MA30476B1 - Derives de type cyclohexylpyrazole-lactame comme inhibiteurs de la 11-beta-hydroxysteroïde deshydrogenase de type 1 - Google Patents
Derives de type cyclohexylpyrazole-lactame comme inhibiteurs de la 11-beta-hydroxysteroïde deshydrogenase de type 1Info
- Publication number
- MA30476B1 MA30476B1 MA31396A MA31396A MA30476B1 MA 30476 B1 MA30476 B1 MA 30476B1 MA 31396 A MA31396 A MA 31396A MA 31396 A MA31396 A MA 31396A MA 30476 B1 MA30476 B1 MA 30476B1
- Authority
- MA
- Morocco
- Prior art keywords
- beta
- cyclohexylpyrazole
- inhibitors
- compounds
- hydroxysteroid dehydrogenase
- Prior art date
Links
- 102000008645 11-beta-Hydroxysteroid Dehydrogenase Type 1 Human genes 0.000 title 1
- 108010088011 11-beta-Hydroxysteroid Dehydrogenase Type 1 Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 230000000694 effects Effects 0.000 abstract 2
- 208000031226 Hyperlipidaemia Diseases 0.000 abstract 1
- 206010020772 Hypertension Diseases 0.000 abstract 1
- 208000001145 Metabolic Syndrome Diseases 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 201000001421 hyperglycemia Diseases 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
La présente invention concerne de nouveaux composés de formule I : (I) ayant une activité antagoniste de la 11(bêta)-HSD de type 1, ainsi que des procédés servant à préparer de tels composés. Dans un autre mode de réalisation, l'invention concerne des compositions pharmaceutiques comprenant des composés de formule I, ainsi que des procédés d'utilisation des composés et des compositions pour traiter le diabète, l'hyperglycémie, l'obésité, l'hypertension, l'hyperlipidémie, un syndrome métabolique et d'autres affections associées à l'activité de la 11(bêta)-HSD de type 1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US74532006P | 2006-04-21 | 2006-04-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30476B1 true MA30476B1 (fr) | 2009-06-01 |
Family
ID=38595048
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA31396A MA30476B1 (fr) | 2006-04-21 | 2008-11-20 | Derives de type cyclohexylpyrazole-lactame comme inhibiteurs de la 11-beta-hydroxysteroïde deshydrogenase de type 1 |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US7981918B2 (fr) |
| EP (1) | EP2029579B1 (fr) |
| JP (1) | JP5161869B2 (fr) |
| KR (1) | KR101055576B1 (fr) |
| CN (1) | CN101426783B (fr) |
| AR (1) | AR060618A1 (fr) |
| AU (1) | AU2007240550B2 (fr) |
| BR (1) | BRPI0710229A2 (fr) |
| CA (1) | CA2647677C (fr) |
| CO (1) | CO6140026A2 (fr) |
| CR (1) | CR10400A (fr) |
| DO (1) | DOP2007000078A (fr) |
| EA (1) | EA015675B1 (fr) |
| EC (1) | ECSP088839A (fr) |
| ES (1) | ES2533263T3 (fr) |
| IL (1) | IL194835A (fr) |
| JO (1) | JO3042B1 (fr) |
| MA (1) | MA30476B1 (fr) |
| MX (1) | MX2008013484A (fr) |
| MY (1) | MY148128A (fr) |
| NO (1) | NO20084403L (fr) |
| NZ (1) | NZ571175A (fr) |
| PE (1) | PE20080362A1 (fr) |
| SV (1) | SV2008003070A (fr) |
| TN (1) | TNSN08405A1 (fr) |
| TW (1) | TWI347321B (fr) |
| UA (1) | UA95798C2 (fr) |
| WO (1) | WO2007124254A2 (fr) |
