PE20090954A1 - Acidos 6-fenilnicotinicos sustituidos como moduladores de ppar-alfa - Google Patents
Acidos 6-fenilnicotinicos sustituidos como moduladores de ppar-alfaInfo
- Publication number
- PE20090954A1 PE20090954A1 PE2008001459A PE2008001459A PE20090954A1 PE 20090954 A1 PE20090954 A1 PE 20090954A1 PE 2008001459 A PE2008001459 A PE 2008001459A PE 2008001459 A PE2008001459 A PE 2008001459A PE 20090954 A1 PE20090954 A1 PE 20090954A1
- Authority
- PE
- Peru
- Prior art keywords
- methyl
- alkyl
- ppar
- methylphenyl
- fluoro
- Prior art date
Links
- 239000002253 acid Substances 0.000 title abstract 2
- 150000007513 acids Chemical class 0.000 title 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 4
- -1 CYANE Chemical class 0.000 abstract 3
- 229910052731 fluorine Inorganic materials 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- RBQVXUUAPXKYAI-UHFFFAOYSA-N 6-(3-fluoro-4-methylphenyl)-2-(2-methylpropyl)-4-(trifluoromethyl)pyridine-3-carboxylic acid Chemical compound FC(F)(F)C1=C(C(O)=O)C(CC(C)C)=NC(C=2C=C(F)C(C)=CC=2)=C1 RBQVXUUAPXKYAI-UHFFFAOYSA-N 0.000 abstract 1
- JJOSJYSVRXSBNW-UHFFFAOYSA-N 6-(3-fluoro-4-methylphenyl)-2-methyl-4-(2-methylpropyl)pyridine-3-carboxylic acid Chemical compound CC1=C(C(O)=O)C(CC(C)C)=CC(C=2C=C(F)C(C)=CC=2)=N1 JJOSJYSVRXSBNW-UHFFFAOYSA-N 0.000 abstract 1
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical class O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 102000003728 Peroxisome Proliferator-Activated Receptors Human genes 0.000 abstract 1
- 108090000029 Peroxisome Proliferator-Activated Receptors Proteins 0.000 abstract 1
- XIPUIGPNIDKXJU-UHFFFAOYSA-N [CH]1CC1 Chemical group [CH]1CC1 XIPUIGPNIDKXJU-UHFFFAOYSA-N 0.000 abstract 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical class C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 208000030159 metabolic disease Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
- C07D213/80—Acids; Esters in position 3
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Communicable Diseases (AREA)
- Vascular Medicine (AREA)
- Psychiatry (AREA)
- Immunology (AREA)
- Psychology (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Virology (AREA)
- Gastroenterology & Hepatology (AREA)
Abstract
REFERIDA A UN DERIVADO DE ACIDO FENIL-NICOTINICO DE FORMULA (I), DONDE UNO DE A Y D REPRESENTA N Y EL OTRO REPRESENTA CR7; R7 ES H, METILO O ETILO; R1 ES ALQUILO C3-C10, CICLOALQUILO C3-C7, -NRARB, ENTRE OTROS; RA ES H O ALQUILO C1-C3; RB ES ALQUILO C1-C10, CICLOALQUILO C3-C7, ENTRE OTROS; R2 ES ALQUILO C1-C3 OPCIONALMENTE SUSTITUIDO CON FLUOR O CICLOPROPILO; R3 ES H O F; R4 ES H, Cl, F O METILO; R5 ES H, HALOGENO, NITRO, CIANO, METILO, ENTRE OTROS; R6 ES H, F, Cl O METILO. SON COMPUESTOS PREFERIDOS: ACIDO 6-(3-FLUORO-4-METILFENIL)-2-ISOBUTIL-4-(TRIFLUOROMETIL)NICOTINICO, ACIDO 6-(3-FLUORO-4-METILFENIL)-2-ISOPROPOXI-4-(TRIFLUOROMETIL)NICOTINICO, ACIDO 6-(3-FLUORO-4-METILFENIL)-4-ISOBUTIL-2-METILNICOTINICO, ENTRE OTROS. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA Y A UN PROCEDIMIENTO DE PREPARACION. DICHOS COMPUESTOS SON MODULADORES DEL RECEPTOR ACTIVADO POR EL PROLIFERADOR DE PEROXISOMA (PPAR-ALFA) Y SON UTILES EN EL TRATAMIENTO DE ENFERMEDADES CARDIOVASCULARES, ENFERMEDADES METABOLICAS, ENTRE OTRAS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102007042754A DE102007042754A1 (de) | 2007-09-07 | 2007-09-07 | Substituierte 6-Phenylnikotinsäuren und ihre Verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20090954A1 true PE20090954A1 (es) | 2009-07-24 |
Family
ID=40032794
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2008001459A PE20090954A1 (es) | 2007-09-07 | 2008-08-28 | Acidos 6-fenilnicotinicos sustituidos como moduladores de ppar-alfa |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US8143411B2 (es) |
| EP (1) | EP2197846A1 (es) |
