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NO20081428L - Tetrahydroquinolinones and their use as modulators of metabotropic glutamate receptors - Google Patents

Tetrahydroquinolinones and their use as modulators of metabotropic glutamate receptors

Info

Publication number
NO20081428L
NO20081428L NO20081428A NO20081428A NO20081428L NO 20081428 L NO20081428 L NO 20081428L NO 20081428 A NO20081428 A NO 20081428A NO 20081428 A NO20081428 A NO 20081428A NO 20081428 L NO20081428 L NO 20081428L
Authority
NO
Norway
Prior art keywords
modulators
tetrahydroquinolinones
metabotropic glutamate
glutamate receptors
compounds
Prior art date
Application number
NO20081428A
Other languages
Norwegian (no)
Inventor
Wojciech Danysz
Ivars Kalvinsh
Valerjans Kauss
Aigars Jirgensons
Christopher Graham Raphael Parsons
Maksims Vanejevs
Ieva Jaunzeme
Markus Henrich
Tanja Weil
Claudia Jatzke
Original Assignee
Merz Pharma Gmbh & Co Kgaa
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 Merz Pharma Gmbh & Co Kgaa filed Critical Merz Pharma Gmbh & Co Kgaa
Publication of NO20081428L publication Critical patent/NO20081428L/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/20—Oxygen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/472—Non-condensed isoquinolines, e.g. papaverine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/472—Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
    • A—HUMAN NECESSITIES
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    • 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
    • C07D401/06—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 carbon chain containing only aliphatic carbon atoms
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    • 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
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    • C07D413/06—Heterocyclic 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 linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic 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
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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic 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
    • C07D417/02—Heterocyclic 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 two hetero rings
    • C07D417/06—Heterocyclic 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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

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Abstract

Oppfinnelsen gjelder etynylsubstituerte tetrahydrokinolinonderivater, så vel som deres farmasøytisk akseptable salter. Oppfinnelsen gj elder videre en fremgangsmåte for fremstilling av slike forbindelser. Forbindelsene ifølge oppfinnelsen er gruppe I-mGluR-modulatorer og er følgelig anvendbare for kontroll og forebyggelse av akutte og/eller kroniske, nevrologiske forstyrrelser .The invention relates to ethynyl-substituted tetrahydroquinolinone derivatives, as well as their pharmaceutically acceptable salts. The invention further relates to a process for the preparation of such compounds. The compounds of the invention are group I mGluR modulators and are consequently useful for the control and prevention of acute and / or chronic neurological disorders.

NO20081428A 2005-08-24 2008-03-18 Tetrahydroquinolinones and their use as modulators of metabotropic glutamate receptors NO20081428L (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
PCT/GB2005/003285 WO2007023242A1 (en) 2005-08-24 2005-08-24 Tetrahydroquinolinones and their use as modulators of metabotropic glutamate receptors
PCT/GB2006/003170 WO2007023290A1 (en) 2005-08-24 2006-08-24 Tetrahydroquinolinones and their use as modulators of metabotropic glutamate receptors

Publications (1)

Publication Number Publication Date
NO20081428L true NO20081428L (en) 2008-03-18

Family

ID=36273537

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20081428A NO20081428L (en) 2005-08-24 2008-03-18 Tetrahydroquinolinones and their use as modulators of metabotropic glutamate receptors

Country Status (15)

Country Link
EP (1) EP1931635A1 (en)
JP (1) JP2009506018A (en)
KR (1) KR20080031972A (en)
CN (1) CN101223142A (en)
AR (1) AR056044A1 (en)
AU (1) AU2006283359B2 (en)
BR (1) BRPI0615059A2 (en)
CA (1) CA2610873C (en)
EA (1) EA200800660A1 (en)
IL (1) IL189617A (en)
MX (1) MX2008001871A (en)
NO (1) NO20081428L (en)
TW (1) TWI329635B (en)
WO (2) WO2007023242A1 (en)
ZA (1) ZA200710668B (en)

