MA50509A - Agonistes de triazole fusionnés du récepteur apj - Google Patents

Agonistes de triazole fusionnés du récepteur apj

Info

Publication number
MA50509A
MA50509A MA050509A MA50509A MA50509A MA 50509 A MA50509 A MA 50509A MA 050509 A MA050509 A MA 050509A MA 50509 A MA50509 A MA 50509A MA 50509 A MA50509 A MA 50509A
Authority
MA
Morocco
Prior art keywords
apj receptor
receptor fused
fused triazole
agonists
triazole agonists
Prior art date
Application number
MA050509A
Other languages
English (en)
Inventor
Paul John Dransfield
James S Harvey
Zhihua Ma
Ankit Sharma
Original Assignee
Amgen Inc
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 Amgen Inc filed Critical Amgen Inc
Publication of MA50509A publication Critical patent/MA50509A/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D498/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/0803Compounds with Si-C or Si-Si linkages
    • C07F7/081Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
MA050509A 2017-11-03 2018-10-25 Agonistes de triazole fusionnés du récepteur apj MA50509A (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201762581078P 2017-11-03 2017-11-03
US201862662516P 2018-04-25 2018-04-25

Publications (1)

Publication Number Publication Date
MA50509A true MA50509A (fr) 2021-06-02

Family

ID=64362636

Family Applications (1)

Application Number Title Priority Date Filing Date
MA050509A MA50509A (fr) 2017-11-03 2018-10-25 Agonistes de triazole fusionnés du récepteur apj

Country Status (4)

Country Link
US (1) US11149040B2 (fr)
EP (1) EP3704122B1 (fr)
MA (1) MA50509A (fr)
WO (1) WO2019089335A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10689367B2 (en) * 2016-11-16 2020-06-23 Amgen Inc. Triazole pyridyl compounds as agonists of the APJ receptor
MA52487A (fr) 2018-05-01 2021-03-10 Amgen Inc Pyrimidinones substituées en tant qu'agonistes du récepteur apj

