MA27667A1 - Analogues de la prostaglandine comme antagonistes du recepteur de ep4 - Google Patents
Analogues de la prostaglandine comme antagonistes du recepteur de ep4Info
- Publication number
- MA27667A1 MA27667A1 MA28497A MA28497A MA27667A1 MA 27667 A1 MA27667 A1 MA 27667A1 MA 28497 A MA28497 A MA 28497A MA 28497 A MA28497 A MA 28497A MA 27667 A1 MA27667 A1 MA 27667A1
- Authority
- MA
- Morocco
- Prior art keywords
- receptor antagonists
- prostaglandin analogs
- prostaglandin
- analogs
- glaucoma
- Prior art date
Links
- 150000003180 prostaglandins Chemical class 0.000 title 1
- 239000002464 receptor antagonist Substances 0.000 title 1
- 229940044551 receptor antagonist Drugs 0.000 title 1
- 208000010412 Glaucoma Diseases 0.000 abstract 1
- 102000008866 Prostaglandin E receptors Human genes 0.000 abstract 1
- 108010088540 Prostaglandin E receptors Proteins 0.000 abstract 1
- 239000000556 agonist Substances 0.000 abstract 1
- 230000004410 intraocular pressure Effects 0.000 abstract 1
- 230000003389 potentiating effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D211/74—Oxygen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
- A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- A61P7/10—Antioedematous agents; Diuretics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D211/74—Oxygen atoms
- C07D211/76—Oxygen atoms attached in position 2 or 6
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/04—1,3-Oxazines; Hydrogenated 1,3-oxazines
- C07D265/06—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings
- C07D265/08—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D265/10—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with oxygen atoms directly attached to ring carbon atoms
-
- 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
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
AGONISTE DU RECEPTEUR EP4, COMPOSITIONS ET METHODES POUR CELLES-LA Cette invention concerne des agonistes sélectifs puissants du sous-type EP4 des récepteurs E2 de la prostaglandine, leur usage ou une composition de ceux-là dans le traitement du glaucome et autres affections, qui sont liées à une pression intraoculaire élevée dans l'oeil d'un patient.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45770003P | 2003-03-26 | 2003-03-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA27667A1 true MA27667A1 (fr) | 2005-12-01 |
Family
ID=33098243
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA28497A MA27667A1 (fr) | 2003-03-26 | 2005-09-14 | Analogues de la prostaglandine comme antagonistes du recepteur de ep4 |
Country Status (22)
| Country | Link |
|---|---|
| US (4) | US7053085B2 (fr) |
| EP (1) | EP1613621B1 (fr) |
| JP (1) | JP4866992B2 (fr) |
| KR (1) | KR20060002873A (fr) |
| CN (1) | CN1764659A (fr) |
| AR (1) | AR040806A1 (fr) |
| AT (1) | ATE474837T1 (fr) |
| BR (1) | BRPI0408690A (fr) |
| CA (1) | CA2519938C (fr) |
| CL (1) | CL2004000655A1 (fr) |
| DE (1) | DE602004028229D1 (fr) |
| EC (1) | ECSP056037A (fr) |
| ES (1) | ES2347434T3 (fr) |
