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
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 102000016622 Dipeptidyl Peptidase 4 Human genes 0.000 abstract 2
- 101000930822 Giardia intestinalis Dipeptidyl-peptidase 4 Proteins 0.000 abstract 2
- 208000008589 Obesity Diseases 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Diabetes (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Peptides Or Proteins (AREA)
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) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| AU2008233548B2 (en) | 2007-04-03 | 2011-12-01 | Mitsubishi Tanabe Pharma Corporation | Combined use of dipeptidyl peptidase IV inhibitor compound and sweetener |
| 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 |
| CN102026993A (zh) * | 2007-12-05 | 2011-04-20 | 阿斯利康(瑞典)有限公司 | 新化合物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 |
| UY31968A (es) | 2008-07-09 | 2010-01-29 | Sanofi Aventis | Nuevos derivados heterocíclicos, sus procesos para su preparación, y sus usos terapéuticos |
| 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 |
| CA2754712A1 (en) * | 2009-03-13 | 2010-09-16 | Sun Chemical B.V. | Cyclic carbamate compounds useful in energy-curable compositions |
| MX2012001729A (es) | 2009-08-26 | 2012-06-13 | Sanofi Sa | Nuevos hidratos cristalinos de fluoroglicosido heteroaromatico, productos farmaceuticos que comprenden estos compuestos, y su empleo. |
| 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 |
| PH12013500343A1 (en) * | 2010-09-03 | 2015-01-23 | Lg Chemical Ltd | Production method of intermediate compound 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 |
| 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 |
| WO2012120053A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| EP2683700B1 (de) | 2011-03-08 | 2015-02-18 | Sanofi | Tetrasubstituierte 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 |
| WO2012170702A1 (en) | 2011-06-08 | 2012-12-13 | Arena Pharmaceuticals, Inc. | Modulators of the gpr119 receptor and the treatment of disorders related thereto |
| 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 |
| US20150297573A1 (en) | 2012-10-24 | 2015-10-22 | INSERM (Institut National de la Santé et de la Recherche Médicale) | TPL2 KINASE INHIBITORS FOR PREVENTING OR TREATING DIABETES AND FOR PROMOTING Beta-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 |
| ES2805743T3 (es) | 2015-03-24 | 2021-02-15 | Inst Nat Sante Rech Med | Método y composición farmacéutica para uso en el tratamiento de la diabetes |
| RU2018133288A (ru) | 2016-02-23 | 2020-03-24 | Индиана Юниверсити Рисерч Энд Текнолоджи Корпорейшн | Комбинированные терапии для лечения спинальной мышечной атрофии |
| KR102068754B1 (ko) * | 2017-04-20 | 2020-01-21 | 주식회사 엘지화학 | 의약품 합성용 중간체 화합물의 제조 방법 |
| PE20210839A1 (es) * | 2017-11-16 | 2021-05-06 | Lg Chemical Ltd | Metodo de produccion de un compuesto intermedio para sintetizar un medicamento |
| CN108191647B (zh) * | 2018-02-22 | 2020-09-29 | 江苏尚莱特医药化工材料有限公司 | 2,2-二氟二羧酸二烷基酯的合成方法 |
| CN111537622B (zh) * | 2019-11-29 | 2021-11-26 | 杭州华东医药集团新药研究院有限公司 | 一种度格列汀及其盐的杂质的检测方法 |
| KR20250097733A (ko) | 2023-12-21 | 2025-06-30 | 이니스트에스티 주식회사 | 디펩티딜 펩티데이즈-iv (dpp-iv) 억제제의 신규한 염, 이의 제조 방법 및 이를 포함하는 약제학적 조성물 |
| KR20250155700A (ko) | 2024-04-24 | 2025-10-31 | 주식회사 다산제약 | 제미글립틴 산부가염 제조방법 및 이를 유효성분으로 포함하는 dpp-4 저해용 조성물 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CO5150173A1 (es) | 1998-12-10 | 2002-04-29 | Novartis Ag | Compuestos n-(glicilo sustituido)-2-cianopirrolidinas inhibidores de peptidasa de dipeptidilo-iv (dpp-iv) los cuales son efectivos en el tratamiento de condiciones mediadas por la inhibicion de dpp-iv |
