KR100702368B1 - 프로스타노이드 작용제로서의 2 피롤리돈 유도체 - Google Patents
프로스타노이드 작용제로서의 2 피롤리돈 유도체 Download PDFInfo
- Publication number
- KR100702368B1 KR100702368B1 KR1020047000756A KR20047000756A KR100702368B1 KR 100702368 B1 KR100702368 B1 KR 100702368B1 KR 1020047000756 A KR1020047000756 A KR 1020047000756A KR 20047000756 A KR20047000756 A KR 20047000756A KR 100702368 B1 KR100702368 B1 KR 100702368B1
- Authority
- KR
- South Korea
- Prior art keywords
- oxo
- hydroxy
- pyrrolidin
- compound
- enyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 CCOC(COCC=CC*(C(CC1)C(*)=O)C1=O)=O Chemical compound CCOC(COCC=CC*(C(CC1)C(*)=O)C1=O)=O 0.000 description 2
- CTHZICXYLKQMKI-FOSBLDSVSA-N CCCCC[C@@H](/C=C/[C@@H](CC1)[C@@H](C/C=C\CCCC(O)=O)C1=O)O Chemical compound CCCCC[C@@H](/C=C/[C@@H](CC1)[C@@H](C/C=C\CCCC(O)=O)C1=O)O CTHZICXYLKQMKI-FOSBLDSVSA-N 0.000 description 1
- ANOSANQSQYFRKI-UHFFFAOYSA-N CCOC(COCCCCN)=C Chemical compound CCOC(COCCCCN)=C ANOSANQSQYFRKI-UHFFFAOYSA-N 0.000 description 1
- IDJGICDLEQWBMA-UHFFFAOYSA-N OCC(CCC1=O)N1OCc1ccccc1 Chemical compound OCC(CCC1=O)N1OCc1ccccc1 IDJGICDLEQWBMA-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
- C07D207/27—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
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- 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
-
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- 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
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- 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
-
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P11/06—Antiasthmatics
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- 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
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
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- A—HUMAN NECESSITIES
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- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A—HUMAN NECESSITIES
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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- 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
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- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A61P31/04—Antibacterial agents
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- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- 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
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- 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
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- 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
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- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- 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
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/273—2-Pyrrolidones with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/46—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Physical Education & Sports Medicine (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Transplantation (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Vascular Medicine (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Dermatology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US30576201P | 2001-07-16 | 2001-07-16 | |
| US60/305,762 | 2001-07-16 | ||
| PCT/EP2002/007733 WO2003007941A1 (en) | 2001-07-16 | 2002-07-11 | 2 pyrrolidone derivatives as prostanoid agonists |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20040017317A KR20040017317A (ko) | 2004-02-26 |
| KR100702368B1 true KR100702368B1 (ko) | 2007-04-02 |
Family
ID=23182225
