IN2014CN02515A - - Google Patents

Info

Publication number
IN2014CN02515A
IN2014CN02515A IN2515CHN2014A IN2014CN02515A IN 2014CN02515 A IN2014CN02515 A IN 2014CN02515A IN 2515CHN2014 A IN2515CHN2014 A IN 2515CHN2014A IN 2014CN02515 A IN2014CN02515 A IN 2014CN02515A
Authority
IN
India
Prior art keywords
directed
present
diseases
involved
prevention
Prior art date
Application number
Other languages
English (en)
Inventor
Scott D Kuduk
Jason W Skudlarek
Original Assignee
Merck Sharp & Dohme
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 Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of IN2014CN02515A publication Critical patent/IN2014CN02515A/en

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Classifications

    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • 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
    • 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)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Anesthesiology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
IN2515CHN2014 2011-10-19 2012-10-17 IN2014CN02515A (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161548883P 2011-10-19 2011-10-19
PCT/US2012/060479 WO2013059222A1 (fr) 2011-10-19 2012-10-17 Antagonistes des récepteurs de l'orexine à base de 2-pyrydyloxy-4-nitrile

Publications (1)

Publication Number Publication Date
IN2014CN02515A true IN2014CN02515A (fr) 2015-07-31

Family

ID=47116466

Family Applications (1)

Application Number Title Priority Date Filing Date
IN2515CHN2014 IN2014CN02515A (fr) 2011-10-19 2012-10-17

Country Status (11)

Country Link
US (1) US9156819B2 (fr)
EP (1) EP2768823B1 (fr)
JP (1) JP5947906B2 (fr)
CN (1) CN103874695B (fr)
AR (1) AR088352A1 (fr)
AU (1) AU2012326275B2 (fr)
BR (1) BR112014009486A2 (fr)
CA (1) CA2852425C (fr)
IN (1) IN2014CN02515A (fr)
TW (1) TW201317228A (fr)
WO (1) WO2013059222A1 (fr)

Families Citing this family (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9440982B2 (en) 2012-02-07 2016-09-13 Eolas Therapeutics, Inc. Substituted prolines/piperidines as orexin receptor antagonists
CA2863413A1 (fr) 2012-02-07 2013-08-15 Eolas Therapeutics, Inc. Piperidines/prolines substituees en tant qu'antagonistes du recepteur de l'orexine
EP2908812A4 (fr) * 2012-10-16 2016-04-20 Merck Sharp & Dohme Antagonistes de type 2-pyridyloxy-3-ester-4-nitrile des récepteurs d'orexines
US9546152B2 (en) * 2012-10-23 2017-01-17 Merck Sharp & Dohme Corp. 2-pyridyloxy-3-substituted-4-nitrile orexin receptor antagonists
WO2014085208A1 (fr) * 2012-11-27 2014-06-05 Merck Sharp & Dohme Corp. Composés de 2-pyridylamino-4-nitrile-pipéridinyl, antagonistes des récepteurs de l'orexine
EP2934516A4 (fr) * 2012-12-20 2016-07-20 Merck Sharp & Dohme Antagonistes des récepteurs de l'orexine 3-ester-4-substitués
US9556145B2 (en) * 2012-12-20 2017-01-31 Merck Sharp & Dohme Corp. 2-pyridyloxy-4-ester orexin receptor antagonists
US9643955B2 (en) * 2012-12-20 2017-05-09 Merck Sharp & Dohme Corp. 2-pyridyloxy-3-nitrile-4-substituted orexin receptor antagonists
TW201444821A (zh) * 2013-03-13 2014-12-01 Janssen Pharmaceutica Nv 經取代之哌啶化合物及其作為食慾素受體調節劑之用途
TWI621618B (zh) 2013-03-13 2018-04-21 比利時商健生藥品公司 經取代2-氮雜雙環類及其作為食慾素受體調控劑之用途
TW201444849A (zh) 2013-03-13 2014-12-01 Janssen Pharmaceutica Nv 經取代的7-氮雜雙環類及其作為食慾激素受體調節劑之用途
WO2014176142A1 (fr) * 2013-04-23 2014-10-30 Merck Sharp & Dohme Corp. Antagonistes des récepteurs de l'orexine substitués par un groupe hydroxy
WO2015018029A1 (fr) 2013-08-08 2015-02-12 Merck Sharp & Dohme Corp. Composés oxazole antagonistes des récepteurs d'orexine
WO2015018027A1 (fr) 2013-08-08 2015-02-12 Merck Sharp & Dohme Corp. Antagonistes thiazoles des récepteurs de l'orexine