Family Cites Families (149)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4160452A (en) 1977-04-07 1979-07-10 Alza Corporation Osmotic system having laminated wall comprising semipermeable lamina and microporous lamina
US4256108A (en) 1977-04-07 1981-03-17 Alza Corporation Microporous-semipermeable laminated osmotic system
US4265874A (en) 1980-04-25 1981-05-05 Alza Corporation Method of delivering drug with aid of effervescent activity generated in environment of use
DE3334455A1 (de) 1983-03-04 1984-09-06 Bayer Ag, 5090 Leverkusen Guanidin - derivate
DE3825867A1 (de) 1988-03-04 1989-09-14 Bayer Ag Heterocyclisch substituierte sulfonylaminoazole und ihre verwendung als herbizide
EP0409332A3 (en) 1989-07-19 1991-08-07 Merck & Co. Inc. Substituted triazoles as angiotensin ii antagonists
DE3928605A1 (de) 1989-08-30 1991-03-07 Bayer Ag Substituierte sulfonylaminoazole
EP0515546A4 (en) 1990-02-13 1993-05-12 Merck & Co. Inc. Triazole angiotensin ii antagonists incorporating a substituted benzyl element
JPH0511439A (ja) 1990-09-13 1993-01-22 Fuji Photo Film Co Ltd 光重合性組成物
DE4035141A1 (de) 1990-11-06 1992-05-07 Bayer Ag Substituierte sulfonylaminotriazolylpyrimidine
SK278998B6 (sk) 1991-02-01 1998-05-06 Merck Sharp & Dohme Limited Deriváty imidazolu, triazolu a tetrazolu, spôsob i
SE9103397D0 (sv) 1991-11-18 1991-11-18 Kabi Pharmacia Ab Nya substituerade salicylsyror
AU669160B2 (en) 1992-03-13 1996-05-30 Merck Sharp & Dohme Limited Imidazole, triazole and tetrazole derivatives
US5411839A (en) 1993-01-15 1995-05-02 Eastman Kodak Company Image formation in color reversal materials using strong inhibitors
ATE205205T1 (de) 1995-02-03 2001-09-15 Upjohn Co Durch hetero-aromatische ring substituierte phenyloxazolidinone als antimikrobielles mittel
US5563026A (en) 1995-04-28 1996-10-08 Eastman Kodak Company Color negative element having improved green record printer compatibility
JP3788676B2 (ja) 1997-11-11 2006-06-21 富士写真フイルム株式会社 有機エレクトロルミネツセンス素子材料およびそれを使用した有機エレクトロルミネツセンス素子
CA2315735A1 (fr) 1998-02-13 1999-08-19 Michael R. Barbachyn Derives d'isoxazoline aminophenyle substitues utilises comme agents antimicrobiens
WO1999046371A2 (fr) 1998-03-11 1999-09-16 Board Of Regents, The University Of Texas System Induction de l'expression de genes apoptotiques ou cytotoxiques par co-apport de genes a mediation adenovirale
HUP0202682A3 (en) 1999-09-10 2003-03-28 Merck & Co Inc Tyrosine kinase inhibitors, pharmaceutical compositions containing them and their use
US6555693B2 (en) 2000-03-16 2003-04-29 Genesoft, Inc. Charged compounds comprising a nucleic acid binding moiety and uses therefor
DE60119714T2 (de) 2000-03-23 2006-09-07 Takeda Chemical Industries, Ltd. Peptidderivat
RU2002133666A (ru) 2000-05-19 2007-05-10 Мерк Патент ГмбХ (DE) Производные триазола
EP1359911A2 (fr) 2000-12-29 2003-11-12 Alteon, Inc. Procede de traitement de troubles fibrogenes et autres symptomes de type ivc
EP1353674A1 (fr) 2000-12-29 2003-10-22 Alteon, Inc. Methode de traitement du glaucome ivb
US6727364B2 (en) 2001-04-30 2004-04-27 The Procter & Gamble Company Triazole compounds useful in treating diseases associated with unwanted cytokine activity
US6787555B2 (en) 2001-04-30 2004-09-07 The Procter & Gamble Company Triazole compounds useful in treating diseases associated with unwanted cytokine activity
US6790846B2 (en) 2001-05-24 2004-09-14 The Procter & Gamble Company Isoxazolone compounds useful in treating diseases associated with unwanted cytokine activity
JP2003005356A (ja) 2001-06-20 2003-01-08 Fuji Photo Film Co Ltd 電子線又はx線用ネガ型レジスト組成物
DE10138569A1 (de) 2001-08-06 2003-04-30 Bayer Ag Regulation des APJ-Rezeptors
JP2003321456A (ja) 2002-04-30 2003-11-11 Fuji Photo Film Co Ltd 5−アミノ−4−含窒素芳香族ヘテロ環置換ピラゾール類の製造方法