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020047000756A Expired - Fee Related KR100702368B1 (ko) | 2001-07-16 | 2002-07-11 | 프로스타노이드 작용제로서의 2 피롤리돈 유도체 |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US6849657B2 (enExample) |
| EP (1) | EP1408961B1 (enExample) |
| JP (2) | JP4211605B2 (enExample) |
| KR (1) | KR100702368B1 (enExample) |
| CN (1) | CN100371322C (enExample) |
| AT (1) | ATE366571T1 (enExample) |
| AU (1) | AU2002328338C1 (enExample) |
| BR (1) | BR0211167A (enExample) |
| CA (1) | CA2451393C (enExample) |
| DE (1) | DE60221130T2 (enExample) |
| DK (1) | DK1408961T3 (enExample) |
| ES (1) | ES2289140T3 (enExample) |
| GT (1) | GT200200152A (enExample) |
| MX (1) | MXPA04000454A (enExample) |
| PA (1) | PA8550501A1 (enExample) |
| PE (1) | PE20030286A1 (enExample) |
| PL (1) | PL215425B1 (enExample) |
| PT (1) | PT1408961E (enExample) |
| RU (1) | RU2296122C2 (enExample) |
| WO (1) | WO2003007941A1 (enExample) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60221130T2 (de) * | 2001-07-16 | 2008-03-13 | F. Hoffmann-La Roche Ag | 2 pyrrolidon-derivate als prostanoid-agonisten |
| CA2454584C (en) * | 2001-07-23 | 2009-09-22 | Ono Pharmaceutical Co., Ltd. | Pharmaceutical composition for treatment of diseases associated with decrease in bone mass comprising ep4 agonist as active ingredient |
| JP2005519879A (ja) * | 2001-12-03 | 2005-07-07 | メルク エンド カムパニー インコーポレーテッド | Ep4受容体作動剤とその組成物および方法 |
| WO2003074483A1 (en) * | 2002-03-05 | 2003-09-12 | Ono Pharmaceutical Co., Ltd. | 8-azaprostaglandin derivative compounds and drugs containing the compounds as the active ingredient |
| US6573294B1 (en) | 2002-05-14 | 2003-06-03 | Allergan, Inc. | 8-azaprostaglandin analogs as agents for lowering intraocular pressure |
| WO2003103604A2 (en) | 2002-06-01 | 2003-12-18 | Applied Research Systems Ars Holding N.V | Gamma lactams as prostaglandin agonists and use thereof |
| US8114391B2 (en) | 2002-12-26 | 2012-02-14 | Dow Corning Toray Company, Ltd. | Hair care composition |
| JP2006515015A (ja) * | 2003-01-10 | 2006-05-18 | エフ.ホフマン−ラ ロシュ アーゲー | プロスタグランジンアゴニストとしての2−ピペリドン誘導体 |
| EP1603874B1 (en) | 2003-03-03 | 2008-05-07 | Laboratoires Serono SA | G-lactam derivatives as prostaglandin agonists |
| US6734206B1 (en) | 2003-06-02 | 2004-05-11 | Allergan, Inc. | 3-oxa-8-azaprostaglandin analogs as agents for lowering intraocular pressure |
| US6734201B1 (en) | 2003-06-02 | 2004-05-11 | Allergan, Inc. | 8-Azaprostaglandin carbonate and thiocarbonate analogs as therapeutic agents |
| ES2381377T3 (es) * | 2004-06-04 | 2012-05-25 | Allergan, Inc. | Análogos de piperidinilprostaglandina como agentes hipotensores oculares |
| JP5128954B2 (ja) | 2004-12-06 | 2013-01-23 | メルク セローノ ソシエテ アノニム | Dp1受容体アゴニストとして使用されるピロリジン−2−オン誘導体 |
| JP5014978B2 (ja) * | 2005-01-27 | 2012-08-29 | 旭化成ファーマ株式会社 | ヘテロ6員環化合物及びその用途 |
| US7531533B2 (en) | 2005-01-27 | 2009-05-12 | Asahi Kasei Pharma Corporation | 6-Membered heterocyclic compound and use thereof |
| US8524731B2 (en) * | 2005-03-07 | 2013-09-03 | The University Of Chicago | Use of opioid antagonists to attenuate endothelial cell proliferation and migration |
| US8372912B2 (en) * | 2005-08-12 | 2013-02-12 | Eastman Chemical Company | Polyvinyl chloride compositions |
| CN101511958B (zh) * | 2006-08-30 | 2012-09-05 | 伊士曼化工公司 | 乙酸乙烯酯聚合物组合物中作为增塑剂的对苯二甲酸酯 |
| PL2057243T3 (pl) | 2006-08-30 | 2013-04-30 | Eastman Chem Co | Kompozycje szczeliwa z nowym plastyfikatorem |
| EP2147672A4 (en) | 2007-05-08 | 2011-11-02 | Nat University Corp Hamamatsu University School Of Medicine | CYTOTOXIC T CELL ACTIVATOR WITH AN EP4 AGONIST |
| US20120142684A1 (en) * | 2010-12-02 | 2012-06-07 | Allergan, Inc. | Compounds and methods for skin repair |