| HR (1) | HRP20050845A2 (fr) |
| IS (1) | IS7999A (fr) |
| MA (1) | MA27667A1 (fr) |
| MX (1) | MXPA05010189A (fr) |
| NO (1) | NO20054951L (fr) |
| PE (1) | PE20050522A1 (fr) |
| RU (1) | RU2005132930A (fr) |
| TW (1) | TW200427670A (fr) |
| WO (2) | WO2004085431A1 (fr) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7053085B2 (en) * | 2003-03-26 | 2006-05-30 | Merck & Co. Inc. | EP4 receptor agonist, compositions and methods thereof |
| CA2511255C (fr) * | 2003-01-10 | 2009-04-07 | F. Hoffmann-La Roche Ag | Derives de 2-piperidone agonistes de la prostaglandine |
| US6977260B2 (en) | 2004-01-22 | 2005-12-20 | Allergan, Inc. | Piperidinyl prostaglandin E analogs |
| US7326716B2 (en) | 2003-06-06 | 2008-02-05 | Allergan, Inc. | Treatment of inflammatory bowel disease |
| BRPI0411057A (pt) * | 2003-06-06 | 2006-07-25 | Allergan Inc | análogos de prostaglandina e de piperidinila |
| US7179820B2 (en) | 2003-06-06 | 2007-02-20 | Allergan, Inc. | Piperidinyl prostaglandin E analogs |
| AU2004268012B2 (en) | 2003-09-02 | 2008-11-20 | Merck & Co., Inc. | Ophthalmic compositions for treating ocular hypertension |
| DE602004020079D1 (de) | 2003-09-04 | 2009-04-30 | Merck & Co Inc | Ophthalmische zusammensetzungen zur behandlung der okularen hypertonie |
| AU2004271978B2 (en) | 2003-09-04 | 2009-02-05 | Merck & Co., Inc. | Ophthalmic compositions for treating ocular hypertension |
| US7427614B2 (en) | 2004-07-02 | 2008-09-23 | Allergan, Inc. | Prostaglandin analogs |
| CN1988903A (zh) * | 2004-07-20 | 2007-06-27 | 默克公司 | 用于治疗高眼压症的眼用组合物 |
| AU2005299473B2 (en) * | 2004-10-26 | 2012-06-28 | Allergan, Inc. | Therapeutic and delivery methods of prostaglandin EP4 agonists |
| US7994195B2 (en) * | 2004-11-04 | 2011-08-09 | Allergan, Inc. | Therapeutic substituted piperidone compounds |
| US7531533B2 (en) | 2005-01-27 | 2009-05-12 | Asahi Kasei Pharma Corporation | 6-Membered heterocyclic compound and use thereof |
| CN101133037B (zh) * | 2005-01-27 | 2012-05-09 | 旭化成制药株式会社 | 六元杂环化合物及其用途 |
| AU2006275270A1 (en) * | 2005-08-03 | 2007-02-08 | Merck Frosst Canada Ltd | EP4 receptor agonist, compositions and methods thereof |
| US20090270395A1 (en) * | 2005-08-03 | 2009-10-29 | John Colucci | EP4 Receptor Agonist, Compositions and Methods Thereof |
| UY30121A1 (es) | 2006-02-03 | 2007-08-31 | Glaxo Group Ltd | Nuevos compuestos |
| US7498447B2 (en) | 2006-05-24 | 2009-03-03 | Allergan, Inc. | Therapeutic compounds |
| US7550448B2 (en) | 2006-05-24 | 2009-06-23 | Allergan, Inc. | Therapeutic compounds |
| WO2008027341A2 (fr) * | 2006-08-30 | 2008-03-06 | Merck & Co., Inc. | Formulations ophtalmiques locales |
| WO2008027340A2 (fr) * | 2006-08-30 | 2008-03-06 | Merck & Co., Inc. | Formulations ophtalmiques locales |
| EP2679221B1 (fr) | 2006-10-20 | 2020-09-23 | Children's Medical Center Corporation | Procédé pour améliorer la régénération tissulaire |
| CN101168514B (zh) * | 2006-10-26 | 2011-12-07 | 上海药明康德新药开发有限公司 | 光学活性α-氨基辛二酸酯和α-氨基辛二酸单酯的合成方法 |
| US20080167377A1 (en) | 2006-12-15 | 2008-07-10 | Alessandra Gaiba | Novel compounds |
