PE20181487A1 - Heteroarilhidroxipirimidinonas como agonistas del receptor de apelina (apj) - Google Patents

Heteroarilhidroxipirimidinonas como agonistas del receptor de apelina (apj)

Info

Publication number
PE20181487A1
PE20181487A1 PE2018001129A PE2018001129A PE20181487A1 PE 20181487 A1 PE20181487 A1 PE 20181487A1 PE 2018001129 A PE2018001129 A PE 2018001129A PE 2018001129 A PE2018001129 A PE 2018001129A PE 20181487 A1 PE20181487 A1 PE 20181487A1
Authority
PE
Peru
Prior art keywords
apj
heteroarylhydroxypirimidinones
receptor agonists
compounds
apelin receptor
Prior art date
Application number
PE2018001129A
Other languages
English (en)
Inventor
Michael C Myers
R Michael Lawrence
Donna M Bilder
Wei Meng
Zulan Pi
Robert Paul Brigance
Heather Finlay
Original Assignee
Bristol Myers Squibb Co
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 Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of PE20181487A1 publication Critical patent/PE20181487A1/es

Links

Classifications

    • 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
    • C07D403/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • C07D417/14Heterocyclic 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 three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Cardiology (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hospice & Palliative Care (AREA)
  • Epidemiology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pyridine Compounds (AREA)

Abstract

Se refiere a compuestos de formula (I), donde: alk es C1-6 alquilo sustituido con 1-5 R7; el anillo A es un heteroarilo de 5 a 6 miembros; el anillo B se selecciona de C3-6 cicloalquilo, arilo, carbociclilo, entre otros; R1 se selecciona de H, halogeno, NO2, entre otros; R2 se selecciona de C1-5 alquilo sustituido con 0-3 Re donde Re se selecciona independientemente de C1-6 alquilo, C2-6 alquenilo, entre otros. Dichos compuestos son utiles como agonistas de APJ siendo utiles en el tratamiento de cardiopatia coronaria, apoplejia, insuficiencia cardiaca, entre otros. Entre los compuestos preferidos tenemos los siguientes: 5-(5-(benzo[d]isoxazol-3-ilmetil)-1,3,4-oxadiazol-2-il)-2-butil-1-(2,6-dimetoxifenil)-6-hidroxipirimidin-4(1H)-ona; 5-(5-(benzo[d]isoxazol-3-ilmetil)-1,3,4-oxadiazol-2-il)-2-butil-1-(2,6-diciclopropilfenil)-6-hidroxipirimidin-4(1H)-ona; entre otros.
PE2018001129A 2015-12-16 2016-12-15 Heteroarilhidroxipirimidinonas como agonistas del receptor de apelina (apj) PE20181487A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201562267997P 2015-12-16 2015-12-16

Publications (1)

Publication Number Publication Date
PE20181487A1 true PE20181487A1 (es) 2018-09-18

Family

ID=57708840

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2018001129A PE20181487A1 (es) 2015-12-16 2016-12-15 Heteroarilhidroxipirimidinonas como agonistas del receptor de apelina (apj)

Country Status (21)

