CL2009000815A1 - Compuestos derivados de fenilhidroximetilpirrolidina, agonista del recptor adrenergico beta 3; composicion farmaceutica que los comprende; uso en el tratamiento de vejiga hiperactiva, incontinencia urinaria por impulso y urgencia urinaria. - Google Patents
Compuestos derivados de fenilhidroximetilpirrolidina, agonista del recptor adrenergico beta 3; composicion farmaceutica que los comprende; uso en el tratamiento de vejiga hiperactiva, incontinencia urinaria por impulso y urgencia urinaria.Info
- Publication number
- CL2009000815A1 CL2009000815A1 CL2009000815A CL2009000815A CL2009000815A1 CL 2009000815 A1 CL2009000815 A1 CL 2009000815A1 CL 2009000815 A CL2009000815 A CL 2009000815A CL 2009000815 A CL2009000815 A CL 2009000815A CL 2009000815 A1 CL2009000815 A1 CL 2009000815A1
- Authority
- CL
- Chile
- Prior art keywords
- treatment
- phenylhydroxymethylpyrrolidine
- beta
- pharmaceutical composition
- receptor agonist
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- XRIRRAZNVLMQOP-UHFFFAOYSA-N (2-phenylpyrrolidin-1-yl)methanol Chemical compound OCN1CCCC1C1=CC=CC=C1 XRIRRAZNVLMQOP-UHFFFAOYSA-N 0.000 title 1
- 206010020853 Hypertonic bladder Diseases 0.000 title 1
- 206010027566 Micturition urgency Diseases 0.000 title 1
- 208000009722 Overactive Urinary Bladder Diseases 0.000 title 1
- 208000000921 Urge Urinary Incontinence Diseases 0.000 title 1
- 208000020629 overactive bladder Diseases 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 229940126158 β3 adrenergic receptor agonist Drugs 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 230000004913 activation Effects 0.000 abstract 1
- 108040005346 beta3-adrenergic receptor activity proteins Proteins 0.000 abstract 1
- 229940126214 compound 3 Drugs 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/428—Thiazoles condensed with carbocyclic rings
-
- 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
-
- 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
-
- 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
- A61P13/06—Anti-spasmodics
-
- 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
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- 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
- A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyrrole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyridine Compounds (AREA)
Abstract
COMPUESTO DERIVADO DE FENILHIDROXIMETILPIRROLIDINA DE FÓRMULA IA, O UNA DE SUS SALES FARMACÉUTICAMENTE ACEPTABLES, O UN ESTEREOISÓMERO DEL MISMO, O UNA SAL FARMACÉUTICAMENTE ACEPTABLE DEL ESTEREOISÓMERO DEL MISMO DONDE R3 Y N SON COMO SE DEFINEN EN LA MEMORIA DESCRIPTIVA COMPOSICIÓN FARMACÉUTICA QUE COMPRENDE DICHO COMPUESTO Y UN VEHICULO FARMACÉUTICAMENTE ACEPTABLE; Y USO DE UNA CANTIDAD TERAPÉUTICAMENTE EFICAZ DE DICHO COMPUESTO QUE SIRVE PARA PREPARAR UN MEDICAMENTO ÚTIL PARA EL TRATAMIENTO O PREVENCIÓN DE UNA ENFERMEDAD O TRASTORNO MEDIADO POR LA ACTIVACIÓN DEL ADRENOCEPTOR ß3 .
