CN101080411B - 作为mch受体拮抗剂的噻唑并吡啶酮衍生物 - Google Patents
作为mch受体拮抗剂的噻唑并吡啶酮衍生物 Download PDFInfo
- Publication number
- CN101080411B CN101080411B CN2005800431124A CN200580043112A CN101080411B CN 101080411 B CN101080411 B CN 101080411B CN 2005800431124 A CN2005800431124 A CN 2005800431124A CN 200580043112 A CN200580043112 A CN 200580043112A CN 101080411 B CN101080411 B CN 101080411B
- Authority
- CN
- China
- Prior art keywords
- phenyl
- thiazole
- chloro
- group
- pyridine
- 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.)
- Expired - Fee Related
Links
- 0 CC(C(N(C(*)=N1)C(C=C2)=C*(*3)C3=C2NC)=O)=C1I Chemical compound CC(C(N(C(*)=N1)C(C=C2)=C*(*3)C3=C2NC)=O)=C1I 0.000 description 1
- GQYOZWVZNQTYNC-UHFFFAOYSA-O CC(C)[SH+]1(C(C)C)OC(CCN(C2)c(ccc(N(CCc3c4[s]c(-c(cc5)ccc5Cl)n3)C4=O)c3)c3OC)C2C1C Chemical compound CC(C)[SH+]1(C(C)C)OC(CCN(C2)c(ccc(N(CCc3c4[s]c(-c(cc5)ccc5Cl)n3)C4=O)c3)c3OC)C2C1C GQYOZWVZNQTYNC-UHFFFAOYSA-O 0.000 description 1
- SCUUDAOOUDRPQX-UHFFFAOYSA-N CC(C)[Si+](C(C)C)(C1C)Oc(c(OC)c2)c1cc2NC(c1c(CCO)nc(-c(cc2)ccc2Cl)[s]1)=O Chemical compound CC(C)[Si+](C(C)C)(C1C)Oc(c(OC)c2)c1cc2NC(c1c(CCO)nc(-c(cc2)ccc2Cl)[s]1)=O SCUUDAOOUDRPQX-UHFFFAOYSA-N 0.000 description 1
- OMRWOBGMYHILOW-UHFFFAOYSA-N CCOC(CCc(c(OC)c1)ccc1N)O Chemical compound CCOC(CCc(c(OC)c1)ccc1N)O OMRWOBGMYHILOW-UHFFFAOYSA-N 0.000 description 1
- VVJXRBOQZCFBSR-UHFFFAOYSA-N CN(C)CCN(C)c1nc2cc(N)ccc2[o]1 Chemical compound CN(C)CCN(C)c1nc2cc(N)ccc2[o]1 VVJXRBOQZCFBSR-UHFFFAOYSA-N 0.000 description 1
- VWJRLGRYQWHZGT-UHFFFAOYSA-N CN1CC(COc(ccc(N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)c2)c2OC)OCC1 Chemical compound CN1CC(COc(ccc(N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)c2)c2OC)OCC1 VWJRLGRYQWHZGT-UHFFFAOYSA-N 0.000 description 1
- XQPFGASPZUVUPY-UHFFFAOYSA-N CN1CCN(Cc(c(OC)c2)ccc2NC(c2c(CCO)nc(-c(cc3)ccc3Cl)[s]2)=O)CC1 Chemical compound CN1CCN(Cc(c(OC)c2)ccc2NC(c2c(CCO)nc(-c(cc3)ccc3Cl)[s]2)=O)CC1 XQPFGASPZUVUPY-UHFFFAOYSA-N 0.000 description 1
- SKLYKGOZUXHSND-UHFFFAOYSA-N COC(COc(ccc(NC(c1c(CCO)nc(-c(cc2)ccc2Cl)[s]1)=O)c1)c1OC)OC Chemical compound COC(COc(ccc(NC(c1c(CCO)nc(-c(cc2)ccc2Cl)[s]1)=O)c1)c1OC)OC SKLYKGOZUXHSND-UHFFFAOYSA-N 0.000 description 1
- DLIGTJBUYQROFH-UHFFFAOYSA-N COCCc1c(C(OC)=O)[s]c(-c(cc2)ccc2Cl)n1 Chemical compound COCCc1c(C(OC)=O)[s]c(-c(cc2)ccc2Cl)n1 DLIGTJBUYQROFH-UHFFFAOYSA-N 0.000 description 1
- VMRWRVIZZURJHB-UHFFFAOYSA-N COc(cc1)ccc1-c1nc(CCO)c(C(O)=O)[s]1 Chemical compound COc(cc1)ccc1-c1nc(CCO)c(C(O)=O)[s]1 VMRWRVIZZURJHB-UHFFFAOYSA-N 0.000 description 1
- WBVDHGRIJZAOEW-UHFFFAOYSA-N COc(cc1)ccc1-c1nc(CCO)c[s]1 Chemical compound COc(cc1)ccc1-c1nc(CCO)c[s]1 WBVDHGRIJZAOEW-UHFFFAOYSA-N 0.000 description 1
