MA28336A1 - Nouveau derive de benzimidazole a substitution 2-heteroaryle - Google Patents
Nouveau derive de benzimidazole a substitution 2-heteroaryleInfo
- Publication number
- MA28336A1 MA28336A1 MA29214A MA29214A MA28336A1 MA 28336 A1 MA28336 A1 MA 28336A1 MA 29214 A MA29214 A MA 29214A MA 29214 A MA29214 A MA 29214A MA 28336 A1 MA28336 A1 MA 28336A1
- Authority
- MA
- Morocco
- Prior art keywords
- prevention
- benzimidazole derivative
- formula
- atom
- nitrogen
- Prior art date
Links
- 150000001556 benzimidazoles Chemical class 0.000 title 1
- 238000006467 substitution reaction Methods 0.000 title 1
- 230000002265 prevention Effects 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 206010012601 diabetes mellitus Diseases 0.000 abstract 2
- 229940124828 glucokinase activator Drugs 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 206010003210 Arteriosclerosis Diseases 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 206010029333 Neurosis Diseases 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 208000017442 Retinal disease Diseases 0.000 abstract 1
- 206010038923 Retinopathy Diseases 0.000 abstract 1
- 208000011775 arteriosclerosis disease Diseases 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 230000001684 chronic effect Effects 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 208000017169 kidney disease Diseases 0.000 abstract 1
- 208000031225 myocardial ischemia Diseases 0.000 abstract 1
- 208000015238 neurotic disease Diseases 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- 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
- C07D401/14—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 three or more hetero rings
-
- 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
- A61K31/4196—1,2,4-Triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- 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
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- 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
- C07D413/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Child & Adolescent Psychology (AREA)
- Emergency Medicine (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Il est proposé un activateur de la glucokinase et un remède et/ou moyen de prévention pour le diabète, et un remède et/ou moyen de prévention pour les complications chroniques du diabète telles que rétinopathie, néphropathie, névrose, cardiopathie ischémique, artérioslérose, et un remède et/ou un moyen de prévention pour l'obésité. Un activateur de la glucokinase caractérisé en ce qu'il contient un dérivé 2-hétéroaryle-benzimidazole substitué ayant la formule générale (I-0) ou son sel phartnaceutiquement acceptable : dans cette formule, X représente un atonie de carbone ou un atome d'azote ; X1, X2, X3 et X4 représentent chacun indépendamment un atome de carbone ou un atome d'azote ; l'anneau A représente un anneau hétéro-aromatique à 5 ou 6 éléments porteur d'azote de formule (II) : R1 représente un aryle, etc.; R2 représente un hydroxy etc.; R3 représente un -C1-6 alkyle, etc.; R4 représente un ¿C1-6 alkyle, etc.; X5 représente -O-, etc.; a représente un nombre entier égal à 1, 2 ou 3; q représente un nombre entier allant de 0 à 2; m indique un nombre entier allant de 0 à 2,
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003436992 | 2003-12-29 | ||
| JP2004235696 | 2004-08-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA28336A1 true MA28336A1 (fr) | 2006-12-01 |
Family
ID=34742165
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA29214A MA28336A1 (fr) | 2003-12-29 | 2006-07-27 | Nouveau derive de benzimidazole a substitution 2-heteroaryle |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US7728025B2 (fr) |