| ZA (1) | ZA200808686B (fr) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8088776B2 (en) * | 2006-04-21 | 2012-01-03 | Eli Lilly And Company | Biphenyl amide lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
| BRPI0710273A2 (pt) | 2006-04-21 | 2011-08-09 | Lilly Co Eli | composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, e, intermediário |
| ATE472542T1 (de) * | 2006-04-24 | 2010-07-15 | Lilly Co Eli | 11-beta-hydroxysteroid-dehydrogenase-1-hemmer |
| ATE543798T1 (de) | 2006-04-24 | 2012-02-15 | Lilly Co Eli | Cyclohexyl-substituierte pyrrolidinone als hemmer von 11-beta-hydroxysteroiddehydrogenase 1 |
| CA2649650C (fr) | 2006-04-24 | 2014-01-14 | Eli Lilly And Company | Pyrolidinones substitues en tant qu'inhibiteurs de l'enzyme 11-beta-hydroxysteroide dehydrogenase de type 1 |
| US7968585B2 (en) | 2006-04-25 | 2011-06-28 | Eli Lilly And Company | Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
| EP2021337B1 (fr) | 2006-04-25 | 2010-01-13 | Eli Lilly And Company | Inhibiteurs de la 11-beta-hydroxystéroïde déshydrogénase 1 |
| AU2007244863B2 (en) * | 2006-04-25 | 2012-01-19 | Eli Lilly And Company | Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
| MX2008013844A (es) * | 2006-04-28 | 2008-11-10 | Lilly Co Eli | Pirrolidinonas substituidas con pieridinilo como inhibidores de 11-beta-hidroxiesteroide deshidrogenasa 1. |
| US8835426B2 (en) | 2007-02-26 | 2014-09-16 | Vitae Pharmaceuticals, Inc. | Cyclic urea and carbamate inhibitors of 11β-hydroxysteroid dehydrogenase 1 |
| EP2025674A1 (fr) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Tetrahydronaphthaline substituée, son procédé de fabrication et son utilisation en tant que médicament |
| AR069207A1 (es) | 2007-11-07 | 2010-01-06 | Vitae Pharmaceuticals Inc | Ureas ciclicas como inhibidores de la 11 beta - hidroxi-esteroide deshidrogenasa 1 |
| CA2708303A1 (fr) | 2007-12-11 | 2009-06-18 | Vitae Pharmaceuticals, Inc. | Inhibiteurs cycliques d'uree de la 11.beta.-hydroxysteroide dehydrogenase 1 |
| KR20110002492A (ko) | 2008-05-01 | 2011-01-07 | 비타이 파마슈티컬즈, 인코포레이티드 | 11베타-하이드록시스테로이드 탈수소효소 1의 고리형 억제제 |
| WO2010011314A1 (fr) | 2008-07-25 | 2010-01-28 | Boehringer Ingelheim International Gmbh | Inhibiteurs cycliques de la 11 bêta-hydroxystéroïde déshydrogénase 1 |
| US8846668B2 (en) | 2008-07-25 | 2014-09-30 | Vitae Pharmaceuticals, Inc. | Inhibitors of 11beta-hydroxysteroid dehydrogenase 1 |
| CA2729993A1 (fr) | 2008-07-25 | 2010-01-28 | Boehringer Ingelheim International Gmbh | Synthese d'inhibiteurs de la 11beta-hydroxysteroide dehydrogenase de typtype 1 |
| US8598163B2 (en) * | 2009-02-04 | 2013-12-03 | Vitae Pharmaceuticals, Inc. | Derivatives of [1,3]Oxazin-2-one useful for the treatment of metabolic diseases such as lipid disorders |
| JP5679997B2 (ja) | 2009-02-04 | 2015-03-04 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 11β−ヒドロキシステロイドデヒドロゲナーゼ1の環状阻害剤 |
| US8507493B2 (en) | 2009-04-20 | 2013-08-13 | Abbvie Inc. | Amide and amidine derivatives and uses thereof |
| UA109255C2 (ru) | 2009-04-30 | 2015-08-10 | Берінгер Інгельхайм Інтернешнл Гмбх | Циклические ингибиторы 11бета-гидроксистероиддегидрогеназы 1 |