- UAZFWESTBFIFDL-UHFFFAOYSA-N COc1c(CCCN2CCCC2)ccc(N(C=Cc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)c1 Chemical compound COc1c(CCCN2CCCC2)ccc(N(C=Cc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)c1 UAZFWESTBFIFDL-UHFFFAOYSA-N 0.000 description 1
- DJPGJWARKQIVBZ-UHFFFAOYSA-N COc1cc(N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)ccc1C#CCN1CCCC1 Chemical compound COc1cc(N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)ccc1C#CCN1CCCC1 DJPGJWARKQIVBZ-UHFFFAOYSA-N 0.000 description 1
- VNEUFXZFBLLCIP-UHFFFAOYSA-N COc1cc([N+]([O-])=O)ccc1C#CCN1CCCC1 Chemical compound COc1cc([N+]([O-])=O)ccc1C#CCN1CCCC1 VNEUFXZFBLLCIP-UHFFFAOYSA-N 0.000 description 1
- MFRDDZGIVQDKLU-UHFFFAOYSA-N Cc1c(cc(cc2)N(CCc3c4[s]c(-c(cc5)ccc5Cl)n3)C4=O)c2nc(NCCN2CCOCC2)c1 Chemical compound Cc1c(cc(cc2)N(CCc3c4[s]c(-c(cc5)ccc5Cl)n3)C4=O)c2nc(NCCN2CCOCC2)c1 MFRDDZGIVQDKLU-UHFFFAOYSA-N 0.000 description 1
- OZKQOANCAJSUNN-UHFFFAOYSA-N Cc1cc2cc(NC(c3c(CCO)nc(-c(cc4)ccc4Cl)[s]3)=O)ccc2[n]1CCN1CCCC1 Chemical compound Cc1cc2cc(NC(c3c(CCO)nc(-c(cc4)ccc4Cl)[s]3)=O)ccc2[n]1CCN1CCCC1 OZKQOANCAJSUNN-UHFFFAOYSA-N 0.000 description 1
- XXFYJRAHTMINDY-UHFFFAOYSA-N Cc1ncc(COc(ccc(N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)c2)c2OC)[s]1 Chemical compound Cc1ncc(COc(ccc(N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)c2)c2OC)[s]1 XXFYJRAHTMINDY-UHFFFAOYSA-N 0.000 description 1
- GBJNVKDIPGIVIH-UHFFFAOYSA-N O=C(c1c(CC2)nc(-c(cc3)ccc3Cl)[s]1)N2c1ccc2[n](Cc3ccncc3)ccc2c1 Chemical compound O=C(c1c(CC2)nc(-c(cc3)ccc3Cl)[s]1)N2c1ccc2[n](Cc3ccncc3)ccc2c1 GBJNVKDIPGIVIH-UHFFFAOYSA-N 0.000 description 1
- SJWSZTXWVAMNOJ-UHFFFAOYSA-N O=C(c1c(CC2)nc(-c(cc3)ccc3Cl)[s]1)N2c1ccc2[n](Cc3ncccc3)ccc2c1 Chemical compound O=C(c1c(CC2)nc(-c(cc3)ccc3Cl)[s]1)N2c1ccc2[n](Cc3ncccc3)ccc2c1 SJWSZTXWVAMNOJ-UHFFFAOYSA-N 0.000 description 1
- ODFKDMCXOMWGEU-UHFFFAOYSA-N O=C1N(CCOCc2ccccc2)CCOC1 Chemical compound O=C1N(CCOCc2ccccc2)CCOC1 ODFKDMCXOMWGEU-UHFFFAOYSA-N 0.000 description 1
- VOEUEYOLZCMCDQ-UHFFFAOYSA-N O=C1OCCc2c1[s]c(-c(cc1)ccc1Cl)n2 Chemical compound O=C1OCCc2c1[s]c(-c(cc1)ccc1Cl)n2 VOEUEYOLZCMCDQ-UHFFFAOYSA-N 0.000 description 1
- FQOGSTGLRLMQOV-UHFFFAOYSA-N [O-][N+](c(cc1N2)ccc1OC2=S)=O Chemical compound [O-][N+](c(cc1N2)ccc1OC2=S)=O FQOGSTGLRLMQOV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P11/06—Antiasthmatics
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- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
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- A—HUMAN NECESSITIES
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- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