CA2496565C (fr) 2002-08-23 2013-04-02 Ribapharm Inc. Inhibiteurs non nucleosidiques de transcriptases inverses
US7084145B2 (en) 2002-10-25 2006-08-01 Pfizer Inc. Triazole compounds useful in therapy
US7361669B2 (en) 2003-01-02 2008-04-22 Millennium Pharmaceuticals, Inc. Compositions and method for inhibiting TGF-β
US20040167188A1 (en) 2003-02-14 2004-08-26 Zhili Xin Protein-tyrosine phosphatase inhibitors and uses thereof
US7169797B2 (en) 2003-02-14 2007-01-30 Abbott Laboratories Protein-tyrosine phosphatase inhibitors and uses thereof
WO2004078923A2 (fr) 2003-02-28 2004-09-16 Plexxikon, Inc. Structure cristalline de pyk2 et ses utilisations
WO2005004818A2 (fr) 2003-07-09 2005-01-20 Imclone Systems Incorporated Composes heterocycliques et leur utilisation comme agents anticancereux
WO2005016929A1 (fr) 2003-08-15 2005-02-24 Astrazeneca Ab Heterocycles fusionnes utilises en tant qu'inhibiteurs de la glutamate racemase (muri)
EP1677786A1 (fr) 2003-10-18 2006-07-12 Bayer HealthCare AG Derives de 2-(phenylmethyl)thio-4-phenyl-4h-1,2,4-triazole substitues en 5 et composes associes utilises en tant que gaba-agonistes dans le traitement de l'incontinence urinaire et des maladies associees
JP2005170939A (ja) 2003-11-20 2005-06-30 Takeda Chem Ind Ltd 糖尿病の予防・治療剤
WO2005073193A1 (fr) 2004-01-23 2005-08-11 Amgen Inc. Ligands du recepteur vanilloide et leur utilisation dans des traitements
US7297168B2 (en) 2004-02-02 2007-11-20 The Procter & Gamble Company Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
DE102004008141A1 (de) 2004-02-19 2005-09-01 Abbott Gmbh & Co. Kg Guanidinverbindungen und ihre Verwendung als Bindungspartner für 5-HT5-Rezeptoren
BRPI0509172A (pt) 2004-03-26 2007-08-28 Amphora Discovery Corp pelo menos uma entidade quìmica, composição farmacêutica, métodos para tratar um paciente, para inibir pelo menos uma enzima que utiliza atp, e para tratar pelo menos uma doença, uso de pelo menos uma entidade quìmica, e, método para a fabricação de um medicamento
US20080153869A1 (en) 2004-06-14 2008-06-26 Bressi Jerome C Kinase Inhibitors
US7399317B2 (en) 2004-08-26 2008-07-15 The Procter & Gamble Company Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
US7776897B2 (en) 2004-09-16 2010-08-17 Astellas Pharma Inc. Triazole derivative or salt thereof
ME01498B (me) 2004-11-18 2014-04-20 Synta Pharmaceuticals Corp Jedinjenja triazola koja modulišu aktivnost hsp90
US20060156480A1 (en) 2005-01-14 2006-07-20 The Procter & Gamble Company Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
JPWO2006080533A1 (ja) 2005-01-31 2008-06-19 持田製薬株式会社 3−アミノ−1,2,4−トリアゾール誘導体
US8399464B2 (en) 2005-03-09 2013-03-19 Nippon Kayaku Kabushiki Kaisha HSP90 inhibitor
CN101160291B (zh) 2005-03-09 2012-09-05 日本化药株式会社 作为hsp90抑制剂的三唑衍生物
JP2008533193A (ja) 2005-03-21 2008-08-21 ファイザー・リミテッド オキシトシン拮抗薬としての置換トリアゾール誘導体
AU2006235759B2 (en) 2005-04-06 2011-07-28 Msd K.K. 1,4-substituted piperazine derivative
WO2007007688A1 (fr) 2005-07-08 2007-01-18 Mochida Pharmaceutical Co., Ltd. Dérivé de 3,5-diamino-1,2,4-triazole
EP1922068A4 (fr) 2005-08-16 2010-08-11 Icagen Inc Inhibiteurs des canaux sodium sensibles au voltage
EP2308852A1 (fr) 2005-08-21 2011-04-13 Abbott GmbH & Co. KG Composés 5-cycle-heteroaromates et leur utilisation en tant que partenaires de liaison des récepteurs 5-HT5
US8673848B2 (en) 2012-01-27 2014-03-18 Novartis Ag Synthetic apelin mimetics for the treatment of heart failure
EP2013180A1 (fr) 2006-04-19 2009-01-14 Laboratoires Serono SA Nouveaux dérivés d'arylaminopyridine substitués par un hétéroaryle, en tant qu'inhibiteurs de mek
US20080125587A1 (en) 2006-05-25 2008-05-29 Chimmanamada Dinesh U Synthesis of triazole compounds that modulate HSP90 activity
CA2653336C (fr) 2006-05-25 2014-10-28 Synta Pharmaceuticals Corp. Methode pour traiter un lymphome non hodgkinien
