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
Application number
CL2009000815A
Other languages
English (en)
Inventor
Richard Berger
Lehua Chang
Scott D Edmondson
Stephen D Goble
Sookhee Nicole Ha
Nam Fung Kar
Ihor E Kopka
Bing Li
Gregori J Morriello
Chris R Moyes
Dong-Ming Shen
Liping Wang
Cheng Zhu
Original Assignee
Schering Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Schering Corp filed Critical Schering Corp
Publication of CL2009000815A1 publication Critical patent/CL2009000815A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/425Thiazoles
    • A61K31/428Thiazoles condensed with carbocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/06Anti-spasmodics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/10Drugs for disorders of the urinary system of the bladder
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/12Antidiuretics, e.g. drugs for diabetes insipidus
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Urology & Nephrology (AREA)
  • Diabetes (AREA)
  • Epidemiology (AREA)
  • Hematology (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 .
CL2009000815A 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. CL2009000815A1 (es)

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 (38)

Country Link
US (3) US8399480B2 (es)
EP (1) EP2276756B9 (es)
JP (3) JP4783867B2 (es)
KR (3) KR101331771B1 (es)
CN (2) CN102056917B (es)
AR (1) AR072043A1 (es)
AT (1) ATE535521T1 (es)
AU (1) AU2009231714B2 (es)
BR (1) BRPI0909768B1 (es)
CA (1) CA2719876C (es)
CL (1) CL2009000815A1 (es)
CO (1) CO6331440A2 (es)
CR (2) CR11751A (es)
CY (1) CY1112552T1 (es)
DO (2) DOP2010000294A (es)
EA (1) EA020135B1 (es)
EC (1) ECSP10010518A (es)
ES (1) ES2376278T3 (es)
GE (1) GEP20125666B (es)
HK (1) HK1147099A1 (es)
HN (1) HN2010002030A (es)
HR (1) HRP20120129T2 (es)
IL (1) IL208215A (es)
MA (1) MA32257B1 (es)
ME (1) ME01988B (es)
MX (1) MX2010010929A (es)
NI (1) NI201000164A (es)
NZ (1) NZ588266A (es)
PE (1) PE20091825A1 (es)
PL (1) PL2276756T3 (es)
PT (1) PT2276756E (es)
RS (1) RS52175B (es)
SG (1) SG188883A1 (es)
SI (1) SI2276756T1 (es)
SV (1) SV2010003687A (es)
TW (1) TWI378098B (es)
WO (2) WO2009124167A1 (es)
ZA (1) ZA201006720B (es)

