AR066104A1 - Derivados de triazolopiridin - carboxamidas y triazolopirimidin-carboxamidas, su preparacion y su aplicacion en terapeutica - Google Patents
Derivados de triazolopiridin - carboxamidas y triazolopirimidin-carboxamidas, su preparacion y su aplicacion en terapeuticaInfo
- Publication number
- AR066104A1 AR066104A1 ARP080101598A ARP080101598A AR066104A1 AR 066104 A1 AR066104 A1 AR 066104A1 AR P080101598 A ARP080101598 A AR P080101598A AR P080101598 A ARP080101598 A AR P080101598A AR 066104 A1 AR066104 A1 AR 066104A1
- Authority
- AR
- Argentina
- Prior art keywords
- carboxamidas
- derivatives
- preparation
- application
- group
- Prior art date
Links
- 239000003814 drug Substances 0.000 title 1
- 208000002193 Pain Diseases 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- 208000000094 Chronic Pain Diseases 0.000 abstract 1
- 208000032928 Dyslipidaemia Diseases 0.000 abstract 1
- 208000017170 Lipid metabolism disease Diseases 0.000 abstract 1
- 206010028813 Nausea Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 208000012886 Vertigo Diseases 0.000 abstract 1
- 206010047700 Vomiting Diseases 0.000 abstract 1
- 230000001154 acute effect Effects 0.000 abstract 1
- 208000005298 acute pain Diseases 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 206010015037 epilepsy Diseases 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 208000015181 infectious disease Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 230000008693 nausea Effects 0.000 abstract 1
- 230000000626 neurodegenerative effect Effects 0.000 abstract 1
- 230000000926 neurological effect Effects 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 230000007170 pathology Effects 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
- 231100000889 vertigo Toxicity 0.000 abstract 1
- 230000008673 vomiting Effects 0.000 abstract 1
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
- C07D471/04—Ortho-condensed systems
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- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P13/10—Drugs for disorders of the urinary system of the bladder
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A—HUMAN NECESSITIES
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- A61P25/20—Hypnotics; Sedatives
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- A—HUMAN NECESSITIES
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
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- A61P37/02—Immunomodulators
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- A—HUMAN NECESSITIES
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Obesity (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pulmonology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Cardiology (AREA)
- Ophthalmology & Optometry (AREA)
- Virology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Otolaryngology (AREA)
- Heart & Thoracic Surgery (AREA)
- Anesthesiology (AREA)
- Child & Adolescent Psychology (AREA)
Abstract