| GB2446652A (en) * | 2007-02-16 | 2008-08-20 | Inion Ltd | Osteogenic compounds |
| EP2147672A4 (fr) | 2007-05-08 | 2011-11-02 | Nat University Corp Hamamatsu University School Of Medicine | Activateur de cellule t cytotoxique comprenant un agoniste ep4 |
| CN101679262A (zh) * | 2007-06-07 | 2010-03-24 | 安斯泰来制药株式会社 | 吡啶酮化合物 |
| GB0721611D0 (en) | 2007-11-02 | 2007-12-12 | Glaxo Group Ltd | Novel compounds |
| CN101468985A (zh) * | 2007-12-28 | 2009-07-01 | 中国人民解放军军事医学科学院毒物药物研究所 | 5-(3-芳杂环取代苯基)四氮唑类化合物及其抗hiv/aids的应用 |
| US8633310B2 (en) * | 2008-02-19 | 2014-01-21 | Allergan, Inc. | Therapeutic substituted lactams |
| US7964596B2 (en) | 2008-03-07 | 2011-06-21 | Allergan, Inc. | Therapeutic compounds |
| WO2011047048A1 (fr) | 2009-10-14 | 2011-04-21 | Gemmus Pharma, Inc. | Traitement par polythérapie pour infections virales |
| CA2738045C (fr) * | 2010-05-28 | 2019-02-19 | Simon Fraser University | Composes conjugues, leurs procedes de fabrication et leurs utilisations |
| KR102456567B1 (ko) | 2013-08-09 | 2022-10-19 | 알데릭스, 인코포레이티드 | 인산염 수송을 억제하기 위한 화합물 및 방법 |
| US9650414B1 (en) | 2014-05-30 | 2017-05-16 | Simon Fraser University | Dual-action EP4 agonist—bisphosphonate conjugates and uses thereof |
| CN107849072B (zh) | 2015-06-12 | 2020-12-15 | 西蒙弗雷泽大学 | 酰胺连接的ep4激动剂-二膦酸盐化合物及其用途 |
| WO2017126635A1 (fr) * | 2016-01-22 | 2017-07-27 | 武田薬品工業株式会社 | Composé hétérocyclique et utilisation de celui-ci |
| PT3733665T (pt) | 2017-12-25 | 2022-10-21 | Asahi Kasei Pharma Corp | Compostos contendo unidade de 2-oxo-1,3,4-tiadiazinan-3-ilo com atividade agonista do recetor ep4 |
| WO2020237096A1 (fr) | 2019-05-21 | 2020-11-26 | Ardelyx, Inc. | Combinaison pour baisser le phosphate sérique chez un patient |
| CN111269193B (zh) * | 2020-04-02 | 2022-05-24 | 湖南海利常德农药化工有限公司 | 一种苯并[e][1,3]噁嗪-2,4-二酮的制备方法 |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1524818A (en) | 1974-11-29 | 1978-09-13 | Beecham Group Ltd | 12-azaprostaglandins |
| US4177346A (en) | 1976-08-06 | 1979-12-04 | Pfizer Inc. | 1,5-Disubstituted-2-pyrrolidones |
| EP0008186A1 (fr) | 1978-08-08 | 1980-02-20 | Beecham Group Plc | Diamides cycliques, procédé pour leur préparation et leurs compositions pharmaceutiques |
| FR2534580A1 (fr) * | 1982-10-13 | 1984-04-20 | Synthelabo | Derives de phenyl-1 piperidino-2 propanol, leur preparation, et medicaments qui les contiennent |
| US5151444B1 (en) * | 1987-09-18 | 1999-07-06 | R Tech Ueno Ltd | Ocular hypotensive agents |
| US4960771A (en) * | 1988-07-12 | 1990-10-02 | Rajadhyaksha Vithal J | Oxazolidinone penetration enhancing compounds |
| DE1300150T1 (de) * | 1988-09-06 | 2003-09-18 | Pharmacia Ab, Stockholm | Prostaglandin-Derivate zur Behandlung von Glaukom oder Augenüberdruck |
| US5296504A (en) * | 1988-09-06 | 1994-03-22 | Kabi Pharmacia | Prostaglandin derivatives for the treatment of glaucoma or ocular hypertension |
| US5352708A (en) * | 1992-09-21 | 1994-10-04 | Allergan, Inc. | Non-acidic cyclopentane heptanoic acid, 2-cycloalkyl or arylalkyl derivatives as therapeutic agents |