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- A61P9/12—Antihypertensives
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Ophthalmology & Optometry (AREA)
- Endocrinology (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Anesthesiology (AREA)
- Rheumatology (AREA)
- Emergency Medicine (AREA)
- Vascular Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Gynecology & Obstetrics (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US63714304P | 2004-12-17 | 2004-12-17 | |
| US60/637,143 | 2004-12-17 | ||
| PCT/US2005/045866 WO2006066174A1 (en) | 2004-12-17 | 2005-12-16 | Thiazolopyridinone derivates as mch receptor antagonists |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101080411A CN101080411A (zh) | 2007-11-28 |
| CN101080411B true CN101080411B (zh) | 2011-11-02 |
Family
ID=36123161
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2005800431124A Expired - Fee Related CN101080411B (zh) | 2004-12-17 | 2005-12-16 | 作为mch受体拮抗剂的噻唑并吡啶酮衍生物 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US7902356B2 (https=) |
| EP (1) | EP1828207B1 (https=) |
| JP (1) | JP5072602B2 (https=) |
| CN (1) | CN101080411B (https=) |
| AT (1) | ATE446962T1 (https=) |
| AU (1) | AU2005316314B2 (https=) |
| BR (1) | BRPI0519124A2 (https=) |
| CA (1) | CA2589695A1 (https=) |
| DE (1) | DE602005017423D1 (https=) |
| ES (1) | ES2333243T3 (https=) |
| MX (1) | MX2007007227A (https=) |
| WO (1) | WO2006066174A1 (https=) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2582327A1 (en) | 2004-10-01 | 2006-04-13 | Takao Suzuki | 2-arylcarboxamide-nitrogeneous heterocycle compound |
| CA2639910A1 (en) | 2006-01-25 | 2007-08-02 | Synta Pharmaceuticals Corp. | Thiazole and thiadiazole compounds for inflammation and immune-related uses |
| MX2008015662A (es) * | 2006-06-08 | 2009-01-12 | Lilly Co Eli | Nuevos receptores antagonistas de la hormona concentradora de melanina (mch). |
| CN101558075A (zh) * | 2006-12-14 | 2009-10-14 | 伊莱利利公司 | 5-[4-(氮杂环丁烷-3-基氧基)-苯基]-2-苯基-5H-噻唑并[5,4-c]吡啶-4-酮衍生物及其作为MCH受体拮抗剂的用途 |
| US8198307B2 (en) * | 2007-05-11 | 2012-06-12 | Korea Research Institute Of Chemical Technology | Imidazole derivatives having aryl piperidine substituent, method for preparation thereof and pharmaceutical compositions containing same |
| DE102007028925A1 (de) | 2007-06-22 | 2008-12-24 | Saltigo Gmbh | Verfahren zur Herstellung von 2-Phenoxyacetalen und den daraus korrespondierenden 2-Phenoxycarbaldehyden |
| US20090076275A1 (en) * | 2007-09-19 | 2009-03-19 | David Robert Bolin | Diacylglycerol acyltransferase inhibitors |
| WO2010024258A1 (ja) | 2008-08-29 | 2010-03-04 | 塩野義製薬株式会社 | Pi3k阻害活性を有する縮環アゾール誘導体 |