AU2012200157B2 (en) 2006-05-25 2014-08-21 Synta Pharmaceuticals Corp. Method for treating proliferative disorders associated with protooncogene products
AU2007267859B2 (en) 2006-05-25 2012-04-12 Synta Pharmaceuticals Corp. Triazole compounds that modulate Hsp90 activity
US8318790B2 (en) 2006-05-25 2012-11-27 Synta Pharmaceuticals Corp. Triazole compounds that modulate HSP90 activity
TW200800260A (en) 2006-05-25 2008-01-01 Synta Pharmaceuticals Corp Method for treating proliferative disorders associated with protooncogene products
US8778977B2 (en) 2006-06-30 2014-07-15 Sunesis Pharmaceuticals, Inc. Pyridinonyl PDK1 inhibitors
US7718683B2 (en) 2006-07-14 2010-05-18 Chemocentryx, Inc. Triazolyl phenyl benzenesulfonamides
DE602007012261D1 (de) 2006-07-14 2011-03-10 Chemocentryx Inc Triazolyl-pyridyl-benzolsulfonamide als ccr2- oder ccr9-modulatoren zur behandlung von atherosklerose
AU2007284537B2 (en) 2006-08-17 2012-04-12 Synta Pharmaceuticals Corp. Triazole compounds that modulate HSP90 activity
US20110046125A1 (en) 2006-10-19 2011-02-24 Synta Pharmaceuticals Corp. Method for treating infections
WO2008057246A2 (fr) 2006-10-26 2008-05-15 Synta Pharmaceuticals Corp. Procédé de traitement de troubles inflammatoires
US7638541B2 (en) 2006-12-28 2009-12-29 Metabolex Inc. 5-ethyl-2-{4-[4-(4-tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidin-1-yl}-pyrimidine
DK2118077T3 (en) 2007-02-08 2015-03-09 Synta Pharmaceuticals Corp Triazole compounds that modulate HSP90 ACTIVITY
US7909187B2 (en) 2007-02-20 2011-03-22 Lonzell Montgomery Modular baby bottle system
WO2008112199A1 (fr) 2007-03-12 2008-09-18 Synta Pharmaceuticals Corp. Procédé d'inhibition de la topoisomérase ii
WO2008153730A2 (fr) 2007-05-25 2008-12-18 Synta Pharmaceuticals Corp. Méthode de traitement des maladies prolifératives associées à des mutations dans c-met
CN101801942B (zh) 2007-07-17 2013-03-27 美国艾森生物科学公司 杂环化合物和作为抗癌剂的用途
BRPI0815116A2 (pt) 2007-08-13 2015-01-27 Synta Pharmaceuticals Corp Compostos de triazol que modulam a atividade da hsp90
TW200922564A (en) 2007-09-10 2009-06-01 Curis Inc CDK inhibitors containing a zinc binding moiety
WO2009075890A2 (fr) 2007-12-12 2009-06-18 Synta Pharmaceuticals Corp. Composés triazole qui modulent l'activité de hsp90
CA2710194C (fr) 2007-12-19 2014-04-22 Amgen Inc. Inhibiteurs de la p13 kinase
DE102008013587A1 (de) 2008-03-11 2009-09-17 Bayer Schering Pharma Aktiengesellschaft Heteroaryl-substituierte Dicyanopyridine und ihre Verwendung
EP2103602A1 (fr) 2008-03-17 2009-09-23 AEterna Zentaris GmbH Nouveaux dérivés de triazole 1,2,4 et leur processus de fabrication
MX338530B (es) 2008-06-03 2016-04-21 Siga Technologies Inc Inhibidores de molecula pequeña para el tratamiento o prevencion de infeccion de virus del dengue.
AU2009266956B2 (en) 2008-07-01 2014-03-20 Genentech, Inc. Bicyclic heterocycles as MEK kinase inhibitors
KR20110028376A (ko) 2008-07-01 2011-03-17 제넨테크, 인크. Mek 키나제 억제제로서의 이소인돌론 유도체 및 사용 방법
US8106083B2 (en) 2008-08-08 2012-01-31 Synta Pharmaceuticals Corp. Triazole compounds that modulate HSP90 activity
DE102008038221A1 (de) 2008-08-18 2010-02-25 Merck Patent Gmbh 7-Azaindolderivate
US9339480B2 (en) 2008-11-26 2016-05-17 Satiogen Pharmaceuticals, Inc. Bile acid recycling inhibitors for treatment of obesity and diabetes
DE102008059702A1 (de) 2008-12-01 2010-06-02 Byk-Chemie Gmbh Verfahren zur Herstellung rheologisch wirksamer Harnstoffurethane in organischen Salzen
EP2438052A1 (fr) 2009-06-05 2012-04-11 Oslo University Hospital HF Dérivés d'azole en tant qu'inhibiteurs de la voie wnt
JP2012529511A (ja) 2009-06-08 2012-11-22 アブラクシス バイオサイエンス リミテッド ライアビリティー カンパニー トリアジン誘導体類及びそれらの治療応用
AR077851A1 (es) 2009-12-11 2011-09-28 Exelixis Inc Agonistas del tgr5
