IS7999A - Prostaglandín hliðstæður sem EP4 viðtaka mótlyf - Google Patents
Prostaglandín hliðstæður sem EP4 viðtaka mótlyfInfo
- Publication number
- IS7999A IS7999A IS7999A IS7999A IS7999A IS 7999 A IS7999 A IS 7999A IS 7999 A IS7999 A IS 7999A IS 7999 A IS7999 A IS 7999A IS 7999 A IS7999 A IS 7999A
- Authority
- IS
- Iceland
- Prior art keywords
- receptor antagonist
- prostaglandin analogues
- prostaglandin
- analogues
- antagonist
- Prior art date
Links
- 101150109738 Ptger4 gene Proteins 0.000 title 1
- 229940006138 antiglaucoma drug and miotics prostaglandin analogues Drugs 0.000 title 1
- 239000002464 receptor antagonist Substances 0.000 title 1
- 229940044551 receptor antagonist Drugs 0.000 title 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
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Pain & Pain Management (AREA)
- Gastroenterology & Hepatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Oncology (AREA)
- Immunology (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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45770003P | 2003-03-26 | 2003-03-26 | |
| PCT/CA2004/000471 WO2004085431A1 (en) | 2003-03-26 | 2004-03-26 | Prostaglandin analogs as ep4 receptor antagonists |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IS7999A true IS7999A (is) | 2005-08-25 |
Family
ID=33098243
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IS7999A IS7999A (is) | 2003-03-26 | 2005-08-25 | Prostaglandín hliðstæður sem EP4 viðtaka mótlyf |
Country Status (22)
| Country | Link |
|---|---|
| US (4) | US7053085B2 (is) |
| EP (1) | EP1613621B1 (is) |
| JP (1) | JP4866992B2 (is) |
| KR (1) | KR20060002873A (is) |
| CN (1) | CN1764659A (is) |
| AR (1) | AR040806A1 (is) |
| AT (1) | ATE474837T1 (is) |
| BR (1) | BRPI0408690A (is) |
| CA (1) | CA2519938C (is) |
| CL (1) | CL2004000655A1 (is) |
| DE (1) | DE602004028229D1 (is) |
| EC (1) | ECSP056037A (is) |
| ES (1) | ES2347434T3 (is) |
| HR (1) | HRP20050845A2 (is) |
| IS (1) | IS7999A (is) |
| MA (1) | MA27667A1 (is) |
| MX (1) | MXPA05010189A (is) |
| NO (1) | NO20054951L (is) |
| PE (1) | PE20050522A1 (is) |
| RU (1) | RU2005132930A (is) |
| TW (1) | TW200427670A (is) |
| WO (2) | WO2004085431A1 (is) |
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 |
| RU2311409C2 (ru) * | 2003-01-10 | 2007-11-27 | Ф.Хоффманн-Ля Рош Аг | Производные 2-пиперидона в качестве агонистов простагландина |
| US7179820B2 (en) * | 2003-06-06 | 2007-02-20 | Allergan, Inc. | Piperidinyl prostaglandin E analogs |
| BRPI0411057A (pt) * | 2003-06-06 | 2006-07-25 | Allergan Inc | análogos de prostaglandina e de piperidinila |
| 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 |
| CN1845914A (zh) | 2003-09-02 | 2006-10-11 | 默克公司 | 用于治疗眼压过高的眼用组合物 |
| WO2005025568A1 (en) | 2003-09-04 | 2005-03-24 | Merck & Co., Inc. | Ophthalmic compositions for treating ocular hypertension |
| KR20060090801A (ko) | 2003-09-04 | 2006-08-16 | 머크 앤드 캄파니 인코포레이티드 | 고안압증 치료용 안용 조성물 |
| CA2571786A1 (en) * | 2004-07-02 | 2006-02-09 | 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 |
| JP2008518013A (ja) * | 2004-10-26 | 2008-05-29 | アラーガン、インコーポレイテッド | プロスタグランジンep4アゴニストによる処置方法およびデリバリー方法 |