Families Citing this family (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20091825A1 (es) 2008-04-04 2009-12-04 Merck & Co Inc Hidroximetil pirrolidinas como agonistas del receptor adrenergico beta 3
WO2011025774A1 (en) * 2009-08-27 2011-03-03 Merck Sharp & Dohme Corp. Novel pyrrolidine derived beta 3 adrenergic receptor agonists
NZ599233A (en) * 2009-10-07 2013-04-26 Merck Sharp & Dohme Combination therapy using a beta 3 adrenergic receptor agonist and an antimuscarinic agent
AU2011245499B2 (en) * 2010-04-30 2014-09-25 Merck Sharp & Dohme Corp. Novel beta 3 adrenergic receptor agonists
CA2805427A1 (en) * 2010-07-23 2012-01-26 Merck Sharp & Dohme Corp. Novel pyrrolidine derived beta 3 adrenergic receptor agonists
AU2011285928B9 (en) * 2010-08-03 2018-08-02 B3Ar Therapeutics, Inc. Combinations of beta - 3 adrenergic receptor agonists and muscarinic receptor antagonists for treating overactive bladder
US9907767B2 (en) 2010-08-03 2018-03-06 Velicept Therapeutics, Inc. Pharmaceutical compositions and the treatment of overactive bladder
US9522129B2 (en) 2010-08-03 2016-12-20 Velicept Therapeutics, Inc. Pharmaceutical Combination
GB2484713A (en) 2010-10-21 2012-04-25 Optovate Ltd Illumination apparatus
EP2742030B1 (de) * 2011-08-11 2016-07-27 Bayer Intellectual Property GmbH 1,2,4-triazolyl-substituierte ketoenole zum einsatz im pflanzenschutz
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
ES2584427T3 (es) 2011-10-27 2016-09-27 Merck Sharp & Dohme Corp. Proceso para la preparación de agonistas beta 3 y productos intermedios
WO2013074650A1 (en) 2011-11-18 2013-05-23 Codexis, Inc. Biocatalysts for the preparation of hydroxy substituted carbamates
TW201338772A (zh) * 2012-02-09 2013-10-01 Altherx Inc 藥學組合物
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
US9784726B2 (en) 2013-01-08 2017-10-10 Atrogi Ab Screening method, a kit, a method of treatment and a compound for use in a method of treatment
BR112015023328A2 (pt) 2013-03-13 2017-07-18 Flatley Discovery Lab compostos de piridazinona e métodos para o tratamento de fibrose cística
WO2014150639A1 (en) * 2013-03-15 2014-09-25 Merck Sharp & Dohme Corp. Process for preparing beta 3 agonists and intermediates
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
WO2015191907A1 (en) 2014-06-11 2015-12-17 VenatoRx Pharmaceuticals, Inc. Beta-lactamase inhibitors
KR20170086659A (ko) 2014-12-03 2017-07-26 벨리셉트 테라퓨틱스, 인크. 하부 요로 증상을 위한 변형 방출형 솔라베그론을 이용한 조성물 및 방법
KR20170103962A (ko) 2015-01-20 2017-09-13 머크 샤프 앤드 돔 코포레이션 인자 xia 억제제
IL310527A (en) 2015-10-23 2024-03-01 B3Ar Therapeutics Inc Zwitterion solvegron and its uses
EP3463307A4 (en) * 2016-06-03 2020-01-15 Velicept Therapeutics, Inc. COMPOSITIONS AND METHODS FOR USE OF SOLABEGRON WITH MODIFIED RELEASE FOR SYMPTOMS OF THE LOWER URINARY PATHWAYS
GB201705365D0 (en) 2017-04-03 2017-05-17 Optovate Ltd Illumination apparatus
GB201705364D0 (en) 2017-04-03 2017-05-17 Optovate Ltd Illumination apparatus
EP3630783A4 (en) 2017-05-26 2021-03-03 Venatorx Pharmaceuticals, Inc. PENICILLIN BINDING PROTEIN INHIBITORS
US20210077496A1 (en) 2017-06-06 2021-03-18 Urovant Sciences Gmbh Dosing of vibegron for treatment of overactive bladder
CN117695286A (zh) 2017-06-06 2024-03-15 住友制药(苏州)有限公司 使用维贝隆以治疗膀胱过度活动症
GB201714736D0 (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
GB201714734D0 (en) 2017-09-13 2017-10-25 Atrogi Ab New compounds and uses
GB201714740D0 (en) 2017-09-13 2017-10-25 Atrogi Ab New compounds and uses
US11376253B2 (en) 2017-12-21 2022-07-05 Kyorin Pharmaceutical Co., Ltd. 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
AU2019273837A1 (en) 2018-05-23 2020-11-19 Urovant Sciences Gmbh Use of vibegron to treat pain associated with irritable bowel syndrome
KR20210102892A (ko) 2018-12-05 2021-08-20 유로반트 사이언시즈 게엠베하 과민성 방광 증상의 치료를 위한 비베그론
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
AU2020243514A1 (en) 2019-03-18 2021-08-26 Urovant Sciences Gmbh Use of vibegron to treat overactive bladder
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
EP4018236A4 (en) 2019-08-23 2023-09-13 RealD Spark, LLC DEVICE FOR DIRECTIONAL LIGHTING AND VISIBILITY DISPLAY
EP4028804A4 (en) 2019-09-11 2023-10-25 RealD Spark, LLC DEVICE FOR DIRECTIONAL LIGHTING AND VISIBILITY DISPLAY
US11163101B2 (en) 2019-09-11 2021-11-02 Reald Spark, Llc Switchable illumination apparatus and privacy display
JP2022550540A (ja) 2019-10-03 2022-12-02 リアルディー スパーク エルエルシー 受動光学ナノ構造を備える照明装置
JP2022550938A (ja) 2019-10-03 2022-12-06 リアルディー スパーク エルエルシー 受動光学ナノ構造を含む照射装置
CN115136065A (zh) 2020-02-20 2022-09-30 瑞尔D斯帕克有限责任公司 照明和显示设备
MX2023007413A (es) 2020-12-22 2023-07-21 Urovant Sciences Gmbh Metodos para monitorear digoxina con el uso de vibegron para tratar veiiga hiperactiva.
WO2022175848A1 (en) 2021-02-16 2022-08-25 Urovant Sciences Gmbh Methods of treating heart failure with vibegron
GB202113588D0 (en) 2021-09-23 2021-11-10 Atrogi Ab New compounds and methods
GB202205895D0 (en) 2022-04-22 2022-06-08 Atrogi Ab New medical uses
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)

* Cited by examiner, † Cited by third party
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
ATE500827T1 (de) * 2002-11-07 2011-03-15 Astellas Pharma Inc Mittel zur behandlung von blasenhyperaktivität mit einem essigsäureanilid-derivat als wirkstoff
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

