MA30291B1 - Derives de l'azolopyridin-3-one en tant qu'inhibiteurs de la lipase endotheliale - Google Patents
Derives de l'azolopyridin-3-one en tant qu'inhibiteurs de la lipase endothelialeInfo
- Publication number
- MA30291B1 MA30291B1 MA31257A MA31257A MA30291B1 MA 30291 B1 MA30291 B1 MA 30291B1 MA 31257 A MA31257 A MA 31257A MA 31257 A MA31257 A MA 31257A MA 30291 B1 MA30291 B1 MA 30291B1
- Authority
- MA
- Morocco
- Prior art keywords
- azolopyridin
- inhibitors
- derivatives
- endothelial lipase
- lipase
- Prior art date
Links
- 102100031375 Endothelial lipase Human genes 0.000 title abstract 3
- 101710087274 Endothelial lipase Proteins 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 title abstract 3
- FCACETKNGAHGMV-UHFFFAOYSA-N pyrrolo[3,2-b]pyridin-3-one Chemical class C1=CN=C2C(=O)C=NC2=C1 FCACETKNGAHGMV-UHFFFAOYSA-N 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000126 substance Substances 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
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- Pulmonology (AREA)
- Reproductive Health (AREA)
- Virology (AREA)
- Dermatology (AREA)
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- Pain & Pain Management (AREA)
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- Urology & Nephrology (AREA)
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- Ophthalmology & Optometry (AREA)
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Abstract
Titre : Dérivés de l'azolopyridin-3-one en tant qu'inhibiteurs de la lipase endothéliale La présente invention concerne des dérivés de l'azolopyridin-3-one de formule générale I avec les significations indiquées dans la description, leurs sels pharmaceutiquement utilisables et leur utilisation comme substances médicinales. Les composés sont des inhibiteurs de la lipase endothéliale.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006014688A DE102006014688A1 (de) | 2006-03-28 | 2006-03-28 | Azolopyridin-3-on-derivate als Inhibitoren von Lipasen und Phospholipasen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30291B1 true MA30291B1 (fr) | 2009-03-02 |
Family
ID=38190768
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA31257A MA30291B1 (fr) | 2006-03-28 | 2008-09-25 | Derives de l'azolopyridin-3-one en tant qu'inhibiteurs de la lipase endotheliale |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US8148395B2 (fr) |
| EP (1) | EP2001879B1 (fr) |
| JP (1) | JP2009531357A (fr) |
| KR (1) | KR20080104032A (fr) |
| CN (1) | CN101415706A (fr) |
| AR (1) | AR060158A1 (fr) |
| AU (1) | AU2007229709A1 (fr) |
| BR (1) | BRPI0709217A2 (fr) |
| CA (1) | CA2647425A1 (fr) |
| DE (1) | DE102006014688A1 (fr) |
| MA (1) | MA30291B1 (fr) |
| MX (1) | MX2008012127A (fr) |
| NO (1) | NO20084418L (fr) |
| RU (1) | RU2008142535A (fr) |
| TW (1) | TW200813049A (fr) |
| WO (1) | WO2007110216A1 (fr) |
| ZA (1) | ZA200807135B (fr) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2025674A1 (fr) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Tetrahydronaphthaline substituée, son procédé de fabrication et son utilisation en tant que médicament |
| UY31968A (es) | 2008-07-09 | 2010-01-29 | Sanofi Aventis | Nuevos derivados heterocíclicos, sus procesos para su preparación, y sus usos terapéuticos |
| US8957219B2 (en) | 2008-10-17 | 2015-02-17 | Shionogi & Co., Ltd. | Acetic acid amide derivative having inhibitory activity on endothelial lipase |