La presente se refiere a los derivados de triazolopiridin-carboxamidas y triazolopirimidin-carboxamidas, de formula general (1) en la que A y X representan, independientemente uno del otro, un átomo de nitrogeno o un grupo CH, R1 representa un grupoarilo o heteroarilo, opcionalmente sustituido con uno o varios grupos elegidos entre un átomo de halogeno, un grupo alquilo C1-6, haloalquiIo C1-6, alcoxi C1-6, haloalcoxi C1-6, R2 representa un grupo arilo, opcionalmente sustituido con uno o vanosgrupos elegidos entre un átomo de halogeno, un grupo metilo, trifluorometilo, metoxi, trifluorometoxi. Procedimiento de preparacion y aplicacion en terapéutica, para prevenir o tratar dolores agudos o cronicos, vértigo, vomitos, náuseas,dislipidemia, patologías neurologicas y psiquiátricas, neurodegenerativas, epilepsia, enfermedades cardiovasculares, cáncer, infecciones.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0702808A FR2915198B1 (fr) | 2007-04-18 | 2007-04-18 | Derives de triazolopyridine-carboxamides et triazolopyridine -carboxamides, leur preparation et leur application en therapeutique. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR066104A1 true AR066104A1 (es) | 2009-07-22 |
Family
ID=38776328
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080101598A AR066104A1 (es) | 2007-04-18 | 2008-04-18 | Derivados de triazolopiridin - carboxamidas y triazolopirimidin-carboxamidas, su preparacion y su aplicacion en terapeutica |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US7863279B2 (es) |
| EP (1) | EP2146992A1 (es) |
| JP (1) | JP2010524908A (es) |
| KR (1) | KR20090130061A (es) |
| CN (1) | CN101663304A (es) |
| AR (1) | AR066104A1 (es) |
| AU (1) | AU2008257324A1 (es) |
| BR (1) | BRPI0810412A2 (es) |
| CA (1) | CA2683936A1 (es) |
| CL (1) | CL2008001103A1 (es) |
| FR (1) | FR2915198B1 (es) |
| IL (1) | IL201471A0 (es) |
| MX (1) | MX2009011213A (es) |
| RU (1) | RU2009142434A (es) |
| TW (1) | TW200901992A (es) |
| UY (1) | UY31037A1 (es) |
| WO (1) | WO2008145843A1 (es) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2915198B1 (fr) * | 2007-04-18 | 2009-12-18 | Sanofi Aventis | Derives de triazolopyridine-carboxamides et triazolopyridine -carboxamides, leur preparation et leur application en therapeutique. |
| EP2382012A2 (en) * | 2008-12-24 | 2011-11-02 | Bial-Portela & CA, S.A. | Pharmaceutical compounds |
| AR076381A1 (es) | 2009-04-22 | 2011-06-08 | Janssen Pharmaceutica Nv | Azetidinil diamidas como inhibidores de monoacilglicerol lipasa |
| CN102656172B (zh) * | 2009-09-09 | 2016-03-23 | 大日本住友制药株式会社 | 8-氧代二氢嘌呤衍生物 |
| WO2011085216A2 (en) | 2010-01-08 | 2011-07-14 | Ironwood Pharmaceuticals, Inc. | Use of faah inhibitors for treating parkinson's disease and restless legs syndrome |
| WO2011123719A2 (en) | 2010-03-31 | 2011-10-06 | Ironwood Pharmaceuticals, Inc. | Use of faah inhibitors for treating abdominal, visceral and pelvic pain |
| DK2571878T3 (en) | 2010-05-17 | 2019-02-11 | Indian Incozen Therapeutics Pvt Ltd | Hitherto unknown 3,5-DISUBSTITUTED-3H-IMIDAZO [4,5-B] PYRIDINE AND 3,5- DISUBSTITUTED -3H- [1,2,3] TRIAZOL [4,5-B] PYRIDINE COMPOUNDS AS MODULATORS OF PROTEIN CHINES |
| KR20140001206A (ko) | 2010-09-27 | 2014-01-06 | 얀센 파마슈티카 엔.브이. | 모노아실글리세롤 리파아제 억제제로서의 옥소피페라진-아제티딘 아미드 및 옥소다이아제핀-아제티딘 아미드 |
| US8513423B2 (en) | 2010-10-22 | 2013-08-20 | Janssen Pharmaceutica, Nv | Piperidin-4-yl-azetidine diamides as monoacylglycerol lipase inhibitors |
