PE20061354A1 - Compuestos 2-amino-4-oxobutil como inhibidores de la dipeptidil peptidas-iv - Google Patents
Compuestos 2-amino-4-oxobutil como inhibidores de la dipeptidil peptidas-ivInfo
- Publication number
- PE20061354A1 PE20061354A1 PE2006000351A PE2006000351A PE20061354A1 PE 20061354 A1 PE20061354 A1 PE 20061354A1 PE 2006000351 A PE2006000351 A PE 2006000351A PE 2006000351 A PE2006000351 A PE 2006000351A PE 20061354 A1 PE20061354 A1 PE 20061354A1
- Authority
- PE
- Peru
- Prior art keywords
- nil
- amino
- dihydro
- compounds
- oxobutil
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/4436—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom
-
- 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
-
- 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
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Abstract
SE REFIERE A COMPUESTOS 2-AMINO-4-OXOBUTIL DE FORMULA (I), EN DONDE A ES i) EN DONDE R1 ES H O ALQUILO(C1-C4) OPCIONALMENTE SUSTITUIDO; X ES C O N; ii) 3-(R2)-4,5-DIHIDRO-7H-ISOOXAZOL[3,4-c]PIRIDI-6-NIL; iii) 3,4-DIHIDRO-1H-ISOQUINOLI-1-NIL; iv) 2-(R3)-4-(R3')-5,8-DIHIDROPIRIDO[3,4-d]-PIRIMIDI-7-NIL; v) 2-()-6,7-DIHIDRO[1,3]TIAZOLO[4,5-C]PIRIDI-5(4H)-NIL; ENTRE OTROS y B ES UN GRUPO DE FORMULA 8); 9); 10) O 11). SON COMPUESTOS PREFERIDOS: 3-[2S-AMINO-4-OXO-4-(3-TRIFLUOROMETIL-5,6-DIHIDRO-8H-[1,2,4]TRIAZOLO[4,3-a]PIRAZI-7-NIL)-BUTIL]-OXAZOLIDI-2-NONA, 1-[2S-AMINO-4-OXO-4-(3-TRIFLUOROMETIL-5,6-DIHIDRO-8H-[1,2,4]TRIAZOLO[4,3-a]PIRAZI-7-NIL)-BUTIL]-PIPERIDI-2-NONA, 1-{(2S)-2-AMINO-4-OXO-4-[2-FENIL-4-(TRIFLUOROMETIL)-5,8-DIHIDROPIRIDO[3,4-d]PIRIMIDI-7(6H)-NIL]BUTIL}-5,5-DIFLUOROPIPERIDI-2-NONA, ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. ESTOS COMPUESTOS SON INHIBIDORES DE LA DIPEPTIDIL PEPTIDASA-IV (DPP-IV), POR LO QUE SON UTILES EN EL TRATAMIENTO DE DIABETES MELLITUS O LA OBESIDAD
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR20050027756 | 2005-04-01 | ||
KR20050053761 | 2005-06-22 | ||
KR20050085980 | 2005-09-15 | ||
KR20050122361 | 2005-12-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20061354A1 true PE20061354A1 (es) | 2007-01-02 |
Family
ID=37053586
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2006000351A PE20061354A1 (es) | 2005-04-01 | 2006-03-30 | Compuestos 2-amino-4-oxobutil como inhibidores de la dipeptidil peptidas-iv |
Country Status (28)
Country | Link |
---|---|
US (1) | US7879848B2 (es) |
EP (1) | EP1863812B1 (es) |
JP (1) | JP4977685B2 (es) |
KR (3) | KR100776623B1 (es) |
CN (1) | CN101151265B (es) |
AR (1) | AR053195A1 (es) |
AT (1) | ATE473976T1 (es) |
AU (1) | AU2006229520B2 (es) |
BR (1) | BRPI0609424B8 (es) |
CA (1) | CA2602248C (es) |
DE (1) | DE602006015443D1 (es) |
DK (1) | DK1863812T3 (es) |
EA (1) | EA012591B1 (es) |
ES (1) | ES2349178T3 (es) |
IL (1) | IL185479A (es) |
MA (1) | MA29586B1 (es) |
MX (1) | MX2007012175A (es) |
MY (1) | MY150102A (es) |
NZ (1) | NZ560789A (es) |
PE (1) | PE20061354A1 (es) |
PL (1) | PL1863812T3 (es) |
PT (1) | PT1863812E (es) |
SI (1) | SI1863812T1 (es) |
TW (1) | TWI357902B (es) |
UA (1) | UA89396C2 (es) |
UY (1) | UY29448A1 (es) |
WO (1) | WO2006104356A1 (es) |
ZA (1) | ZA200708304B (es) |
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WO2007148185A2 (en) | 2006-06-21 | 2007-12-27 | Pfizer Products Inc. | Substituted 3 -amino- pyrrolidino-4 -lactams as dpp inhibitors |
CA2666193A1 (en) | 2006-08-08 | 2008-02-14 | Sanofi-Aventis | Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, process for preparing them, medicaments comprising these compounds, and their use |
KR20120030570A (ko) | 2007-04-03 | 2012-03-28 | 미쓰비시 타나베 파마 코퍼레이션 | 디펩티딜 펩티다아제 4 저해 화합물과 감미료와의 병용 |
CN101357922B (zh) * | 2007-08-02 | 2011-05-18 | 山东轩竹医药科技有限公司 | 新的dpp-iv抑制剂 |
EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
EP2227461A1 (en) * | 2007-12-05 | 2010-09-15 | AstraZeneca AB (Publ) | New compounds iii |
EP2220086A4 (en) * | 2007-12-21 | 2010-12-22 | Lg Life Sciences Ltd | DIPEPTIDYLPEPTIDASE IV-INHIBITABLE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS THEREFOR AS ACTIVE AGENT |
CL2008003653A1 (es) | 2008-01-17 | 2010-03-05 | Mitsubishi Tanabe Pharma Corp | Uso de un inhibidor de sglt derivado de glucopiranosilo y un inhibidor de dppiv seleccionado para tratar la diabetes; y composicion farmaceutica. |