| EP (1) | EP1702919B1 (fr) |
| JP (1) | JP4707560B2 (fr) |
| KR (1) | KR20060105872A (fr) |
| AU (1) | AU2004309287B2 (fr) |
| BR (1) | BRPI0418212A (fr) |
| CA (1) | CA2553160C (fr) |
| EC (1) | ECSP066682A (fr) |
| IL (1) | IL176451A0 (fr) |
| IS (1) | IS8509A (fr) |
| MA (1) | MA28336A1 (fr) |
| NO (1) | NO20063475L (fr) |
| NZ (1) | NZ548128A (fr) |
| RU (1) | RU2329261C2 (fr) |
| WO (1) | WO2005063738A1 (fr) |
Families Citing this family (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0102299D0 (sv) | 2001-06-26 | 2001-06-26 | Astrazeneca Ab | Compounds |
| SE0102764D0 (sv) | 2001-08-17 | 2001-08-17 | Astrazeneca Ab | Compounds |
| GB0226931D0 (en) | 2002-11-19 | 2002-12-24 | Astrazeneca Ab | Chemical compounds |
| GB0226930D0 (en) | 2002-11-19 | 2002-12-24 | Astrazeneca Ab | Chemical compounds |
| TW200600086A (en) | 2004-06-05 | 2006-01-01 | Astrazeneca Ab | Chemical compound |
| KR20070085371A (ko) | 2004-10-16 | 2007-08-27 | 아스트라제네카 아베 | 페녹시 벤즈아미드 화합물의 제조 방법 |
| CA2586056C (fr) | 2004-11-02 | 2012-03-13 | Banyu Pharmaceutical Co., Ltd. | Derives de benzimidazole aryloxy-substitues |
| TW200714597A (en) | 2005-05-27 | 2007-04-16 | Astrazeneca Ab | Chemical compounds |
| CA2614746C (fr) | 2005-07-09 | 2011-05-10 | Astrazeneca Ab | Derives d'heteroaryl benzamide utilises en tant qu'activateurs de la glk dans le traitement du diabete |
| EP1905769B1 (fr) * | 2005-07-13 | 2017-03-29 | Msd K.K. | Dérivé du benzimidazole à substitution par un hétérocycle |
| JP2007063225A (ja) | 2005-09-01 | 2007-03-15 | Takeda Chem Ind Ltd | イミダゾピリジン化合物 |
| EP1928874A1 (fr) * | 2005-09-16 | 2008-06-11 | AstraZeneca AB | Composés hétérobicycliques utilisés comme activateurs de la glucokinase |
| JP2009509988A (ja) | 2005-09-29 | 2009-03-12 | サノフィ−アベンティス | フェニル−及びピリジニル−1,2,4−オキサジアゾロン誘導体、その製造方法、及び医薬品としてのその使用 |
| US7625890B2 (en) | 2005-11-10 | 2009-12-01 | Smithkline Beecham Corp. | Substituted imidazo[4,5-c]pyridine compounds as Akt inhibitors |
| JP2009515997A (ja) * | 2005-11-18 | 2009-04-16 | タケダ サン ディエゴ インコーポレイテッド | グルコキナーゼ活性剤 |
| TW200738621A (en) | 2005-11-28 | 2007-10-16 | Astrazeneca Ab | Chemical process |
| ATE545637T1 (de) * | 2005-12-15 | 2012-03-15 | Astrazeneca Ab | Substituierte diphenylether, -amine, -sulfide und methane zur behandlung von atemwegserkrankungen |
| US7560551B2 (en) | 2006-01-23 | 2009-07-14 | Amgen Inc. | Aurora kinase modulators and method of use |
| AU2007208351C1 (en) * | 2006-01-23 | 2011-07-07 | Amgen Inc. | Aurora kinase modulators and method of use |
| PE20080359A1 (es) | 2006-04-19 | 2008-06-06 | Novartis Ag | Compuestos de benzoxazol y benzotiazol 6-0-sustituidos y metodos de inhibicion de la senalizacion de csf-1r |
| PE20110235A1 (es) | 2006-05-04 | 2011-04-14 | Boehringer Ingelheim Int | Combinaciones farmaceuticas que comprenden linagliptina y metmorfina |
| EP2077267A4 (fr) * | 2006-10-18 | 2010-04-07 | Takeda Pharmaceutical | Composé hétérocyclique fusionné |
| TW200825063A (en) | 2006-10-23 | 2008-06-16 | Astrazeneca Ab | Chemical compounds |
| SA07280576B1 (ar) | 2006-10-26 | 2011-06-22 | استرازينيكا ايه بي | مركبات بنزويل أمينو سيكليل غير متجانسة بأعتبارها عوامل منشطة للجلوكوكيناز |
| UY30822A1 (es) | 2006-12-21 | 2008-07-31 | Astrazeneca Ab | Fnueva forma cristalina de 3-{[5-azetidin-1-ylcabonyl)pyrazin-2-yl]oxy}-5-[1-methylethyloxy]-n-1h-pyrazol-3-ylbenzamida, composiciones conteniéndola, procesos de preparacion y aplicaciones |
| JPWO2008136428A1 (ja) * | 2007-04-27 | 2010-07-29 | 武田薬品工業株式会社 | 含窒素5員複素環化合物 |