| WO2011011123A1 (fr) | 2009-06-11 | 2011-01-27 | Vitae Pharmaceuticals, Inc. | Inhibiteurs cycliques de la 11-bêta-hydroxystéroïde déshydrogénase 1 basée sur la structure 1,3-oxazinan-2-one |
| WO2011002910A1 (fr) | 2009-07-01 | 2011-01-06 | Vitae Pharmaceuticals, Inc. | Inhibiteurs cycliques de la 11-bêta-hydroxystéroïde déshydrogénase 1 |
| EP2496589B1 (fr) | 2009-11-05 | 2014-03-05 | Boehringer Ingelheim International GmbH | Nouveaux ligands de phosphore chiraux |
| WO2011068927A2 (fr) * | 2009-12-04 | 2011-06-09 | Abbott Laboratories | Inhibiteurs de la 11-β-hydroxystéroïde déshydrogénase de type 1 (11b-hsd1) et leurs utilisations |
| WO2011107494A1 (fr) | 2010-03-03 | 2011-09-09 | Sanofi | Nouveaux dérivés aromatiques de glycoside, médicaments contenants ces composés, et leur utilisation |
| EP2576570A1 (fr) | 2010-05-26 | 2013-04-10 | Boehringer Ingelheim International GmbH | Dérivés d'acide 2-oxo-1,2-dihydropyridin-4-yle boronique |
| EP2582698B1 (fr) | 2010-06-16 | 2016-09-14 | Vitae Pharmaceuticals, Inc. | Hétérocycles à 5, 6 et 7 chaînons substitués, médicaments contenant ces composés et leur utilisation |
| EP2582709B1 (fr) | 2010-06-18 | 2018-01-24 | Sanofi | Dérivés d'azolopyridin-3-one en tant qu'inhibiteurs de lipases et de phospholipases |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| WO2011161128A1 (fr) | 2010-06-25 | 2011-12-29 | Boehringer Ingelheim International Gmbh | Azaspirohexanones comme inhibiteurs de 11-β-hsd1 pour le traitement de troubles métaboliques |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| CA2813671A1 (fr) | 2010-11-02 | 2012-05-10 | Boehringer Ingelheim International Gmbh | Combinaisons pharmaceutiques destinees au traitement de troubles du metabolisme |
| WO2012120056A1 (fr) | 2011-03-08 | 2012-09-13 | Sanofi | Dérivés oxathiazine tétra-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation |
| EP2683704B1 (fr) | 2011-03-08 | 2014-12-17 | Sanofi | Dérivés oxathiazine ramifiés, procédé pour leur préparation, utilisation en tant que médicament, agents pharmaceutiques contenant ces dérivés et leur utilisation |
| WO2012120055A1 (fr) | 2011-03-08 | 2012-09-13 | Sanofi | Dérivés oxathiazine di- et tri-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation |
| WO2012120054A1 (fr) | 2011-03-08 | 2012-09-13 | Sanofi | Dérivés oxathiazine di- et tri-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation |
| EP2766349B1 (fr) | 2011-03-08 | 2016-06-01 | Sanofi | Dérivés d'oxathiazine substitués par des carbocycles ou des hétérocycles, leur procédé de préparation, médicaments contenant ces composés et leur utilisation |
| WO2013037390A1 (fr) | 2011-09-12 | 2013-03-21 | Sanofi | Dérivés amides d'acide 6-(4-hydroxyphényl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique en tant qu'inhibiteurs de kinase |
| EP2760862B1 (fr) | 2011-09-27 | 2015-10-21 | Sanofi | Dérivés d'amide d'acide 6-(4-hydroxyphényl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique utilisés comme inhibiteurs de kinase |