| WO2006052630A1 (en) * | 2004-11-04 | 2006-05-18 | Allergan, Inc. | Therapeutic substituted piperidone compounds |
| EP1847533B1 (en) * | 2005-01-27 | 2013-08-14 | Asahi Kasei Pharma Corporation | Six-membered heterocyclic compound and the use thereof |
| US7531533B2 (en) | 2005-01-27 | 2009-05-12 | Asahi Kasei Pharma Corporation | 6-Membered heterocyclic compound and use thereof |
| EP1912957A4 (en) * | 2005-08-03 | 2009-05-13 | Merck Frosst Canada Ltd | EP4 RECEPTOR AGONIST, COMPOSITIONS AND METHODS |
| EP1912977A4 (en) * | 2005-08-03 | 2009-10-21 | Merck Frosst Canada Ltd | EP4 RECEPTOR AGONIST, COMPOSITIONS AND METHODS |
| UY30121A1 (es) | 2006-02-03 | 2007-08-31 | Glaxo Group Ltd | Nuevos compuestos |
| US7550448B2 (en) * | 2006-05-24 | 2009-06-23 | Allergan, Inc. | Therapeutic compounds |
| US7498447B2 (en) | 2006-05-24 | 2009-03-03 | Allergan, Inc. | Therapeutic compounds |
| WO2008027341A2 (en) * | 2006-08-30 | 2008-03-06 | Merck & Co., Inc. | Topical ophthalmic formulations |
| WO2008027340A2 (en) * | 2006-08-30 | 2008-03-06 | Merck & Co., Inc. | Topical ophthalmic formulations |
| EP3824885A1 (en) | 2006-10-20 | 2021-05-26 | Children's Medical Center Corporation | Method to enhance tissue regeneration |
| 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 |
| AU2007331471C1 (en) | 2006-12-15 | 2013-07-25 | Glaxo Group Limited | Benzamide derivatives as EP4 receptor agonists |
| GB2446652A (en) * | 2007-02-16 | 2008-08-20 | Inion Ltd | Osteogenic compounds |
| AU2008246579A1 (en) | 2007-05-08 | 2008-11-13 | National University Corporation, Hamamatsu University School Of Medicine | Cytotoxic T cell activator comprising EP4 agonist |
| US20100179137A1 (en) * | 2007-06-07 | 2010-07-15 | Takashi Kamikubo | Pyridone compound |
| 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 (en) | 2009-10-14 | 2011-04-21 | Gemmus Pharma, Inc. | Combination therapy treatment for viral infections |
| CA2738045C (en) | 2010-05-28 | 2019-02-19 | Simon Fraser University | Conjugate compounds, methods of making same, and uses thereof |
| AU2014305843B2 (en) | 2013-08-09 | 2019-08-29 | Ardelyx, Inc. | Compounds and methods for inhibiting phosphate transport |
| 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 (ja) * | 2016-01-22 | 2017-07-27 | 武田薬品工業株式会社 | 複素環化合物およびその用途 |
| CN111511736B (zh) | 2017-12-25 | 2023-03-24 | 旭化成制药株式会社 | 含氮6元环化合物 |
| EP4706758A3 (en) | 2019-05-21 | 2026-05-06 | Ardelyx, Inc. | Methods for inhibiting phosphate transport |
| 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 (en) | 1978-08-08 | 1980-02-20 | Beecham Group Plc | Cyclic diamides, a process for their preparation and their pharmaceutical compositions |
| 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 |
| US5296504A (en) * | 1988-09-06 | 1994-03-22 | Kabi Pharmacia | Prostaglandin derivatives for the treatment of glaucoma or ocular hypertension |
| WO1990002553A1 (en) * | 1988-09-06 | 1990-03-22 | Pharmacia Ab | 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 |
| US6586468B1 (en) | 1998-09-14 | 2003-07-01 | Ono Pharmaceutical Co., Ltd. | ω-substituted phenyl-prostaglandin E derivatives and drugs containing the same as the active ingredient |