| JP (1) | JP2010538025A (es) |
| KR (1) | KR20100066545A (es) |
| AU (1) | AU2008298021A1 (es) |
| BR (1) | BRPI0816372A2 (es) |
| CA (1) | CA2698471A1 (es) |
| CL (1) | CL2008002537A1 (es) |
| DE (1) | DE102007042754A1 (es) |
| MX (1) | MX2010002565A (es) |
| NZ (1) | NZ583697A (es) |
| PA (1) | PA8794401A1 (es) |
| PE (1) | PE20090954A1 (es) |
| TW (1) | TW200914002A (es) |
| UY (1) | UY31310A1 (es) |
| WO (1) | WO2009033561A1 (es) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ567892A (en) | 2005-11-08 | 2010-12-24 | Vertex Pharma | Heterocyclic modulators of ATP-binding cassette transporters containing cycloalkyl or heterocycloalkyl groups |
| NZ581259A (en) | 2007-05-09 | 2012-07-27 | Vertex Pharma | Modulators of cystic fibrosis transmembrane conductance regulator |
| PL2225230T3 (pl) | 2007-12-07 | 2017-08-31 | Vertex Pharmaceuticals Incorporated | Stałe postacie kwasu 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioksol-5-ilo)cyklopropanokarboksyamido)-3-metylopirydyn-2-ylo)benzoesowego |
| DK2639224T3 (en) * | 2007-12-07 | 2016-10-17 | Vertex Pharma | A process for the preparation of cycloalkylcarboxiamido-pyridinbenzoesyrer |
| NZ720282A (en) | 2008-02-28 | 2017-12-22 | Vertex Pharma | Heteroaryl derivatives as cftr modulators |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| DK3150198T3 (da) | 2010-04-07 | 2021-11-01 | Vertex Pharma | Farmaceutiske sammensætninger af 3-(6-(1-(2,2-difluorbenzo[d][1,3]dioxol-5-yl)-cyclopropancarboxamido)-3-methylpyriodin-2-yl)benzoesyre og indgivelse deraf |
| 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 |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| 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 |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| 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 |
| WO2013045413A1 (en) | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| US9113629B2 (en) * | 2013-03-15 | 2015-08-25 | Dow Agrosciences Llc | 4-amino-6-(4-substituted-phenyl)-picolinates and 6-amino-2-(4-substituted-phenyl)-pyrimidine-4-carboxylates and their use as herbicides |
| PL3068392T3 (pl) | 2013-11-12 | 2021-07-19 | Vertex Pharmaceuticals Incorporated | Proces wytwarzania kompozycji farmaceutycznych do leczenia chorób, w których pośredniczy cftr |
| CN107110831B (zh) | 2014-11-18 | 2020-02-21 | 弗特克斯药品有限公司 | 进行高通量试验高效液相色谱的方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3655679A (en) * | 1969-06-25 | 1972-04-11 | Merck & Co Inc | Certain aryl pyridine carboxylic acid derivatives |
| US5217982A (en) | 1990-09-25 | 1993-06-08 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Compounds having antihypertensive properties |
| WO1997026265A1 (en) | 1996-01-17 | 1997-07-24 | Novo Nordisk A/S | Fused 1,2,4-thiadiazine and fused 1,4-thiazine derivatives, their preparation and use |
| US6225310B1 (en) | 1996-01-17 | 2001-05-01 | Novo Nordisk A/S | Fused 1,2,4-thiadiazine derivatives, their preparation and use |
| US6380218B1 (en) | 1997-04-04 | 2002-04-30 | Pfizer Inc | Nicotinamide derivatives |
| KR20010021936A (ko) | 1997-07-16 | 2001-03-15 | 한센 핀 베네드, 안네 제헤르, 웨이콥 마리안느 | 융합된 1,2,4-티아디아진 유도체, 그의 제조와 사용 |
| DE19834047A1 (de) | 1998-07-29 | 2000-02-03 | Bayer Ag | Substituierte Pyrazolderivate |
| DE19834044A1 (de) | 1998-07-29 | 2000-02-03 | Bayer Ag | Neue substituierte Pyrazolderivate |
| DE19943634A1 (de) | 1999-09-13 | 2001-04-12 | Bayer Ag | Neuartige Dicarbonsäurederivate mit pharmazeutischen Eigenschaften |
| DE19943635A1 (de) | 1999-09-13 | 2001-03-15 | Bayer Ag | Neuartige Aminodicarbonsäurederivate mit pharmazeutischen Eigenschaften |
| DE19943636A1 (de) | 1999-09-13 | 2001-03-15 | Bayer Ag | Neuartige Dicarbonsäurederivate mit pharmazeutischen Eigenschaften |
| DE19943639A1 (de) | 1999-09-13 | 2001-03-15 | Bayer Ag | Dicarbonsäurederivate mit neuartigen pharmazeutischen Eigenschaften |
