AR040806A1 - Derivados de piperidi-2-ona 1,6 disustituidos, composicion farmaceutica que la comprende y metodo de tratamiento - Google Patents
Derivados de piperidi-2-ona 1,6 disustituidos, composicion farmaceutica que la comprende y metodo de tratamientoInfo
- Publication number
- AR040806A1 AR040806A1 AR20040100984A ARP040100984A AR040806A1 AR 040806 A1 AR040806 A1 AR 040806A1 AR 20040100984 A AR20040100984 A AR 20040100984A AR P040100984 A ARP040100984 A AR P040100984A AR 040806 A1 AR040806 A1 AR 040806A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- heterocyclyl
- cycloalkyl
- aryl
- substituted
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 150000002431 hydrogen Chemical class 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 1
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 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
- 230000002378 acidificating effect Effects 0.000 abstract 1
- 239000000556 agonist Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 230000004406 elevated intraocular pressure Effects 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- -1 nitro, amino Chemical group 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
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- 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)
- Animal Behavior & Ethology (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)
- Life Sciences & Earth Sciences (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)
- Heart & Thoracic Surgery (AREA)
- Oncology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Gastroenterology & Hepatology (AREA)
- Endocrinology (AREA)
- Cardiology (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)
Abstract
Se refiere a agonistas selectivos del subtipo EP4 de los receptores E2 de las prostaglandinas, su uso, o el de una formulación de los mismos en el tratamiento de glaucoma y otras afecciones, las cuales se refieren a presión intraocular elevada en el ojo de un paciente. Reivindicación 1: Un compuesto que tiene la fórmula estructural (1), o una sal, enantiómero diestereoisómero, profármaco del mismo o mezcla de los mismos, farmacéuticamente aceptable, en el que, U representa H, alquilo C1-3 o no se presenta cuando W es =O; W representa OH o =O, lo que proporciona que U no está presente cuando W es =O; Z representa (CH2)n, o CH=CH; R1 representa (CH2)phidroxi, (CH2)pCO2R10, o (CH2)nheterociclil, estando dicho heterociclilo no sustituido o sustituido con de 1 a 3 grupos de Ra y conteniendo opcionalmente un grupo hidroxilo ácido; R2 representa independientemente alquilo C1-10, alquilo, (CH2)mariloC6-10, (CH2)mheterocicliloC5-10, (CH2)mheterocicliloC3-10, (CH2)mcicloalquiloC3-8, dicho alquilo, cicloalquilo, heterociclialquilo, arilo o heterociclilo no sustituido o sustituido con 1-3 grupos de Ra; R3 y R4 representan independientemente hidrógeno, halógeno, o alquilo C1-6; R6 representa hidrógeno, o alquilo C1-4; R10 representa hidrógeno, alquilo C1-10, cicloalquilo C3-10, (CH2)pariloC6-10, (CH2)pheterocicliloC5-10; Ra representa alcoxi C1-6, alquilo C1-6, CF3, nitro, amino, ciano, alquilamino C1-6, halógeno, o Ra también representa arilos y heterociclilo, S alquilo C1-6, S arilo C6-10, S heterociclilo C5-10, O arilo C6-10, O heterociclilo C5-10, CO2R6, CH2OalquiloC1-6, CH2alquiloC1-6, CH2Oarilo, CH2Sarilo; representa un enlace doble o simple; p representa 0-3; n representa 0-4; y m representa 0-8.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45770003P | 2003-03-26 | 2003-03-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR040806A1 true AR040806A1 (es) | 2005-04-20 |
Family
ID=33098243
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AR20040100984A AR040806A1 (es) | 2003-03-26 | 2004-03-24 | Derivados de piperidi-2-ona 1,6 disustituidos, composicion farmaceutica que la comprende y metodo de tratamiento |
Country Status (22)
| Country | Link |
|---|---|
| US (4) | US7053085B2 (es) |
| EP (1) | EP1613621B1 (es) |
| JP (1) | JP4866992B2 (es) |