| UA74912C2 (en) * | 2001-07-06 | 2006-02-15 | Merck & Co Inc | Beta-aminotetrahydroimidazo-(1,2-a)-pyrazines and tetratriazolo-(4,3-a)-pyrazines as inhibitors of dipeptylpeptidase for the treatment or prevention of diabetes |
| US6861440B2 (en) * | 2001-10-26 | 2005-03-01 | Hoffmann-La Roche Inc. | DPP IV inhibitors |
| WO2003057144A2 (en) * | 2001-12-26 | 2003-07-17 | Guilford Pharmaceuticals | Change inhibitors of dipeptidyl peptidase iv |
| EP1490335B1 (en) * | 2002-03-25 | 2007-09-19 | Merck & Co., Inc. | Beta-amino heterocyclic dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| CA2483843A1 (en) * | 2002-04-29 | 2003-11-13 | Merck & Co. Inc. | Tetrahydropyranyl cyclopentyl tetrahydroisoquinoline modulators of chemokine receptor activity |
| AU2003251869A1 (en) * | 2002-07-15 | 2004-02-02 | Merck & Co., Inc. | Piperidino pyrimidine dipeptidyl peptidase inhibitors for the treatment of diabetes |
| JP2004285325A (ja) * | 2002-12-17 | 2004-10-14 | Fuji Photo Film Co Ltd | パターン形成方法及び物質付着パターン材料 |
| WO2004058266A1 (en) * | 2002-12-20 | 2004-07-15 | Merck & Co., Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| JP4564952B2 (ja) | 2003-01-17 | 2010-10-20 | メルク・シャープ・エンド・ドーム・コーポレイション | 糖尿病の治療および予防のためのジペプチジルペプチダーゼ阻害薬としての3−アミノ−4−フェニルブタン酸誘導体 |
| CA2513684A1 (en) * | 2003-01-31 | 2004-08-19 | Merck & Co., Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| EP1732885A1 (en) | 2004-02-23 | 2006-12-20 | Trustees Of Tufts College | Lactams as conformationally constrained peptidomimetic inhibitors |
| US7291427B2 (en) * | 2004-03-19 | 2007-11-06 | Fujifilm Corporation | Surface graft material, conductive pattern material, and production method thereof |
| DE102004020908A1 (de) * | 2004-04-28 | 2005-11-17 | Grünenthal GmbH | Substituierte 5,6,7,8,-Tetrahydro-pyrido[4,3-d]pyrimidin-2-yl- und 5,6,7,8,-Tetrahydro-chinazolin-2-yl-Verbindungen |
| DE102005016170A1 (de) * | 2005-04-07 | 2006-10-12 | Grünenthal GmbH | 4,5,6,7- Tetrahydro-isoxazolo(4,5c)pyridin-Verbindungen und deren Verwendung zur Herstellung von Arzneimitteln |
| AU2006244206A1 (en) * | 2005-05-10 | 2006-11-16 | Vertex Pharmaceuticals Incorporated | Bicyclic derivatives as modulators of ion channels |
| US20090176825A1 (en) * | 2006-05-16 | 2009-07-09 | Fitch Duke M | Prolyl hydroxylase inhibitors |
| JP2011509961A (ja) * | 2008-01-17 | 2011-03-31 | グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | 置換スルホンアミド誘導体 |
-
2006
- 2006-03-21 TW TW095109718A patent/TWI357902B/zh active
- 2006-03-29 AR ARP060101214A patent/AR053195A1/es active IP Right Grant
- 2006-03-30 EA EA200701854A patent/EA012591B1/ru unknown
- 2006-03-30 DK DK06732744.5T patent/DK1863812T3/da active
- 2006-03-30 MY MYPI20061446A patent/MY150102A/en unknown
- 2006-03-30 US US11/910,370 patent/US7879848B2/en active Active
- 2006-03-30 AU AU2006229520A patent/AU2006229520B2/en active Active
- 2006-03-30 UY UY29448A patent/UY29448A1/es not_active Application Discontinuation
- 2006-03-30 NZ NZ560789A patent/NZ560789A/en unknown
- 2006-03-30 PL PL06732744T patent/PL1863812T3/pl unknown
- 2006-03-30 WO PCT/KR2006/001169 patent/WO2006104356A1/en not_active Ceased
- 2006-03-30 AT AT06732744T patent/ATE473976T1/de active
- 2006-03-30 ES ES06732744T patent/ES2349178T3/es active Active
- 2006-03-30 PE PE2006000351A patent/PE20061354A1/es active IP Right Grant
- 2006-03-30 DE DE602006015443T patent/DE602006015443D1/de active Active
- 2006-03-30 EP EP06732744A patent/EP1863812B1/en active Active
- 2006-03-30 CA CA2602248A patent/CA2602248C/en active Active
- 2006-03-30 MX MX2007012175A patent/MX2007012175A/es active IP Right Grant
