NO20084663L - 1,3,4-oksadiazol-derivater som DGAT1 inhibitorer - Google Patents
1,3,4-oksadiazol-derivater som DGAT1 inhibitorerInfo
- Publication number
- NO20084663L NO20084663L NO20084663A NO20084663A NO20084663L NO 20084663 L NO20084663 L NO 20084663L NO 20084663 A NO20084663 A NO 20084663A NO 20084663 A NO20084663 A NO 20084663A NO 20084663 L NO20084663 L NO 20084663L
- Authority
- NO
- Norway
- Prior art keywords
- oxadiazole derivatives
- dgat1 inhibitors
- dgat1
- acetyl
- inhibitors
- Prior art date
Links
- 150000005072 1,3,4-oxadiazoles Chemical class 0.000 title 1
- 229940127193 DGAT1 inhibitor Drugs 0.000 title 1
- ZSLZBFCDCINBPY-ZSJPKINUSA-N acetyl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)C)O[C@H]1N1C2=NC=NC(N)=C2N=C1 ZSLZBFCDCINBPY-ZSJPKINUSA-N 0.000 abstract 4
- 102000002148 Diacylglycerol O-acyltransferase Human genes 0.000 abstract 2
- 108010001348 Diacylglycerol O-acyltransferase Proteins 0.000 abstract 2
- -1 cyano, methyl Chemical group 0.000 abstract 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 229940100228 acetyl coenzyme a Drugs 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
- C07D271/113—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4245—Oxadiazoles
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Diabetes (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Child & Adolescent Psychology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US80929706P | 2006-05-30 | 2006-05-30 | |
| PCT/GB2007/001981 WO2007138304A1 (fr) | 2006-05-30 | 2007-05-29 | Dérivés du 1,3,4-oxadiazole en tant qu'inhibiteurs de dgat1 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20084663L true NO20084663L (no) | 2008-12-12 |
Family
ID=38308729
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20084663A NO20084663L (no) | 2006-05-30 | 2008-11-05 | 1,3,4-oksadiazol-derivater som DGAT1 inhibitorer |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US8003676B2 (fr) |
| EP (1) | EP2041099A1 (fr) |
| JP (1) | JP2009538891A (fr) |
| KR (1) | KR20090010092A (fr) |
| CN (1) | CN101460470B (fr) |
| AU (1) | AU2007266890B2 (fr) |
| BR (1) | BRPI0712796A2 (fr) |
| CA (1) | CA2651663A1 (fr) |
| IL (1) | IL195125A0 (fr) |
| MX (1) | MX2008015226A (fr) |
| NO (1) | NO20084663L (fr) |
| NZ (1) | NZ572585A (fr) |
| WO (1) | WO2007138304A1 (fr) |
| ZA (1) | ZA200809689B (fr) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2007007101A (es) * | 2004-12-14 | 2007-08-21 | Astrazeneca Ab | Derivados de oxadiazol como inhibidores de acil coa:diacilglicerol aciltransferasa. |
| AR058562A1 (es) | 2005-12-22 | 2008-02-13 | Astrazeneca Ab | Derivados de pirimido [4,5 b] (1,4) oxazinas , procedimientos de obtencion y su uso como inhibidores de acetil coa y dgat 1 |
| WO2007126957A2 (fr) | 2006-03-31 | 2007-11-08 | Novartis Ag | Nouveaux composés |
| BRPI0712802A2 (pt) | 2006-05-30 | 2012-10-23 | Astrazeneca Ab | composto, métodos para produzir uma inibição da atividade de dgat1, e para tratar diabete melito e/ou obesidade em um animal de sangue quente, uso de um composto, composição farmacêutica, e, processo para preparar um composto |
| CA2651663A1 (fr) | 2006-05-30 | 2007-12-06 | Astrazeneca Ab | Composes chimiques |
| JP2009539818A (ja) * | 2006-06-08 | 2009-11-19 | アストラゼネカ アクチボラグ | ベンゾイミダゾールおよび糖尿病の処置のためのその使用 |