WO2015088864A1 (fr) 2013-12-09 2015-06-18 Merck Sharp & Dohme Corp. Composés 2-pyridyloxy-3-ester-4-éther antagonistes des récepteurs de l'orexine
US9586934B2 (en) 2013-12-09 2017-03-07 Merck Sharp & Dohme Corp. 2-pyridyloxy-4-methyl orexin receptor antagonists
US9617246B2 (en) 2013-12-18 2017-04-11 Merck Sharp & Dohme Corp. Thioether-piperidinyl orexin receptor antagonists
US9676751B2 (en) 2013-12-20 2017-06-13 Merck Sharp & Dohme Corp. 2-amino-3-ester-pyridl orexin receptor antagonists
AU2015226679B2 (en) * 2014-03-06 2017-05-25 Shanghai Haiyan Pharmaceutical Technology Co. Ltd Piperidine derivatives as orexin receptor antagonist
JP6663909B2 (ja) 2014-08-13 2020-03-13 エオラス セラピューティクス, インコーポレイテッド オレキシンレセプターモジュレーターとしてのジフルオロピロリジン
AU2015314851B2 (en) 2014-09-11 2020-01-02 Janssen Pharmaceutica Nv Substituted 2-azabicycles and their use as orexin receptor modulators
WO2016065584A1 (fr) 2014-10-30 2016-05-06 Merck Sharp & Dohme Corp. Antagonistes pipéridine oxadiazole et pipéridine thiadiazole du récepteur de l'orexine
WO2016065586A1 (fr) 2014-10-30 2016-05-06 Merck Sharp & Dohme Corp. Pyrazole, triazole et tétrazole antagonistes des récepteurs de l'orexine
WO2016065587A1 (fr) 2014-10-30 2016-05-06 Merck Sharp & Dohme Corp. Composés pyrazoles antagonistes des récepteurs de l'orexine
WO2016065585A1 (fr) 2014-10-30 2016-05-06 Merck Sharp & Dohme Corp. Composés pipéridines isoxazoles et isothiazoles antagonistes des récepteurs de l'orexine
WO2016065583A1 (fr) 2014-10-30 2016-05-06 Merck Sharp & Dohme Corp. Antagonistes du récepteur d'orexine à base d'oxazole
WO2016083315A1 (fr) * 2014-11-24 2016-06-02 INSERM (Institut National de la Santé et de la Recherche Médicale) Utilisation d'antagonistes d'ox1r pour le traitement de maladies intestinales inflammatoires
US9994570B2 (en) 2014-11-26 2018-06-12 Merck Sharp & Dohme Corp. Bridged diazepane orexin receptor antagonists
WO2016085784A1 (fr) 2014-11-26 2016-06-02 Merck Sharp & Dohme Corp. Antagonistes de récepteur d'orexine de type méthyl-diazépane
WO2016086357A1 (fr) 2014-12-02 2016-06-09 Merck Sharp & Dohme Corp. Méthyl oxazoles antagonistes du récepteur d'orexine
WO2016086358A1 (fr) * 2014-12-02 2016-06-09 Merck Sharp & Dohme Corp. Hydroxyméthyl pipéridines antagonistes du récepteur d'orexine
US9987255B2 (en) 2014-12-19 2018-06-05 Merck Sharp & Dohme Corp. 5,5-bicyclic oxazole orexin receptor antagonists
WO2016095205A1 (fr) 2014-12-19 2016-06-23 Merck Sharp & Dohme Corp. Composés hétéroaryle en tant qu'antagonistes du récepteur de l'hypocrétine
WO2016095204A1 (fr) 2014-12-19 2016-06-23 Merck Sharp & Dohme Corp. Composés pyrrolidine en tant qu'antagonistes du récepteur de l'hypocrétine
US9938276B2 (en) 2014-12-19 2018-04-10 Merck Sharp & Dohme Corp. 6,5-bicyclic octahydropyrrolopyridine orexin receptor antagonists
WO2016100161A1 (fr) 2014-12-19 2016-06-23 Merck Sharp & Dohme Corp. Éthylène diamine en tant qu'antagonistes du récepteur de l'hypocrétine
WO2016101118A1 (fr) 2014-12-23 2016-06-30 Merck Sharp & Dohme Corp. Antagonistes des récepteurs d'orexine de type amidoéthylazole
WO2016101119A1 (fr) 2014-12-23 2016-06-30 Merck Sharp & Dohme Corp. Dérivés d'hétéroaryles fusionnés en tant qu'antagonistes des récepteurs des oréxines
CA3005918C (fr) 2015-11-23 2023-10-17 Sunshine Lake Pharma Co., Ltd. Derives d'octahydropyrrolo [3, 4-c] pyrrole et leurs utilisations
US10894789B2 (en) 2016-02-12 2021-01-19 Astrazeneca Ab Halo-substituted piperidines as orexin receptor modulators
WO2017194548A1 (fr) 2016-05-10 2017-11-16 INSERM (Institut National de la Santé et de la Recherche Médicale) Méthodes et compositions pharmaceutiques pour le traitement de maladies inflammatoires auto-immunes
JP6574918B1 (ja) 2017-08-03 2019-09-11 武田薬品工業株式会社 複素環化合物およびその用途