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12306308P | 2008-04-04 | 2008-04-04 | |
| US20604309P | 2009-01-27 | 2009-01-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2009000815A1 true CL2009000815A1 (es) | 2009-08-21 |
Family
ID=40671093
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2009000815A CL2009000815A1 (es) | 2008-04-04 | 2009-04-03 | Compuestos derivados de fenilhidroximetilpirrolidina, agonista del recptor adrenergico beta 3; composicion farmaceutica que los comprende; uso en el tratamiento de vejiga hiperactiva, incontinencia urinaria por impulso y urgencia urinaria. |
Country Status (41)
Families Citing this family (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4891872A (en) | 1988-05-09 | 1990-01-09 | Sussman Martin V | Apparatus for incrementally drawing fibers |
| PE20091825A1 (es) | 2008-04-04 | 2009-12-04 | Merck & Co Inc | Hidroximetil pirrolidinas como agonistas del receptor adrenergico beta 3 |
| IN2012DN00971A (es) * | 2009-08-27 | 2015-04-10 | Merck Sharp & Dohme | |
| IN2012DN02782A (es) * | 2009-10-07 | 2015-09-18 | Merck Sharp & Dohme | |
| US8748433B2 (en) * | 2010-04-30 | 2014-06-10 | Merck Sharp & Dohme Corp. | β3 adrenergic receptor agonists |
| JP5795799B2 (ja) * | 2010-07-23 | 2015-10-14 | メルク・シャープ・エンド・ドーム・コーポレイション | 新規なピロリジン由来ベータ３アドレナリン作動性受容体アゴニスト |
| US9522129B2 (en) | 2010-08-03 | 2016-12-20 | Velicept Therapeutics, Inc. | Pharmaceutical Combination |
| KR20180008918A (ko) * | 2010-08-03 | 2018-01-24 | 앨씨알엑스, 인크. | 과민성 방광 치료를 위한 베타-3 아드레날린 수용체 작용제 및 무스카린 수용체 길항제의 약학적 배합제 |
| US9907767B2 (en) | 2010-08-03 | 2018-03-06 | Velicept Therapeutics, Inc. | Pharmaceutical compositions and the treatment of overactive bladder |
| GB2484713A (en) | 2010-10-21 | 2012-04-25 | Optovate Ltd | Illumination apparatus |
| CN103857661B (zh) * | 2011-08-11 | 2016-11-16 | 拜耳知识产权有限责任公司 | 1,2,4‑三唑基取代的酮烯醇 |
| WO2013062878A1 (en) | 2011-10-27 | 2013-05-02 | Merck Sharp & Dohme Corp. | Process for making beta 3 angonists and intermediates |
| JP6063948B2 (ja) | 2011-10-27 | 2017-01-18 | メルク・シャープ・アンド・ドーム・コーポレーションＭｅｒｃｋ Ｓｈａｒｐ ＆ Ｄｏｈｍｅ Ｃｏｒｐ． | ベータ３アゴニストおよび中間体を製造するプロセス |
| CN104053771B (zh) | 2011-11-18 | 2016-11-09 | 科德克希思公司 | 用于制备羟基取代的氨基甲酸酯的生物催化剂 |
| KR20150020160A (ko) | 2012-02-09 | 2015-02-25 | 앨씨알엑스, 인크. | 과민성 방광의 치료를 위한 무스카린 수용체 길항제 및 베타―3 아드레날린 수용체 작용제의 조합물 |
| JP2015178458A (ja) * | 2012-07-25 | 2015-10-08 | 杏林製薬株式会社 | ベンゼン環縮合含窒素５員複素環式化合物、またはその薬理学的に許容される塩 |
| WO2014108449A1 (en) | 2013-01-08 | 2014-07-17 | Atrogi Ab | A screening method, a kit, a method of treatment and a compound for use in a method of treatment |
| JP6545148B2 (ja) | 2013-03-13 | 2019-07-17 | フラットリー ディスカバリー ラブ，エルエルシー | ピリダジノン化合物及び嚢胞性線維症の治療のための方法 |
| LT2968269T (lt) | 2013-03-15 | 2019-10-25 | Merck Sharp & Dohme | Beta 3 agonistų ir tarpinių junginių gamybos būdas |
| CN103232352B (zh) * | 2013-05-11 | 2015-12-23 | 苏州永健生物医药有限公司 | (r)-4-(2-(2-羟基-2-苯乙胺基)乙基)苯胺基甲酸叔丁基酯 |
| CN103760286A (zh) * | 2014-01-14 | 2014-04-30 | 北京万全德众医药生物技术有限公司 | 一种用高效液相色谱法测定琥珀酸索非那新中间体光学纯度的方法 |
| KR20220065084A (ko) | 2014-06-11 | 2022-05-19 | 베나토알엑스 파마슈티컬스, 인크. | 베타-락타마제 억제제 |
| CN107205964A (zh) | 2014-12-03 | 2017-09-26 | 威力塞帕特治疗股份有限公司 | 使用调节释放索拉贝隆用于下尿路症状的组合物和方法 |