Country Link
US (1) US10669261B2 (es)
EP (1) EP3390400B1 (es)
JP (1) JP6948322B2 (es)
KR (1) KR20180095577A (es)
CN (1) CN108602813B (es)
AR (1) AR107061A1 (es)
AU (1) AU2016372048B2 (es)
BR (1) BR112018012112A2 (es)
CA (1) CA3008630A1 (es)
CL (1) CL2018001621A1 (es)
CO (1) CO2018007221A2 (es)
EA (1) EA036736B1 (es)
ES (1) ES2854733T3 (es)
HK (1) HK1255163A1 (es)
IL (1) IL259947B (es)
MX (1) MX2018007155A (es)
PE (1) PE20181487A1 (es)
SG (1) SG11201804674UA (es)
TW (1) TW201725203A (es)
UY (1) UY37026A (es)
WO (1) WO2017106396A1 (es)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2988147C (en) 2015-06-03 2023-06-13 Bristol-Myers Squibb Company 4-hydroxy-3-(heteroaryl)pyridine-2-one apj agonists for use in the treatment of cardiovascular disorders
BR112018007395A2 (pt) 2015-10-14 2018-10-23 Bristol-Myers Squibb Company 2,4-di-hidróxi-nicotinamidas como agonistas de apj
ES2858312T3 (es) 2015-12-04 2021-09-30 Bristol Myers Squibb Co Agonistas del receptor de apelina y métodos de uso
CO2018006164A2 (es) 2015-12-16 2018-09-20 Loxo Oncology Inc Compuestos útiles como inhibidores de cinasa
AR107973A1 (es) 2016-03-24 2018-07-04 Bristol Myers Squibb Co 6-hidroxi-4-oxo-1,4-dihidropirimidin-5-carboxamidas como agonista de apj
EP3452466B1 (en) 2016-05-03 2020-08-12 Amgen Inc. Heterocyclic triazole compounds as agonists of the apj receptor
CN109311821B (zh) * 2016-06-14 2022-10-14 百时美施贵宝公司 作为apj激动剂的6-羟基-5-(苯基/杂芳基磺酰基)嘧啶-4(1h)-酮
US10889565B2 (en) 2016-06-14 2021-01-12 Bristol-Myers Squibb Company 4-hydroxy-3-sulfonylpyridin-2(1H)-ones as APJ receptor agonists
ES2820223T3 (es) 2016-10-14 2021-04-20 Bristol Myers Squibb Co Agonistas de APJ de 3-sulfonil-5-aminopiridin-2,4-diol
WO2018093577A1 (en) 2016-11-16 2018-05-24 Amgen Inc. Cycloalkyl substituted triazole compounds as agonists of the apj receptor
WO2018097944A1 (en) 2016-11-16 2018-05-31 Amgen Inc. Triazole furan compounds as agonists of the apj receptor
EP3541805B1 (en) 2016-11-16 2020-10-14 Amgen Inc. Heteroaryl-substituted triazoles as apj receptor agonists
WO2018093579A1 (en) 2016-11-16 2018-05-24 Amgen Inc. Triazole phenyl compounds as agonists of the apj receptor
WO2018093580A1 (en) 2016-11-16 2018-05-24 Amgen Inc. Triazole pyridyl compounds as agonists of the apj receptor
WO2018093576A1 (en) 2016-11-16 2018-05-24 Amgen Inc. Alkyl substituted triazole compounds as agonists of the apj receptor
EP3788037A1 (en) 2018-05-01 2021-03-10 Amgen Inc. Substituted pyrimidinones as agonists of the apj receptor