Family Cites Families (214)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3914250A (en) 1974-08-01 1975-10-21 American Home Prod 1,4-Diazepino{8 6,5,4-jk{9 carbazoles
CA1258454A (fr) 1982-08-10 1989-08-15 Leo Alig Phenethanolamines
IT1159765B (it) 1982-09-28 1987-03-04 Zanussi A Spa Industrie Macchina lavabiancheria di tipo modulare
ZA848275B (en) 1983-12-28 1985-08-28 Degussa New piridine-2-ethers or pyridine-2-thioethers having a nitrogen-containing cycloaliphatic ring
MX18467A (es) 1988-11-23 1993-07-01 Pfizer Agentes terapeuticos de quinuclidinas
US5232929A (en) 1990-11-28 1993-08-03 Pfizer Inc. 3-aminopiperidine derivatives and related nitrogen containing heterocycles and pharmaceutical compositions and use
US5081122A (en) 1990-03-05 1992-01-14 Sterling Drug Inc. Antiglaucoma compositions containing 4-arylcarbonyl-1-(4-morpholinyl)-lower-alkyl)-1H-indoles and method of use thereof
US5112820A (en) 1990-03-05 1992-05-12 Sterling Drug Inc. Anti-glaucoma compositions containing 2- and 3-aminomethyl-6-arylcarbonyl- or 6-phenylthio-2,3-dihydropyrrolo-(1,2,3-de)-1,4-benzoxazines and method of use thereof
US5013837A (en) 1990-03-08 1991-05-07 Sterling Drug Inc. 3-Arylcarbonyl-1H-indole-containing compounds
US4973587A (en) 1990-03-08 1990-11-27 Sterling Drug Inc. 3-arylcarbonyl-1-aminoalkyl-1H-indole-containing antiglaucoma method
US5242930A (en) 1991-02-11 1993-09-07 Merck Sharp & Dohme Ltd. Azabicyclic compounds, pharmaceutical compositions containing them and their use in therapy
DK0573522T3 (da) 1991-03-01 1995-03-06 Pfizer 1-Azabicyclo(3,2,2)nonan-3-aminderivater
EP0528495A1 (fr) 1991-08-20 1993-02-24 Merck Sharp & Dohme Ltd. Composés azacycliques, leur préparation et compositions pharmaceutiques les contenant
GB9211193D0 (en) 1992-05-27 1992-07-08 Merck Sharp & Dohme Therapeutic agents
FR2692575B1 (fr) 1992-06-23 1995-06-30 Sanofi Elf Nouveaux derives du pyrazole, procede pour leur preparation et compositions pharmaceutiques les contenant.
US5637699A (en) 1992-06-29 1997-06-10 Merck & Co., Inc. Process for preparing morpholine tachykinin receptor antagonists
US5387595A (en) 1992-08-26 1995-02-07 Merck & Co., Inc. Alicyclic compounds as tachykinin receptor antagonists
US5578593A (en) 1992-12-11 1996-11-26 Merck & Co., Inc. Spiro piperidines and homologs promote release of growth hormone
US5292736A (en) 1993-02-26 1994-03-08 Sterling Winthrop Inc. Morpholinoalkylindenes as antiglaucoma agents
US5496833A (en) 1993-04-13 1996-03-05 Merck Sharp & Dohme Limited Piperidine tachykinin receptor antagonists
PL321136A1 (en) 1994-11-07 1997-11-24 Pfizer Some substituted derivatives of bencylamine as a new class of specific ligands of neuropeptide y1
US5532237A (en) 1995-02-15 1996-07-02 Merck Frosst Canada, Inc. Indole derivatives with affinity for the cannabinoid receptor
US5831115A (en) 1995-04-21 1998-11-03 Abbott Laboratories Inhibitors of squalene synthase and protein farnesyltransferase
US5739106A (en) 1995-06-07 1998-04-14 Rink; Timothy J. Appetite regulating compositions
FR2741621B1 (fr) 1995-11-23 1998-02-13 Sanofi Sa Nouveaux derives de pyrazole, procede pour leur preparation et compositions pharmaceutiques en contenant
WO1997020823A2 (fr) 1995-12-01 1997-06-12 Novartis Ag Antagonistes de recepteurs
WO1997020822A1 (fr) 1995-12-01 1997-06-12 Novartis Ag Quinazolin-2,4-diazirines en tant qu'antagoniste du recepteur du neuropeptide y
AU7692696A (en) 1995-12-01 1997-06-27 Novartis Ag Heteroaryl derivatives
AU1328197A (en) 1995-12-01 1997-06-19 Synaptic Pharmaceutical Corporation Aryl sulfonamide and sulfamide derivatives and uses thereof
AU7626496A (en) 1995-12-01 1997-06-27 Ciba-Geigy Ag Heteroaryl compounds
TW432073B (en) 1995-12-28 2001-05-01 Pfizer Pyrazolopyridine compounds
WO1997028149A1 (fr) 1996-02-02 1997-08-07 Merck & Co., Inc. Procede pour augmenter les niveaux de cholesterol hdl
WO1997029079A1 (fr) 1996-02-06 1997-08-14 Japan Tobacco Inc. Composes chimiques et utilisation pharmaceutique
GB9606805D0 (en) 1996-03-30 1996-06-05 Glaxo Wellcome Inc Medicaments
US6043246A (en) 1996-12-03 2000-03-28 Banyu Pharmaceutical Co., Ltd. Urea derivatives
DE69719544T2 (de) 1996-12-12 2003-11-06 Banyu Pharma Co Ltd Pyrazolderivate
CA2274593A1 (fr) 1996-12-13 1998-06-18 Banyu Pharmaceutical Co., Ltd. Derives d'aminopyrazole
WO1998027063A1 (fr) 1996-12-16 1998-06-25 Banyu Pharmaceutical Co., Ltd. Derives d'aminopyrazole
US6100259A (en) 1997-01-21 2000-08-08 Smithkline Beecham Corporation Cannabinoid receptor modulators
CN1246845A (zh) 1997-02-04 2000-03-08 纳幕尔杜邦公司 杀菌的羧酰胺