Also Published As

Publication number Publication date
JP5432846B2 (ja) 2014-03-05
HN2010002030A (es) 2012-08-13
PE20091825A1 (es) 2009-12-04
SV2010003687A (es) 2011-03-23
KR20120104257A (ko) 2012-09-20
KR101288798B1 (ko) 2013-07-23
NZ588266A (en) 2011-11-25
EP2276756B1 (en) 2011-11-30
PL2276756T3 (pl) 2012-04-30
KR20100126860A (ko) 2010-12-02
IL208215A0 (en) 2010-12-30
DOP2010000294A (es) 2010-12-31
CR20120282A (es) 2012-07-03
TW200944521A (en) 2009-11-01
ECSP10010518A (es) 2010-11-30
JP2011201897A (ja) 2011-10-13
HRP20120129T1 (en) 2012-03-31
AU2009231714B2 (en) 2011-11-03
KR20120118086A (ko) 2012-10-25
BRPI0909768B1 (pt) 2019-01-15
GEP20125666B (en) 2012-10-10
SI2276756T1 (sl) 2012-04-30
US20110028481A1 (en) 2011-02-03
US8653260B2 (en) 2014-02-18
ES2376278T3 (es) 2012-03-12
JP4783870B1 (ja) 2011-09-28
PT2276756E (pt) 2012-02-03
ZA201006720B (en) 2011-05-25
JP2011510023A (ja) 2011-03-31
EP2276756B9 (en) 2012-08-15
EA020135B1 (ru) 2014-08-29
HK1147099A1 (en) 2011-07-29
TWI378098B (en) 2012-12-01
CR11751A (es) 2010-11-22
DOP2013000267A (es) 2014-01-31
US20090253705A1 (en) 2009-10-08
NI201000164A (es) 2011-06-21
MA32257B1 (fr) 2011-04-01
CN102056917A (zh) 2011-05-11
ME01988B (me) 2012-08-31
AR072043A1 (es) 2010-08-04
CA2719876C (en) 2013-10-01
CO6331440A2 (es) 2011-10-20
KR101331771B1 (ko) 2013-11-22
CN102391255B (zh) 2014-07-09
US20120258963A1 (en) 2012-10-11
EA201071169A1 (ru) 2011-04-29
CY1112552T1 (el) 2016-02-10
HRP20120129T2 (hr) 2012-09-30
ATE535521T1 (de) 2011-12-15
EP2276756B8 (en) 2012-04-11
EP2276756A1 (en) 2011-01-26
JP4783867B2 (ja) 2011-09-28
SG188883A1 (en) 2013-04-30
CA2719876A1 (en) 2009-10-08
WO2009124166A1 (en) 2009-10-08
RS52175B (en) 2012-08-31
BRPI0909768A2 (pt) 2015-10-06
HRP20120129T8 (en) 2012-04-30
CN102391255A (zh) 2012-03-28
WO2009124167A1 (en) 2009-10-08
AU2009231714A1 (en) 2009-10-08
MX2010010929A (es) 2010-11-12
CN102056917B (zh) 2014-11-05
JP2012020961A (ja) 2012-02-02
IL208215A (en) 2014-04-30
US8399480B2 (en) 2013-03-19
US8247415B2 (en) 2012-08-21

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.
ES2649340T3 (es) Administración de fármacos activados por hipoxia y agentes antiangiogénicos para el tratamiento del cáncer
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
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.
AR117814A1 (es) Compuestos moduladores de fxr (nr1h4)
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.
PE20090113A1 (es) Compuestos triciclicos como moduladores del receptor de glucocorticoides, composiciones y procedimientos
PE20210667A1 (es) Derivados de benzamida para la inhibicion de la actividad abl1, abl2 y bcr-abl1
ECSP12011799A (es) Compuestos de espiropiperidina y uso farmacéutico de los mismos
CO6390101A2 (es) Compuestos purina
ECSP11011560A (es) Derivados amino-propiónicos sustituidos como inhibidores de neprilisina
CR20120591A (es) Derivados de aminopirimidina como moduladores de la lrrk2
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.
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.
UY31554A1 (es) Nuevos inhibidores de acetil coenzima a carboxilasa y usos en tratamientos de obesidad y diabetes mellitus
CL2009000662A1 (es) Compuestos derivados de 1,2,4-triazol trisustituidos, moduladores del receptor de acetilcolina nicotinicos; composicion farmaceutica; su proceso de preparacion; y uso para la prevencion o el tratamiento de trastornos psicoticos, trastornos o enfermedades de daño intelectual, o enfermedades o trastornos inflamatorios.
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
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
AR077138A1 (es) Composiciones farmaceuticas utiles para tratar el vhc
CO6430439A2 (es) Agonistas del receptor de esfingosina -1- fosfato
UY31672A1 (es) "agonistas de receptores muscarínicos composiciones farmacéuticas métodos de tratamiento de los mismos, y procedimientos para su preparación"
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.
CL2012003341A1 (es) Composicion farmaceutica de administracion oral que compende bendamustina o un ester, una sal o un solvato de la misma, y un excipiente que es un agente tensioactivo no ionico e hidrofilico; combinacion farmaceutica; y su uso para el tratamiento de leucemia linfocitica cronica y el mieloma multiple, entre otras enfermedades.
CL2011001829A1 (es) 3'-n-desmetil-4''-o-(2-dietilaminoetanoil)-6-o-metil-9a-aza-9a-homoeritromicina a, sus sales y formas cristalinas 1, 2 y 3; proceso de preparacion; uso para tratar enfermedades inflamatorias; composicion farmaceutica; y composicion que ademas comprende otro compuesto activo.