| BR112017015431A2 (pt) * | 2015-01-20 | 2018-01-16 | Merck Sharp & Dohme | composto, composição farmacêutica, métodos para inibir a formação de trombos no sangue ou tratar uma formação de trombos no sangue, para impedir a formação de trombos no sangue, para tratar tromboembolismo venoso e embolia pulmonar, para tratar trombose venosa profunda e para tratar ataque tromboembólico, e, uso de um composto |
| WO2017070689A2 (en) | 2015-10-23 | 2017-04-27 | Velicept Therapeutics, Inc. | Solabegron zwitterion and uses thereof |
| WO2017210700A1 (en) * | 2016-06-03 | 2017-12-07 | Velicept Therapeutics, Inc. | Compositions and methods of using modified release solabegron for lower urinary tract symptoms |
| GB201705364D0 (en) | 2017-04-03 | 2017-05-17 | Optovate Ltd | Illumination apparatus |
| GB201705365D0 (en) | 2017-04-03 | 2017-05-17 | Optovate Ltd | Illumination apparatus |
| WO2018218154A1 (en) | 2017-05-26 | 2018-11-29 | VenatoRx Pharmaceuticals, Inc. | Penicillin-binding protein inhibitors |
| KR20200012939A (ko) | 2017-06-06 | 2020-02-05 | 유로반트 사이언시즈 게엠베하 | 과민성 방광의 치료를 위한 비베그론의 투약 |
| EP4410295A3 (en) | 2017-06-06 | 2024-10-16 | Urovant Sciences GmbH | Use of vibegron to treat overactive bladder |
| GB201714740D0 (en) | 2017-09-13 | 2017-10-25 | Atrogi Ab | New compounds and uses |
| GB201714734D0 (en) | 2017-09-13 | 2017-10-25 | Atrogi Ab | New compounds and uses |
| GB201714745D0 (en) | 2017-09-13 | 2017-10-25 | Atrogi Ab | New compounds and uses |
| GB201714736D0 (en) | 2017-09-13 | 2017-10-25 | Atrogi Ab | New compounds and uses |
| GB201718307D0 (en) | 2017-11-05 | 2017-12-20 | Optovate Ltd | Display apparatus |
| MY201379A (en) * | 2017-12-21 | 2024-02-21 | Kyorin Seiyaku Kk | An agent for treating nocturnal pollakiuria |
| GB201800574D0 (en) | 2018-01-14 | 2018-02-28 | Optovate Ltd | Illumination apparatus |
| GB201803767D0 (en) | 2018-03-09 | 2018-04-25 | Optovate Ltd | Illumination apparatus |
| GB201807747D0 (en) | 2018-05-13 | 2018-06-27 | Optovate Ltd | Colour micro-LED display apparatus |
| CA3098536A1 (en) | 2018-05-23 | 2019-11-28 | Urovant Sciences Gmbh | Use of vibegron to treat pain associated with irritable bowel syndrome |
| US12173018B2 (en) | 2018-05-25 | 2024-12-24 | VenatoRx Pharmaceuticals, Inc. | Penicillin-binding protein inhibitors |
| NZ774649A (en) * | 2018-12-05 | 2025-07-25 | Urovant Sciences Gmbh | Vibegron for the treatment of overactive bladder symptoms |
| CN109503500A (zh) * | 2018-12-17 | 2019-03-22 | 天津药明康德新药开发有限公司 | 一种2-(2-氧代吡嗪-1(2h)-基)乙酸的合成方法 |
| CN109734712B (zh) * | 2019-01-30 | 2020-10-20 | 广东东阳光药业有限公司 | 芳基或杂芳基取代的吡咯烷酰胺衍生物及其用途 |
| EP3941473A1 (en) | 2019-03-18 | 2022-01-26 | Urovant Sciences GmbH | Use of vibegron to treat overactive bladder |
| GB201903832D0 (en) | 2019-03-20 | 2019-05-01 | Atrogi Ab | New compounds and methods |
| TW202102883A (zh) | 2019-07-02 | 2021-01-16 | 美商瑞爾Ｄ斯帕克有限責任公司 | 定向顯示設備 |
| US11294233B2 (en) | 2019-08-23 | 2022-04-05 | ReaID Spark, LLC | Directional illumination apparatus and privacy display |
| EP4028804A4 (en) | 2019-09-11 | 2023-10-25 | RealD Spark, LLC | DEVICE FOR DIRECTIONAL LIGHTING AND VISIBILITY DISPLAY |
| EP4028805A4 (en) | 2019-09-11 | 2023-10-18 | RealD Spark, LLC | SWITCHABLE LIGHTING FIXTURE AND PRIVACY DISPLAY |
