-09-11 | 2013-06-27 | Эбботт Лэборетриз | N-ОКСИДЫ ОКТАГИДРО-ПИРРОЛО[3,4-b]ПИРРОЛА |
| AR068745A1 (es) * | 2007-10-08 | 2009-12-02 | Panacea Biotec Ltd | Una composicion en forma de dosificacion farmaceutica oral de unidad de alta dosis de micofenolato sodico, metodo para utilizar dicha composicion y sus usos |
| ES2392122T3 (es) * | 2007-10-17 | 2012-12-04 | Sanofi | N-fenil-pirrolidinilmetilpirrolidin amidas sustituidas y uso terapéutico de las mismas |
| PL2212283T3 (pl) * | 2007-10-17 | 2012-01-31 | Sanofi Sa | Podstawione karboksyamidy N-fenylobipirolidyny i ich zastosowanie terapeutyczne |
| US8034806B2 (en) * | 2007-11-02 | 2011-10-11 | Vanderbilt University | Bicyclic mGluR5 positive allosteric modulators and methods of making and using same |
| WO2010003624A2 (en) | 2008-07-09 | 2010-01-14 | Sanofi-Aventis | Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof |
| US8586607B2 (en) | 2008-07-28 | 2013-11-19 | Syddansk Universitet | Compounds for the treatment of metabolic diseases |
| AR074466A1 (es) * | 2008-12-05 | 2011-01-19 | Sanofi Aventis | Piperidina espiro pirrolidinona y piperidinona sustituidas y su uso terapeutico en enfermedades mediadas por la modulacion de los receptores h3. |
| WO2010147234A1 (en) * | 2009-06-18 | 2010-12-23 | Banyu Pharmaceutical Co.,Ltd. | Diarylamide-spirodiamine derivative |
| KR101116234B1 (ko) | 2009-10-29 | 2014-03-06 | (주)퓨쳐켐 | (3-플루오로-2-히드록시)프로필 작용기가 도입된 아릴 유도체 또는 이의 약학적으로 허용가능한 염, 이의 제조방법 및 이를 유효성분으로 함유하는 퇴행성 뇌질환의 진단 또는 치료용 약학적 조성물 |
| TW201206910A (en) | 2010-05-11 | 2012-02-16 | Sanofi Aventis | Substituted N-heterocycloalkyl bipyrrolidinylphenyl amide derivatives, preparation and therapeutic use thereof |
| TW201206889A (en) * | 2010-05-11 | 2012-02-16 | Sanofi Aventis | Substituted N-alkyl and N-acyl tetrahydro-isoquinoline derivatives, preparation and therapeutic use thereof |
| TW201206444A (en) | 2010-05-11 | 2012-02-16 | Sanofi Aventis | Substituted N-heteroaryl tetrahydro-isoquinoline derivatives, preparation and therapeutic use thereof |
| WO2011143148A1 (en) * | 2010-05-11 | 2011-11-17 | Sanofi | Substituted n-heteroaryl spirolactam bipyrrolidines, preparation and therapeutic use thereof |
| AR083718A1 (es) | 2010-05-11 | 2013-03-20 | Sanofi Aventis | Fenil cicloalquil pirrolidina (piperidina) espirolactamas y amidas sustituidas, preparacion y uso terapeutico de las mismas |
| EP2569294B1 (en) | 2010-05-11 | 2015-03-11 | Sanofi | Substituted n-heteroaryl bipyrrolidine carboxamides, preparation and therapeutic use thereof |
| UY33463A (es) | 2010-06-24 | 2012-01-31 | Takeda Pharmaceutical | Compuestos heterocíclicos fusionados |
| US9134238B2 (en) * | 2010-12-01 | 2015-09-15 | Nalco Company | Method for determination of system parameters for reducing crude unit corrosion |
| TWI570122B (zh) * | 2011-06-22 | 2017-02-11 | 武田藥品工業股份有限公司 | 稠合雜環化合物之結晶 |
| CN103086894B (zh) * | 2013-02-25 | 2014-10-01 | 武汉迪可表面技术有限公司 | 一种电镀添加剂3-甲基-3-氨基丁炔的合成方法 |
| PE20160286A1 (es) | 2013-08-08 | 2016-05-22 | Galapagos Nv | DERIVADOS DE TIENO [2,3-c] PIRANO Y SUS COMPOSICIONES FARMACEUTICAS PARA EL TRATAMIENTO DE LA FIBROSIS QUISTICA |
| US20210017174A1 (en) | 2018-03-07 | 2021-01-21 | Bayer Aktiengesellschaft | Identification and use of erk5 inhibitor |
| MA53188A1 (fr) * | 2018-10-11 | 2021-12-31 | Basf As | Composés aromatiques et leurs utilisations pharmaceutiques |
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| US4329353A (en) * | 1980-10-22 | 1982-05-11 | Janssen Pharmaceutica, N.V. | 1-(4-Aryl-cyclohexyl)piperidine derivatives, method of use thereof and pharmaceutical compositions thereof |