| US5922773A (en) | 1992-12-04 | 1999-07-13 | The Children's Medical Center Corp. | Glaucoma treatment |
| US5510383A (en) * | 1993-08-03 | 1996-04-23 | Alcon Laboratories, Inc. | Use of cloprostenol, fluprostenol and their salts and esters to treat glaucoma and ocular hypertension |
| JPH10265454A (ja) | 1997-01-27 | 1998-10-06 | Ono Pharmaceut Co Ltd | 3,7−ジチアプロスタン酸誘導体、それらの製造方法およびそれらを有効成分として含有する薬剤 |
| US6043275A (en) * | 1998-04-16 | 2000-03-28 | Ono Pharmaceutical Co., Ltd. | 3,7-dithiaprostanoic acid derivative |
| KR20010074981A (ko) | 1998-09-14 | 2001-08-09 | 우에노 도시오 | ω치환된 페닐프로스타그란딘 E 유도체 및 그 유도체를유효 성분으로 하는 약제 |
| EP1121133A1 (fr) | 1998-10-15 | 2001-08-08 | Merck & Co., Inc. | Methodes de stimulation de la formation osseuse |
| AU2183900A (en) * | 1998-12-24 | 2000-07-31 | Alcon Laboratories, Inc. | Ep4 receptor agonists for treatment of dry eye |
| GEP20043203B (en) | 1999-12-22 | 2004-03-25 | Pfizer Prod Inc | EP4 Receptor Selective Agonists in the Treatment of Osteoporosis |
| BR0017157A (pt) | 2000-03-17 | 2002-11-26 | Alcon Inc | Derivados de 6-hidroxi-indazol para o tratamento de glaucoma |
| CN1366458A (zh) | 2000-03-31 | 2002-08-28 | 东丽株式会社 | 毛发生长和毛发形成调节剂 |
| AU2001290250A1 (en) | 2000-09-21 | 2002-04-02 | Ono Pharmaceutical Co. Ltd. | Ep4 receptor agonists containing 8-azaprostaglandin derivatives as the active ingredient |
| OA12533A (en) | 2000-11-27 | 2006-06-05 | Pfizer Prod Inc | Ep4 receptor selective agonists in the treatment of osteoporosis. |
| CA2434495A1 (fr) | 2001-01-30 | 2002-08-08 | Merck & Co., Inc. | Compositions ophtalmiques pouvant traiter l'hypertension oculaire |
| WO2002077168A2 (fr) | 2001-03-22 | 2002-10-03 | Merck & Co., Inc. | Souris deficientes en mch1r |
| WO2003047417A2 (fr) | 2001-12-03 | 2003-06-12 | Merck & Co., Inc. | Agoniste du recepteur ep4, compositions et procedes associes |
| EP1461026A2 (fr) | 2001-12-03 | 2004-09-29 | Merck & Co., Inc. | Methode de traitement de l'hypertension oculaire |
| US20050256117A1 (en) | 2002-06-14 | 2005-11-17 | Meng Hsin Chen | Ophthalmic compositions for treating ocular hypertension |
| EP1515730A4 (fr) | 2002-06-17 | 2005-07-20 | Merck & Co Inc | Nouveaux inhibiteurs de canaux maxi k, methodes d'utilisation et procede de fabrication associe |
| WO2003105724A2 (fr) | 2002-06-17 | 2003-12-24 | Merck & Co., Inc. | Nouveaux bloqueurs de canaux maxi k, methodes d'utilisation et procedes de fabrication associes |
| US7053085B2 (en) * | 2003-03-26 | 2006-05-30 | Merck & Co. Inc. | EP4 receptor agonist, compositions and methods thereof |
| CA2511255C (fr) * | 2003-01-10 | 2009-04-07 | F. Hoffmann-La Roche Ag | Derives de 2-piperidone agonistes de la prostaglandine |
| US6747037B1 (en) * | 2003-06-06 | 2004-06-08 | Allergan, Inc. | Piperidinyl prostaglandin E analogs |
-
2004
- 2004-03-10 US US10/797,257 patent/US7053085B2/en not_active Ceased
- 2004-03-24 AR AR20040100984A patent/AR040806A1/es not_active Application Discontinuation