Family Cites Families (52)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2263639A (en) 1992-01-28 1993-08-04 Merck & Co Inc Substituted pyrimidinones as neurotensin antagonists
US6174998B1 (en) 1996-03-12 2001-01-16 Roche Diagnostics Gmbh C-nucleoside derivatives and their use in the detection of nucleic acids
JPH08311041A (ja) 1995-03-16 1996-11-26 Takeda Chem Ind Ltd 複素環化合物およびその剤
CZ298812B6 (cs) 1996-07-01 2008-02-13 Dr. Reddy's Laboratories Limited Azolidindionové deriváty, způsob jejich přípravy, farmaceutické kompozice s jejich obsahem a jejich použití v léčbě diabetu a příbuzných nemocí
US6369067B1 (en) 1997-10-27 2002-04-09 Dr. Reddy's Research Foundation Monocyclic compounds and their use in medicine: process for their preparation and pharmaceutical compositions containing them
JP4095804B2 (ja) * 2000-02-16 2008-06-04 スミスクライン ビーチャム ピー エル シー Ldl−pla2阻害剤としてのピリミジン−4−オン誘導体
WO2002006242A2 (en) 2000-07-18 2002-01-24 Neurogen Corporation 5-substituted 2-aryl-4-pyrimidinones
WO2002081454A1 (en) 2001-04-09 2002-10-17 Dr. Reddy's Laboratories Ltd. Derivatives of aryl acids, their use in medicine, process for their preparation and pharmaceutical compositions containing them
BR0309892A2 (pt) 2002-05-09 2011-04-05 Cytokinetics Inc composto, composição, métodos para modular a atividade da cinesina de ksp, para inibir a ksp, e para o tratamento de uma doença proliferativa celular, e, uso de um composto
CA2483627A1 (en) 2002-05-23 2003-12-04 Merck & Co., Inc. Mitotic kinesin inhibitors
US20070167621A1 (en) 2003-04-03 2007-07-19 Pharmacia Corporation Substituted pyrimidinones
JP2006524223A (ja) 2003-04-23 2006-10-26 ファルマシア・アンド・アップジョン・カンパニー・エルエルシー Crfアンタゴニストとしての置換されたピリミジノンおよびピリミジンチオン
EP1699777B1 (en) 2003-09-08 2012-12-12 Takeda Pharmaceutical Company Limited Dipeptidyl peptidase inhibitors
JP2007510652A (ja) 2003-11-03 2007-04-26 サイトキネティクス・インコーポレーテッド ピリミジン−4−オン化合物、組成物、および方法
JP2007518711A (ja) 2003-12-19 2007-07-12 メルク エンド カムパニー インコーポレーテッド 有糸分裂キネシン阻害剤
JP4517349B2 (ja) 2004-07-28 2010-08-04 宇部興産株式会社 ピリミジン−4−オン化合物の製造方法
DE102005025315A1 (de) 2005-06-02 2006-12-14 Merck Patent Gmbh Ionische Flüssigkeiten mit niedriger Viskosität
WO2007037543A1 (ja) 2005-09-29 2007-04-05 Banyu Pharmaceutical Co., Ltd. ビアリールアミド誘導体
JP5144532B2 (ja) 2005-11-30 2013-02-13 バーテックス ファーマシューティカルズ インコーポレイテッド c−Met阻害剤及び用法
WO2007124397A2 (en) 2006-04-21 2007-11-01 Trustees Of Boston University Ionic viscoelastics and viscoelastic salts
WO2008052861A2 (de) 2006-10-10 2008-05-08 Proionic Production Of Ionic Substances Gmbh & Co Keg Verfahren zur herstellung von 1,3 -hetero-aromatischen carbonaten
EP2079707B1 (de) 2006-10-10 2014-12-03 proionic GmbH & Co KG Verfahren zur umsetzung von 1,3-hetero-aromatischen 2-carboxylaten mit wasser
JP2010519204A (ja) 2007-02-16 2010-06-03 アムジエン・インコーポレーテツド 窒素含有複素環ケトン類およびそれらのc−Met阻害薬としての使用
EP2279192B1 (en) 2008-05-28 2013-10-30 Merck Patent GmbH Ionic liquids
DE102008031480A1 (de) 2008-07-03 2010-01-07 Merck Patent Gmbh Salze enthaltend ein Pyrimidincarbonsäure-Derivat
US20110253929A1 (en) 2008-12-22 2011-10-20 Basf Se Mixtures of hydrophobic and hydrophilic ionic liquids and use thereof in liquid ring compressors