| US11652195B2 (en) | 2019-10-03 | 2023-05-16 | Reald Spark, Llc | Illumination apparatus comprising passive optical nanostructures |
| US11162661B2 (en) | 2019-10-03 | 2021-11-02 | Reald Spark, Llc | Illumination apparatus comprising passive optical nanostructures |
| WO2021168090A1 (en) | 2020-02-20 | 2021-08-26 | Reald Spark, Llc | Illumination and display apparatus |
| CN116133660B (zh) * | 2020-07-22 | 2025-05-02 | 詹森药业有限公司 | 可用作因子XIa抑制剂的化合物 |
| WO2022137178A1 (en) | 2020-12-22 | 2022-06-30 | Urovant Sciences Gmbh | Methods of monitoring digoxin with concomitant use of vibegron to treat overactive bladder |
| TW202245781A (zh) | 2021-02-16 | 2022-12-01 | 瑞士商優洛凡特科學公司 | 用維貝格龍（ｖｉｂｅｇｒｏｎ）治療心臟衰竭之方法 |
| US12158602B2 (en) | 2021-06-22 | 2024-12-03 | Reald Spark, Llc | Illumination apparatus |
| GB202113588D0 (en) | 2021-09-23 | 2021-11-10 | Atrogi Ab | New compounds and methods |
| WO2023168365A1 (en) | 2022-03-02 | 2023-09-07 | Jds Therapeutics, Llc | Polyglutamic acid compositions and methods of using |
| GB202205895D0 (en) | 2022-04-22 | 2022-06-08 | Atrogi Ab | New medical uses |
| CN114920771A (zh) * | 2022-05-13 | 2022-08-19 | 苏州虞美景盛新药开发有限公司 | 一种用于膀胱过度活动症的口服新药的中间体新合成工艺 |
| KR20250088578A (ko) | 2022-10-18 | 2025-06-17 | 보나파이드 헬스, 엘엘씨 | 베타-아드레날린 작용제 및 무스카린 길항제 조성물 및 사용 방법 |
| CN115850286B (zh) * | 2022-12-05 | 2023-08-22 | 奥锐特药业(天津)有限公司 | 一种维贝格龙中间体及其制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6525202B2 (en) | 2000-07-17 | 2003-02-25 | Wyeth | Cyclic amine phenyl beta-3 adrenergic receptor agonists |
| DOP2003000587A (es) * | 2002-02-27 | 2003-08-30 | Pfizer Prod Inc | AGONISTAS DEL RECEPTOR ß3-ADRENERGICO |
| CA2503570C (en) * | 2002-11-07 | 2011-04-19 | Yamanouchi Pharmaceutical Co., Ltd. | Remedy for overactive bladder comprising acetic acid anilide derivative as the active ingredient |
| FR2874011B1 (fr) * | 2004-08-03 | 2007-06-15 | Sanofi Synthelabo | Derives de sulfonamides, leur preparation et leur application en therapeutique |
| PE20091825A1 (es) | 2008-04-04 | 2009-12-04 | Merck & Co Inc | Hidroximetil pirrolidinas como agonistas del receptor adrenergico beta 3 |
-
2009
- 2009-03-27 PE PE2009000460A patent/PE20091825A1/es active IP Right Grant
- 2009-03-30 AR ARP090101127A patent/AR072043A1/es active IP Right Grant
- 2009-04-02 US US12/936,221 patent/US8399480B2/en active Active
- 2009-04-02 SI SI200930188T patent/SI2276756T1/sl unknown
- 2009-04-02 HR HRP20120129AT patent/HRP20120129T2/hr unknown
- 2009-04-02 PT PT09726601T patent/PT2276756E/pt unknown
- 2009-04-02 BR BRPI0909768A patent/BRPI0909768B1/pt active IP Right Grant
- 2009-04-02 JP JP2010543320A patent/JP4783867B2/ja active Active
- 2009-04-02 WO PCT/US2009/039249 patent/WO2009124166A1/en not_active Ceased
- 2009-04-02 WO PCT/US2009/039253 patent/WO2009124167A1/en not_active Ceased
- 2009-04-02 US US12/417,239 patent/US8247415B2/en active Active
- 2009-04-02 PL PL09726601T patent/PL2276756T3/pl unknown
- 2009-04-02 KR KR1020107024750A patent/KR101331771B1/ko active Active
- 2009-04-02 NZ NZ588266A patent/NZ588266A/en unknown
- 2009-04-02 SG SG2013017736A patent/SG188883A1/en unknown
- 2009-04-02 KR KR1020127015876A patent/KR101288798B1/ko not_active Expired - Fee Related
- 2009-04-02 CN CN201110265670.2A patent/CN102391255B/zh active Active