| KR (1) | KR20060002873A (es) |
| CN (1) | CN1764659A (es) |
| AR (1) | AR040806A1 (es) |
| AT (1) | ATE474837T1 (es) |
| BR (1) | BRPI0408690A (es) |
| CA (1) | CA2519938C (es) |
| CL (1) | CL2004000655A1 (es) |
| DE (1) | DE602004028229D1 (es) |
| EC (1) | ECSP056037A (es) |
| ES (1) | ES2347434T3 (es) |
| HR (1) | HRP20050845A2 (es) |
| IS (1) | IS7999A (es) |
| MA (1) | MA27667A1 (es) |
| MX (1) | MXPA05010189A (es) |
| NO (1) | NO20054951L (es) |
| PE (1) | PE20050522A1 (es) |
| RU (1) | RU2005132930A (es) |
| TW (1) | TW200427670A (es) |
| WO (2) | WO2004085431A1 (es) |
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 |
| EP1585729A1 (en) * | 2003-01-10 | 2005-10-19 | F.Hoffmann-La Roche Ag | 2-piperidone derivatives as prostaglandin agonists |
| EP1631355B1 (en) * | 2003-06-06 | 2014-08-13 | Allergan, Inc. | Piperidinyl prostaglandin e analogs |
| US7326716B2 (en) | 2003-06-06 | 2008-02-05 | Allergan, Inc. | Treatment of inflammatory bowel disease |
| US7179820B2 (en) * | 2003-06-06 | 2007-02-20 | Allergan, Inc. | Piperidinyl prostaglandin E analogs |
| US6977260B2 (en) | 2004-01-22 | 2005-12-20 | Allergan, Inc. | Piperidinyl prostaglandin E analogs |
| US7576122B2 (en) | 2003-09-02 | 2009-08-18 | Merck & Co. Inc. | Ophthalmic compositions for treating ocular hypertension |
| CN1845904A (zh) | 2003-09-04 | 2006-10-11 | 默克公司 | 用于治疗高眼压的眼用组合物 |
| AU2004271978B2 (en) | 2003-09-04 | 2009-02-05 | Merck & Co., Inc. | Ophthalmic compositions for treating ocular hypertension |
| WO2006014207A1 (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 |
| WO2006047476A2 (en) * | 2004-10-26 | 2006-05-04 | 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 |
| JP2009502982A (ja) * | 2005-08-03 | 2009-01-29 | メルク フロスト カナダ リミテツド | Ep4受容体アゴニスト、この組成物および方法 |
| JP2009502977A (ja) * | 2005-08-03 | 2009-01-29 | メルク フロスト カナダ リミテツド | Ep4受容体アゴニスト、この組成物および方法 |
| 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 |
| WO2008027340A2 (en) * | 2006-08-30 | 2008-03-06 | Merck & Co., Inc. | Topical ophthalmic formulations |
| WO2008027341A2 (en) * | 2006-08-30 | 2008-03-06 | Merck & Co., Inc. | Topical ophthalmic formulations |
| RU2480213C2 (ru) | 2006-10-20 | 2013-04-27 | Чилдрен'З Медикал Сентер Корпорейшн | Способ стимуляции регенерации тканей |
| 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 |
| JP5069752B2 (ja) | 2006-12-15 | 2012-11-07 | グラクソ グループ リミテッド | Ep4受容体アゴニストとしてのベンズアミド誘導体 |
| GB2446652A (en) * | 2007-02-16 | 2008-08-20 | Inion Ltd | Osteogenic compounds |
| EP2147672A4 (en) | 2007-05-08 | 2011-11-02 | Nat University Corp Hamamatsu University School Of Medicine | CYTOTOXIC T CELL ACTIVATOR WITH AN EP4 AGONIST |
| TW200911245A (en) * | 2007-06-07 | 2009-03-16 | Astellas Pharma Inc | Pyridone derivatives |
| 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 |
| KR20120093955A (ko) | 2009-10-14 | 2012-08-23 | 젬머스 파마 인코포레이티드 | 바이러스 감염에 대한 병용 요법 치료 |
| CA2738045C (en) * | 2010-05-28 | 2019-02-19 | Simon Fraser University | Conjugate compounds, methods of making same, and uses thereof |
| CN114404588A (zh) | 2013-08-09 | 2022-04-29 | 阿德利克斯公司 | 用于抑制磷酸盐转运的化合物和方法 |
| US9650414B1 (en) | 2014-05-30 | 2017-05-16 | Simon Fraser University | Dual-action EP4 agonist—bisphosphonate conjugates and uses thereof |
| EP3307747A4 (en) | 2015-06-12 | 2019-02-27 | Simon Fraser University | AMID LINKED EP4 AGONIST BISPHOSPHONATE COMPOUNDS AND USES THEREOF |
| 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 |
| EP3972599B1 (en) | 2019-05-21 | 2025-10-22 | Ardelyx, Inc. | Combination for lowering serum phosphate in a 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 (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 |
| 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 |
| EP1114816A4 (en) | 1998-09-14 | 2002-09-04 | Ono Pharmaceutical Co | SUBSTITUTED PHENYL-PROSTAGLANDIN E DERIVATIVES- $ g (V) AND MEDICINAL PRODUCTS CONTAINING THEM AS 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 |