| KR20120101551A (ko) | 2009-12-18 | 2012-09-13 | 얀센 파마슈티카 엔.브이. | Mglur5 수용체의 알로스테릭 조절자로서 바이사이클릭 티아졸 |
| CA2782950A1 (en) | 2009-12-18 | 2011-06-23 | Janssen Pharmaceutica Nv | Bicyclic thiazoles as allosteric modulators of mglur5 receptors |
| US8895737B2 (en) | 2010-07-16 | 2014-11-25 | Shashank Shekhar | Process for preparing antiviral compounds |
| BR112013001138A2 (pt) | 2010-07-16 | 2016-07-05 | Abbvie Inc | ligantes de fosfina para reações catalíticas |
| US8975443B2 (en) | 2010-07-16 | 2015-03-10 | Abbvie Inc. | Phosphine ligands for catalytic reactions |
| US9255074B2 (en) | 2010-07-16 | 2016-02-09 | Abbvie Inc. | Process for preparing antiviral compounds |
| CN102532123B (zh) * | 2010-12-29 | 2016-03-09 | 中国医学科学院药物研究所 | 噻唑-5-甲酰胺化合物、及其制法和药物组合物与用途 |
| WO2012109573A1 (en) * | 2011-02-11 | 2012-08-16 | Purdue Research Foundation | Substituted thiazoles for use as antiviral agents |
| CN104350059B (zh) * | 2012-03-27 | 2016-12-07 | 拜耳知识产权有限责任公司 | 具有除草和杀虫活性的噻唑并吡啶酮 |
| EP2848621A4 (en) * | 2012-05-10 | 2016-06-01 | Takeda Pharmaceutical | AROMATIC RING CONNECTION |
| FI3805233T3 (fi) | 2014-01-13 | 2024-04-17 | Aurigene Oncology Ltd | N-(5-(3-hydroksipyrrolidin-1-yyli)-2-morfolinooksatsolo[4,5-b]pyridin-6-yyli)-2-(2-metylipyridin-4-yyli)okatsoli-karboksamidin (r)- (s)-enantiomeerit irak4-estäjänä syövän hoitoon |
| US20150252022A1 (en) * | 2014-03-10 | 2015-09-10 | Innov17 Llc | Retinoic acid receptor-related orphan receptor modulators and uses thereof |
| US20150252051A1 (en) * | 2014-03-10 | 2015-09-10 | Innov17 Llc | Retinoic acid receptor-related orphan receptor modulators and uses thereof |
| BR112018000624A2 (pt) * | 2015-07-15 | 2018-09-18 | Aurigene Discovery Technologies Limited | compostos de indazol e azaindazol como inibidores de irak-4 |
| NZ746901A (en) * | 2016-03-11 | 2023-06-30 | Ac Immune Sa | Bicyclic compounds for diagnosis and therapy |
| DK3600270T3 (da) | 2017-03-31 | 2023-07-10 | Aurigene Oncology Ltd | Forbindelser og sammensætninger til behandling af hæmatologiske lidelser |
| CA3079628A1 (en) | 2017-10-31 | 2019-05-09 | Curis, Inc. | Compounds and compositions for treating hematological disorders |
| CN109928939A (zh) * | 2019-02-27 | 2019-06-25 | 上海卡洛化学有限公司 | 一种2,2,6,6-四甲基吗啉的制备方法 |
| JP2024513227A (ja) | 2021-04-05 | 2024-03-22 | ハリア・セラピューティクス・インコーポレイテッド | Nek7阻害剤 |
| KR20240004476A (ko) | 2021-04-08 | 2024-01-11 | 쿠리스 인코퍼레이션 | 암 치료를 위한 병용 요법 |
| US20250177382A1 (en) | 2021-04-22 | 2025-06-05 | Halia Therapeutics, Inc. | Nek7 inhibitors |
| CN115403456B (zh) * | 2022-09-22 | 2023-11-17 | 成都大学 | 一种合成爱德万甜中间体3-羟基-4-甲氧基苯丙醛的方法 |