RU2203272C2 (ru) 1997-02-21 2003-04-27 Байер Акциенгезелльшафт Замещенные бициклические соединения, исходные и промежуточные продукты для их получения и фармацевтическая композиция на их основе
AU6309698A (en) 1997-03-12 1998-09-29 Banyu Pharmaceutical Co., Ltd. Drugs containing aminopyridine derivatives as the active ingredient
EP0979228A4 (fr) 1997-03-18 2000-05-03 Smithkline Beecham Corp Nouveaux agonistes de recepteurs de cannabinoides
FR2761266B1 (fr) 1997-03-28 1999-07-02 Sanofi Sa Composition pharmaceutique formee par granulation humide pour l'administration orale d'un derive du n-piperidino-3- pyrazolecarboxamide, de ses sels et de leurs solvates
FR2761265B1 (fr) 1997-03-28 1999-07-02 Sanofi Sa Composition pharmaceutique pour l'administration orale d'un derive du n-piperidino-3-pyrazolecarboxamide, de ses sels et de leurs solvates
EP0992239B1 (fr) 1997-04-23 2003-03-12 Banyu Pharmaceutical Co., Ltd. Antagoniste de recepteur de neuropeptide y
US6001836A (en) 1997-05-28 1999-12-14 Bristol-Myers Squibb Company Dihydropyridine NPY antagonists: cyanoguanidine derivatives
KR20010021696A (ko) 1997-07-11 2001-03-15 미즈노 마사루 퀴놀린 화합물 및 그의 의약용도
AR016817A1 (es) 1997-08-14 2001-08-01 Smithkline Beecham Plc Derivados de fenilurea o feniltiourea, procedimiento para su preparacion, coleccion de compuestos, compuestos intermediarios, composicion farmaceutica,metodo de tratamiento y uso de dichos compuestos para la manufactura de un medicamento
AU9185598A (en) 1997-09-25 1999-04-12 Banyu Pharmaceutical Co., Ltd. Novel neuropeptide y receptor antagonists
WO1999027965A1 (fr) 1997-11-28 1999-06-10 Banyu Pharmaceutical Co., Ltd. Agents anti-hyperlipemiques
WO1999051600A1 (fr) 1998-04-02 1999-10-14 Neurogen Corporation DERIVES AMINOALKYLE SUBSTITUES DE 9H-PYRIDINO [2,3-b]INDOLE ET 9H-PYRIMIDINO [4,5-b]INDOLE
ES2223170T3 (es) 1998-04-29 2005-02-16 Ortho-Mcneil Pharmaceutical, Inc. Aminotetralinas n sustituidas, ligandos del receptor y y5 del neuropeptido que sirve para el tratamiento de la obesidad y otros trastornos.
EP1075478B1 (fr) 1998-05-08 2003-04-16 SmithKline Beecham plc Derives de phenyluree et de (phenylthio)uree
US6329395B1 (en) 1998-06-08 2001-12-11 Schering Corporation Neuropeptide Y5 receptor antagonists
HN1998000027A (es) 1998-08-19 1999-06-02 Bayer Ip Gmbh Arilsulfonamidas y analagos
DE19837627A1 (de) 1998-08-19 2000-02-24 Bayer Ag Neue Aminosäureester von Arylsulfonamiden und Analoga
US6358951B1 (en) 1998-08-21 2002-03-19 Pfizer Inc. Growth hormone secretagogues
US6337332B1 (en) 1998-09-17 2002-01-08 Pfizer Inc. Neuropeptide Y receptor antagonists
AU756797B2 (en) 1998-11-10 2003-01-23 Banyu Pharmaceutical Co., Ltd. Spiro-indolines as Y5 receptor antagonists
AU2910600A (en) 1999-02-12 2000-08-29 Smithkline Beecham Plc Phenyl urea and phenyl thiourea derivatives
WO2000047576A1 (fr) 1999-02-12 2000-08-17 Smithkline Beecham Plc Derives de cinnamide utilises en tant qu'antagonistes des recepteurs de l'orexine-1
EP1150977B1 (fr) 1999-02-12 2004-08-25 SmithKline Beecham plc Derives de phenyluree et de phenylthiouree utilises comme antagonistes des recepteurs de l'orexine
PT1183245E (pt) 1999-04-22 2007-07-12 Lundbeck & Co As H Antagonistas selectivos de npy (y5)
US6340683B1 (en) 1999-04-22 2002-01-22 Synaptic Pharmaceutical Corporation Selective NPY (Y5) antagonists (triazines)
CA2373035A1 (fr) 1999-05-05 2000-11-16 Scott Dax Ligands de recepteurs du neuropeptide y derives de 3a,4,5,9b-tetrahydro-1h-benz[e]indol-2-yl amine, utilises pour le traitement de l'obesite et d'autres etats pathologiques
DE60023128T2 (de) 1999-05-12 2006-07-06 Ortho-Mcneil Pharmaceutical, Inc. Pyrazolcarboxamide zur behandlung von fettleibigkeit und anderen erkrankungen
EP1194421B1 (fr) 1999-06-30 2005-10-12 H. Lundbeck A/S Antagonistes selectifs du npy (y5)
WO2001007409A1 (fr) 1999-07-23 2001-02-01 Astrazeneca Uk Limited Derives de carbazole et leur utilisation en tant que ligands du recepteur de neuropeptide y5
HUP0202143A3 (en) 1999-07-28 2003-12-29 Ortho Mcneil Pharm Inc Amine and amide derivatives as ligands for the neuropeptide y y5 receptor pharmaceutical compositions containing them and their use
TWI279402B (en) 1999-08-20 2007-04-21 Banyu Pharma Co Ltd Spiro compounds having NPY antagonistic activities and agents containing the same
US6462053B1 (en) 1999-08-20 2002-10-08 Banyu Pharmaceutical Co., Ltd. Spiro compounds
EP1219294A4 (fr) 1999-09-20 2005-01-26 Antagonistes de l'hormone de concentration de la melanine
CA2386474A1 (fr) 1999-09-20 2001-03-29 Takeda Chemical Industries, Ltd. Antagoniste de l'hormone de concentration de la melanine