CA2829790C (fr) 2010-03-30 2018-06-05 Verseon Corporation Composes aromatiques multisubstitues utilises comme inhibiteurs de la thrombine
US9205086B2 (en) 2010-04-19 2015-12-08 Synta Pharmaceuticals Corp. Cancer therapy using a combination of a Hsp90 inhibitory compounds and a EGFR inhibitor
US20130156755A1 (en) 2010-04-19 2013-06-20 Synta Pharmaceuticals Corp. Cancer therapy using a combination of a hsp90 inhibitory compounds and a vegf inhibitor
US20130172333A1 (en) 2010-05-20 2013-07-04 Synta Pharmaceuticals Corp. Formulation and dosing of hsp90 inhibitory compounds
WO2011150286A2 (fr) 2010-05-26 2011-12-01 Satiogen Pharmaceuticals,Inc. Inhibiteurs et satiogènes de recyclage d'acide biliaire pour traitement du diabète, de l'obésité et d'états inflammatoires gastro-intestinaux
JP5996532B2 (ja) 2010-07-15 2016-09-21 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH 有害生物防除剤としての新規複素環式化合物
US20130266636A1 (en) 2010-08-12 2013-10-10 The Regents Of The University Of California Methods for blocking cell proliferation and treating diseases and conditions responsive to cell growth inhibition
JP2013544874A (ja) 2010-12-08 2013-12-19 オスロ ユニヴァーシティー ホスピタル エイチエフ Wntシグナル伝達経路阻害薬としてのトリアゾール誘導体
US20140045908A1 (en) 2011-02-25 2014-02-13 Synta Pharmaceuticals Corp. Hsp90 inhibitory compounds in treating jak/stat signaling-mediated cancers
US20130034536A1 (en) 2011-08-04 2013-02-07 Lumena Pharmaceuticals, Inc. Bile Acid Recycling Inhibitors for Treatment of Pancreatitis
WO2013032939A1 (fr) 2011-08-26 2013-03-07 Metabolex, Inc. Agonistes bicycliques de gpr131 et leurs utilisations
CN104023718B (zh) 2011-10-28 2017-04-05 鲁美纳医药公司 用于治疗高胆血症和胆汁淤积性肝病的胆汁酸再循环抑制剂
CN104023727B (zh) 2011-10-28 2017-04-05 鲁美纳医药公司 用于治疗小儿胆汁淤积性肝病的胆汁酸再循环抑制剂
AU2012332421A1 (en) 2011-11-02 2014-06-05 Synta Pharmaceuticals Corp. Cancer therapy using a combination of Hsp90 inhibitors with topoisomerase I inhibitors
WO2013067165A1 (fr) 2011-11-02 2013-05-10 Synta Pharmaceuticals Corp. Polythérapie d'inhibiteurs de hsp 90 avec des agents contenant du platine
WO2013074594A1 (fr) 2011-11-14 2013-05-23 Synta Pharmaceuticals Corp. Association thérapeutique d'inhibiteurs de hsp90 et d'inhibiteurs de braf
AU2013208109A1 (en) 2012-01-09 2014-08-14 Anchor Therapeutics, Inc. APJ receptor compounds
CN104169275B (zh) 2012-01-13 2017-06-09 百时美施贵宝公司 用作激酶抑制剂的三唑取代的吡啶化合物
EP2831061A1 (fr) 2012-03-28 2015-02-04 Synta Pharmaceuticals Corp. Dérivés de triazole comme inhibiteurs de hsp90
AU2013271731A1 (en) 2012-06-07 2014-12-18 Georgia State University Research Foundation, Inc. SecA inhibitors and methods of making and using thereof
US20140005181A1 (en) 2012-06-21 2014-01-02 Sanford-Burnham Medical Research Institute Small molecule antagonists of the apelin receptor for the treatment of disease
PL2897939T3 (pl) 2012-09-21 2017-08-31 Sanofi Pochodne amidu kwasu benzoimidazolo-karboksylowego do leczenia chorób metabolicznych i sercowo-naczyniowych
ES2875957T3 (es) 2012-12-20 2021-11-11 Amgen Inc Agonistas del receptor APJ y usos de los mismos
EP2968266B1 (fr) 2013-03-15 2019-05-01 Shifa Biomedical Corporation Composés anti-proprotéine convertase subtilisine kexine de type 9 (anti-pcsk9) dans le traitement et/ou la prévention de maladies cardio-vasculaires
UY35517A (es) 2013-04-04 2014-10-31 Mabxience S A Un procedimiento para aumentar la formación de ácido piroglutamico de una proteína
EP3003322B1 (fr) 2013-05-30 2023-09-13 Washington University Dérivés du mannose et leur utilisation dans le traitement d'infections bactériennes
AU2015233370A1 (en) 2014-03-20 2016-09-22 Centre National De La Recherche Scientifique (Cnrs) Use of compounds inhibiting Apelin / APJ / GP130 signaling for treating cancer