| CN119592965B (zh) * | 2024-12-10 | 2025-09-26 | 西安交通大学 | 一种基于电合成的羟基酮类化合物的制备方法及其制备的羟基酮类化合物 |
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| US20030158177A1 (en) * | 2000-05-16 | 2003-08-21 | Yuji Ishihara | Melanin-concentrating hormone antagonist |
| WO2004004726A1 (en) * | 2002-07-08 | 2004-01-15 | Astrazeneca Ab | Mchir antagonists |
| WO2004052848A1 (en) * | 2002-12-11 | 2004-06-24 | Eli Lilly And Company | Novel mch receptor antagonists |
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| JPH0867678A (ja) * | 1993-11-10 | 1996-03-12 | Takeda Chem Ind Ltd | 複素環アミド化合物、その製造法および剤 |
| JP2002371059A (ja) * | 2000-05-16 | 2002-12-26 | Takeda Chem Ind Ltd | メラニン凝集ホルモン拮抗剤 |
| GB0124627D0 (en) | 2001-10-15 | 2001-12-05 | Smithkline Beecham Plc | Novel compounds |
| US20040214856A1 (en) * | 2003-04-23 | 2004-10-28 | Pfizer Inc | Cannabinoid receptor ligands and uses thereof |
| WO2005047293A1 (en) | 2003-11-07 | 2005-05-26 | Neurocrine Biosciences, Inc. | Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto |
| MX2007007226A (es) * | 2004-12-17 | 2007-08-21 | Lilly Co Eli | Antagonistas receptores novedosos de hormona concentradora de melanina (mch). |
| EP1987020B1 (en) | 2006-02-15 | 2012-10-03 | Sanofi | Azacyclyl-substituted aryldihydroisoquinolinones, process for their preparation and their use as medicaments |
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- 2005-12-16 EP EP05854554A patent/EP1828207B1/en not_active Expired - Lifetime
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- 2005-12-16 BR BRPI0519124-6A patent/BRPI0519124A2/pt not_active IP Right Cessation
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030158177A1 (en) * | 2000-05-16 | 2003-08-21 | Yuji Ishihara | Melanin-concentrating hormone antagonist |
| WO2004004726A1 (en) * | 2002-07-08 | 2004-01-15 | Astrazeneca Ab | Mchir antagonists |
| WO2004052848A1 (en) * | 2002-12-11 | 2004-06-24 | Eli Lilly And Company | Novel mch receptor antagonists |
Also Published As
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|---|---|
| CN101080411A (zh) | 2007-11-28 |
| JP2008524250A (ja) | 2008-07-10 |
| AU2005316314B2 (en) | 2011-06-23 |
| JP5072602B2 (ja) | 2012-11-14 |
| MX2007007227A (es) | 2007-08-21 |
| AU2005316314A1 (en) | 2006-06-22 |
| US7902356B2 (en) | 2011-03-08 |
| WO2006066174A1 (en) | 2006-06-22 |
| EP1828207A1 (en) | 2007-09-05 |
| ATE446962T1 (de) | 2009-11-15 |
| DE602005017423D1 (de) | 2009-12-10 |
| EP1828207B1 (en) | 2009-10-28 |
| US20090233919A1 (en) | 2009-09-17 |
| ES2333243T3 (es) | 2010-02-18 |
| BRPI0519124A2 (pt) | 2008-12-23 |
| CA2589695A1 (en) | 2006-06-22 |
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