| WO2000021542A1 (en) | 1998-10-15 | 2000-04-20 | Merck & Co., Inc. | Methods for stimulating bone formation |
| AU2183900A (en) * | 1998-12-24 | 2000-07-31 | Alcon Laboratories, Inc. | Ep4 receptor agonists for treatment of dry eye |
| AP2001002357A0 (en) | 1999-12-22 | 2001-12-31 | Pfizer Prod Inc | EP4 receptor selective agonists in the treatment of osteoporosis. |
| PL358481A1 (en) | 2000-03-17 | 2004-08-09 | Alcon Inc. | 6-hydroxy-indazole derivatives for treating glaucoma |
| WO2001072268A1 (en) | 2000-03-31 | 2001-10-04 | Toray Industries, Inc. | Hair growth or hair formation controlling agents |
| WO2002024647A1 (en) | 2000-09-21 | 2002-03-28 | Ono Pharmaceutical Co., Ltd. | Ep4 receptor agonists containing 8-azaprostaglandin derivatives as the active ingredient |
| PT1339678E (pt) | 2000-11-27 | 2007-11-30 | Pfizer Prod Inc | Agonistas selectivos do receptor ep4 no tratamento de osteoporose |
| JP2004530647A (ja) | 2001-01-30 | 2004-10-07 | メルク エンド カムパニー インコーポレーテッド | 高眼圧治療用眼薬組成物 |
| EP1373545A4 (en) | 2001-03-22 | 2005-07-20 | Merck & Co Inc | Mch1r deficient mice |
| CA2466757A1 (en) | 2001-12-03 | 2003-06-12 | Merck & Co., Inc. | Method for treating ocular hypertension |
| US20040204590A1 (en) | 2001-12-03 | 2004-10-14 | Ogidigben Miller J. | Ep4 receptor agonist, compositions and methods thereof |
| CA2488802A1 (en) | 2002-06-14 | 2003-12-24 | Merck & Co., Inc. | Ophthalmic compositions for treating ocular hypertension |
| JP2005538061A (ja) | 2002-06-17 | 2005-12-15 | メルク エンド カムパニー インコーポレーテッド | 新規maxi−kチャネルブロッカー、その使用方法および製造方法 |
| AU2003247533B2 (en) | 2002-06-17 | 2008-09-18 | Merck & Co., Inc. | Novel maxi-k channel blockers, methods of use and process for making the same |
| US7053085B2 (en) * | 2003-03-26 | 2006-05-30 | Merck & Co. Inc. | EP4 receptor agonist, compositions and methods thereof |
| RU2311409C2 (ru) | 2003-01-10 | 2007-11-27 | Ф.Хоффманн-Ля Рош Аг | Производные 2-пиперидона в качестве агонистов простагландина |
| 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 PE PE2004000303A patent/PE20050522A1/es not_active Application Discontinuation
- 2004-03-24 AR AR20040100984A patent/AR040806A1/es not_active Application Discontinuation
- 2004-03-25 TW TW093108108A patent/TW200427670A/zh unknown
- 2004-03-26 CA CA2519938A patent/CA2519938C/en not_active Expired - Lifetime
- 2004-03-26 CL CL200400655A patent/CL2004000655A1/es unknown
- 2004-03-26 WO PCT/CA2004/000471 patent/WO2004085431A1/en not_active Ceased
- 2004-03-26 WO PCT/CA2004/000470 patent/WO2004085430A1/en not_active Ceased
- 2004-03-26 AT AT04723484T patent/ATE474837T1/de not_active IP Right Cessation
- 2004-03-26 HR HR20050845A patent/HRP20050845A2/xx not_active Application Discontinuation
- 2004-03-26 BR BRPI0408690-2A patent/BRPI0408690A/pt not_active Application Discontinuation
- 2004-03-26 MX MXPA05010189A patent/MXPA05010189A/es unknown
- 2004-03-26 EP EP04723484A patent/EP1613621B1/en not_active Expired - Lifetime
- 2004-03-26 RU RU2005132930/04A patent/RU2005132930A/ru not_active Application Discontinuation
- 2004-03-26 ES ES04723484T patent/ES2347434T3/es not_active Expired - Lifetime
- 2004-03-26 JP JP2006504090A patent/JP4866992B2/ja not_active Expired - Lifetime