| JP5301456B2 (ja) | 2007-11-12 | 2013-09-25 | Msd株式会社 | ヘテロアリールオキシキナゾリン誘導体 |
| PT2239253E (pt) * | 2008-02-06 | 2013-09-17 | Daiichi Sankyo Co Ltd | Novo derivado de fenilpirrole |
| EP2294066B9 (fr) | 2008-04-28 | 2015-03-11 | Janssen Pharmaceutica, N.V. | Benzoimidazoles comme inhibiteurs de la prolyl hydroxylase |
| CA2732165A1 (fr) | 2008-08-04 | 2010-02-11 | Astrazeneca Ab | Agents therapeutiques 414 |
| JP2012500181A (ja) | 2008-08-15 | 2012-01-05 | Msd株式会社 | アセチルピロリジニルインドール誘導体 |
| US8609699B2 (en) * | 2008-08-29 | 2013-12-17 | Msd K.K. | Oxotetrahydrofuran-2-yl-benzimidazole derivative |
| US8703778B2 (en) | 2008-09-26 | 2014-04-22 | Intellikine Llc | Heterocyclic kinase inhibitors |
| GB0902434D0 (en) | 2009-02-13 | 2009-04-01 | Astrazeneca Ab | Chemical process |
| GB0902406D0 (en) | 2009-02-13 | 2009-04-01 | Astrazeneca Ab | Crystalline polymorphic form |
| AR076221A1 (es) * | 2009-04-09 | 2011-05-26 | Astrazeneca Ab | Derivado de pirazol [4,5-e] pirimidina y su uso para tratar diabetes y obesidad |
| AR076220A1 (es) | 2009-04-09 | 2011-05-26 | Astrazeneca Ab | Derivados de pirazol [4,5 - e] pirimidina |
| UY32799A (es) | 2009-07-24 | 2011-02-28 | Novartis Ag | Derivados de oxazina y su uso en el tratamiento de trastornos neurológicos |
| BR112012010738A2 (pt) | 2009-11-06 | 2019-09-24 | Univ Vanderbilt | ''aril e heteroaril sulfonas como potenciadores alostéricos de mglur4,composições e métodos de tratamento de disfunção neurológica'' |
| PH12012501104A1 (en) * | 2009-12-04 | 2014-10-14 | Nissan Chemical Ind Ltd | 2-pyridone compounds |
| KR20120118008A (ko) * | 2009-12-18 | 2012-10-25 | 아이데닉스 파마슈티칼스, 인코포레이티드 | 5,5-융합 아릴렌 또는 헤테로아릴렌 간염 c 바이러스 억제제 |
| WO2011080176A1 (fr) | 2009-12-31 | 2011-07-07 | Novartis Ag | Derives de pyrazine et leur utilisation dans le traitement de troubles neurologiques |
| PH12012500361A1 (en) | 2010-07-13 | 2012-01-19 | Novartis Ag | Oxazine derivatives and their use in the treatment of neurological disorders |
| CN103429589A (zh) | 2011-01-12 | 2013-12-04 | 诺瓦提斯公司 | 噁嗪衍生物及其在治疗神经障碍中的用途 |
| US9273034B2 (en) | 2011-10-25 | 2016-03-01 | Janssen Pharmaceutica Nv | Meglumine salt formulations of 1-(5,6-dichloro-1H-benzo[D]imidazol-2-yl)-1H-pyrazole-4-carboxylic acid |
| WO2015035223A1 (fr) | 2013-09-09 | 2015-03-12 | Peloton Therapeutics, Inc. | Aryléthers et utilisations de ceux-ci |
| US10278942B2 (en) | 2015-03-11 | 2019-05-07 | Peloton Therapeutics, Inc. | Compositions for use in treating pulmonary arterial hypertension |
| WO2016145045A1 (fr) | 2015-03-11 | 2016-09-15 | Peloton Therapeutics, Inc. | Compositions s'utilisant dans le traitement du glioblastome |
| WO2016144826A1 (fr) | 2015-03-11 | 2016-09-15 | Peloton Therapeutics, Inc. | Pyridines substituées et leurs utilisations |
| US10807948B2 (en) | 2015-03-11 | 2020-10-20 | Peloton Therapeutics, Inc. | Aromatic compounds and uses thereof |
| WO2016168510A1 (fr) | 2015-04-17 | 2016-10-20 | Peloton Therapeutics, Inc. | Thérapie combinée avec un inhibiteur de hif-2-alpha et un agent immunothérapeutique, et applications corresponantes |
| CN108349979B (zh) | 2015-11-02 | 2021-04-09 | 詹森药业有限公司 | [1,2,4]三唑并[1,5-a]嘧啶-7-基化合物 |
| EA039102B1 (ru) | 2016-11-02 | 2021-12-03 | Янссен Фармацевтика Нв | Соединения [1,2,4]триазоло[1,5-a]пиримидина в качестве ингибиторов pde2 |
| CN109890824B (zh) | 2016-11-02 | 2022-05-24 | 詹森药业有限公司 | 作为pde2抑制剂的[1,2,4]三唑并[1,5-a]嘧啶化合物 |
| MY193511A (en) | 2016-11-02 | 2022-10-17 | Janssen Pharmaceutica Nv | [1,2,4]triazolo[1,5-a]pyrimidine derivatives as pde2 inhibitors |
| KR20240035820A (ko) | 2021-07-09 | 2024-03-18 | 플렉시움 인코포레이티드 | Ikzf2를 조절하는 아릴 화합물 및 약학 조성물 |