- 2004-03-24 PE PE2004000303A patent/PE20050522A1/es not_active Application Discontinuation
- 2004-03-25 TW TW093108108A patent/TW200427670A/zh unknown
- 2004-03-26 HR HR20050845A patent/HRP20050845A2/xx not_active Application Discontinuation
- 2004-03-26 WO PCT/CA2004/000471 patent/WO2004085431A1/fr not_active Ceased
- 2004-03-26 CL CL200400655A patent/CL2004000655A1/es unknown
- 2004-03-26 RU RU2005132930/04A patent/RU2005132930A/ru not_active Application Discontinuation
- 2004-03-26 BR BRPI0408690-2A patent/BRPI0408690A/pt not_active Application Discontinuation
- 2004-03-26 KR KR1020057018107A patent/KR20060002873A/ko not_active Withdrawn
- 2004-03-26 CN CNA200480008186XA patent/CN1764659A/zh active Pending
- 2004-03-26 DE DE602004028229T patent/DE602004028229D1/de not_active Expired - Lifetime
- 2004-03-26 EP EP04723484A patent/EP1613621B1/fr not_active Expired - Lifetime
- 2004-03-26 ES ES04723484T patent/ES2347434T3/es not_active Expired - Lifetime
- 2004-03-26 CA CA2519938A patent/CA2519938C/fr not_active Expired - Lifetime
- 2004-03-26 AT AT04723484T patent/ATE474837T1/de not_active IP Right Cessation
- 2004-03-26 MX MXPA05010189A patent/MXPA05010189A/es unknown
- 2004-03-26 WO PCT/CA2004/000470 patent/WO2004085430A1/fr not_active Ceased
- 2004-03-26 JP JP2006504090A patent/JP4866992B2/ja not_active Expired - Lifetime
-
2005
- 2005-06-07 US US11/146,992 patent/US7238710B2/en not_active Expired - Lifetime
- 2005-08-25 IS IS7999A patent/IS7999A/is unknown
- 2005-09-14 MA MA28497A patent/MA27667A1/fr unknown
- 2005-09-23 EC EC2005006037A patent/ECSP056037A/es unknown
- 2005-10-25 NO NO20054951A patent/NO20054951L/no unknown
-
2007
- 2007-04-26 US US11/796,044 patent/USRE42562E1/en not_active Expired - Lifetime
-
2011
- 2011-06-03 US US13/152,586 patent/US20110237511A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20050227969A1 (en) | 2005-10-13 |
| ES2347434T3 (es) | 2010-10-29 |
| HRP20050845A2 (en) | 2006-05-31 |
| JP2006520758A (ja) | 2006-09-14 |
| EP1613621A1 (fr) | 2006-01-11 |
| BRPI0408690A (pt) | 2006-03-28 |
| JP4866992B2 (ja) | 2012-02-01 |
| US7053085B2 (en) | 2006-05-30 |
| WO2004085430A1 (fr) | 2004-10-07 |
| CA2519938C (fr) | 2010-11-30 |
| USRE42562E1 (en) | 2011-07-19 |
| US20110237511A1 (en) | 2011-09-29 |
| TW200427670A (en) | 2004-12-16 |
| NO20054951D0 (no) | 2005-10-25 |
| DE602004028229D1 (de) | 2010-09-02 |
| IS7999A (is) | 2005-08-25 |
| RU2005132930A (ru) | 2006-02-10 |
| WO2004085431A1 (fr) | 2004-10-07 |
| ECSP056037A (es) | 2006-01-27 |
| PE20050522A1 (es) | 2005-07-06 |
| CL2004000655A1 (es) | 2005-01-21 |
| MXPA05010189A (es) | 2006-02-22 |
| NO20054951L (no) | 2005-12-22 |
| AU2004224261A1 (en) | 2004-10-07 |
| AR040806A1 (es) | 2005-04-20 |
| CN1764659A (zh) | 2006-04-26 |
| EP1613621B1 (fr) | 2010-07-21 |
| CA2519938A1 (fr) | 2004-10-07 |
| US20040198701A1 (en) | 2004-10-07 |
| KR20060002873A (ko) | 2006-01-09 |
| ATE474837T1 (de) | 2010-08-15 |
| US7238710B2 (en) | 2007-07-03 |
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