| AP2002002555A0 (en) | 1999-12-22 | 2002-06-30 | Pfizer Prod Inc | EP4 Receptor selective agonists in the treatment of osteoporosis. |
| AU2001216072A1 (en) | 2000-03-17 | 2001-10-03 | Alcon, Inc. | 6-hydroxy-indazole derivatives for treating glaucoma |
| CA2374731A1 (en) | 2000-03-31 | 2001-10-04 | Toray Industries, Inc. | Agent for modulating growth or generation of hair |
| AU2001290250A1 (en) | 2000-09-21 | 2002-04-02 | Ono Pharmaceutical Co. Ltd. | Ep4 receptor agonists containing 8-azaprostaglandin derivatives as the active ingredient |
| IL155368A0 (en) | 2000-11-27 | 2003-11-23 | Pfizer Prod Inc | Ep4 receptor selective agonists in the treatment of osteoporosis |
| CA2434495A1 (en) | 2001-01-30 | 2002-08-08 | Merck & Co., Inc. | Ophthalmic compositions for treating ocular hypertension |
| CA2441708A1 (en) | 2001-03-22 | 2002-10-03 | Merck & Co., Inc. | Mch1r deficient mice |
| AU2002346561B2 (en) | 2001-12-03 | 2006-08-17 | Merck & Co., Inc. | EP4 receptor agonist, compositions and methods thereof |
| JP2005514378A (ja) | 2001-12-03 | 2005-05-19 | メルク エンド カムパニー インコーポレーテッド | 高眼圧症の治療方法 |
| CA2488802A1 (en) | 2002-06-14 | 2003-12-24 | Merck & Co., Inc. | Ophthalmic compositions for treating ocular hypertension |
| WO2003105868A1 (en) | 2002-06-17 | 2003-12-24 | Merck & Co., Inc. | Novel maxi-k channel blockers, methods of use and process for making the same |
| 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 |
| EP1585729A1 (en) | 2003-01-10 | 2005-10-19 | F.Hoffmann-La Roche Ag | 2-piperidone derivatives as prostaglandin agonists |
| 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 MX MXPA05010189A patent/MXPA05010189A/es unknown
- 2004-03-26 EP EP04723484A patent/EP1613621B1/en not_active Expired - Lifetime
- 2004-03-26 WO PCT/CA2004/000471 patent/WO2004085431A1/en not_active Ceased
- 2004-03-26 KR KR1020057018107A patent/KR20060002873A/ko not_active Withdrawn
- 2004-03-26 ES ES04723484T patent/ES2347434T3/es not_active Expired - Lifetime
- 2004-03-26 CL CL200400655A patent/CL2004000655A1/es unknown
- 2004-03-26 AT AT04723484T patent/ATE474837T1/de not_active IP Right Cessation
- 2004-03-26 RU RU2005132930/04A patent/RU2005132930A/ru not_active Application Discontinuation
- 2004-03-26 HR HR20050845A patent/HRP20050845A2/xx not_active Application Discontinuation
- 2004-03-26 WO PCT/CA2004/000470 patent/WO2004085430A1/en not_active Ceased
- 2004-03-26 CN CNA200480008186XA patent/CN1764659A/zh active Pending
- 2004-03-26 BR BRPI0408690-2A patent/BRPI0408690A/pt not_active Application Discontinuation
- 2004-03-26 JP JP2006504090A patent/JP4866992B2/ja not_active Expired - Lifetime
- 2004-03-26 DE DE602004028229T patent/DE602004028229D1/de not_active Expired - Lifetime
- 2004-03-26 CA CA2519938A patent/CA2519938C/en 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 |
| RU2005132930A (ru) | 2006-02-10 |
| MA27667A1 (fr) | 2005-12-01 |
| BRPI0408690A (pt) | 2006-03-28 |
| WO2004085430A1 (en) | 2004-10-07 |
| NO20054951L (no) | 2005-12-22 |
| ECSP056037A (es) | 2006-01-27 |
| KR20060002873A (ko) | 2006-01-09 |
| EP1613621A1 (en) | 2006-01-11 |
| EP1613621B1 (en) | 2010-07-21 |
| DE602004028229D1 (de) | 2010-09-02 |
| TW200427670A (en) | 2004-12-16 |
| IS7999A (is) | 2005-08-25 |
| JP2006520758A (ja) | 2006-09-14 |
| PE20050522A1 (es) | 2005-07-06 |
| CL2004000655A1 (es) | 2005-01-21 |
| HRP20050845A2 (en) | 2006-05-31 |
| NO20054951D0 (no) | 2005-10-25 |
| US7053085B2 (en) | 2006-05-30 |
| ES2347434T3 (es) | 2010-10-29 |
| ATE474837T1 (de) | 2010-08-15 |
| USRE42562E1 (en) | 2011-07-19 |
| MXPA05010189A (es) | 2006-02-22 |
| JP4866992B2 (ja) | 2012-02-01 |
| WO2004085431A1 (en) | 2004-10-07 |
| US20040198701A1 (en) | 2004-10-07 |
| CN1764659A (zh) | 2006-04-26 |
| AU2004224261A1 (en) | 2004-10-07 |
| CA2519938C (en) | 2010-11-30 |
| US20110237511A1 (en) | 2011-09-29 |
| US7238710B2 (en) | 2007-07-03 |
| CA2519938A1 (en) | 2004-10-07 |
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| FA | Abandonment or withdrawal |