US6414002B1 (en) 1999-09-22 2002-07-02 Bristol-Myers Squibb Company Substituted acid derivatives useful as antidiabetic and antiobesity agents and method
YU23602A (sh) 1999-09-30 2004-09-03 Neurogen Corporation Amino supstituisani pirazolo /1,5/a/-1,5-pirimidini i pirazolo /1,5-a/-1,3,5-triazini
WO2001023389A2 (fr) 1999-09-30 2001-04-05 Neurogen Corporation Hétérocycles à substitution alkylène-diamine
CZ20021067A3 (cs) 1999-09-30 2002-11-13 Neurogen Corporation Určité alkylendiaminové substituované pyrazolo[1,5-a]- 1,5-pyrimidiny a pyrazolo[1,5-a]-1,3,5-triaziny
BR0017025A (pt) 1999-12-16 2003-01-07 Schering Corp Antagonistas do receptor y5 do neuropeptìdeo y de imidazola substituìda
AU779442B2 (en) 2000-01-20 2005-01-27 Eisai Co. Ltd. Novel piperidine compounds and drugs containing the same
WO2001056592A1 (fr) 2000-02-01 2001-08-09 Novo Nordisk A/S Utilisation de composes pour la regulation de l'absorption de nourriture
WO2001058869A2 (fr) 2000-02-11 2001-08-16 Bristol-Myers Squibb Company Modulateurs de recepteurs aux cannabinoides, leurs procedes de preparation et utilisations de modulateurs de recepteurs aux cannabinoides pour le traitement de maladies respiratoires et non respiratoires
ES2236178T3 (es) 2000-02-22 2005-07-16 Banyu Pharmaceutical Co., Ltd. Nuevos compuestos de imidazolina.
US6531478B2 (en) 2000-02-24 2003-03-11 Cheryl P. Kordik Amino pyrazole derivatives useful for the treatment of obesity and other disorders
FR2805818B1 (fr) 2000-03-03 2002-04-26 Aventis Pharma Sa Derives d'azetidine, leur preparation et les compositions pharmaceutiques les contenant
FR2805817B1 (fr) 2000-03-03 2002-04-26 Aventis Pharma Sa Compositions pharmaceutiques contenant des derives d'azetidine, les nouveaux derives d'azetidine et leur preparation
FR2805810B1 (fr) 2000-03-03 2002-04-26 Aventis Pharma Sa Compositions pharmaceutiques contenant des derives de 3- amino-azetidine, les nouveaux derives et leur preparation
EP1132389A1 (fr) 2000-03-06 2001-09-12 Vernalis Research Limited Nouveaux dérivés de l'azaindole pour le traitement de l'obésité
JP4009460B2 (ja) 2000-03-14 2007-11-14 アクテリオン ファマシューティカルズ リミテッド 1,2,3,4−テトラヒドロイソキノリン誘導体
EP1142886A1 (fr) 2000-04-07 2001-10-10 Aventis Pharma Deutschland GmbH Percyquinine, procédé pour sa production et son utilisation comme produit pharmaceutique
CA2407149C (fr) 2000-04-28 2010-10-12 Takeda Chemical Industries, Ltd. Antagonistes de l'hormone concentrant la melanine
GB0010757D0 (en) 2000-05-05 2000-06-28 Astrazeneca Ab Chemical compounds
GB0011013D0 (en) 2000-05-09 2000-06-28 Astrazeneca Ab Chemical compounds
WO2001085173A1 (fr) 2000-05-10 2001-11-15 Bristol-Myers Squibb Company Derives d'alkylamine d'antagonistes de dihydropyridine npy
US6444675B2 (en) 2000-05-10 2002-09-03 Bristol-Myers Squibb Company 4-alkyl and 4-cycloalkyl derivatives of dihydropyridine NPY antagonists
US6432960B2 (en) 2000-05-10 2002-08-13 Bristol-Myers Squibb Company Squarate derivatives of dihydropyridine NPY antagonists
WO2001085693A1 (fr) 2000-05-11 2001-11-15 Banyu Pharmaceutical Co., Ltd. Dérivés n-acyltétrahydroisoquinoline
AU5959201A (en) 2000-05-11 2001-11-20 Bristol Myers Squibb Co Tetrahydroisoquinoline analogs useful as growth hormone secretagogues
AU2001256733A1 (en) 2000-05-16 2001-11-26 Takeda Chemical Industries Ltd. Melanin-concentrating hormone antagonist
AU2001259056A1 (en) 2000-05-17 2001-11-26 Eli Lilly And Company Method for selectively inhibiting ghrelin action
US6391881B2 (en) 2000-05-19 2002-05-21 Bristol-Myers Squibb Company Thiourea derivatives of dihydropyridine NPY antagonists
SE0001899D0 (sv) 2000-05-22 2000-05-22 Pharmacia & Upjohn Ab New compounds
AU2001272476A1 (en) 2000-06-16 2001-12-24 Smithkline Beecham Plc Piperidines for use as orexin receptor antagonists
JP2004504303A (ja) 2000-07-05 2004-02-12 シナプティック・ファーマスーティカル・コーポレーション 選択的メラニン凝集ホルモン−1(mch1)受容体アンタゴニストおよびその使用
AU2001279294A1 (en) 2000-07-06 2002-01-21 Neurogen Corporation Melanin concentrating hormone receptor ligands
AU2001283938A1 (en) 2000-07-24 2002-02-05 Ardana Bioscience Limited Ghrelin antagonists
BR0112918A (pt) 2000-07-31 2003-07-01 Hoffmann La Roche Composto, utilização do mesmo, processo de tratamento de distúrbios, processo para a preparação de composto, composição farmacêutica que compreende esse composto, processo para preparar uma composição e processo de tratamento de obesidade em um ser humano
AU2001294547A1 (en) 2000-09-14 2002-03-26 Schering Corporation Substituted urea neuropeptide y y5 receptor antagonists