- 2006-03-30 UA UAA200710765A patent/UA89396C2/ru unknown
- 2006-03-30 BR BRPI0609424A patent/BRPI0609424B8/pt active IP Right Grant
- 2006-03-30 PT PT06732744T patent/PT1863812E/pt unknown
- 2006-03-30 KR KR1020060029138A patent/KR100776623B1/ko active Active
- 2006-03-30 JP JP2008503954A patent/JP4977685B2/ja active Active
- 2006-03-30 CN CN200680009935XA patent/CN101151265B/zh active Active
- 2006-03-30 SI SI200331873T patent/SI1863812T1/sl unknown
-
2007
- 2007-08-23 IL IL185479A patent/IL185479A/en active IP Right Grant
- 2007-08-28 KR KR1020070086444A patent/KR100830902B1/ko active Active
- 2007-08-28 KR KR1020070086486A patent/KR100794184B1/ko active Active
- 2007-09-28 ZA ZA200708304A patent/ZA200708304B/xx unknown
- 2007-10-30 MA MA30343A patent/MA29586B1/fr unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PE20061354A1 (es) | Compuestos 2-amino-4-oxobutil como inhibidores de la dipeptidil peptidas-iv | |
| PE20060316A1 (es) | Derivados de prolina como inhibidores de dipeptidil peptidasa-iv | |
| PE20071104A1 (es) | Aminotetrahidropiranos como inhibidores de dipeptidil peptidasa-iv (dpp-4) | |
| PE20050696A1 (es) | SAL DIHIDROGENOFOSFATO DE 4-OXO-4-[3-(TRIFLUOROMETIL)-5,6-DIHIDRO[1,2,4]TRIAZOLO[4,3-a]PIRAZIN-7(8H)-IL]-1-(2,4,5-TRIFLUOROFENIL)BUTAN-2-AMINA COMO INHIBIDOR DE LA DIPEPTIDIL PEPTIDASA IV | |
| PE20070367A1 (es) | Compuestos de espiropiperidina como inhibidores de la enzima beta secretasa | |
| PE20030654A1 (es) | Butanoil-5,6,7,8-tetrahidro (imidazo o triazo) piracinas como inhibidores de dipeptidil peptidasa iv | |
| PE20091353A1 (es) | Nuevos compuestos heterociclicos | |
| PE20090370A1 (es) | Derivados de heterociclo fusionado como inhibidores de quinasa | |
| PE20110922A1 (es) | DERIVADOS DE PIRAZOLO[4,3-e]PIRIMIDIN COMO INHIBIDORES DE LA FOSFODIESTERASA 1 (PDE1) | |
| PE20060210A1 (es) | 8-[3-amino-piperidin-1-il]-xantinas como inhibidores de dpp-iv | |
| PE20110944A1 (es) | DERIVADOS DE PIRAZOLO[3,4-d]PIRIMIDINA COMO INHIBIDORES PDE1 | |
| PE20060555A1 (es) | Derivados de pirrol-oxindol como moduladores del receptor de progesterona | |
| PE20060486A1 (es) | Derivados de pirrol-oxindol como moduladores del receptor de progesterona | |
| PE20121150A1 (es) | Inhibidores de jak2 y su uso en el tratamiento de enfermedades mieloproliferativas y cancer | |
| AR070526A1 (es) | Derivados de urea de benzomorfanos y estructuras relacionadas, una composicion farmaceutica que incluye al compuesto y un procedimiento de preparacion del mismo | |
| PE20080139A1 (es) | Compuestos de pirrolotriazina anilina como inhibidores de cinasa | |
| PE20120121A1 (es) | Derivados de imidazopirazina como inhibidores de syk | |
| PE20091211A1 (es) | Derivados de pirazolopirimidina como moduladores de pde9a | |
| PE20081377A1 (es) | Compuestos de tiazol pirazolopirimidina | |
| PE20110222A1 (es) | Inhibidores de dipeptidilpeptidasa iv | |
| PE20040197A1 (es) | Pirazolopiridinas sustituidas con carbamato | |
| PE20061424A1 (es) | Compuestos triciclicos de base 1,6-dihidro-1-3,5,6-tetraaza-as-indaceno y composiciones farmaceuticas que comprenden los mismos | |
| PE20121511A1 (es) | Novedosos derivados biciclicos de triazol sustituidos como moduladores de gamma secretasa | |
| PE20120209A1 (es) | DERIVADOS DE IMIDAZO-[1,2-a]-PIRAZOLO [4,3-e]PIRIMIDINA O PIRIMIDO-[1,2-a]-PIRAZOLO [4,3-e]PIRIMIDINA COMO INHIBIDORES DE FOSFODIESTERASA 1 (PDE1) | |
| PE20091056A1 (es) | PIRIDO[3,2-e]PIRAZINAS, SU PROCEDIMIENTO DE PREPARACION Y USO COMO INHIBIDORES DE FOSFODIESTERASA 10 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant, registration |