US10590407B2 (en) 2014-04-24 2020-03-17 Nanyang Technological University Asx-specific protein ligase
WO2015184011A2 (fr) 2014-05-28 2015-12-03 Sanford-Burnham Medical Research Institute Agonistes du récepteur de l'apéline et leurs procédés d'utilisation
BR112016028119A2 (pt) 2014-06-06 2017-08-22 Res Triangle Inst Agonistas receptores de apelina (apj) e usos dos mesmos
US20160058705A1 (en) 2014-08-28 2016-03-03 Jayakumar Rajadas Compositions and methods for treating cardiovascular and pulmonary diseases and disorders with apelin
JP6758294B2 (ja) 2014-12-23 2020-09-23 アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル アペリン受容体により媒介される疾患の処置における代謝的に安定なアペリン類似体
US10426818B2 (en) 2015-03-24 2019-10-01 Inserm (Institut National De La Sante Et De La Recherche Medicale) Method and pharmaceutical composition for use in the treatment of diabetes
WO2016176473A1 (fr) 2015-04-28 2016-11-03 Sanford-Burnham Medical Researc Institute Agonistes du récepteur de l'apéline et leurs méthodes d'utilisation
CA2985542C (fr) 2015-05-20 2023-10-10 Amgen Inc. Triazoles agonistes du recepteur apj
SI3303330T1 (sl) 2015-06-03 2019-08-30 Bristol-Myers Squibb Company Agonisti 4-hidroksi-3-(heteroaril)piridin-2-on apj za uporabo pri zdravljenju kardiovaskularnih motenj
BR112018007395A2 (pt) 2015-10-14 2018-10-23 Bristol-Myers Squibb Company 2,4-di-hidróxi-nicotinamidas como agonistas de apj
EP3380970B1 (fr) 2015-11-24 2023-01-04 Sanford Burnham Prebys Medical Discovery Institute Nouveaux dérivés azolés comme agoniste du récepteur de l'apéline
PE20181269A1 (es) 2015-12-04 2018-08-03 Bristol Myers Squibb Co Agonistas del receptor de apelina y metodos de uso
EP3386976A1 (fr) 2015-12-09 2018-10-17 Research Triangle Institute, International Agonistes améliorés du récepteur de l'apéline (apj) et leurs utilisations
US9989592B2 (en) 2015-12-18 2018-06-05 Intel IP Corporation Interfaces for wireless debugging
BR112018068341A2 (pt) 2016-03-24 2019-01-15 Bristol-Myers Squibb Company 6-hidróxi-4-oxo-1,4-di-hidropirimidina-5-carboxamidas como agonistas de apj
EP3228630A1 (fr) 2016-04-07 2017-10-11 IMBA-Institut für Molekulare Biotechnologie GmbH Combinaison d'un antagoniste d'apeline et inhibiteur de l'angiogenèse pour le traitement du cancer
EP3452466B1 (fr) 2016-05-03 2020-08-12 Amgen Inc. Composés triazole hétérocycliques utilisés en tant qu'agonistes du récepteur apj
US10889565B2 (en) 2016-06-14 2021-01-12 Bristol-Myers Squibb Company 4-hydroxy-3-sulfonylpyridin-2(1H)-ones as APJ receptor agonists
JP6993357B2 (ja) 2016-06-14 2022-01-13 ブリストル-マイヤーズ スクイブ カンパニー Apjアゴニストとしての6-ヒドロキシ-5-(フェニル/ヘテロアリールスルホニル)ピリミジン-4(1h)-オン
MX2019004214A (es) 2016-10-12 2019-06-10 Res Triangle Inst Agonistas heterociclicos del receptor de apelina (apj) y usos de los mismos.
EP3526198B1 (fr) 2016-10-14 2020-08-12 Bristol-Myers Squibb Company Agonistes d'apj de 3-sulfonyl-5-aminopyridine -2,4-diol
US10689367B2 (en) * 2016-11-16 2020-06-23 Amgen Inc. Triazole pyridyl compounds as agonists of the APJ receptor
WO2018097944A1 (fr) 2016-11-16 2018-05-31 Amgen Inc. Composés de triazole furane utilisés en tant qu'agonistes du récepteur apj
US11020395B2 (en) 2016-11-16 2021-06-01 Amgen Inc. Cycloalkyl substituted triazole compounds as agonists of the APJ receptor
US11046680B1 (en) 2016-11-16 2021-06-29 Amgen Inc. Heteroaryl-substituted triazoles as APJ receptor agonists
MA46824A (fr) 2016-11-16 2019-09-25 Amgen Inc Composés de triazole substitués par alkyle en tant qu'agonistes du récepteur apj
WO2018093579A1 (fr) 2016-11-16 2018-05-24 Amgen Inc. Composés phényle triazole en tant qu'agonistes du récepteur apj
US20190276696A1 (en) 2016-11-23 2019-09-12 Guangzhou Chinaray Optoelectronic Materials Ltd. Formulations for printed electronic devices, preparation methods and uses thereof