TW201100411A (en) 2009-05-21 2011-01-01 Chlorion Pharma Inc Pyrimidines as novel therapeutic agents
CN103140221A (zh) 2010-08-10 2013-06-05 盐野义制药株式会社 新型杂环衍生物和含有其的药物组合物
CN103582647A (zh) 2011-05-31 2014-02-12 默克专利股份有限公司 含有氢基-三氰基-硼酸根阴离子的化合物
TW201311709A (zh) 2011-05-31 2013-03-16 Merck Patent Gmbh 電解質配方
CN102903954B (zh) 2011-07-25 2015-06-03 微宏动力系统(湖州)有限公司 含有离子液体电解质的锂离子二次电池
DE102012006896A1 (de) 2012-04-05 2013-10-10 Merck Patent Gmbh Silikate mit organischen Kationen
CA2875964C (en) 2012-06-07 2018-01-02 Georgia State University Research Foundation, Inc. Seca inhibitors and methods of making and using thereof
DK2897939T3 (en) * 2012-09-21 2017-05-08 Sanofi Sa BENZOIMIDAZOLCARBOXYL ACID AMIDE DERIVATIVES FOR THE TREATMENT OF METABOLIC OR CARDIOVASCULAR DISEASES
WO2014056844A1 (en) 2012-10-10 2014-04-17 Basf Se Ionic liquids based on oxalic acid mono esters
DE102012021452A1 (de) 2012-10-31 2014-04-30 Merck Patent Gmbh Salze mit Trihydroperfluoralkoxybutansulfonat- oder Trihydroperfluoralkoxypropansulfonat-Anion
EP2919785A4 (en) 2012-11-16 2016-10-05 Biocryst Pharm Inc ANTIVIRAL NUCLEOSIDES CONTAINING AZASUCRE
WO2014207100A1 (en) 2013-06-27 2014-12-31 Basf Se A process for coating paper with cellulose using a solution containing cellulose
DE102013016324A1 (de) 2013-10-04 2015-04-09 Merck Patent Gmbh Perfluoralkylfluor- oder Perfluoralkylchlorgermanate
BR112016011663B1 (pt) 2013-11-29 2022-02-22 Proionic Gmbh Processos para cura de um adesivo por meio de irradiação por micro-ondas e paracolagem de um material termoplástico
KR101550846B1 (ko) 2014-01-29 2015-09-07 한국과학기술연구원 단일공정을 이용한 탄소소재의 다원소 도핑방법 및 그 용도
KR101531023B1 (ko) 2014-05-27 2015-06-23 한국과학기술연구원 열분해 가스 도핑에 의한 고강도 고전도성 탄소나노튜브섬유의 제조방법 및 이에 따라 제조된 탄소나노튜브섬유
WO2015184011A2 (en) 2014-05-28 2015-12-03 Sanford-Burnham Medical Research Institute Agonists of the apelin receptor and methods of use thereof
AU2015269247B2 (en) * 2014-06-06 2019-10-24 Research Triangle Institute Apelin receptor (APJ) agonists and uses thereof
WO2016074757A1 (de) 2014-11-11 2016-05-19 Merck Patent Gmbh Verfahren zur herstellung von mono- und bis(perfluoralkyl)fluorophosphatsalzen und deren säuren
CA2988147C (en) * 2015-06-03 2023-06-13 Bristol-Myers Squibb Company 4-hydroxy-3-(heteroaryl)pyridine-2-one apj agonists for use in the treatment of cardiovascular disorders
BR112018007395A2 (pt) 2015-10-14 2018-10-23 Bristol-Myers Squibb Company 2,4-di-hidróxi-nicotinamidas como agonistas de apj
ES2858312T3 (es) 2015-12-04 2021-09-30 Bristol Myers Squibb Co Agonistas del receptor de apelina y métodos de uso
AR107973A1 (es) 2016-03-24 2018-07-04 Bristol Myers Squibb Co 6-hidroxi-4-oxo-1,4-dihidropirimidin-5-carboxamidas como agonista de apj
CN109311821B (zh) 2016-06-14 2022-10-14 百时美施贵宝公司 作为apj激动剂的6-羟基-5-(苯基/杂芳基磺酰基)嘧啶-4(1h)-酮
US10889565B2 (en) 2016-06-14 2021-01-12 Bristol-Myers Squibb Company 4-hydroxy-3-sulfonylpyridin-2(1H)-ones as APJ receptor agonists
ES2820223T3 (es) 2016-10-14 2021-04-20 Bristol Myers Squibb Co Agonistas de APJ de 3-sulfonil-5-aminopiridin-2,4-diol