| WO2025111224A1 (fr) * | 2023-11-21 | 2025-05-30 | Fmc Corporation | Composés bicycliques liés pour lutter contre les nuisibles invertébrés et combattre ceux-ci |
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|---|---|---|---|---|
| NL134354C (fr) * | 1963-05-23 | |||
| US3536809A (en) | 1969-02-17 | 1970-10-27 | Alza Corp | Medication method |
| US3598123A (en) | 1969-04-01 | 1971-08-10 | Alza Corp | Bandage for administering drugs |
| US3845770A (en) | 1972-06-05 | 1974-11-05 | Alza Corp | Osmatic dispensing device for releasing beneficial agent |
| US3916899A (en) | 1973-04-25 | 1975-11-04 | Alza Corp | Osmotic dispensing device with maximum and minimum sizes for the passageway |
| US4008719A (en) | 1976-02-02 | 1977-02-22 | Alza Corporation | Osmotic system having laminar arrangement for programming delivery of active agent |
| EP0726260A1 (fr) | 1995-02-08 | 1996-08-14 | American Cyanamid Company | (1,2,4)Thiadiazoles herbicides |
| PE92198A1 (es) | 1996-08-01 | 1999-01-09 | Banyu Pharma Co Ltd | Derivados de 1,4-piperidina disustituida que contienen fluor |
| KR20010015910A (ko) | 1998-01-23 | 2001-02-26 | 로렌스 티. 마이젠헬더 | 옥사졸리디논 조합 라이브러리, 조성물 및 제조 방법 |
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| US7064215B2 (en) * | 2001-07-03 | 2006-06-20 | Chiron Corporation | Indazole benzimidazole compounds |
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| CA2586056C (fr) | 2004-11-02 | 2012-03-13 | Banyu Pharmaceutical Co., Ltd. | Derives de benzimidazole aryloxy-substitues |
| TW200745031A (en) | 2005-10-13 | 2007-12-16 | Merck & Co Inc | Acyl indoles, compositions containing such compounds and methods of use |
| TW200821284A (en) | 2006-10-03 | 2008-05-16 | Merck & Co Inc | Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use |
-
2004
- 2004-12-28 CA CA2553160A patent/CA2553160C/fr not_active Expired - Fee Related
- 2004-12-28 AU AU2004309287A patent/AU2004309287B2/en not_active Ceased
- 2004-12-28 BR BRPI0418212-0A patent/BRPI0418212A/pt not_active IP Right Cessation
- 2004-12-28 RU RU2006127420/04A patent/RU2329261C2/ru not_active IP Right Cessation
- 2004-12-28 EP EP04808192A patent/EP1702919B1/fr not_active Expired - Lifetime
- 2004-12-28 JP JP2005516745A patent/JP4707560B2/ja not_active Expired - Fee Related
- 2004-12-28 NZ NZ548128A patent/NZ548128A/en unknown
- 2004-12-28 KR KR1020067013089A patent/KR20060105872A/ko not_active Ceased
- 2004-12-28 US US10/582,564 patent/US7728025B2/en not_active Expired - Lifetime
- 2004-12-28 WO PCT/JP2004/019843 patent/WO2005063738A1/fr not_active Ceased
-
2006
- 2006-06-15 IS IS8509A patent/IS8509A/xx unknown
- 2006-06-20 IL IL176451A patent/IL176451A0/en unknown
- 2006-06-28 EC EC2006006682A patent/ECSP066682A/es unknown
- 2006-07-27 MA MA29214A patent/MA28336A1/fr unknown
- 2006-07-28 NO NO20063475A patent/NO20063475L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0418212A (pt) | 2007-04-27 |
| EP1702919A4 (fr) | 2008-11-12 |
| ECSP066682A (es) | 2006-10-25 |
| CA2553160A1 (fr) | 2005-07-14 |
| JP4707560B2 (ja) | 2011-06-22 |
| KR20060105872A (ko) | 2006-10-11 |
| RU2329261C2 (ru) | 2008-07-20 |
| US7728025B2 (en) | 2010-06-01 |
| NZ548128A (en) | 2010-05-28 |
| NO20063475L (no) | 2006-09-28 |
| RU2006127420A (ru) | 2008-02-10 |
| CA2553160C (fr) | 2010-09-28 |
| JPWO2005063738A1 (ja) | 2007-07-19 |
| AU2004309287B2 (en) | 2008-07-31 |
| EP1702919A1 (fr) | 2006-09-20 |
| IL176451A0 (en) | 2006-10-05 |
| EP1702919B1 (fr) | 2012-05-30 |
| US20080070928A1 (en) | 2008-03-20 |
| WO2005063738A1 (fr) | 2005-07-14 |
| IS8509A (is) | 2006-06-15 |
| AU2004309287A1 (en) | 2005-07-14 |
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