| JP6020459B2 (ja) * | 2011-10-18 | 2016-11-02 | アステラス製薬株式会社 | 二環式ヘテロ環化合物 |
| AR099936A1 (es) | 2014-04-04 | 2016-08-31 | Sanofi Sa | Heterociclos condensados sustituidos como moduladores de gpr119 para el tratamiento de la diabetes, obesidad, dislipidemia y trastornos relacionados |
| US10858347B2 (en) | 2015-12-31 | 2020-12-08 | Karyopharm Therapeutics Inc. | Multicyclic compounds and uses thereof |
| CN115916766A (zh) | 2021-02-25 | 2023-04-04 | 阿普塔生物治疗公司 | 新型吡唑衍生物 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004056744A1 (fr) | 2002-12-23 | 2004-07-08 | Janssen Pharmaceutica N.V. | Adamantyl acetamides utilises comme inhibiteurs de la hydroxysteroide deshydrogenase |
| CA2565630C (fr) * | 2004-05-07 | 2013-05-28 | Janssen Pharmaceutica N.V. | Utilisation de derives de pyrrolidin-2-one et de piperidin-2-one comme inhibiteurs de la 11-beta-hydroxysteroide deshydrogenase |
| EP1747198B1 (fr) * | 2004-05-07 | 2008-06-04 | Janssen Pharmaceutica N.V. | Utilisation de derives d'adamantyle pyrrolidin-2-one comme inhibiteurs de la 11-beta-hydroxysteroide deshydrogenase |
| EP1802623A1 (fr) | 2004-10-12 | 2007-07-04 | Novo Nordisk A/S | Composes spiro actifs du type a- hydroxysteroide deshydrogenase de type 1 |
| WO2006049952A1 (fr) | 2004-10-29 | 2006-05-11 | Eli Lilly And Company | Inhibiteurs de la 11-béta-hydroxystéroïde déshydrogénase 1 dérivés de cycloalkyllactames |
| SG161261A1 (en) | 2004-11-10 | 2010-05-27 | Incyte Corp | Lactam compounds and their use as pharmaceuticals |
| ATE399546T1 (de) * | 2004-12-20 | 2008-07-15 | Lilly Co Eli | Cycloalkyl-lactam-derivate als inhibitoren von 11-beta-hydroxysteroiddehydrogenase 1 |
| EP1830840B1 (fr) * | 2004-12-21 | 2008-07-16 | Eli Lilly And Company | Derives de cycloalkyle lactame utilises comme inhibiteurs de la 11-beta-hydroxysteroide deshydrogenase 1 |
| EP1864971A4 (fr) | 2005-03-31 | 2010-02-10 | Takeda Pharmaceutical | Agent prophylactique/therapeutique pour le diabete |
| ES2322727B1 (es) | 2005-07-28 | 2010-04-22 | Universidad Del Pais Vasco | Metodo para cuantificar la union receptor acoplado a proteina g (gpcr)-proteina g mediante el empleo de un array de membranas celulares. |
| US7998959B2 (en) | 2006-01-12 | 2011-08-16 | Incyte Corporation | Modulators of 11-β hydroxyl steroid dehydrogenase type 1, pharmaceutical compositions thereof, and methods of using the same |
| US8088776B2 (en) * | 2006-04-21 | 2012-01-03 | Eli Lilly And Company | Biphenyl amide lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
| BRPI0710273A2 (pt) * | 2006-04-21 | 2011-08-09 | Lilly Co Eli | composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, e, intermediário |
| ATE543798T1 (de) | 2006-04-24 | 2012-02-15 | Lilly Co Eli | Cyclohexyl-substituierte pyrrolidinone als hemmer von 11-beta-hydroxysteroiddehydrogenase 1 |
| CA2649650C (fr) * | 2006-04-24 | 2014-01-14 | Eli Lilly And Company | Pyrolidinones substitues en tant qu'inhibiteurs de l'enzyme 11-beta-hydroxysteroide dehydrogenase de type 1 |
| ATE472542T1 (de) * | 2006-04-24 | 2010-07-15 | Lilly Co Eli | 11-beta-hydroxysteroid-dehydrogenase-1-hemmer |