Also Published As

Publication number Publication date
AU2016372048A1 (en) 2018-08-02
BR112018012112A2 (pt) 2018-12-04
CO2018007221A2 (es) 2018-07-19
SG11201804674UA (en) 2018-06-28
CN108602813A (zh) 2018-09-28
EP3390400B1 (en) 2021-01-20
JP6948322B2 (ja) 2021-10-13
JP2018538304A (ja) 2018-12-27
UY37026A (es) 2017-06-30
MX2018007155A (es) 2018-08-15
CA3008630A1 (en) 2017-06-22
EA201891336A1 (ru) 2019-01-31
HK1255163A1 (zh) 2019-08-09
EP3390400A1 (en) 2018-10-24
IL259947A (en) 2018-07-31
US10669261B2 (en) 2020-06-02
WO2017106396A1 (en) 2017-06-22
TW201725203A (zh) 2017-07-16
AR107061A1 (es) 2018-03-14
US20180362508A1 (en) 2018-12-20
ES2854733T3 (es) 2021-09-22
EA036736B1 (ru) 2020-12-14
CL2018001621A1 (es) 2018-08-03
AU2016372048B2 (en) 2021-02-04
IL259947B (en) 2020-10-29
KR20180095577A (ko) 2018-08-27
CN108602813B (zh) 2021-10-29

Similar Documents

Publication Publication Date Title
PE20181487A1 (es) Heteroarilhidroxipirimidinonas como agonistas del receptor de apelina (apj)
PE20181269A1 (es) Agonistas del receptor de apelina y metodos de uso
CY1122964T1 (el) Ενωσεις πυριμιδινοδιονης εναντι καρδιακων παθησεων
CO2018004344A2 (es) Derivados de heterociclos bicíclicos condensados como agentes de control de plagas
PE20180483A1 (es) Oxiesteroles y metodos de uso de los mismos
PE20161405A1 (es) Analogos de cortistatina y sintesis y usos de los mismos
AR090760A1 (es) Compuestos de benzotiazol y su uso contra el virus de hiv
CO2017002714A2 (es) Ácido 4-(3-fluoro-3-(2-(5,6,7,8-tetrahidro-1,8-naftiridin-2-il)etil)pirrolidin-1-il)-3-(3-(2-metoxietoxi)fenil)butanoico, o una sal del mismo
PE20120034A1 (es) Compuestos derivados de n-fenilpirimidin-2-amina
PE20180506A1 (es) Agonistas de receptor de apelina (apj) de 4-hidroxi-3-(heteroaril) piridin-2-ona como para uso en el tratamiento de trastornos cardiovasculares
PE20181197A1 (es) 2,4-dihidroxi-nicotinamidas como agonistas del receptor de apelina (apj)
PE20142461A1 (es) Moduladores del receptor de estrogeno y sus usos
PE20170664A1 (es) Agonistas del receptor de apelina(apj) y usos de los mismos
CY1125004T1 (el) Ετεροαρυλο υποκατεστημενες βητα-υδροξυαιθυλαμινες για χρηση στη θεραπεια της υπεργλυκαιμιας
AR093818A1 (es) Compuesto de 1-(bencil sustituido)piperazina sustituida
AR092827A1 (es) Compuestos de n-(tetrazol-5-il)- y n-(triazol-5-il)arilcarboxamida sustituidos y su uso como herbicidas
PE20211002A1 (es) Compuestos como moduladores de ror gamma
ECSP18024565A (es) Benzamidas sustituidas con isoxazolinas y análalogos como insecticidas
PE20171511A1 (es) Compuestos de piperidina urea 4-metilsulfonil-sustituidos para el tratamiento de miocardiopatia dilatada (mcd)
AR096339A1 (es) Agonistas del receptor de somatostatina subtipo 4 (sstr4)
PE20141828A1 (es) 6-alquinilo piridinas como mimeticos smac
ECSP20018487A (es) Activadores de piruvato quinasas para usar en el tratamiento de trastornos en la sangre
PE20160589A1 (es) Heteroaril-ciclohexil-tetraazabenzo[e]azulenos como antagonistas de los receptores de vasopresina v1a
PE20151060A1 (es) Nuevos derivados de pirazina como agonistas del receptor cb2
PE20140703A1 (es) Derivados de heteroarilo como moduladores de nachr alfa 7