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PE20091348A1 - Derivados de 1,2,4-triazol amino como moduladores de mglur5 - Google Patents

Derivados de 1,2,4-triazol amino como moduladores de mglur5

Info

Publication number
PE20091348A1
PE20091348A1 PE2008001830A PE2008001830A PE20091348A1 PE 20091348 A1 PE20091348 A1 PE 20091348A1 PE 2008001830 A PE2008001830 A PE 2008001830A PE 2008001830 A PE2008001830 A PE 2008001830A PE 20091348 A1 PE20091348 A1 PE 20091348A1
Authority
PE
Peru
Prior art keywords
methyl
amino
triazole
isoxazol
mglur5
Prior art date
Application number
PE2008001830A
Other languages
English (en)
Inventor
Isaac Methvin
Wallberg Andreas
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of PE20091348A1 publication Critical patent/PE20091348A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/08Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • 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
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/061,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

REFERIDO A UN COMPUESTO DERIVADO DE 1,2,4-TRIAZOL AMINO DE FORMULA I, DONDE X ES (a), (b), ENTRE OTROS, R1 ES METIL, HALOGENO O CIANO, R2 ES H O FLUORO, R3 Y R4 SON CADA UNO C1-C3 ALQUIL O CICLOPROPIL, R5 ES H, ALQUIL C1-C3 O CICLOPROPIL, Z ES (c), (d), ENTRE OTROS, R6 Y R7 SON CADA UNO H, FLUORO, ALQUIL C1-C3 O ALCOXI C1-C3. SON COMPUESTOS PREFERIDOS: 5-{5-[{[5-(3-CLOROFENIL)ISOXAZOL-3-IL]METIL}(CICLOPROPIL)AMINO]-4-METIL-4H-1,2,4-TRIAZOL-3-IL}PIRIDAZIN-3(2H)-ONA, 6-[4-ETIL-5-(METIL{[5-(3-METILFENIL)ISOXAZOL-3-IL]METIL}AMINO)-4H-1,2,4-TRIAZOL-3-IL]PIRIMIDIN-4(3H)-ONA; 2-METIL-5-[4-METIL-5-(METIL{(1S)-1-[5-(3-METILFENIL)ISOXAZOL-3-IL]ETIL}AMINO)-4H-1,2,4-TRIAZOL-3-IL]PIRIDAZIN-3(2H)-ONA. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON MODULADORES DE LOS RECEPTORES DE GLUTAMATO METABOTROPICOS mGLUR5, SIENDO UTILES PARA EL TRATAMIENTO DE DEMENCIA SENIL, ENFERMEDAD DE PARKINSON, ESQUIZOFRENIA, RETINOPATIAS, EPILEPSIA, ENTRE OTROS
PE2008001830A 2007-10-26 2008-10-24 Derivados de 1,2,4-triazol amino como moduladores de mglur5 PE20091348A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US98295607P 2007-10-26 2007-10-26

Publications (1)

Publication Number Publication Date
PE20091348A1 true PE20091348A1 (es) 2009-10-04

Family

ID=40579779

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2008001830A PE20091348A1 (es) 2007-10-26 2008-10-24 Derivados de 1,2,4-triazol amino como moduladores de mglur5

Country Status (21)

Country Link
US (1) US20090111821A1 (es)
EP (1) EP2212316A4 (es)
JP (1) JP2011500798A (es)
KR (1) KR20100089091A (es)
CN (1) CN101918399A (es)
AR (1) AR069030A1 (es)
AU (1) AU2008317544A1 (es)
BR (1) BRPI0818679A2 (es)
CA (1) CA2702974A1 (es)
CL (1) CL2008003182A1 (es)
CR (1) CR11391A (es)
DO (1) DOP2010000124A (es)
EA (1) EA201000656A1 (es)
IL (1) IL205289A0 (es)
MX (1) MX2010004362A (es)
NI (1) NI201000072A (es)
PE (1) PE20091348A1 (es)
TW (1) TW200922585A (es)
UY (1) UY31427A1 (es)
WO (1) WO2009054794A1 (es)
ZA (1) ZA201002854B (es)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2438052A1 (en) * 2009-06-05 2012-04-11 Oslo University Hospital HF Azole derivatives as wtn pathway inhibitors
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
RU2495687C1 (ru) * 2012-06-19 2013-10-20 Государственное бюджетное образовательное учреждение высшего профессионального образования "Северо-Осетинская государственная медицинская академия" Минздравсоцразвития Российской Федерации Способ лечения больных гастроэзофагеальной рефлюксной болезнью
UA113223C2 (xx) * 2012-08-13 2016-12-26 Арилетинілпіримідини
EP2857387A1 (en) 2013-10-07 2015-04-08 Boehringer Ingelheim International Gmbh Process for manufacturing 1,6-dihydro-6-oxo-4-pyridazine carboxylic acid
US9745308B2 (en) 2014-09-12 2017-08-29 Chiesi Farmaceutici S.P.A. Pyridazinone derivatives as phoshoinositide 3-kinases inhibitors
US12435078B2 (en) 2017-09-18 2025-10-07 Gfb (Abc), Llc Pyridazinones and methods of use thereof

