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MA26730A1 - Composes nouveaux antagonistes de npy, procede pour leur preparation et compositions pharmaceutiques les contenant - Google Patents

Composes nouveaux antagonistes de npy, procede pour leur preparation et compositions pharmaceutiques les contenant

Info

Publication number
MA26730A1
MA26730A1 MA25963A MA25963A MA26730A1 MA 26730 A1 MA26730 A1 MA 26730A1 MA 25963 A MA25963 A MA 25963A MA 25963 A MA25963 A MA 25963A MA 26730 A1 MA26730 A1 MA 26730A1
Authority
MA
Morocco
Prior art keywords
preparation
pharmaceutical compositions
compositions containing
antagonist compounds
npy antagonist
Prior art date
Application number
MA25963A
Other languages
English (en)
Inventor
Louis Elliott Richard
Frederick Hank Richard
Hammond Marlys
Original Assignee
Pfizer Prod 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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of MA26730A1 publication Critical patent/MA26730A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Child & Adolescent Psychology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Diabetes (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)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
MA25963A 1999-04-30 2000-04-26 Composes nouveaux antagonistes de npy, procede pour leur preparation et compositions pharmaceutiques les contenant MA26730A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US13202999P 1999-04-30 1999-04-30

Publications (1)

Publication Number Publication Date
MA26730A1 true MA26730A1 (fr) 2004-12-20

Family

ID=22452122

Family Applications (1)

Application Number Title Priority Date Filing Date
MA25963A MA26730A1 (fr) 1999-04-30 2000-04-26 Composes nouveaux antagonistes de npy, procede pour leur preparation et compositions pharmaceutiques les contenant

Country Status (12)

Country Link
US (2) US6355635B1 (fr)
AR (1) AR028824A1 (fr)
AU (1) AU2935200A (fr)
CO (1) CO5170414A1 (fr)
GT (1) GT200000057A (fr)
HN (1) HN2000000041A (fr)
MA (1) MA26730A1 (fr)
PA (1) PA8493701A1 (fr)
PE (1) PE20010118A1 (fr)
TN (1) TNSN00092A1 (fr)
UY (1) UY26130A1 (fr)
WO (1) WO2000066578A1 (fr)

Families Citing this family (38)

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PL356485A1 (en) 1999-12-16 2004-06-28 Schering Corporation Substituted imidazole neuropeptide y y5 receptor antagonists
US6894063B2 (en) * 2000-09-14 2005-05-17 Schering Corporation Substituted urea neuropeptide Y Y5 Receptor antagonists
US20050043256A1 (en) * 2001-07-30 2005-02-24 Isis Pharmaceuticals, Inc. Antisense modulation of stearoyl-CoA desaturase expression
US20050107411A1 (en) * 2001-12-17 2005-05-19 Macneil Douglas J. Method for treating circadian rhythm disruptions
MXPA04007612A (es) * 2002-02-05 2004-11-10 Novo Nordisk As Aril- y heteroarilpiperazinas novedosas.
WO2003077847A2 (fr) 2002-03-12 2003-09-25 Merck & Co., Inc. Amides substitues
CA2502511A1 (fr) * 2002-10-18 2004-05-29 Pfizer Products Inc. Ligands des recepteurs des cannabinoides et applications de ceux-ci
EP1635813A4 (fr) * 2003-06-06 2009-07-01 Merck & Co Inc Polytherapie permettant de traiter la dyslipidemie
ATE461178T1 (de) 2003-07-29 2010-04-15 High Point Pharmaceuticals Llc Pyridazinyl-piperazine und deren verwendung als histamin-h3-rezeptorliganden
WO2005030210A1 (fr) * 2003-09-26 2005-04-07 Pfizer Products Inc. Traitement des dereglements neurologiques lies a des troubles du sommeil paradoxal avec un antagoniste du recepteur y5 du npy
EP1670468A1 (fr) * 2003-09-26 2006-06-21 Pfizer Products Inc. Utilisation d'un antagoniste du recepteur y5 du npy pour le traitement des troubles du rythme circadien
DE102004003812A1 (de) * 2004-01-25 2005-08-11 Aventis Pharma Deutschland Gmbh Arylsubstituierte Heterozyklen, Verfahren ihrer Herstellung und ihre Verwendung als Arzneimittel
US7319108B2 (en) 2004-01-25 2008-01-15 Sanofi-Aventis Deutschland Gmbh Aryl-substituted heterocycles, process for their preparation and their use as medicaments
US20050256124A1 (en) * 2004-04-15 2005-11-17 Neurocrine Biosciences, Inc. Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto
US20060039890A1 (en) * 2004-08-20 2006-02-23 Renshaw Perry F Treatment of psychological and cognitive disorders using a cholesterol -lowering agent in combination with an antidepressant
MX2007003318A (es) 2004-09-20 2007-05-18 Xenon Pharmaceuticals Inc Derivados heterociclicos y su uso como agentes terapeuticos.
TW200626138A (en) 2004-09-20 2006-08-01 Xenon Pharmaceuticals Inc Heterocyclic derivatives and their use as therapeutic agents
CA2580857A1 (fr) 2004-09-20 2006-09-28 Xenon Pharmaceuticals Inc. Derives heterocycliques et leur utilisation en tant qu'agents therapeutiques
MX2007003319A (es) 2004-09-20 2007-06-05 Xenon Pharmaceuticals Inc Derivados heterociclicos y su uso como agentes terapeuticos.
CN101084212A (zh) 2004-09-20 2007-12-05 泽农医药公司 杂环衍生物及其作为硬脂酰CoA去饱和酶介导剂的用途
CA2580855A1 (fr) 2004-09-20 2006-03-30 Xenon Pharmaceuticals Inc. Derives heterocycliques et leur utilisation en tant qu'agents therapeutiques
US8071603B2 (en) 2004-09-20 2011-12-06 Xenon Pharmaceuticals Inc. Heterocyclic derivatives and their use as stearoyl-CoA desaturase inhibitors
US20080064632A1 (en) * 2004-09-24 2008-03-13 Amatruda John M Combination Therapy for the Treatment of Obesity
GB0510141D0 (en) * 2005-05-18 2005-06-22 Addex Pharmaceuticals Sa Novel compounds B3
EP2029138A1 (fr) 2005-06-03 2009-03-04 Xenon Pharmaceuticals Inc. Derives aminothiazole utilises en tant qu'inhibiteurs de la stearoyle-coa desaturase humaine
KR101286569B1 (ko) 2005-07-04 2013-07-23 하이 포인트 파마슈티칼스, 엘엘씨 신규 약제
EP1968596A4 (fr) * 2005-12-22 2010-12-01 Icagen Inc Antagonistes du canal calcique
CA2653062A1 (fr) 2006-05-23 2007-11-29 Transtech Pharma, Inc. Nouveaux medicaments
DK2079732T3 (da) 2006-05-29 2012-01-23 High Point Pharmaceuticals Llc 3-(1,3-benzodioxol-5-yl)-6-(4-cyclopropylpiperazin-1-yl)-pyridazin, dets salte og solvater og dets anvendelse som histamin H3-receptorantagonister
WO2008033575A2 (fr) * 2006-09-15 2008-03-20 Metabolon, Inc. Procédés d'identification de cheminements biochimiques
DK2125797T3 (da) * 2007-03-16 2014-02-10 Actelion Pharmaceuticals Ltd Aminopyridinderivater som s1p1/edg1-receptoragonister
EP2014656A3 (fr) 2007-06-11 2011-08-24 High Point Pharmaceuticals, LLC Nouveaux antagonistes d'hétéocycliques h3
WO2009112033A1 (fr) * 2008-03-12 2009-09-17 Københavns Universitet (University Of Copenhagen) Utilisation d’antagonistes de récepteur npy y5 pour la prévention de l’abus de psychostimulants et d’opioïdes
JP2012510523A (ja) * 2008-12-03 2012-05-10 プレシディオ ファーマシューティカルズ インコーポレイテッド Ｈｃｖｎｓ５ａの阻害剤
PH12013501268A1 (en) 2010-12-17 2016-04-01 Mitsubishi Tanabe Pharma Corp Continuous arycyclic compound
US9546155B2 (en) 2012-06-15 2017-01-17 Mitsubishi Tanabe Pharma Corporation Aromatic heterocyclic compound
US10328064B2 (en) * 2014-12-23 2019-06-25 Fgh Biotech, Inc. Compositions of fatostatin based heterocyclic compounds and uses thereof
CA3160364C (fr) * 2019-11-19 2024-11-05 Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften E.V. Composes et utilisation pour le diagnostic, le traitement et la prevention de maladies associees a l'agregation d'alpha-synucleine