| JP2010536839A (ja) * | 2007-08-17 | 2010-12-02 | アストラゼネカ アクチボラグ | 化合物979 |
| AR066169A1 (es) | 2007-09-28 | 2009-07-29 | Novartis Ag | Derivados de benzo-imidazoles, utiles para trastornos asociados con la actividad de dgat |
| CN101932562B (zh) | 2007-12-20 | 2013-06-12 | 阿斯利康(瑞典)有限公司 | 作为dgat1抑制剂190的氨基甲酰基化合物 |
| WO2010023609A1 (fr) | 2008-08-25 | 2010-03-04 | Piramal Life Sciences Limited | Dérivés d’oxazole, d’oxadiazole et de thiazole comme inhibiteurs de la diacylglycérol acyltransférase |
| MX2011006672A (es) * | 2008-12-19 | 2011-07-20 | Astrazeneca Ab | Derivados de 1,3,4-oxadiazol y sus usos para tratar diabetes. |
| DK3366686T3 (da) | 2009-03-20 | 2020-11-23 | Metabasis Therapeutics Inc | Inhibitorer af diacylglycerol-o-acyltransferase 1 (dgat-1) og anvendelser deraf |
| MX2011011178A (es) | 2009-04-21 | 2011-12-06 | Astellas Pharma Inc | Compuesto de diaciletilendiamina. |
| WO2010146395A1 (fr) * | 2009-06-19 | 2010-12-23 | Astrazeneca Ab | Carboxamides de pyrazine utiles comme inhibiteurs de la dgat1 |
| FR2963005B1 (fr) * | 2010-07-23 | 2012-08-17 | Sanofi Aventis | Derives d'oxadiazoles et de pyridazines, leur preparation et leur application en therapeutique |
| 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 |
| 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 |
| 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 |
| 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 |
| WO2013056679A1 (fr) * | 2011-10-21 | 2013-04-25 | Beijing Hanmi Pharmaceutical Co., Ltd | Nouveaux dérivés amino-hétéroaryle |
| CN107667025B (zh) | 2015-06-22 | 2020-10-16 | 大陆汽车有限责任公司 | 具有可控屏蔽显示器的透明显示器 |
| CN118243845B (zh) * | 2024-03-13 | 2026-03-06 | 浙江大学 | 一种评估脂质吸收的再酯化测定方法及应用 |
Family Cites Families (80)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3245989A (en) * | 1962-12-15 | 1966-04-12 | Acraf | 3-aminophenyl-5-aminoloweralkyl-1, 2, 4-oxadiazoles |
| US4983731A (en) * | 1989-03-17 | 1991-01-08 | Nebraska Department Of Economic Development | Separation and purification of sugar esters |
| US5491172A (en) * | 1993-05-14 | 1996-02-13 | Warner-Lambert Company | N-acyl sulfamic acid esters (or thioesters), N-acyl sulfonamides, and N-sulfonyl carbamic acid esters (or thioesters) as hypercholesterolemic agents |
| IL109431A (en) | 1993-05-14 | 2001-01-11 | Warner Lambert Co | Pharmaceutical compositions containing n-acyl sulfamic acid esters (or thioesters), n-acyl sulfonamides, and n-sulfonyl carbamic acid esters (or thioesters), for regulating plasma cholesterol concentration, and certain such novel compounds |
| US20030167483A1 (en) * | 1998-06-24 | 2003-09-04 | Farese Robert V. | Diacylglycerol O-acyltransferase |
| WO2000058491A1 (fr) | 1999-03-25 | 2000-10-05 | The Kitasato Institute | Nouvelles substances kf-1040t4a, kf-1040t4b, kf-1040t5a et kf-1040t5b et leur procede de production |
| TW518218B (en) | 1999-05-27 | 2003-01-21 | Merck Patent Gmbh | Pharmaceutical compositions comprising 1-[4-(5-cyanoindol-3-yl)butyl]-4-(2-carbamoylbenzofuran-5-yl)piperazine or its physiologically acceptable salts for use in the treatment of sub-type anxiety disorders |
| GB0021670D0 (en) | 2000-09-04 | 2000-10-18 | Astrazeneca Ab | Chemical compounds |