- 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 KR KR1020057018107A patent/KR20060002873A/ko not_active Withdrawn
-
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 |
|---|---|
| ECSP056037A (es) | 2006-01-27 |
| CL2004000655A1 (es) | 2005-01-21 |
| RU2005132930A (ru) | 2006-02-10 |
| USRE42562E1 (en) | 2011-07-19 |
| CA2519938C (en) | 2010-11-30 |
| NO20054951D0 (no) | 2005-10-25 |
| MXPA05010189A (es) | 2006-02-22 |
| CN1764659A (zh) | 2006-04-26 |
| CA2519938A1 (en) | 2004-10-07 |
| AU2004224261A1 (en) | 2004-10-07 |
| JP4866992B2 (ja) | 2012-02-01 |
| WO2004085430A1 (en) | 2004-10-07 |
| US7053085B2 (en) | 2006-05-30 |
| US20110237511A1 (en) | 2011-09-29 |
| EP1613621B1 (en) | 2010-07-21 |
| ATE474837T1 (de) | 2010-08-15 |
| HRP20050845A2 (en) | 2006-05-31 |
| US7238710B2 (en) | 2007-07-03 |
| US20040198701A1 (en) | 2004-10-07 |
| BRPI0408690A (pt) | 2006-03-28 |
| EP1613621A1 (en) | 2006-01-11 |
| DE602004028229D1 (de) | 2010-09-02 |
| AR040806A1 (es) | 2005-04-20 |
| PE20050522A1 (es) | 2005-07-06 |
| KR20060002873A (ko) | 2006-01-09 |
| JP2006520758A (ja) | 2006-09-14 |
| US20050227969A1 (en) | 2005-10-13 |
| TW200427670A (en) | 2004-12-16 |
| MA27667A1 (fr) | 2005-12-01 |
| ES2347434T3 (es) | 2010-10-29 |
| WO2004085431A1 (en) | 2004-10-07 |
| NO20054951L (no) | 2005-12-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IS7999A (is) | Prostaglandín hliðstæður sem EP4 viðtaka mótlyf | |
| CY2013035I1 (el) | Μεθοδοι χρησης συνθεσεων αμινοπυριδινης παρατεταμενης αποδεσμευσης | |
| IS2905B (is) | Afleiður (þíó) karbamóýl-sýklóhexans sem mótlyf D3/D2 viðtaka | |
| IS8501A (is) | Azatvíhringja heteróhringir sem kannabínóníð-viðtakastillar | |
| MA28841B1 (fr) | Analogues tetrapeptidiques | |
| EP2096917A4 (en) | Cyclopamine ANALOG | |
| MA28857B1 (fr) | Analogues de pipérazinyl-pyridine biaryliques substitués | |
| IS8345A (is) | 6-útskipt anilínópúrín sem RTK-tálmar | |
| IL184816A0 (en) | 2-phenyl-indoles as prostaglandin d2 receptor antagonists | |
| DK1819670T3 (da) | 12-Aryl-prostaglandinanaloger | |
| IS2756B (is) | Samrunnin heteróhringssambönd sem stillar fyrir viðtaka serótóníns | |
| IL182090A0 (en) | 2,6-substituted-4-monosubstitutedamino-pyrimidine as prostaglandin d2 receptor antagonists | |
| DK1501809T3 (da) | Trizolderivater som tachykininreceptorantagonister | |
| DE602005004011D1 (de) | Hydroisoindolin-tachykininrezeptorantagonisten | |
| NO20054669D0 (no) | Substituerte kinobenzoxazinanaloger | |
| IS8117A (is) | 3-Flúr-píperidín sem NMDA/NR2B mótlyf | |
| DK1776090T3 (da) | Stabiliseret prostaglandinsammensætning | |
| IS2456B (is) | Ímídasókínólínafleiður sem adenósín A3 viðtakabindlar | |
| IS8291A (is) | Pýrról-2,5-tvíþíónafleiður sem lifrar X viðtakastillar | |
| ATE406366T1 (de) | Gehinderte himbacinanaloga als thrombinrezeptorantagonisten | |
| DE602005001661D1 (de) | Vermessungsgerät | |
| EP1888618A4 (en) | Analogs of glycyl-prolyl-glutamate | |
| IS8278A (is) | Sýkóprópýl afleiður sem NK3 viðtaka mótlyf | |
| EP1898905A4 (en) | HYDROISOINDOLIN-tachykinin receptor Antagonist | |
| IS7452A (is) | Prógesterón viðtakastillar sem ekki eru steratengdir |