| TW201321003A (zh) | 2011-08-02 | 2013-06-01 | Ono Pharmaceutical Co | 左心室擴張機能改善劑 |
| WO2014015247A1 (en) | 2012-07-19 | 2014-01-23 | Cayman Chemical Company, Inc. | Difluorolactam compounds as ep4 receptor-selective agonists for use in the treatment of ep4-mediated disease and conditions |
| JP6317807B2 (ja) | 2013-03-15 | 2018-04-25 | ケイマン ケミカル カンパニー, インコーポレーテッド | Ep4媒介性の疾病及び病態の治療に使用するためのep4受容体選択性アゴニストとしてのラクタム化合物 |
| WO2014144610A1 (en) | 2013-03-15 | 2014-09-18 | Cayman Chemical Company, Inc. | Lactam compounds as ep4 receptor-selective agonists for use in the treatment of ep4-mediated diseases and conditions |
| US9914725B2 (en) | 2013-03-15 | 2018-03-13 | Cayman Chemical Company, Inc. | Methods of synthesizing a difluorolactam analog |
| CA2910398A1 (en) | 2013-07-19 | 2015-01-22 | Cayman Chemical Company, Inc. | Methods, systems, and compositions for promoting bone growth |
| ES2929799T3 (es) | 2017-12-25 | 2022-12-01 | Asahi Kasei Pharma Corp | Compuestos que contienen resto de 2-oxo-1,3,4-tiadiazinan-3-ilo con actividad agonista del receptor EP4 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2618341A1 (de) * | 1975-04-28 | 1976-11-11 | Syntex Inc | Neue dl-8-aza-9-keto-15-hydroxy- prostan- und -prost-13-trans-ensaeuren, deren 15-methylderivate und pharmazeutisch zulaessige, nicht toxische niederalkylester und salze der carbonsaeurefunktion sowie verfahren zur herstellung solcher verbindungen |
| EP1097922A1 (en) * | 1998-07-15 | 2001-05-09 | Ono Pharmaceutical Co., Ltd. | 5-thia-omega-substituted phenyl-prostaglandin e derivatives, process for producing the same and drugs containing the same as the active ingredient |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3975399A (en) * | 1974-08-06 | 1976-08-17 | E. I. Du Pont De Nemours And Company | 1,5-Disubstituted-2-pyrrolidinones, -3-pyrrolin-2-ones, and -4-pyrrolin-2-ones |
| US4113873A (en) * | 1975-04-26 | 1978-09-12 | Tanabe Seiyaku Co. Ltd. | 8-azaprostanoic acid derivatives |
| DE2556326A1 (de) | 1975-12-13 | 1977-06-23 | Hoechst Ag | Neue pyrrolidone und verfahren zu ihrer herstellung |
| DE2528664A1 (de) | 1975-06-27 | 1977-01-13 | Hoechst Ag | Pyrrolidone und verfahren zu ihrer herstellung |
| IL49325A (en) * | 1976-03-31 | 1979-11-30 | Labaz | 8-aza-11-deoxy-pge1 derivatives,their preparation and pharmaceutical compositions containing them |
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| JP2571250B2 (ja) * | 1987-01-19 | 1997-01-16 | 三共株式会社 | プロスタグランジン化合物 |
| SE9702681D0 (sv) * | 1997-07-10 | 1997-07-10 | Pharmacia & Upjohn Ab | Method and composition for treatment of impotence |
| JP2002527400A (ja) | 1998-10-15 | 2002-08-27 | メルク エンド カムパニー インコーポレーテッド | 骨形成刺激方法 |
| CA2346038A1 (en) | 1998-10-15 | 2000-04-20 | Merck & Co., Inc. | Methods for inhibiting bone resorption |
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| TWI247606B (en) * | 1999-11-24 | 2006-01-21 | Ono Pharmaceutical Co | Treating agent for osteopenic diseases |
| MXPA02006322A (es) * | 1999-12-22 | 2002-12-13 | Pfizer Prod Inc | Agonistas selectivos del receptor ep4 en el tratamiento de la osteoporosis. |
| ATE327751T1 (de) * | 2000-01-31 | 2006-06-15 | Pfizer Prod Inc | Verwendung von aktivatoren des prostaglandinrezeptores 4 zur behandlung von akuter oder chronischer niereninsuffizienz |
| AU2001235990A1 (en) * | 2000-02-28 | 2001-09-03 | Fumie Sato | Prostaglandin e derivatives |
| AU2001290250A1 (en) | 2000-09-21 | 2002-04-02 | Ono Pharmaceutical Co. Ltd. | Ep4 receptor agonists containing 8-azaprostaglandin derivatives as the active ingredient |
| MXPA03004623A (es) * | 2000-11-27 | 2003-09-05 | Pfizer Prod Inc | Agonistas selectivos del receptor ep4 en el tratamiento de la osteoporosis. |