| CA2369967A1 (fr) | 2001-02-12 | 2002-08-12 | Joseph Anthony Cornicelli | Methodes de traitement de maladies et de troubles relies au facteur nucleaire-kappa b |
| JP2002284741A (ja) | 2001-03-23 | 2002-10-03 | Kitasato Inst:The | ローズリピン誘導体 |
| DE10223273A1 (de) | 2002-05-24 | 2003-12-04 | Aventis Pharma Gmbh | Diarylcycloalkylderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| JP4436129B2 (ja) * | 2001-08-31 | 2010-03-24 | サノフィ−アベンティス・ドイチュラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | ジアリールシクロアルキル誘導体、その製造法及びppar−活性剤としてのその使用 |
| FR2840301B1 (fr) | 2002-05-29 | 2007-03-23 | Sanofi Synthelabo | Derives de phenyl-cyclohexyl-propanolamine, leur preparation et leur applicaton en therapeutique |
| MXPA05000279A (es) * | 2002-07-09 | 2005-03-31 | Squibb Bristol Myers Co | Derivados heterociclicos sustituidos utiles como agentes antidiabeticos y antiobesidad y metodo. |
| EP1541563A4 (fr) | 2002-07-10 | 2007-11-07 | Ono Pharmaceutical Co | Antagoniste du ccr4 et utilisation medicinale correspondante |
| DE50312261D1 (de) * | 2002-07-12 | 2010-02-04 | Sanofi Aventis Deutschland | Heterozyklisch substituierte benzoylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
| JP4164645B2 (ja) | 2002-08-09 | 2008-10-15 | 株式会社大塚製薬工場 | Dgat阻害剤 |
| AU2003265659A1 (en) | 2002-08-23 | 2004-03-11 | University Of Connecticut | Novel biphenyl and biphenyl-like cannabinoids |
| US7189712B2 (en) | 2002-10-10 | 2007-03-13 | Smithkline Beecham Corporation | 1,3-Oxazole compounds for the treatment of cancer |
| AU2003293006A1 (en) | 2002-11-22 | 2004-06-18 | Japan Tobacco Inc. | Fused bicyclic nitrogen-containing heterocycles |
| SG2012000667A (en) | 2003-01-08 | 2015-03-30 | Univ Washington | Antibacterial agents |
| EP1611120A4 (fr) | 2003-04-07 | 2008-04-23 | Cortical Pty Ltd | Nouvelles m thodes de traitement des maladies inflammatoires |
| AR044152A1 (es) | 2003-05-09 | 2005-08-24 | Bayer Corp | Derivados de alquilarilo, metodo de preparacion y uso para el tratamiento de la obesidad |
| EP1628666B1 (fr) | 2003-05-14 | 2015-09-23 | NeuroGenetic Pharmaceuticals, Inc. | Composes et leurs utilisations pour la modulation de l'amyloide-beta |
| EP1653969A4 (fr) * | 2003-08-07 | 2006-12-20 | Japan Tobacco Inc | Derives de pyrrolo 1,2-b pyridazine |
| EP1661889A4 (fr) | 2003-09-05 | 2009-08-05 | Ono Pharmaceutical Co | Antagoniste du recepteur de la chimiokine et son utilisation a des fins medicales |
| US20050143464A1 (en) | 2003-09-22 | 2005-06-30 | Use-Techno Corporation | Insulin secretion potentiator |
| BRPI0415500A (pt) | 2003-10-17 | 2007-04-10 | Incyte Corp | hidroxamatos cìclicos substituìdos como inibidores de metaloproteinases de matriz |
| GB0325192D0 (en) | 2003-10-29 | 2003-12-03 | Astrazeneca Ab | Method of use |
| US20050101660A1 (en) | 2003-11-11 | 2005-05-12 | The Skinny Drink Company | Composition for prevention and treatment of obesity, cardiovascular and coronary artery disease |
| US7507832B2 (en) * | 2003-12-22 | 2009-03-24 | Eli Lilly And Company | Triazole PPAR modulators |
| JP2005206492A (ja) | 2004-01-21 | 2005-08-04 | Sankyo Co Ltd | スルホンアミド化合物 |
| KR20060114376A (ko) | 2004-01-30 | 2006-11-06 | 니뽄 다바코 산교 가부시키가이샤 | 식욕 감퇴 화합물 |
| EP1760071A4 (fr) | 2004-06-23 | 2008-03-05 | Ono Pharmaceutical Co | Composé ayant une activité de liaison aux récepteurs s1p et utilisation de celui-ci |