CN101486689B (zh) * | 2008-01-18 | 2011-08-10 | 山东轩竹医药科技有限公司 | 具有磺酰胺基甲酰胺哌嗪结构的dpp-iv抑制剂 |
EP2310372B1 (en) | 2008-07-09 | 2012-05-23 | Sanofi | Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof |
JO2870B1 (en) * | 2008-11-13 | 2015-03-15 | ميرك شارب اند دوهم كورب | Amino Tetra Hydro Pirans as Inhibitors of Peptide Dipeptide IV for the Treatment or Prevention of Diabetes |
WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
KR20110136850A (ko) * | 2009-03-13 | 2011-12-21 | 썬 케미칼 비.브이. | 에너지-경화성 조성물에 유용한 사이클릭 카바메이트 화합물 |
EP2470552B1 (en) | 2009-08-26 | 2013-11-13 | Sanofi | Novel crystalline heteroaromatic fluoroglycoside hydrates, pharmaceuticals comprising these compounds and their use |
US8871760B2 (en) * | 2009-09-21 | 2014-10-28 | Roche Palo Alto Llc | [1,2,4]triazolo[3,4-C][1,4]oxazines as P2X7 modulators |
WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
CN102260265B (zh) * | 2010-05-24 | 2015-09-02 | 上海阳帆医药科技有限公司 | 六氢吡咯[3,4-b]吡咯衍生物、其制备方法及其用途 |
EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
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 |
CA2810393C (en) * | 2010-09-03 | 2016-04-12 | Lg Life Sciences Ltd. | Method of preparing 3-amino-4-(2-oxo-piperidin-1-yl)-butyric acid derivative for synthesizing medicament |
TWI519533B (zh) * | 2010-11-01 | 2016-02-01 | Lg生命科學有限公司 | 1-{(2S)-2-胺基-4-[2,4-雙(三氟甲基)-5,8-二氫吡啶并[3,4-d]嘧啶-7(6H)-基]-4-側氧丁基}-5,5-二氟哌啶-2-酮酒石酸鹽之水合物 |
EP2683705B1 (de) | 2011-03-08 | 2015-04-22 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
WO2012120052A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
US8710050B2 (en) | 2011-03-08 | 2014-04-29 | Sanofi | Di and tri- substituted oxathiazine derivatives, method for the production, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
US8871758B2 (en) | 2011-03-08 | 2014-10-28 | Sanofi | Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof |
EP2683704B1 (de) | 2011-03-08 | 2014-12-17 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
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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 |
EP2911655A1 (en) | 2012-10-24 | 2015-09-02 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Tpl2 kinase inhibitors for preventing or treating diabetes and for promoting -cell survival |
CN105085528A (zh) * | 2014-05-15 | 2015-11-25 | 成都贝斯凯瑞生物科技有限公司 | 作为二肽基肽酶-iv抑制剂的氨基四氢吡喃衍生物 |
WO2016151018A1 (en) | 2015-03-24 | 2016-09-29 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Method and pharmaceutical composition for use in the treatment of diabetes |
BR112018017077A2 (pt) | 2016-02-23 | 2018-12-26 | Univ Indiana Res & Tech Corp | terapias de combinação para tratamento de atrofia muscular espinhal |
KR102068754B1 (ko) * | 2017-04-20 | 2020-01-21 | 주식회사 엘지화학 | 의약품 합성용 중간체 화합물의 제조 방법 |
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- 2006-03-21 TW TW095109718A patent/TWI357902B/zh active
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- 2006-03-30 UY UY29448A patent/UY29448A1/es not_active Application Discontinuation
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- 2006-03-30 CN CN200680009935XA patent/CN101151265B/zh active Active
- 2006-03-30 US US11/910,370 patent/US7879848B2/en active Active
- 2006-03-30 CA CA2602248A patent/CA2602248C/en active Active
- 2006-03-30 JP JP2008503954A patent/JP4977685B2/ja active Active
- 2006-03-30 DE DE602006015443T patent/DE602006015443D1/de active Active
- 2006-03-30 KR KR1020060029138A patent/KR100776623B1/ko active IP Right Grant
- 2006-03-30 BR BRPI0609424A patent/BRPI0609424B8/pt active IP Right Grant
- 2006-03-30 AT AT06732744T patent/ATE473976T1/de active
- 2006-03-30 PL PL06732744T patent/PL1863812T3/pl unknown
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- 2007-08-23 IL IL185479A patent/IL185479A/en active IP Right Grant
- 2007-08-28 KR KR1020070086486A patent/KR100794184B1/ko active IP Right Grant
- 2007-08-28 KR KR1020070086444A patent/KR100830902B1/ko active IP Right Grant
- 2007-09-28 ZA ZA200708304A patent/ZA200708304B/xx unknown
- 2007-10-30 MA MA30343A patent/MA29586B1/fr unknown
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