| AU2007244863B2 (en) * | 2006-04-25 | 2012-01-19 | Eli Lilly And Company | Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
| US7968585B2 (en) * | 2006-04-25 | 2011-06-28 | Eli Lilly And Company | Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
| EP2021337B1 (fr) | 2006-04-25 | 2010-01-13 | Eli Lilly And Company | Inhibiteurs de la 11-beta-hydroxystéroïde déshydrogénase 1 |
| MX2008013844A (es) | 2006-04-28 | 2008-11-10 | Lilly Co Eli | Pirrolidinonas substituidas con pieridinilo como inhibidores de 11-beta-hidroxiesteroide deshidrogenasa 1. |
| CL2008001839A1 (es) | 2007-06-21 | 2009-01-16 | Incyte Holdings Corp | Compuestos derivados de 2,7-diazaespirociclos, inhibidores de 11-beta hidroxil esteroide deshidrogenasa tipo 1; composicion farmaceutica que comprende a dichos compuestos; utiles para tratar la obesidad, diabetes, intolerancia a la glucosa, diabetes tipo ii, entre otras enfermedades. |
-
2007
- 2007-04-05 NZ NZ571175A patent/NZ571175A/en not_active IP Right Cessation
- 2007-04-05 MY MYPI20084205A patent/MY148128A/en unknown
- 2007-04-05 WO PCT/US2007/066069 patent/WO2007124254A2/fr not_active Ceased
- 2007-04-05 CA CA2647677A patent/CA2647677C/fr not_active Expired - Fee Related
- 2007-04-05 BR BRPI0710229-1A patent/BRPI0710229A2/pt active Search and Examination
- 2007-04-05 MX MX2008013484A patent/MX2008013484A/es active IP Right Grant
- 2007-04-05 US US12/297,375 patent/US7981918B2/en not_active Expired - Fee Related
- 2007-04-05 CN CN2007800142829A patent/CN101426783B/zh not_active Expired - Fee Related
- 2007-04-05 UA UAA200812290A patent/UA95798C2/ru unknown
- 2007-04-05 EP EP07760191.2A patent/EP2029579B1/fr active Active
- 2007-04-05 KR KR1020087025618A patent/KR101055576B1/ko not_active Expired - Fee Related
- 2007-04-05 EA EA200870460A patent/EA015675B1/ru not_active IP Right Cessation
- 2007-04-05 JP JP2009506680A patent/JP5161869B2/ja not_active Expired - Fee Related
- 2007-04-05 ES ES07760191.2T patent/ES2533263T3/es active Active
- 2007-04-05 AU AU2007240550A patent/AU2007240550B2/en not_active Ceased
- 2007-04-18 JO JOP/2007/0149A patent/JO3042B1/ar active
- 2007-04-19 TW TW096113852A patent/TWI347321B/zh not_active IP Right Cessation
- 2007-04-19 DO DO2007000078A patent/DOP2007000078A/es unknown
- 2007-04-20 AR ARP070101715A patent/AR060618A1/es not_active Application Discontinuation
- 2007-04-20 PE PE2007000491A patent/PE20080362A1/es not_active Application Discontinuation
-
2008
- 2008-10-10 ZA ZA200808686A patent/ZA200808686B/xx unknown
- 2008-10-17 TN TNP2008000405A patent/TNSN08405A1/en unknown
- 2008-10-17 CO CO08110816A patent/CO6140026A2/es unknown
- 2008-10-20 NO NO20084403A patent/NO20084403L/no not_active Application Discontinuation
- 2008-10-21 EC EC2008008839A patent/ECSP088839A/es unknown
- 2008-10-21 SV SV2008003070A patent/SV2008003070A/es unknown
- 2008-10-22 IL IL194835A patent/IL194835A/en not_active IP Right Cessation
- 2008-10-24 CR CR10400A patent/CR10400A/es unknown
- 2008-11-20 MA MA31396A patent/MA30476B1/fr unknown
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