| RU2013123274A (ru) | 2010-10-22 | 2014-11-27 | Янссен Фармацевтика Нв | Аминопирролидиназетидиндиамиды как ингибиторы моноацилглицеринлипазы |
| CA2815350A1 (en) * | 2010-10-22 | 2012-04-26 | Janssen Pharmaceutica Nv | Piperidin-4-yl-azetidine diamides as monoacylglycerol lipase inhibitors |
| JP2014076947A (ja) * | 2011-02-03 | 2014-05-01 | Dainippon Sumitomo Pharma Co Ltd | 2−オキシ置換8−オキソジヒドロプリン誘導体 |
| CN103957916A (zh) * | 2011-09-30 | 2014-07-30 | 詹森药业有限公司 | 用于治疗代谢疾病和相关失调的单酰甘油脂肪酶抑制剂 |
| KR20140072897A (ko) * | 2011-09-30 | 2014-06-13 | 얀센 파마슈티카 엔.브이. | (1-(4-플루오로페닐)-1h-인돌-5-일)-(3-(4-(티아졸-2-카르보닐)피페라진-1-일)아제티딘-1-일)메탄온의 결정성 하이드로클로라이드 염,및 통증 및 대사 장애의 치료에 있어서의 이의 용도 |
| MX2014003883A (es) | 2011-09-30 | 2014-08-27 | Janssen Pharmaceutica Nv | Inhibidores de monoacilglicerol lipasa para el tratamiento de enfermedades metabolicas y transtornos relacionados. |
| CN107082779A (zh) * | 2012-03-30 | 2017-08-22 | 理森制药股份公司 | 作为c‑met 蛋白激酶调节剂的新化合物 |
| JP6936796B2 (ja) * | 2015-07-06 | 2021-09-22 | ロダン・セラピューティクス,インコーポレーテッド | ヒストンデアセチラーゼのヘテロハロ阻害剤 |
| WO2017007755A1 (en) | 2015-07-06 | 2017-01-12 | Rodin Therapeutics, Inc. | Heterobicyclic n-aminophenyl-amides as inhibitors of histone deacetylase |
| TN2017000544A1 (en) | 2015-07-31 | 2019-04-12 | Pfizer | 1,1,1-trifluoro-3-hydroxypropan-2-yl carbamate derivatives and 1,1,1-trifluoro-4-hydroxybutan-2-yl carbamate derivatives as magl inhibitors |
| ES2992063T3 (es) | 2016-11-28 | 2024-12-09 | Praxis Prec Medicines Inc | Compuestos y procedimientos de uso de los mismos |
| WO2018098491A1 (en) | 2016-11-28 | 2018-05-31 | Praxis Precision Medicines, Inc. | Compounds and their methods of use |
| AU2018207402B2 (en) | 2017-01-11 | 2023-09-28 | Alkermes, Inc. | Bicyclic inhibitors of histone deacetylase |
| SG11201906417RA (en) | 2017-01-20 | 2019-08-27 | Pfizer | 1,1,1-trifluoro-3-hydroxypropan-2-yl carbamate derivatives as magl inhibitors |
| JP2020506903A (ja) | 2017-01-23 | 2020-03-05 | ファイザー・インク | Magl阻害薬としての複素環式スピロ化合物 |
| US11492345B2 (en) | 2017-02-13 | 2022-11-08 | Praxis Precision Medicines, Inc. | Compounds and their methods of use |
| WO2018187480A1 (en) * | 2017-04-04 | 2018-10-11 | Praxis Precision Medicines, Inc. | Compounds and their methods of use |
| WO2019032528A1 (en) | 2017-08-07 | 2019-02-14 | Rodin Therapeutics, Inc | BICYCLIC HISTONE DEACETYLASE INHIBITORS |
| WO2019035951A1 (en) | 2017-08-15 | 2019-02-21 | Praxis Precision Medicines, Inc. | COMPOUNDS AND THEIR METHODS OF USE |
| CN112423760A (zh) | 2018-05-30 | 2021-02-26 | 普拉克西斯精密药物股份有限公司 | 离子通道调节剂 |
| EA202092908A1 (ru) | 2018-09-28 | 2021-05-14 | Праксис Пресижн Медсинз, Инк. | Модуляторы ионных каналов |
| US11773099B2 (en) | 2019-05-28 | 2023-10-03 | Praxis Precision Medicines, Inc. | Compounds and their methods of use |
| US11505554B2 (en) | 2019-05-31 | 2022-11-22 | Praxis Precision Medicines, Inc. | Substituted pyridines as ion channel modulators |
| US11279700B2 (en) | 2019-05-31 | 2022-03-22 | Praxis Precision Medicines, Inc. | Ion channel modulators |
| US11767325B2 (en) | 2019-11-26 | 2023-09-26 | Praxis Precision Medicines, Inc. | Substituted [1,2,4]triazolo[4,3-a]pyrazines as ion channel modulators |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0100624D0 (en) * | 2001-01-10 | 2001-02-21 | Vernalis Res Ltd | Chemical compounds VII |