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9420355D0 (en) * 1994-10-10 1994-11-23 Univ Nottingham Preparation of protein microspheres, films and coatings
JP4060884B2 (ja) * 1995-08-28 2008-03-12 昭和薬品化工株式会社 局所麻酔用組成物
US5962536A (en) * 1998-07-31 1999-10-05 Komer; Gene Injectable propofol formulations
WO2005077345A1 (en) * 2004-02-03 2005-08-25 Astrazeneca Ab Compounds for the treatment of gastro-esophageal reflux disease
RU2006127575A (ru) * 2004-02-18 2008-03-27 Астразенека Аб (Se) Соединение триазола и их применение в качестве антагонистов метаботропного рецептора глутамата
MXPA06009019A (es) * 2004-02-18 2007-03-08 Astrazeneca Ab Compuestos de tetrazol y su uso como antagonistas del receptor de glutamato metabotropico.
AR058807A1 (es) * 2005-09-29 2008-02-27 Astrazeneca Ab 5-(fenilisoxazoletoxi)-triazol-3-il piridinas sustituidas, para el tratamiento de trastornos mediados por el receptor mglur5
JP2009515997A (ja) * 2005-11-18 2009-04-16 タケダ サン ディエゴ インコーポレイテッド グルコキナーゼ活性剤
HRP20110054T1 (hr) * 2006-03-24 2011-02-28 Eisai R&D Management Co. Derivat triazolona
TW200808777A (en) * 2006-05-05 2008-02-16 Astrazeneca Ab MGLUR5 modulators III
TW200811179A (en) * 2006-05-05 2008-03-01 Astrazeneca Ab mGluR5 modulators VI
TW200808800A (en) * 2006-05-05 2008-02-16 Astrazeneca Ab MGluR5 modulators V
TW200811157A (en) * 2006-05-05 2008-03-01 Astrazeneca Ab mGluR5 modulators I
TW200811156A (en) * 2006-05-05 2008-03-01 Astrazeneca Ab mGluR5 modulators IV
TW200811137A (en) * 2006-05-05 2008-03-01 Astrazeneca Ab mGluR5 modulators II
TW200821305A (en) * 2006-10-05 2008-05-16 Astrazeneca Ab MGluR5 modulators
CA2710345C (en) * 2007-12-21 2016-11-15 Merck Serono S.A. Triazole oxadiazoles derivatives
EP2276746A1 (en) * 2008-04-10 2011-01-26 Basf Se Substituted pyridazinylmethyl sulfonamides

Also Published As

Publication number Publication date
EP2212316A4 (en) 2012-06-27
AU2008317544A1 (en) 2009-04-30
MX2010004362A (es) 2010-04-30
DOP2010000124A (es) 2010-10-15
AR069030A1 (es) 2009-12-23
BRPI0818679A2 (pt) 2015-04-14
NI201000072A (es) 2011-03-24
CL2008003182A1 (es) 2009-11-27
EA201000656A1 (ru) 2010-12-30
CA2702974A1 (en) 2009-04-30
CN101918399A (zh) 2010-12-15
CR11391A (es) 2010-08-05
TW200922585A (en) 2009-06-01
WO2009054794A1 (en) 2009-04-30
JP2011500798A (ja) 2011-01-06
UY31427A1 (es) 2009-05-29
ZA201002854B (en) 2011-10-26
US20090111821A1 (en) 2009-04-30
EP2212316A1 (en) 2010-08-04
KR20100089091A (ko) 2010-08-11
IL205289A0 (en) 2010-12-30

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