| DE60221130T2 (de) * | 2001-07-16 | 2008-03-13 | F. Hoffmann-La Roche Ag | 2 pyrrolidon-derivate als prostanoid-agonisten |
-
2002
- 2002-07-11 DE DE60221130T patent/DE60221130T2/de not_active Expired - Lifetime
- 2002-07-11 DK DK02762347T patent/DK1408961T3/da active
- 2002-07-11 WO PCT/EP2002/007733 patent/WO2003007941A1/en not_active Ceased
- 2002-07-11 ES ES02762347T patent/ES2289140T3/es not_active Expired - Lifetime
- 2002-07-11 EP EP02762347A patent/EP1408961B1/en not_active Expired - Lifetime
- 2002-07-11 PL PL367696A patent/PL215425B1/pl not_active IP Right Cessation
- 2002-07-11 KR KR1020047000756A patent/KR100702368B1/ko not_active Expired - Fee Related
- 2002-07-11 CN CNB028142675A patent/CN100371322C/zh not_active Expired - Fee Related
- 2002-07-11 JP JP2003513549A patent/JP4211605B2/ja not_active Expired - Fee Related
- 2002-07-11 AT AT02762347T patent/ATE366571T1/de active
- 2002-07-11 AU AU2002328338A patent/AU2002328338C1/en not_active Ceased
- 2002-07-11 BR BR0211167-5A patent/BR0211167A/pt not_active IP Right Cessation
- 2002-07-11 MX MXPA04000454A patent/MXPA04000454A/es active IP Right Grant
- 2002-07-11 RU RU2004104627/04A patent/RU2296122C2/ru not_active IP Right Cessation
- 2002-07-11 CA CA2451393A patent/CA2451393C/en not_active Expired - Fee Related
- 2002-07-11 PT PT02762347T patent/PT1408961E/pt unknown
- 2002-07-15 GT GT200200152A patent/GT200200152A/es unknown
- 2002-07-15 PE PE2002000629A patent/PE20030286A1/es not_active Application Discontinuation
- 2002-07-15 PA PA20028550501A patent/PA8550501A1/es unknown
- 2002-07-16 US US10/197,279 patent/US6849657B2/en not_active Expired - Lifetime
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2008
- 2008-06-13 JP JP2008155799A patent/JP5003601B2/ja not_active Expired - Fee Related
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| Publication number | Priority date | Publication date | Assignee | Title |
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| DE2618341A1 (de) * | 1975-04-28 | 1976-11-11 | Syntex Inc | Neue dl-8-aza-9-keto-15-hydroxy- prostan- und -prost-13-trans-ensaeuren, deren 15-methylderivate und pharmazeutisch zulaessige, nicht toxische niederalkylester und salze der carbonsaeurefunktion sowie verfahren zur herstellung solcher verbindungen |
| EP1097922A1 (en) * | 1998-07-15 | 2001-05-09 | Ono Pharmaceutical Co., Ltd. | 5-thia-omega-substituted phenyl-prostaglandin e derivatives, process for producing the same and drugs containing the same as the active ingredient |
Also Published As
| Publication number | Publication date |
|---|---|
| DE60221130D1 (de) | 2007-08-23 |
| CN100371322C (zh) | 2008-02-27 |
| EP1408961B1 (en) | 2007-07-11 |
| DE60221130T2 (de) | 2008-03-13 |
| JP5003601B2 (ja) | 2012-08-15 |
| EP1408961A1 (en) | 2004-04-21 |
| ES2289140T3 (es) | 2008-02-01 |
| RU2004104627A (ru) | 2005-07-10 |
| WO2003007941A1 (en) | 2003-01-30 |
| PT1408961E (pt) | 2007-10-10 |
| PE20030286A1 (es) | 2003-03-25 |
| MXPA04000454A (es) | 2004-03-18 |
| CN1529593A (zh) | 2004-09-15 |
| BR0211167A (pt) | 2004-08-10 |
| AU2002328338C1 (en) | 2009-01-08 |
| JP4211605B2 (ja) | 2009-01-21 |
| JP2004538280A (ja) | 2004-12-24 |
| PL215425B1 (pl) | 2013-12-31 |
| US6849657B2 (en) | 2005-02-01 |
| ATE366571T1 (de) | 2007-08-15 |
| JP2008303222A (ja) | 2008-12-18 |
| GT200200152A (es) | 2003-06-19 |
| PL367696A1 (en) | 2005-03-07 |
| CA2451393C (en) | 2011-01-04 |
| DK1408961T3 (da) | 2007-11-05 |
| AU2002328338B2 (en) | 2008-04-24 |
| PA8550501A1 (es) | 2003-06-30 |
| CA2451393A1 (en) | 2003-01-30 |
| KR20040017317A (ko) | 2004-02-26 |
| US20030064964A1 (en) | 2003-04-03 |
| RU2296122C2 (ru) | 2007-03-27 |
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