Also Published As

Publication number Publication date
US20200308189A1 (en) 2020-10-01
US11149040B2 (en) 2021-10-19
WO2019089335A1 (fr) 2019-05-09
EP3704122B1 (fr) 2021-09-01
EP3704122A1 (fr) 2020-09-09

Similar Documents

Publication Publication Date Title
HK1253366A1 (zh) Apj受體的三唑激動劑
DK3953327T3 (da) Melanocortin-4-receptor-agonister
CL2018000920A1 (es) Conjugados de anticuerpos que comprenden agonistas de receptor similares
DK3762380T3 (da) Phenylpyrrolidinon-formylpeptid-2-receptoragonister
DK3368060T3 (da) Glugacon-receptor-agonister
ES2981193T3 (es) Anticuerpos antisirpalpha
HK1255163A1 (zh) 作為apj受體激動劑的雜芳基羥基嘧啶酮
DK3440105T3 (da) T-cellereceptorer
DK3440106T3 (da) T-cellereceptorer
DK3494133T3 (da) Anti-kras-g12d-t-cellereceptorer
DK3283110T3 (da) Antistoffer rettet mod interleukin-36-receptor (il-36r)
DK3294764T3 (da) Kimæriske antigenreceptor sammensætninger
DK3606961T3 (da) Garp-tgf-beta-antistoffer
DK3713928T3 (da) Hidtil ukendte bradykinin-b2-receptorantagonister
DK3334457T3 (da) Humaniserede anti-CCR7-receptorantistoffer
ZA202101537B (en) Anti-trem-2 agonist antibodies
DK3334721T3 (da) Cgrp-receptorantagonister
ES2982217T3 (es) Antagonistas de DP
GB201619637D0 (en) C3a receptor agonists
MA50509A (fr) Agonistes de triazole fusionnés du récepteur apj
DK3581572T3 (da) Adenosin-A3-receptormodulatorer
MA46464A (fr) Polymorphes de l'agoniste de récepteur muscarinique
IT201800003973A1 (it) Dispositivo per la fusione interspinosa
GB201817943D0 (en) Galanin-2 receptor agonists
UA37486S (uk) Опакування - етикетка для міні-круасанів