| KR20120123325A (ko) | 2009-12-15 | 2012-11-08 | 시오노기세야쿠 가부시키가이샤 | 혈관 내피 리파아제 저해 활성을 갖는 옥사디아졸 유도체 |
| WO2011107494A1 (fr) | 2010-03-03 | 2011-09-09 | Sanofi | Nouveaux dérivés aromatiques de glycoside, médicaments contenants ces composés, et leur utilisation |
| US8450350B2 (en) | 2010-05-05 | 2013-05-28 | Infinity Pharmaceuticals, Inc. | Triazoles as inhibitors of fatty acid synthase |
| CA2798330A1 (fr) | 2010-05-05 | 2011-11-10 | Infinity Pharmaceuticals, Inc. | Tetrazolones utilises en tant qu'inhibiteurs d'acide gras synthase (fasn) |
| 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 |
| 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 |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| EP2612669A4 (fr) | 2010-08-31 | 2014-05-14 | Snu R&Db Foundation | Utilisation de la reprogrammation f tale d'un agoniste des ppar |
| 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 |
| 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 |
| 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 |
| EP2683699B1 (fr) | 2011-03-08 | 2015-06-24 | Sanofi | Dérivés oxathiazine di- et tri-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation |
| EP2567959B1 (fr) | 2011-09-12 | 2014-04-16 | Sanofi | Dérivés d'amide d'acide 6-(4-hydroxy-phényl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique en tant qu'inhibiteurs de kinase |
| 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 |
| EP2760828B1 (fr) | 2011-09-27 | 2015-10-21 | Bristol-Myers Squibb Company | Composés de pyrrolinone-carboxamide utiles en tant qu'inhibiteurs de lipase endothéliale |
| US9493412B2 (en) | 2011-09-27 | 2016-11-15 | Bristol-Myers Squibb Company | Pyrrolinone carboxamide compounds useful as endothelial lipase inhibitors |
| EP2760829B1 (fr) | 2011-09-27 | 2016-05-18 | Bristol-Myers Squibb Company | Dérivés de pyrrolinone-carboxamide utiles comme inhibiteurs de lipase endothéliale |
| WO2013045413A1 (fr) | 2011-09-27 | 2013-04-04 | Sanofi | Dérivés d'amide d'acide 6-(4-hydroxyphényl)-3-alkyl-1h-pyrazolo[3,4-b] pyridine-4-carboxylique utilisés comme inhibiteurs de kinase |
| WO2013049104A1 (fr) | 2011-09-30 | 2013-04-04 | Bristol-Myers Squibb Company | Pyridinedione carboxamides convenant comme inhibiteurs de la lipase endothéliale |
| EP2760840B1 (fr) | 2011-09-30 | 2015-08-12 | Bristol-Myers Squibb Company | Inhibiteurs quinoléinone carboxamide de lipase endothéliale |
| WO2013048930A1 (fr) | 2011-09-30 | 2013-04-04 | Bristol-Myers Squibb Company | Inhibiteurs pyridinedione carboxamide de lipase endothéliale |
| PT2794618T (pt) | 2011-12-20 | 2017-01-17 | Sanofi Sa | Isotiazolopiridina-2-carboxamidas e seu uso como produtos farmacêuticos |
| EP2844643B1 (fr) | 2012-04-03 | 2016-11-30 | Bristol-Myers Squibb Company | Inhibiteurs pyrimidinedione carboxamide de la lipase endothéliale |
| US9394260B2 (en) | 2012-04-03 | 2016-07-19 | Bristol-Myers Squibb Company | Pyrimidinone carboxamide inhibitors of endothelial lipase |
| AR092854A1 (es) | 2012-07-09 | 2015-05-06 | Bristol Myers Squibb Co | Benzotiazoles que contienen sulfonilo como inhibidores de la lipasa endotelial |
| US9139578B2 (en) | 2012-07-09 | 2015-09-22 | Bristol-Myers Squibb Company | Amide or urea containing benzothiazole inhibitors of endothelial lipase |
| WO2014015088A1 (fr) | 2012-07-19 | 2014-01-23 | Bristol-Myers Squibb Company | Inhibiteurs de lipase endothéliale à base de benzothiazole liés à une amine, l'urée ou un sulfone amide |