PT1326851E (pt) 2000-10-13 2004-11-30 Lilly Co Eli Dipeptidos substituidos como secretagogues da hormona do crescimento
AU2167002A (en) 2000-10-16 2002-06-11 Hoffmann La Roche Indoline derivatives and their use as 5-ht2 receptor ligands
WO2002036596A2 (fr) 2000-11-03 2002-05-10 Wyeth Cycloalkyl[b][1,4]diazepino[6,7,1-hi]indoles et derives
AU2426602A (en) 2000-11-20 2002-05-27 Biovitrum Ab Piperazinylpyrazine compounds as agonist or antagonist of serotonin 5ht-2 receptor
NZ525699A (en) 2000-11-20 2005-03-24 Biovitrum Ab Piperazinylpyrazines compounds as antagonists of serotonin 5-HT2 receptor
AU2002224885A1 (en) 2000-11-28 2002-06-11 Smithkline Beecham Plc Morpholine derivatives as antagonists of orexin receptors
ES2249384T3 (es) 2000-12-12 2006-04-01 Neurogen Corporation Espiro(isobenzofuran-1,4'-piperadin)-3-onas y 3h-espirobenzofuran-1,4-piperidinas.
GB0030710D0 (en) 2000-12-15 2001-01-31 Hoffmann La Roche Piperazine derivatives
ES2316486T3 (es) 2000-12-21 2009-04-16 Schering Corporation Antagonsitas de los receptores y5 del neuropeptido y heteroaril-urea.
CN1273451C (zh) 2000-12-22 2006-09-06 先灵公司 哌啶mch拮抗剂及其治疗肥胖症的用途
BR0116605A (pt) 2000-12-27 2003-09-30 Hoffmann La Roche Composto, processo para a preparação de um composto, composição farmacêutica que compreende o mesmo, sua utilização e processo para o tratamento e profilaxia de distúrbios do sistema nervoso central, distúrbios cardiovasculares, distúrbios gastrintestinais e apnéia do sono
WO2002051232A2 (fr) 2000-12-27 2002-07-04 Actelion Pharmaceuticals Ltd. Nouvelles benzazepines et derives heterocycliques associes
IL157179A0 (en) 2001-02-02 2004-02-08 Takeda Chemical Industries Ltd Fused heterocyclic compounds
CN100537527C (zh) 2001-03-21 2009-09-09 法马科皮亚公司 具有mch调节活性的芳基和二芳基化合物
US6900329B2 (en) 2001-03-21 2005-05-31 Schering Corporation MCH antagonists and their use in the treatment of obesity
SI1373216T1 (en) 2001-03-22 2005-06-30 Solvay Pharmaceuticals B.V. 4,5-dihydro-1h-pyrazole derivatives having cb1-antagonistic activity
AR035234A1 (es) 2001-04-12 2004-05-05 Pharmacopeia Drug Discovery Aril y biaril-piperidinas con actividad moduladora mch, metodo para preparar dichos compuestos, composiciones farmaceuticas, metodo para preparar las composiciones farmaceuticas y el uso de dichos compuestos para la manufactura de un medicamento
US6573287B2 (en) 2001-04-12 2003-06-03 Bristo-Myers Squibb Company 2,1-oxazoline and 1,2-pyrazoline-based inhibitors of dipeptidyl peptidase IV and method
EP1435955A2 (fr) 2001-05-05 2004-07-14 SmithKline Beecham P.L.C. Derives d'amines cycliques n-aroyl utilises comme antagonistes du recepteur d'orexine
US7432270B2 (en) 2001-05-05 2008-10-07 Smithkline Beecham P.L.C. N-aroyl cyclic amines
FR2824825B1 (fr) 2001-05-15 2005-05-06 Servier Lab Nouveaux derives d'alpha-amino-acides, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
WO2002094825A1 (fr) 2001-05-22 2002-11-28 Banyu Pharmaceutical Co., Ltd. Nouveau derive de spiropiperidine
IL158941A0 (en) 2001-05-22 2004-05-12 Neurogen Corp Melanin concentrating hormone receptor ligands: substituted 1-benzyl-4-aryl piperazine analogues
ATE381539T1 (de) 2001-06-20 2008-01-15 Merck & Co Inc Dipeptidylpeptidase-hemmer zur behandlung von diabetes
JP2005500308A (ja) 2001-06-20 2005-01-06 メルク エンド カムパニー インコーポレーテッド 糖尿病を治療するためのジペプチジルペプチダーゼ阻害剤
GB0115517D0 (en) 2001-06-25 2001-08-15 Ferring Bv Novel antidiabetic agents
ATE370943T1 (de) 2001-06-27 2007-09-15 Smithkline Beecham Corp Fluoropyrrolidine als dipeptidyl-peptidase inhibitoren
US7196201B2 (en) 2001-06-27 2007-03-27 Smithkline Beecham Corporation Pyrrolidines as dipeptidyl peptidase inhibitors
CA2419888A1 (fr) 2001-06-27 2003-01-09 Probiodrug Ag Structures peptidiques utiles pour la modulation competitive de la catalyse de dipeptidyle peptidase iv
DE60222667T2 (de) 2001-06-27 2008-07-17 Smithkline Beecham Corp. Fluorpyrrolidine als dipeptidylpeptidaseinhibitoren
JP4399256B2 (ja) 2001-06-28 2010-01-13 スミスクライン ビーチャム ピー エル シー オレキシン受容体アンタゴニストとしてのn−アロイル環状アミン誘導体
GB0115862D0 (en) 2001-06-28 2001-08-22 Smithkline Beecham Plc Compounds
EP1404675B1 (fr) 2001-07-03 2008-03-12 Novo Nordisk A/S Derives de purine inhibiteurs de dpp-iv pour le traitement du diabete
KR20040027870A (ko) 2001-07-05 2004-04-01 시냅틱 파마세틱칼 코포레이션 Mch 선택적인 안타고니스트로서의 치환 아닐린 피페리딘
UA74912C2 (en) 2001-07-06 2006-02-15 Merck & Co Inc Beta-aminotetrahydroimidazo-(1,2-a)-pyrazines and tetratriazolo-(4,3-a)-pyrazines as inhibitors of dipeptylpeptidase for the treatment or prevention of diabetes
