GT200800226A - Derivados de acido benzoazepin-oxi-acetico como agonistas de receptores activados por proliferador de peroxisoma delta usados para incrementar la lipoproteina de alta densidad-colesterol, reducir la lipoproteina de baja densidad-colesterol y reducir - Google Patents
Derivados de acido benzoazepin-oxi-acetico como agonistas de receptores activados por proliferador de peroxisoma delta usados para incrementar la lipoproteina de alta densidad-colesterol, reducir la lipoproteina de baja densidad-colesterol y reducirInfo
- Publication number
- GT200800226A GT200800226A GT200800226A GT200800226A GT200800226A GT 200800226 A GT200800226 A GT 200800226A GT 200800226 A GT200800226 A GT 200800226A GT 200800226 A GT200800226 A GT 200800226A GT 200800226 A GT200800226 A GT 200800226A
- Authority
- GT
- Guatemala
- Prior art keywords
- colesterol
- lipoprotein
- redesteru
- peroxisoma
- benzoazepin
- Prior art date
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- C07D233/06—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
- C07D233/08—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms with alkyl radicals, containing more than four carbon atoms, directly attached to ring carbon atoms
- C07D233/12—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms with alkyl radicals, containing more than four carbon atoms, directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
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- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D223/16—Benzazepines; Hydrogenated benzazepines
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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
- C07D401/06—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 only aliphatic carbon atoms
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- C07D403/06—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 linked by a carbon chain containing only aliphatic carbon atoms
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- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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Abstract
LA INVENCIÓN ESTÁ DIRIGIDA A COMPUESTOS DE LA FÓRMULA (I) ÚTILES COMO AGONISTAS DE PPAR; TAMBIÉN SE DESCRIBEN COMPOSICIONES FARMACÉUTICAS Y MÉTODOS PARA TRATAR UNA O MÁS CONDICIONES INCLUYENDO, PERO SIN LIMITARSE A, DIABETES, NEFROPATÍA, NEUROPATÍA, RETINOPATÍA, SÍNDROME DE OVARIO POLICÍSTICO, HIPERTENSIÓN, ISQUEMIA, ACCIDENTE VASCULAR CEREBRAL, TRASTORNO INTESTINAL METABÓLICO X, HIPER-LDL-COLESTEROLEMIA, DISLIPIDEMIA (INCLUYENDO HIPERTRIGLICERIDEMIA, HIPERCOLESTEROLEMIA, HIPERLIPIDEMIA MIXTA, E HIPO-HDL-COLESTEROLEMIA), ATEROSCLEROSIS, OBESIDAD Y TRASTORNOS RELACIONADOS CON EL METABOLISMO DE LÍPIDOS Y COMPLICACIONES DE HOMEOSTASIS DE ENERGÍA DE LOS MISMOS, USANDO COMPUESTOS DE LA INVENCIÓN. T2008
Applications Claiming Priority (1)
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US79300106P | 2006-04-18 | 2006-04-18 |
Publications (1)
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GT200800226A true GT200800226A (es) | 2009-03-13 |
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ID=38610435
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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GT200800226A GT200800226A (es) | 2006-04-18 | 2008-10-21 | Derivados de acido benzoazepin-oxi-acetico como agonistas de receptores activados por proliferador de peroxisoma delta usados para incrementar la lipoproteina de alta densidad-colesterol, reducir la lipoproteina de baja densidad-colesterol y reducir |
Country Status (30)
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US (2) | US7678786B2 (es) |
EP (1) | EP2010289B1 (es) |
JP (1) | JP5232771B2 (es) |
KR (1) | KR101472370B1 (es) |
CN (1) | CN101479008B (es) |
AR (1) | AR060489A1 (es) |
AT (1) | ATE535282T1 (es) |
AU (1) | AU2007237928B2 (es) |
BR (1) | BRPI0711695A2 (es) |
CA (1) | CA2649700C (es) |
CO (1) | CO6160296A2 (es) |
CR (1) | CR10447A (es) |
EA (1) | EA016583B1 (es) |
EC (1) | ECSP088841A (es) |
ES (1) | ES2375754T3 (es) |
GT (1) | GT200800226A (es) |
HK (1) | HK1124797A1 (es) |
HN (1) | HN2008001559A (es) |
IL (1) | IL194850A (es) |
JO (1) | JO3444B1 (es) |
MX (1) | MX2008013534A (es) |
MY (1) | MY144637A (es) |
NO (1) | NO344334B1 (es) |
NZ (1) | NZ571998A (es) |
PE (1) | PE20080188A1 (es) |
TW (1) | TWI404712B (es) |
UA (1) | UA96150C2 (es) |
UY (1) | UY30288A1 (es) |
WO (1) | WO2007121432A2 (es) |
ZA (1) | ZA200809790B (es) |
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EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
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WO2009097995A1 (de) * | 2008-02-07 | 2009-08-13 | Sanofi-Aventis | Neue phenyl-substituierte imidazolidine, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
KR20110022620A (ko) | 2008-05-30 | 2011-03-07 | 다케다 야쿠힌 고교 가부시키가이샤 | 복소환 화합물 |
WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
US9051290B2 (en) | 2010-04-28 | 2015-06-09 | Leo Pharma A/S | Biaryl phosphodiesterase inhibitors |
US8933024B2 (en) | 2010-06-18 | 2015-01-13 | Sanofi | Azolopyridin-3-one derivatives as inhibitors of lipases and 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 |
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 |
CN104086528A (zh) | 2010-07-15 | 2014-10-08 | 拜耳知识产权有限责任公司 | 作为杀虫剂的新杂环化合物 |
CA2809958A1 (en) | 2010-08-31 | 2012-03-08 | Snu R & Db Foundation | Use of the fetal reprogramming of a ppar ? agonist |
US8828994B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Di- and tri-substituted oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
US8828995B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
US8901114B2 (en) | 2011-03-08 | 2014-12-02 | Sanofi | Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof |
WO2012120056A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
EP2683699B1 (de) | 2011-03-08 | 2015-06-24 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
WO2013124381A1 (en) | 2012-02-24 | 2013-08-29 | Nestec S.A. | Peltatin for use in the treatment of metabolic disorders |
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US9695137B2 (en) * | 2013-03-14 | 2017-07-04 | The University Of Toledo | Analogs of peroxisome proliferator activated receptor (PPAR) agonists, and methods of using the same |
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