| TW200606137A (en) * | 2004-07-02 | 2006-02-16 | Sankyo Co | Urea derivatives |
| WO2006019020A1 (fr) | 2004-08-16 | 2006-02-23 | Sankyo Company, Limited | Urées de substitution |
| MX2007004217A (es) | 2004-10-15 | 2007-06-11 | Bayer Pharmaceuticals Corp | Preparacion y uso de derivados de acido bifenil-4-il-carbonilamino para el tratamiento de obesidad. |
| WO2006054370A1 (fr) | 2004-11-16 | 2006-05-26 | Use-Techno Corporation | Agents d’inhibition de la gluconeogenese |
| MX2007007101A (es) * | 2004-12-14 | 2007-08-21 | Astrazeneca Ab | Derivados de oxadiazol como inhibidores de acil coa:diacilglicerol aciltransferasa. |
| WO2006082952A1 (fr) | 2005-02-01 | 2006-08-10 | Takeda Pharmaceutical Company Limited | Composé amide |
| CN101115711A (zh) | 2005-02-07 | 2008-01-30 | 霍夫曼-拉罗奇有限公司 | 二酰基甘油酰基转移酶(dgat)的抑制剂 |
| CN101198333A (zh) | 2005-04-19 | 2008-06-11 | 拜尔药品公司 | 芳烷基酸衍生物及其用途 |
| CN101171231A (zh) | 2005-05-10 | 2008-04-30 | 霍夫曼-拉罗奇有限公司 | 二酰基甘油酰基转移酶抑制剂 |
| EP1893592A1 (fr) * | 2005-06-11 | 2008-03-05 | AstraZeneca AB | Dérivés d oxadiazole en tant qu inhibiteurs de la diacylglycérol acyltransférase (dgat) |
| WO2007007588A1 (fr) | 2005-07-08 | 2007-01-18 | Ono Pharmaceutical Co., Ltd. | Compose comportant un groupe cyclique ayant un noyau plan |
| JP2009505962A (ja) | 2005-07-29 | 2009-02-12 | バイエル・ヘルスケア・エルエルシー | 肥満を治療するためのビフェニルアミノ酸誘導体の製造および使用 |
| JP2007131584A (ja) | 2005-11-11 | 2007-05-31 | Sankyo Co Ltd | 新規ベンゾオキサゾール誘導体 |
| EP1963313B1 (fr) * | 2005-11-28 | 2012-11-14 | Madrigal Pharmaceuticals, Inc. | Inhibiteurs de diacylglycérol acyltransférase (dgat) |
| JP2007191471A (ja) | 2005-12-21 | 2007-08-02 | Sankyo Co Ltd | ウレア誘導体を含有する医薬 |
| AR058562A1 (es) * | 2005-12-22 | 2008-02-13 | Astrazeneca Ab | Derivados de pirimido [4,5 b] (1,4) oxazinas , procedimientos de obtencion y su uso como inhibidores de acetil coa y dgat 1 |
| WO2007074753A1 (fr) | 2005-12-27 | 2007-07-05 | Daiichi Sankyo Company, Limited | Produit pharmaceutique comprenant un dérivé de l'urée substitué |
| WO2007126957A2 (fr) | 2006-03-31 | 2007-11-08 | Novartis Ag | Nouveaux composés |
| CN101541747B (zh) | 2006-04-21 | 2012-11-14 | 伊莱利利公司 | 作为11-β-羟基甾族化合物脱氢酶1的抑制剂的联苯基酰胺内酰胺衍生物 |
| US20080064717A1 (en) | 2006-05-19 | 2008-03-13 | Rajesh Iyengar | Inhibitors of diacylglycerol O-acyltransferase type 1 enzyme |
| US20080015227A1 (en) | 2006-05-19 | 2008-01-17 | Kym Philip R | Inhibitors of diacylglycerol O-acyltransferase type 1 enzyme |
| CA2651663A1 (fr) | 2006-05-30 | 2007-12-06 | Astrazeneca Ab | Composes chimiques |
| BRPI0712802A2 (pt) | 2006-05-30 | 2012-10-23 | Astrazeneca Ab | composto, métodos para produzir uma inibição da atividade de dgat1, e para tratar diabete melito e/ou obesidade em um animal de sangue quente, uso de um composto, composição farmacêutica, e, processo para preparar um composto |
| CN101460469A (zh) * | 2006-06-06 | 2009-06-17 | 阿斯利康(瑞典)有限公司 | 化合物 |
| JP2009539818A (ja) | 2006-06-08 | 2009-11-19 | アストラゼネカ アクチボラグ | ベンゾイミダゾールおよび糖尿病の処置のためのその使用 |
| GB0611507D0 (en) | 2006-06-10 | 2006-07-19 | Astrazeneca Ab | Chemical compounds |
| GB0611506D0 (en) * | 2006-06-10 | 2006-07-19 | Astrazeneca Ab | Chemical compounds |
| GB0611552D0 (en) | 2006-06-12 | 2006-07-19 | Astrazeneca Ab | Chemical compounds |