| DE10247680B4 (de) * | 2002-10-12 | 2005-09-01 | Aventis Pharma Deutschland Gmbh | Neue bicyclische Inhibitoren der Hormon Sensitiven Lipase |
| DE102004005172A1 (de) * | 2004-02-02 | 2005-08-18 | Aventis Pharma Deutschland Gmbh | Indazolderivate als Inhibitoren der Hormon Sensitiven Lipase |
| US7632837B2 (en) * | 2005-06-17 | 2009-12-15 | Bristol-Myers Squibb Company | Bicyclic heterocycles as cannabinoid-1 receptor modulators |
| DE102005049954A1 (de) * | 2005-10-19 | 2007-05-31 | Sanofi-Aventis Deutschland Gmbh | Triazolopyridin-derivate als Inhibitoren von Lipasen und Phospholipasen |
| FR2915198B1 (fr) * | 2007-04-18 | 2009-12-18 | Sanofi Aventis | Derives de triazolopyridine-carboxamides et triazolopyridine -carboxamides, leur preparation et leur application en therapeutique. |
| FR2915199B1 (fr) * | 2007-04-18 | 2010-01-22 | Sanofi Aventis | Derives de triazolopyridine-carboxamides et triazolopyrimidine-carboxamides, leur preparation et leur application en therapeutique. |
-
2007
- 2007-04-18 FR FR0702808A patent/FR2915198B1/fr not_active Expired - Fee Related
-
2008
- 2008-04-16 WO PCT/FR2008/000536 patent/WO2008145843A1/fr not_active Ceased
- 2008-04-16 RU RU2009142434/04A patent/RU2009142434A/ru not_active Application Discontinuation
- 2008-04-16 BR BRPI0810412-3A2A patent/BRPI0810412A2/pt not_active IP Right Cessation
- 2008-04-16 EP EP08787965A patent/EP2146992A1/fr not_active Withdrawn
- 2008-04-16 CN CN200880012579A patent/CN101663304A/zh active Pending
- 2008-04-16 MX MX2009011213A patent/MX2009011213A/es active IP Right Grant
- 2008-04-16 CA CA002683936A patent/CA2683936A1/fr not_active Abandoned
- 2008-04-16 JP JP2010503551A patent/JP2010524908A/ja active Pending
- 2008-04-16 KR KR1020097021601A patent/KR20090130061A/ko not_active Withdrawn
- 2008-04-16 AU AU2008257324A patent/AU2008257324A1/en not_active Abandoned
- 2008-04-17 CL CL2008001103A patent/CL2008001103A1/es unknown
- 2008-04-17 TW TW097114003A patent/TW200901992A/zh unknown
- 2008-04-18 UY UY31037A patent/UY31037A1/es not_active Application Discontinuation
- 2008-04-18 AR ARP080101598A patent/AR066104A1/es unknown
-
2009
- 2009-10-12 IL IL201471A patent/IL201471A0/en unknown
- 2009-10-13 US US12/577,777 patent/US7863279B2/en not_active Expired - Fee Related
-
2010
- 2010-11-30 US US12/956,892 patent/US20110071162A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| FR2915198B1 (fr) | 2009-12-18 |
| CA2683936A1 (fr) | 2008-12-04 |
| RU2009142434A (ru) | 2011-05-27 |
| KR20090130061A (ko) | 2009-12-17 |
| IL201471A0 (en) | 2010-05-31 |
| AU2008257324A1 (en) | 2008-12-04 |
| US7863279B2 (en) | 2011-01-04 |
| US20100041670A1 (en) | 2010-02-18 |
| CN101663304A (zh) | 2010-03-03 |
| MX2009011213A (es) | 2009-11-02 |
| CL2008001103A1 (es) | 2009-01-16 |
| UY31037A1 (es) | 2008-11-28 |
| JP2010524908A (ja) | 2010-07-22 |
| TW200901992A (en) | 2009-01-16 |
| FR2915198A1 (fr) | 2008-10-24 |
| EP2146992A1 (fr) | 2010-01-27 |
| WO2008145843A1 (fr) | 2008-12-04 |
| US20110071162A1 (en) | 2011-03-24 |
| BRPI0810412A2 (pt) | 2014-10-14 |
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