WO2003007887A2 (fr) 2001-07-20 2003-01-30 Merck & Co., Inc. Imidazoles substitues servant de modulateurs de recepteurs de cannabinoides
BRPI0104510B8 (pt) 2001-07-27 2021-05-25 Embrapa Pesquisa Agropecuaria peptídeos antibióticos da família das phylloseptinas isolados da secreção da pele de phylloseptina hypocondrialis e composição antimicrobiana relacionada
HUP0401108A2 (hu) 2001-08-07 2004-09-28 Banyu Pharmaceutical Co., Ltd. Spirovegyületek, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények
GB0124463D0 (en) 2001-10-11 2001-12-05 Smithkline Beecham Plc Compounds
GB0126292D0 (en) 2001-11-01 2002-01-02 Smithkline Beecham Plc Compounds
GB0127145D0 (en) 2001-11-10 2002-01-02 Smithkline Beecham Compounds
GB0130393D0 (en) 2001-12-19 2002-02-06 Smithkline Beecham Plc Compounds
GB0130335D0 (en) 2001-12-19 2002-02-06 Smithkline Beecham Plc Compounds
GB0130341D0 (en) 2001-12-19 2002-02-06 Smithkline Beecham Plc Compounds
JP2005320249A (ja) 2002-05-01 2005-11-17 Banyu Pharmaceut Co Ltd 2−アミノピラジン誘導体の製造方法
TWI283241B (en) 2002-05-29 2007-07-01 Tanabe Seiyaku Co Novel piperidine compound
AR040241A1 (es) 2002-06-10 2005-03-23 Merck & Co Inc Inhibidores de la 11-beta-hidroxiesteroide deshidrogrenasa 1 para el tratamiento de la diabetes obesidad y dislipidemia
US7105526B2 (en) 2002-06-28 2006-09-12 Banyu Pharmaceuticals Co., Ltd. Benzimidazole derivatives
CA2460051A1 (fr) 2002-07-09 2004-01-15 Actelion Pharmaceuticals Ltd. Derives de 7,8,9,10-tetrahydro-6h-azepino, 6,7,8,9-tetrahydro-pyrido et 2,3-dihydro-2h-pyrrolo[2,1-b]-quinazolinone
EP1539747B1 (fr) 2002-09-18 2006-11-02 Glaxo Group Limited Amines cycliques n-aroyle utilisees comme antagonistes du recepteur d'orexine
US6869966B2 (en) 2002-09-30 2005-03-22 Banyu Pharmaceutical Co., Ltd. N-substituted-2-oxodihydropyridine derivatives
US20060166966A1 (en) 2002-10-08 2006-07-27 Cameron Black 4-amino-azepan-3-one compounds as cathepsin k inhibitors useful in the treatment of osteoporosis
CA2498091C (fr) 2002-10-11 2011-03-22 Actelion Pharmaceuticals Ltd. Derives d'acide sulfonylaminoacetique
GB0225884D0 (en) 2002-11-06 2002-12-11 Glaxo Group Ltd Novel compounds
GB0225938D0 (en) 2002-11-06 2002-12-11 Glaxo Group Ltd Novel compounds
MY134457A (en) 2002-11-22 2007-12-31 Merck & Co Inc Substituted amides
AU2003299648A1 (en) 2002-12-12 2004-06-30 Janssen Pharmaceutica, N.V. Substituted 4-phenyl-(1,3)-dioxanes
JO2397B1 (en) 2002-12-20 2007-06-17 ميرك شارب اند دوم كوربوريشن Terazol derivatives as beta-hydroxy steroid dihydrogenase-1 inhibitors
CL2004000553A1 (es) 2003-03-20 2005-02-04 Actelion Pharmaceuticals Ltd Uso de compuestos derivados de guanidina como antagonistas del receptor de neuropeptido ff; compuestos derivados de guanidina; procedimientos de preparacion; y composicion farmaceutica que los comprende.
CN100432056C (zh) 2003-03-26 2008-11-12 埃科特莱茵药品有限公司 四氢异喹啉基乙酰胺衍生物作为阿立新受体拮抗剂的应用
JO2355B1 (en) 2003-04-15 2006-12-12 ميرك شارب اند دوم كوربوريشن Hereditary calcitonin polypeptide receptor antagonists
CN1780820A (zh) 2003-04-28 2006-05-31 埃科特莱茵药品有限公司 作为阿立新受体拮抗剂的喹喔啉-3-酮衍生物
JP3939744B2 (ja) 2003-06-11 2007-07-04 メルク エンド カムパニー インコーポレーテッド 置換3−アルキルおよび3−アルケニルアゼチジン誘導体
HUP0304101A3 (en) 2003-12-22 2008-10-28 Sanofi Aventis Pyrazole derivatives, process for producing them, their use, pharmaceutical compositions containing them and their intermediates
HUP0400405A3 (en) 2004-02-10 2009-03-30 Sanofi Synthelabo Pyrimidine derivatives, process for producing them, their use, pharmaceutical compositions containing them and their intermediates
WO2005118548A1 (fr) 2004-03-01 2005-12-15 Actelion Pharmaceuticals Ltd Derives de 1,2,3,4-tétrahydroisoquinoléine substitués
WO2006067224A2 (fr) 2004-12-23 2006-06-29 Biovitrum Ab (Publ) Nouveaux composes
DE102004062544A1 (de) 2004-12-24 2006-07-06 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue substituierte Pyrrolidinone, deren Herstellung und deren Verewendung als Arzneimittel
WO2006110626A1 (fr) 2005-04-12 2006-10-19 Merck & Co., Inc. Antagonistes du récepteur de l’orexine de type amidopropoxyphényle
WO2006113704A2 (fr) * 2005-04-18 2006-10-26 Neurogen Corporation Antagonistes cb1 heteroaryle substitue
WO2006117669A1 (fr) 2005-05-03 2006-11-09 Pfizer Inc. Composes d'amide resorcinol
JP2008542276A (ja) 2005-05-23 2008-11-27 メルク エンド カムパニー インコーポレーテッド プロリンビスアミドオレキシン受容体アンタゴニスト
WO2007019234A2 (fr) 2005-08-04 2007-02-15 Merck & Co., Inc. Antagonistes des recepteurs d'orexine a base de sulfamide d'aminoethane
WO2007025069A2 (fr) 2005-08-26 2007-03-01 Merck & Co., Inc. Diazaspirodecane utilise comme antagonistes de recepteurs d'orexine