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4440774A (en) 1975-03-03 1984-04-03 Merck & Co., Inc. 3-Amino-2-hydroxypropoxyaryl imidazole derivatives
US4853383A (en) 1975-03-03 1989-08-01 Merck & Co., Inc. β-blocking substituted imidazoles
JPH0251150A (ja) * 1988-08-12 1990-02-21 Konica Corp 新規なシアンカプラーを含有するハロゲン化銀写真感光材料
DE3935514A1 (de) * 1989-10-25 1991-05-02 Boehringer Mannheim Gmbh Neue bicyclo-imidazole, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel
DK0448765T3 (da) * 1990-03-30 1994-09-19 Heumann Pharma Gmbh & Co Anvendelse af guanidinderivater til fremstilling af et lægemiddel med NPY-antagonistisk virkning
US6562862B1 (en) 1994-10-20 2003-05-13 Eli Lilly And Company Methods of inhibiting physiological conditions associated with an excess of neuropeptide Y
WO1996014307A1 (fr) 1994-11-07 1996-05-17 Pfizer Inc. Certains derives de benzylamine a substitutions; une nouvelle classe de ligands specifiques du neuropeptide y1
EP0759441A3 (fr) * 1995-06-30 1999-06-30 Eli Lilly And Company Procédés de traitement des pathologies associées aux peptides neuropeptide Y
KR20010020610A (ko) * 1997-07-03 2001-03-15 해피 페너 ; 해리 에이치. 페너 2세 엔피와이 특이적 리간드 유형인 디아릴이미다졸 유도체
CA2325587A1 (fr) * 1998-03-25 1999-09-30 Mendi Higgins Agents anorexigenes a base d'imidazolones: derives phenyles ii

Also Published As

Publication number Publication date
CO5170414A1 (es) 2002-06-27
US6355635B1 (en) 2002-03-12
AR028824A1 (es) 2003-05-28
US20010039277A1 (en) 2001-11-08
WO2000066578A1 (fr) 2000-11-09
AU2935200A (en) 2000-11-17
TNSN00092A1 (fr) 2005-11-10
GT200000057A (es) 2001-10-20
PE20010118A1 (es) 2001-02-03
PA8493701A1 (es) 2002-07-30
HN2000000041A (es) 2001-02-02
US6514966B2 (en) 2003-02-04
UY26130A1 (es) 2000-12-29

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