| JP2009544616A (ja) | 2006-07-21 | 2009-12-17 | 武田薬品工業株式会社 | アミド化合物 |
| US20120065196A1 (en) | 2006-07-21 | 2012-03-15 | Shuji Kitamura | Amide compounds |
| US7569590B2 (en) * | 2006-09-19 | 2009-08-04 | Bristol-Myers Squibb Company | Use of thianecarboxamides as dgat inhibitors |
| KR100811100B1 (ko) | 2006-09-27 | 2008-03-06 | 한국생명공학연구원 | 벤즈아졸 유도체를 유효성분으로 함유하는 대사성 질환예방 및 치료용 약학적 조성물 |
| KR100795462B1 (ko) | 2006-09-27 | 2008-01-16 | 한국생명공학연구원 | 인돌 유도체, 이의 제조방법 및 이를 유효성분으로함유하는 대사성 질환 예방 및 치료용 약학적 조성물 |
| BRPI0717845A2 (pt) | 2006-10-04 | 2015-06-16 | Hoffmann La Roche | Uso de compostos, composições farmacêuticas e métodos para o tratamento e/ou profilaxia de enfermidades que podem ser tratadas com agentes de elevação de colesterol-hdl e compostos |
| WO2008046216A1 (fr) | 2006-10-18 | 2008-04-24 | Methylgene, Inc. | Inhibiteurs de kinase et leurs utilisations |
| AR063311A1 (es) | 2006-10-18 | 2009-01-21 | Novartis Ag | Compuestos organicos |
| WO2008058402A1 (fr) | 2006-11-17 | 2008-05-22 | Queen's University At Kingston | Composés et procédés pour traiter des troubles de repliement de protéine |
| BRPI0719352A2 (pt) | 2006-11-29 | 2017-10-24 | Abbott Lab | inibidores de enzima diacilglicerol o-aciltransferase tipo 1 |
| JP2010512410A (ja) | 2006-12-11 | 2010-04-22 | ノバルティス アーゲー | 心筋虚血を予防または処置するための方法 |
| US20100093733A1 (en) | 2007-02-15 | 2010-04-15 | Prosidion Limited | Amide and urea derivatives for the treatment of metabolic diseases |
| GB0707662D0 (en) | 2007-04-20 | 2007-05-30 | Astrazeneca Ab | Chemical compounds |
| CA2685529A1 (fr) * | 2007-04-30 | 2008-11-06 | Abbott Laboratories | Inhibiteurs d'enzyme diacylglycerol o-acyltransferase de type 1 |
| US8058299B2 (en) * | 2007-05-22 | 2011-11-15 | Via Pharmaceuticals, Inc. | Diacylglycerol acyltransferase inhibitors |
| CN101932562B (zh) * | 2007-12-20 | 2013-06-12 | 阿斯利康(瑞典)有限公司 | 作为dgat1抑制剂190的氨基甲酰基化合物 |
| JP2010132590A (ja) | 2008-12-03 | 2010-06-17 | Astellas Pharma Inc | オキサジアゾール化合物 |
| MX2011006672A (es) * | 2008-12-19 | 2011-07-20 | Astrazeneca Ab | Derivados de 1,3,4-oxadiazol y sus usos para tratar diabetes. |
-
2007
- 2007-05-29 CA CA002651663A patent/CA2651663A1/fr not_active Abandoned
- 2007-05-29 CN CN2007800202196A patent/CN101460470B/zh not_active Expired - Fee Related
- 2007-05-29 AU AU2007266890A patent/AU2007266890B2/en not_active Ceased
- 2007-05-29 MX MX2008015226A patent/MX2008015226A/es not_active Application Discontinuation
- 2007-05-29 BR BRPI0712796-0A patent/BRPI0712796A2/pt not_active IP Right Cessation
- 2007-05-29 KR KR1020087029466A patent/KR20090010092A/ko not_active Withdrawn
- 2007-05-29 JP JP2009512663A patent/JP2009538891A/ja active Pending
- 2007-05-29 US US12/302,192 patent/US8003676B2/en not_active Expired - Fee Related
- 2007-05-29 WO PCT/GB2007/001981 patent/WO2007138304A1/fr not_active Ceased
- 2007-05-29 EP EP07732997A patent/EP2041099A1/fr not_active Withdrawn
- 2007-05-29 NZ NZ572585A patent/NZ572585A/en not_active IP Right Cessation
-
2008
- 2008-11-05 NO NO20084663A patent/NO20084663L/no not_active Application Discontinuation
- 2008-11-05 IL IL195125A patent/IL195125A0/en unknown
- 2008-11-13 ZA ZA200809689A patent/ZA200809689B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2009538891A (ja) | 2009-11-12 |
| AU2007266890A1 (en) | 2007-12-06 |