- 2009-04-02 ES ES09726601T patent/ES2376278T3/es active Active
- 2009-04-02 EA EA201071169A patent/EA020135B1/ru not_active IP Right Cessation
- 2009-04-02 CA CA2719876A patent/CA2719876C/en active Active
- 2009-04-02 RS RS20120042A patent/RS52175B/sr unknown
- 2009-04-02 GE GEAP200911992A patent/GEP20125666B/en unknown
- 2009-04-02 AU AU2009231714A patent/AU2009231714B2/en active Active
- 2009-04-02 CN CN200980121149.2A patent/CN102056917B/zh active Active
- 2009-04-02 AT AT09726601T patent/ATE535521T1/de active
- 2009-04-02 MX MX2010010929A patent/MX2010010929A/es active IP Right Grant
- 2009-04-02 EP EP09726601A patent/EP2276756B9/en active Active
- 2009-04-02 ME MEP-2012-549A patent/ME01988B/me unknown
- 2009-04-02 KR KR1020127026256A patent/KR20120118086A/ko not_active Withdrawn
- 2009-04-03 TW TW098111302A patent/TWI378098B/zh active
- 2009-04-03 CL CL2009000815A patent/CL2009000815A1/es unknown
-
2010
- 2010-07-14 JP JP2010159938A patent/JP5432846B2/ja active Active
- 2010-09-16 IL IL208215A patent/IL208215A/en active IP Right Grant
- 2010-09-20 ZA ZA2010/06720A patent/ZA201006720B/en unknown
- 2010-09-30 SV SV2010003687A patent/SV2010003687A/es unknown
- 2010-09-30 HN HN2010002030A patent/HN2010002030A/es unknown
- 2010-10-01 NI NI201000164A patent/NI201000164A/es unknown
- 2010-10-01 DO DO2010000294A patent/DOP2010000294A/es unknown
- 2010-10-04 CO CO10122821A patent/CO6331440A2/es active IP Right Grant
- 2010-10-04 EC EC2010010518A patent/ECSP10010518A/es unknown
- 2010-10-22 CR CR11751A patent/CR11751A/es unknown
- 2010-10-29 MA MA33292A patent/MA32257B1/fr unknown
-
2011
- 2011-05-13 JP JP2011107738A patent/JP4783870B1/ja active Active
-
2012
- 2012-02-29 CY CY20121100209T patent/CY1112552T1/el unknown
- 2012-05-25 CR CR20120282A patent/CR20120282A/es unknown
- 2012-06-20 US US13/527,934 patent/US8653260B2/en active Active
-
2013
- 2013-11-15 DO DO2013000267A patent/DOP2013000267A/es unknown
-
2024
- 2024-12-11 NL NL301305C patent/NL301305I2/nl unknown
- 2024-12-12 NO NO2024055C patent/NO2024055I1/no unknown
- 2024-12-12 FR FR24C1051C patent/FR24C1051I1/fr active Active
- 2024-12-16 FI FIC20240046C patent/FIC20240046I1/fi unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CL2009000815A1 (es) | Compuestos derivados de fenilhidroximetilpirrolidina, agonista del recptor adrenergico beta 3; composicion farmaceutica que los comprende; uso en el tratamiento de vejiga hiperactiva, incontinencia urinaria por impulso y urgencia urinaria. | |
| UY31863A (es) | Combinaciones de drogas que comprenden un inhibidor de dgat y un agonista de ppar | |
| SV2011004077A (es) | Derivados aminobutiricos sustituidos como inhibidores de neprilisina | |
| UY31672A1 (es) | "agonistas de receptores muscarínicos composiciones farmacéuticas métodos de tratamiento de los mismos, y procedimientos para su preparación" | |
| CL2008000836A1 (es) | Compuestos derivados de tiazolidina, antagonistas del receptor de orexina; composicion farmaceutica que los comprende; y su uso en el tratamiento de neurosis emocional, depresion grave, trastornos psicoticos, alzheimer, parkinson, dolor, entre otras. | |
| UY30809A1 (es) | Derivados de n-[3-[4-fenil)piperidin-1-carbonil]fenil]sulfonamidas sustituidas, procesos de preparacion y aplicaciones | |