| WO2014042939A1 (fr) | 2012-09-11 | 2014-03-20 | Bristol-Myers Squibb Company | Inhibiteurs de lipase endothéliale de type benzothiazole lié à une cétone |
| US10173991B2 (en) | 2014-01-07 | 2019-01-08 | Bristol-Myers Squibb Company | Sulfone amide linked benzothiazole inhibitors of endothelial lipase |
| US20160304496A1 (en) | 2015-04-17 | 2016-10-20 | Abbvie Inc. | Indazolones as modulators of tnf signaling |
| AR104291A1 (es) | 2015-04-17 | 2017-07-12 | Abbvie Inc | Moduladores tricíclicos de la señalización por tnf |
| US9879016B2 (en) | 2015-04-17 | 2018-01-30 | Abbvie Inc. | Indazolones as modulators of TNF signaling |
| US10597370B2 (en) | 2016-06-06 | 2020-03-24 | Bristol-Myers Squibb Company | 2-(benzothiazol-2-yl)-2-cyano-acetamide derivatives and their use as endothelial lipase inhibitors |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2003286711A1 (en) * | 2002-10-25 | 2004-05-13 | Vertex Pharmaceuticals Incorporated | Indazolinone compositions useful as kinase inhibitors |
| DE602004023062D1 (en) * | 2003-03-31 | 2009-10-22 | Lilly Co Eli | 3-oxo-1,3-dihydro-indazol-2-carbonsäureamid derivate als phospholipase inhibitoren |
| US7217727B2 (en) * | 2003-04-01 | 2007-05-15 | Eli Lilly And Company | Phospholipase inhibitors |
| DE102004005172A1 (de) * | 2004-02-02 | 2005-08-18 | Aventis Pharma Deutschland Gmbh | Indazolderivate als Inhibitoren der Hormon Sensitiven Lipase |
-
2006
- 2006-03-28 DE DE102006014688A patent/DE102006014688A1/de not_active Withdrawn
-
2007
- 2007-03-26 BR BRPI0709217-2A patent/BRPI0709217A2/pt not_active IP Right Cessation
- 2007-03-26 JP JP2009501924A patent/JP2009531357A/ja not_active Abandoned
- 2007-03-26 WO PCT/EP2007/002649 patent/WO2007110216A1/fr not_active Ceased
- 2007-03-26 CN CNA2007800116186A patent/CN101415706A/zh active Pending
- 2007-03-26 EP EP07723595.0A patent/EP2001879B1/fr active Active
- 2007-03-26 RU RU2008142535/04A patent/RU2008142535A/ru not_active Application Discontinuation
- 2007-03-26 CA CA002647425A patent/CA2647425A1/fr not_active Abandoned
- 2007-03-26 MX MX2008012127A patent/MX2008012127A/es not_active Application Discontinuation
- 2007-03-26 TW TW096110267A patent/TW200813049A/zh unknown
- 2007-03-26 KR KR1020087023679A patent/KR20080104032A/ko not_active Withdrawn
- 2007-03-26 AU AU2007229709A patent/AU2007229709A1/en not_active Abandoned
- 2007-03-27 AR ARP070101271A patent/AR060158A1/es not_active Application Discontinuation
-
2008
- 2008-08-19 ZA ZA200807135A patent/ZA200807135B/xx unknown
- 2008-09-22 US US12/235,047 patent/US8148395B2/en not_active Expired - Fee Related
- 2008-09-25 MA MA31257A patent/MA30291B1/fr unknown
- 2008-10-21 NO NO20084418A patent/NO20084418L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| ZA200807135B (en) | 2009-05-27 |
| AR060158A1 (es) | 2008-05-28 |
| US8148395B2 (en) | 2012-04-03 |
| EP2001879A1 (fr) | 2008-12-17 |
| NO20084418L (no) | 2008-12-23 |
| KR20080104032A (ko) | 2008-11-28 |
| AU2007229709A1 (en) | 2007-10-04 |
| EP2001879B1 (fr) | 2013-08-21 |
| BRPI0709217A2 (pt) | 2011-07-12 |
| RU2008142535A (ru) | 2010-05-10 |
| CN101415706A (zh) | 2009-04-22 |
| JP2009531357A (ja) | 2009-09-03 |
| TW200813049A (en) | 2008-03-16 |
| US20090054478A1 (en) | 2009-02-26 |
| MX2008012127A (es) | 2008-10-03 |
| DE102006014688A1 (de) | 2007-10-04 |
| CA2647425A1 (fr) | 2007-10-04 |
| WO2007110216A1 (fr) | 2007-10-04 |
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