| ATE198328T1 (de) * | 1992-09-28 | 2001-01-15 | Hoechst Ag | Antiarrhythmische und cardioprotektive substituierte 1(2h)-isochinoline, verfahren zu deren herstellung, diese enthaltende arzneimittel und ihre anwendung für die herstellung eines arzneimittels zur behandlung von herzinsuffizienzen |
| GB0124627D0 (en) * | 2001-10-15 | 2001-12-05 | Smithkline Beecham Plc | Novel compounds |
| AU2002352878B2 (en) * | 2001-11-27 | 2007-11-22 | Merck Sharp & Dohme Corp. | 2-Aminoquinoline compounds |
| DE10238865A1 (de) * | 2002-08-24 | 2004-03-11 | Boehringer Ingelheim International Gmbh | Neue Carbonsäureamid-Verbindungen mit MCH-antagonistischer Wirkung, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| AU2003287880A1 (en) * | 2002-12-11 | 2004-06-30 | 7Tm Pharma A/S | Cyclic quinoline compounds for use in mch receptor related disorders |
| EP1618112A1 (en) * | 2003-04-11 | 2006-01-25 | SmithKline Beecham Corporation | Heterocyclic mchr1 antagonists |
| MXPA06003997A (es) * | 2003-10-23 | 2006-07-05 | Glaxo Group Ltd | Derivados de 3-(4-aminofenil) tienopirimid-4-ona como antagonistas mch r1 para el tratamiento de obesidad, diabetes, depresion y ansiedad. |
| WO2005103039A1 (en) * | 2004-04-15 | 2005-11-03 | Neurocrine Biosciences, Inc. | 2- (3-aminopyrrolidin-1-yl) pyridines as melanin-concentrating hormone receptor an tagonists |
-
2007
- 2007-02-13 WO PCT/EP2007/001212 patent/WO2007093364A1/en not_active Ceased
- 2007-02-13 JP JP2008554653A patent/JP5175228B2/ja not_active Expired - Fee Related
- 2007-02-13 TW TW096105359A patent/TW200800908A/zh unknown
- 2007-02-13 NZ NZ570503A patent/NZ570503A/en unknown
- 2007-02-13 BR BRPI0707872-2A patent/BRPI0707872A2/pt not_active IP Right Cessation
- 2007-02-13 EP EP07711518A patent/EP1987020B1/en active Active
- 2007-02-13 CN CNA2007800057794A patent/CN101384583A/zh active Pending
- 2007-02-13 RU RU2008136898/04A patent/RU2008136898A/ru not_active Application Discontinuation
- 2007-02-13 KR KR1020087019922A patent/KR20080095877A/ko not_active Withdrawn
- 2007-02-13 CA CA002636873A patent/CA2636873A1/en not_active Abandoned
- 2007-02-13 AU AU2007214709A patent/AU2007214709A1/en not_active Abandoned
- 2007-02-15 UY UY30166A patent/UY30166A1/es not_active Application Discontinuation
- 2007-02-15 AR ARP070100658A patent/AR059458A1/es not_active Application Discontinuation
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2008
- 2008-07-08 ZA ZA200805939A patent/ZA200805939B/xx unknown
- 2008-07-17 CR CR10160A patent/CR10160A/es not_active Application Discontinuation
- 2008-08-10 IL IL193340A patent/IL193340A0/en unknown
- 2008-08-11 TN TNP2008000326A patent/TNSN08326A1/en unknown
- 2008-08-13 EC EC2008008680A patent/ECSP088680A/es unknown
- 2008-08-14 US US12/191,662 patent/US8822495B2/en not_active Expired - Fee Related
- 2008-08-14 NI NI200800217A patent/NI200800217A/es unknown
- 2008-08-15 MA MA31180A patent/MA30221B1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ZA200805939B (en) | 2009-12-30 |
| AR059458A1 (es) | 2008-04-09 |
| NI200800217A (es) | 2010-02-10 |
| JP2009526793A (ja) | 2009-07-23 |
| WO2007093364A1 (en) | 2007-08-23 |
| NZ570503A (en) | 2010-07-30 |
| MA30221B1 (fr) | 2009-02-02 |
| IL193340A0 (en) | 2009-05-04 |
| UY30166A1 (es) | 2007-09-28 |
| CR10160A (es) | 2008-10-06 |
| AU2007214709A1 (en) | 2007-08-23 |
| TW200800908A (en) | 2008-01-01 |
| US20090264403A1 (en) | 2009-10-22 |
| RU2008136898A (ru) | 2010-03-20 |
| EP1987020A1 (en) | 2008-11-05 |
| EP1987020B1 (en) | 2012-10-03 |
| TNSN08326A1 (en) | 2009-12-29 |
| BRPI0707872A2 (pt) | 2011-05-10 |
| US8822495B2 (en) | 2014-09-02 |
| CA2636873A1 (en) | 2007-08-23 |
| ECSP088680A (es) | 2008-09-29 |
| JP5175228B2 (ja) | 2013-04-03 |
| CN101384583A (zh) | 2009-03-11 |
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