| PE20090113A1 (es) | Compuestos triciclicos como moduladores del receptor de glucocorticoides, composiciones y procedimientos | |
| CL2012001366A1 (es) | Compuestos derivados de carboxamida n-((2-morfolino-5-ariltiazol-4-il)metil), moduladores de receptores nicotinicos alfa 7; composicion farmaceutica; proceso para prepararla; combinacion farmaceutica; y su uso para el tratamiento de la enfermedad de alzheimer, demencia, esquizofrenia, enfermedad de parkinson, entre otras. | |
| ECSP12011799A (es) | Compuestos de espiropiperidina y uso farmacéutico de los mismos | |
| CO6390101A2 (es) | Compuestos purina | |
| PE20210667A1 (es) | Derivados de benzamida para la inhibicion de la actividad abl1, abl2 y bcr-abl1 | |
| CR20110616A (es) | Derivados amino-propiónicos sustituidos como inhibidores de neprilisina | |
| AR093244A1 (es) | Compuestos de benceno sustituidos utilizables en el tratamiento de trastornos mediados por ezh2 | |
| CL2011000835A1 (es) | Compuestos derivados de espiro-oxindol; moduladores de los canales de sodio; composicion farmaceutica que comprende a dicho compuesto; y uso en el tratamiento del dolor, depresion, enfermedades cardiovasculares, respiratorias, psiquiatricas, entre otras. | |
| AR117814A1 (es) | Compuestos moduladores de fxr (nr1h4) | |
| AR071788A1 (es) | Derivados de 3-aminocarbazol, composiciones farmaceuticas que los contienen, metodo de preparacion y uso de los mismos para tratar y/o prevenir trastornos asociados con la produccion de prostaglandina e2(pge2), tales como aterosclerosis, artritis, artrosis y tumores, entre otros. | |
| CL2008003789A1 (es) | Compuestos derivados de bencimidazol sustituido por carboxilo o por hidroxilo, moduladores selectivos del receptor x de farnesoide (fxr); proceso de preparacion; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento de la diabetes, dislipidemia, sindrome metabolico, cancer, alzheimer. | |
| AR070158A1 (es) | Compuesto de benzamida composicion farmaceutica que lo comprende y su uso para la manufactura de un medicamento util para antagonizar selectivamente los rceptores opioides kappa | |
| UY31554A1 (es) | Nuevos inhibidores de acetil coenzima a carboxilasa y usos en tratamientos de obesidad y diabetes mellitus | |
| CL2007003289A1 (es) | Compuestos derivados de biciclocarboxiamida; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento de enfermedades provocadas por la hiperactivacion del receptor vc1 como dolor, enfermedad de vejiga, inflam | |
| AR070025A1 (es) | Uso de derivados de 1-amino-alquilciclohexano para el tratamiento del tinnitus coclear y composicion farmaceutica | |
| CL2016003329A1 (es) | Derivados de indano e indolina y el uso de los mismos como activadores de la guanilato ciclasa soluble | |
| AR077138A1 (es) | Composiciones farmaceuticas utiles para tratar el vhc | |
| MX2011011058A (es) | Antagonistas del receptor ep4 para el tratamiento de cancer. | |
| CL2011001050A1 (es) | Compuesto 2-metil-1-(fenilsulfonil)-4-(piperazin-1-il)-1h-bencimidazol, que es ligando de 5-hidroxitriptamina-6; su composicion farmaceutica; modulador de la actividad de 5-ht6; su uso en el tratamiento de trastornos del sistema nervioso central, tal como psicosis, ansiedad, depresión, epilepsia, entre otros. |