| CN101460470B (zh) | 2011-05-18 |
| AU2007266890B2 (en) | 2011-02-17 |
| MX2008015226A (es) | 2008-12-12 |
| CN101460470A (zh) | 2009-06-17 |
| EP2041099A1 (fr) | 2009-04-01 |
| BRPI0712796A2 (pt) | 2012-10-02 |
| KR20090010092A (ko) | 2009-01-28 |
| WO2007138304A1 (fr) | 2007-12-06 |
| IL195125A0 (en) | 2011-08-01 |
| ZA200809689B (en) | 2010-04-28 |
| US20100029727A1 (en) | 2010-02-04 |
| CA2651663A1 (fr) | 2007-12-06 |
| NZ572585A (en) | 2011-02-25 |
| US8003676B2 (en) | 2011-08-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO20084663L (no) | 1,3,4-oksadiazol-derivater som DGAT1 inhibitorer | |
| NO20084732L (no) | Substituerte 5-fenylamino- 1, 3, 4-oksadiazol-2-ylcarbonylamino-4-fenoksy-cycloheksane karboksylsyre som inhibitorer av acetyl koenzym A diacylglyserol acyltransferase | |
| NO20091858L (no) | Hydrobenzamid derivater som inhibitorer av HSP90 | |
| NO20083434L (no) | Benzamid- og heteroarenderivater | |
| NO20091893L (no) | Nye 1,4-benzotiepin-1,1-dioksidderivater som er substituert med benzylgrupper, fremgangsmater for fremstilling av medisiner inneholdende forbindelsene og anvendelse derav. | |
| ZA200810739B (en) | Pesticide containing novel pyridyl-methanamine derivative or its salt | |
| NO20092033L (no) | Nye forbindelser | |
| EA201001013A1 (ru) | Бис(сульфониламино)производные для применения в терапии | |
| NO20080865L (no) | Spirokromanonderivater som acetyl-koenzym-A-karboksylase(ACC)inhibitorer | |
| TNSN08407A1 (en) | Organic compounds | |
| WO2007122634A3 (fr) | Inhibiteurs de kinase | |
| EA201000805A1 (ru) | Бис-(сульфониламино)производные в терапии 066 | |
| NO20080789L (no) | 1,4-benzotiazepin 1,1-dioksidderivater, fremgangsmate for fremstilling derav, medikamenter inneholdende denne forbindelsen og anvendelse derav som et hypolipid | |
| NO20064297L (no) | Aminoalkoholforbindelse | |
| Bua et al. | Click-tailed benzenesulfonamides as potent bacterial carbonic anhydrase inhibitors for targeting Mycobacterium tuberculosis and Vibrio cholerae | |
| MX2010001848A (es) | Derivados de oxadiazol como inhibidores de diacilglicerolaciltrans ferasa (dgat). | |
| NO20052074L (no) | Substituerte benzoksazinoner og anvendelser derav. | |
| NO20065880L (no) | 3-Amino-l-arylpropylindoler som monoamin-gjenopptagelsesinhibitor | |
| NO20081216L (no) | Amidderivater | |
| NO20072310L (no) | 1,2,4-triazolylaminoaryl (heteroaryl) sulfonamidderivater | |
| ATE529424T1 (de) | 1-ää2-amino-3-(substituiertes alkyl)-3h- benzimidazolylümethylü-3-substituierte-1,3- dihydrobenzimidazol-2-one als replikationshemmer des respiratorischen syncytialvirus | |
| DK1634595T3 (da) | N-Phenylbenzamidderivater som medikamenter til behandling af kronisk obstruktiv lungesygdom (KOL) | |
| NO20074631L (no) | Nye 3-aryl-1,2-benzisoksazolderivater, forbindelser inneholdende de samme og deres anvendelse | |
| NO20055167L (no) | Nye benzotiadiazinforbindelser, fremgangsmate for deres fremstilling og farmasoytiske sammensetninger inneholdende dem | |
| NO20041761L (no) | Nye hydroksyalkylindolokarbazolforbindelser, fremgangsmate for deres fremstilling og farmasoytiske sammensetninger inneholdende dem |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC2A | Withdrawal, rejection or dismissal of laid open patent application |