AR055203A1 (es) * 2005-08-31 2007-08-08 Otsuka Pharma Co Ltd Derivados de benzotiofeno con propiedades antipsicoticas
EP1954276A2 (fr) 2005-11-22 2008-08-13 Merck & Co., Inc. Antagonistes des recepteurs de l'indole orexine
AU2007245037A1 (en) 2006-03-29 2007-11-08 Merck Sharp & Dohme Corp. Diazepan orexin receptor antagonists
US20090105318A1 (en) 2006-03-29 2009-04-23 Coleman Paul J Amidoethylthioether Orexin Receptor Antagonists
EP2007717A1 (fr) 2006-04-11 2008-12-31 Actelion Pharmaceuticals Ltd. Nouveaux composés sulfonamides
EP2013209B1 (fr) 2006-04-26 2011-01-19 Actelion Pharmaceuticals Ltd. Dérivés de pyrazolo-tétrahydropyridine en tant qu'antagonistes des récepteurs d'orexine
US20090192143A1 (en) 2006-07-14 2009-07-30 Cox Christopher D Substituted diazepan orexin receptor antagonists
EP2049526A2 (fr) 2006-07-14 2009-04-22 Merck & Co., Inc. Prolines bis-amides substituées en 2 antagonistes du récepteur de l'oréxine
CA2657623A1 (fr) 2006-07-14 2008-01-17 Merck & Co., Inc. Diazepans pontes antagonistes du recepteur de l'orexine
AU2007285371A1 (en) 2006-08-15 2008-02-21 Actelion Pharmaceuticals Ltd. Azetidine compounds as orexin receptor antagonists
CA2659352A1 (fr) 2006-08-28 2008-03-06 Actelion Pharmaceuticals Ltd Derives de 1,4,5,6,7,8-hexahydro-1,2,5-triaza-azulene en tant qu'antagonistes de recepteur d'orexine
DE602007009284D1 (de) 2006-09-29 2010-10-28 Actelion Pharmaceuticals Ltd 3-aza-bicycloä3.1.0ühexanderivate
ATE496043T1 (de) * 2006-12-01 2011-02-15 Actelion Pharmaceuticals Ltd 3-heteroaryl (amino bzw. amido)-1- (biphenyl bzw. phenylthiazolyl) carbonylpiperdinderivate als orexinrezeptor-inhibitoren
PE20081229A1 (es) 2006-12-01 2008-08-28 Merck & Co Inc Antagonistas de receptor de orexina de diazepam sustituido
EP2131654A4 (fr) * 2007-03-02 2011-02-02 Merck Sharp & Dohme Carboxamides de bipyridine, antagonistes du récepteur de l'orexine
RU2470021C2 (ru) 2007-05-23 2012-12-20 Мерк Шарп Энд Домэ Корп. Пиридилпиперидиновые антагонисты рецептора орексинов
EP2184981A4 (fr) * 2007-08-09 2012-02-01 Merck Sharp & Dohme Antagonistes de récepteurs d'orexine au pyridinecarboxamide
EP2234999A1 (fr) * 2007-12-21 2010-10-06 F. Hoffmann-La Roche AG Dérivés hétéroaryles en tant qu'antagonistes du récepteur à orexine
AR070221A1 (es) * 2008-01-23 2010-03-25 Astrazeneca Ab Derivados de ftalazinona inhibidores de polimerasas, composiciones farmaceuticas que los contienen y usos de los mismos para prevenir y/o tratar tumores cancerigenos,lesiones isquemicas y otras enfermedades asociadas.
WO2009133522A1 (fr) 2008-04-30 2009-11-05 Actelion Pharmaceuticals Ltd Composés de pipéridine et de pyrrolidine
CA2724648A1 (fr) * 2008-05-22 2009-11-26 Merck Sharp & Dohme Corp. Procede de preparation d'un antagoniste des recepteurs de l'orexine
US8623863B2 (en) 2008-10-21 2014-01-07 Merck Sharp & Dohme Corp. Disubstituted azepan orexin receptor antagonists
US8466281B2 (en) 2008-10-21 2013-06-18 Merck Sharp & Dohme Corp. 2,5-disubstituted morpholine orexin receptor antagonists
JP2012506375A (ja) 2008-10-21 2012-03-15 メルク・シャープ・エンド・ドーム・コーポレイション 2,5−二置換ピペリジンオレキシン受容体アンタゴニスト
EP2350066B1 (fr) 2008-10-21 2013-08-28 Merck Sharp & Dohme Corp. Pipéridines 2,5-disubstituées comme antagonistes du récepteur de l orexine
AU2009307918A1 (en) 2008-10-21 2010-04-29 Merck Sharp & Dohme Corp. 2,4-disubstituted pyrrolidine orexin receptor antagonists
EP2350061B1 (fr) * 2008-10-21 2013-08-14 Merck Sharp & Dohme Corp. Antagonistes de récepteur de l'orexine de type pipéridine 2,3-disubstituée
CA2741648A1 (fr) * 2008-10-30 2010-05-06 Merck Sharp & Dohme Corp. Antagonistes carboxamide phenyl 2,5-disubstitue du recepteur de l'orexine
CA2741644C (fr) * 2008-10-30 2013-05-07 Merck Sharp & Dohme Corp. Antagonistes d'isonicotinamide des recepteurs de l'orexine
GB0823467D0 (en) 2008-12-23 2009-01-28 Glaxo Group Ltd Novel Compounds
JP2013502447A (ja) 2009-08-24 2013-01-24 グラクソ グループ リミテッド 睡眠障害の治療のためのオレキシン受容体アンタゴニストとしての5−メチル−ピペリジン誘導体
US9546152B2 (en) * 2012-10-23 2017-01-17 Merck Sharp & Dohme Corp. 2-pyridyloxy-3-substituted-4-nitrile orexin receptor antagonists

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EP2768823B1 (fr) 2017-09-06
US9156819B2 (en) 2015-10-13
CN103874695B (zh) 2017-12-15
US20130102619A1 (en) 2013-04-25
CA2852425A1 (fr) 2013-04-25
AU2012326275A1 (en) 2014-04-17
CN103874695A (zh) 2014-06-18
TW201317228A (zh) 2013-05-01
AU2012326275B2 (en) 2016-12-01
BR112014009486A2 (pt) 2017-05-09
JP5947906B2 (ja) 2016-07-06
AR088352A1 (es) 2014-05-28

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