| AR031176A1 (es) | 2000-11-22 | 2003-09-10 | Bayer Ag | Nuevos derivados de pirazolpiridina sustituidos con piridina |
| DE10110750A1 (de) | 2001-03-07 | 2002-09-12 | Bayer Ag | Neuartige Aminodicarbonsäurederivate mit pharmazeutischen Eigenschaften |
| DE10110749A1 (de) | 2001-03-07 | 2002-09-12 | Bayer Ag | Substituierte Aminodicarbonsäurederivate |
| WO2003082191A2 (en) * | 2002-03-28 | 2003-10-09 | Merck & Co., Inc. | Substituted 2,3-diphenyl pyridines |
| DE10220570A1 (de) | 2002-05-08 | 2003-11-20 | Bayer Ag | Carbamat-substituierte Pyrazolopyridine |
| CA2504941C (en) | 2002-11-08 | 2012-06-26 | Neurogen Corporation | 3-substituted-6-aryl pyridines |
| JP2007513058A (ja) | 2003-09-08 | 2007-05-24 | 武田薬品工業株式会社 | ジペプチジルぺプチダーゼ阻害剤 |
| CN100509802C (zh) * | 2003-11-05 | 2009-07-08 | 霍夫曼-拉罗奇有限公司 | 作为ppar激活剂的杂芳基衍生物 |
| CA2543249C (en) | 2003-11-05 | 2012-08-07 | F. Hoffmann-La Roche Ag | Phenyl derivatives as ppar agonists |
| KR20130083488A (ko) | 2004-09-02 | 2013-07-22 | 제넨테크, 인크. | 헤지호그 신호전달에 대한 피리딜 억제제 |
| DE102005027150A1 (de) | 2005-03-12 | 2006-09-28 | Bayer Healthcare Ag | Pyrimidincarbonsäure-Derivate und ihre Verwendung |
| CA2603345C (en) | 2005-04-01 | 2017-05-02 | Insa Rouen | New heterocyclic compounds, their preparation and their use as medicaments, in particular as anti-alzheimer agents |
| WO2006124874A2 (en) | 2005-05-12 | 2006-11-23 | Kalypsys, Inc. | Inhibitors of b-raf kinase |
| US7932270B2 (en) | 2006-08-01 | 2011-04-26 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
| DE102006043520A1 (de) | 2006-09-12 | 2008-03-27 | Bayer Healthcare Ag | 2-Phenoxynikotinsäure-Derivate und ihre Verwendung |
| DE102006043519A1 (de) | 2006-09-12 | 2008-03-27 | Bayer Healthcare Ag | 4-Phenoxynikotinsäure-Derivate und ihre Verwendung |
| CN101605792A (zh) * | 2007-02-09 | 2009-12-16 | 阿斯利康(瑞典)有限公司 | 氮杂-异吲哚酮和它们作为亲代谢性谷氨酸受体增效剂-613的用途 |
-
2007
- 2007-09-07 DE DE102007042754A patent/DE102007042754A1/de not_active Withdrawn
-
2008
- 2008-08-26 KR KR1020107007500A patent/KR20100066545A/ko not_active Withdrawn
- 2008-08-26 CA CA2698471A patent/CA2698471A1/en not_active Abandoned
- 2008-08-26 NZ NZ583697A patent/NZ583697A/en not_active IP Right Cessation
- 2008-08-26 BR BRPI0816372-3A2A patent/BRPI0816372A2/pt not_active IP Right Cessation
- 2008-08-26 JP JP2010523302A patent/JP2010538025A/ja not_active Withdrawn
- 2008-08-26 WO PCT/EP2008/006969 patent/WO2009033561A1/de not_active Ceased
- 2008-08-26 US US12/676,568 patent/US8143411B2/en active Active
- 2008-08-26 MX MX2010002565A patent/MX2010002565A/es active IP Right Grant
- 2008-08-26 AU AU2008298021A patent/AU2008298021A1/en not_active Abandoned
- 2008-08-26 EP EP08801700A patent/EP2197846A1/de not_active Withdrawn
- 2008-08-27 UY UY31310A patent/UY31310A1/es not_active Application Discontinuation
- 2008-08-28 PA PA20088794401A patent/PA8794401A1/es unknown
- 2008-08-28 PE PE2008001459A patent/PE20090954A1/es not_active Application Discontinuation
- 2008-08-28 CL CL2008002537A patent/CL2008002537A1/es unknown
- 2008-09-05 TW TW097133999A patent/TW200914002A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MX2010002565A (es) | 2010-04-30 |
| PA8794401A1 (es) | 2009-07-23 |
| JP2010538025A (ja) | 2010-12-09 |
| US8143411B2 (en) | 2012-03-27 |
| NZ583697A (en) | 2012-04-27 |
| KR20100066545A (ko) | 2010-06-17 |
| UY31310A1 (es) | 2009-04-30 |
| TW200914002A (en) | 2009-04-01 |
| WO2009033561A8 (de) | 2010-06-10 |
| AU2008298021A1 (en) | 2009-03-19 |
| US20100234432A1 (en) | 2010-09-16 |
| CL2008002537A1 (es) | 2009-03-20 |
| DE102007042754A1 (de) | 2009-03-12 |
| BRPI0816372A2 (pt) | 2015-02-24 |
| EP2197846A1 (de) | 2010-06-23 |
| WO2009033561A1 (de) | 2009-03-19 |
| CA2698471A1 (en) | 2009-03-19 |
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