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US8349852B2 (en) 2009-01-13 2013-01-08 Novartis Ag Quinazolinone derivatives useful as vanilloid antagonists
CN102666551B (en) * 2009-12-18 2014-12-10 詹森药业有限公司 Bicyclic thiazoles as allosteric modulators of MGLUR5 receptors
CA2782950A1 (en) 2009-12-18 2011-06-23 Janssen Pharmaceutica Nv Bicyclic thiazoles as allosteric modulators of mglur5 receptors
CA2784830C (en) 2009-12-18 2018-03-27 Sunovion Pharmaceuticals Inc. Compounds for treating disorders mediated by metabotropic glutamate receptor 5, and methods of use thereof
AR080056A1 (en) 2010-02-01 2012-03-07 Novartis Ag CICLOHEXIL-AMIDA DERIVATIVES AS ANTAGONISTS OF CRF RECEIVERS
EP2531510B1 (en) 2010-02-01 2014-07-23 Novartis AG Pyrazolo[5,1b]oxazole derivatives as crf-1 receptor antagonists
US8835444B2 (en) 2010-02-02 2014-09-16 Novartis Ag Cyclohexyl amide derivatives as CRF receptor antagonists
AR083475A1 (en) 2010-10-18 2013-02-27 Merz Pharma Gmbh & Co Kgaa METABOTROPIC GLUTAMATE RECEIVERS MODULATORS
WO2012139876A1 (en) 2011-04-14 2012-10-18 Merz Pharma Gmbh & Co. Kgaa Enteric formulations of metabotropic glutamate receptor modulators
WO2012172093A1 (en) * 2011-06-17 2012-12-20 Merz Pharma Gmbh & Co. Kgaa Dihydroindolizine derivate as metabotropic glutamate receptor modulators
WO2013050527A1 (en) 2011-10-05 2013-04-11 H. Lundbeck A/S Quinazoline derivatives as pde10a enzyme inhibitors
EP2650284A1 (en) * 2012-04-10 2013-10-16 Merz Pharma GmbH & Co. KGaA Heterocyclic derivatives as metabotropic glutamate receptor modulators
KR101418078B1 (en) * 2013-01-23 2014-07-10 한국과학기술연구원 2-(Substituted ethynyl)quinoline derivatives as mGluR5 antagonists
US9856214B2 (en) 2013-11-15 2018-01-02 The Wistar Institute Of Anatomy And Biology EBNA1 inhibitors and their method of use
KR101579496B1 (en) * 2014-07-03 2015-12-23 한국과학기술연구원 mGluR5 Radiotracer composition
EP3285582B1 (en) * 2015-03-26 2020-11-11 Merck Sharp & Dohme Corp. Phosphate-substituted quinolizine derivatives useful as hiv integrase inhibitors
JP6771491B2 (en) 2015-05-14 2020-10-21 ザ ウィスター インスティテュート オブ アナトミー アンド バイオロジー EBNA1 inhibitor and how to use it
PH12017502158B1 (en) 2015-06-03 2022-04-27 Bristol Meyers Squibb Co 4-hydroxy-3-(heteroaryl)pyridine-2-one apj agonists for use in the treatment of cardiovascular disorders
EP3459939A1 (en) * 2017-09-26 2019-03-27 Pragma Therapeutics Novel heterocyclic compounds as modulators of mglur7
TW201946919A (en) 2018-05-17 2019-12-16 威斯塔研究所 EBNA1 inhibitor crystalline forms, and methods of preparing and using same
CN114929230B (en) * 2019-10-21 2024-11-29 爱思开生物制药株式会社 Use of imidazopyrimidine or imidazotriazine compounds for the prevention, alleviation or treatment of cognitive disorders or for improving cognitive function
EP4049661A4 (en) * 2019-10-21 2023-11-08 SK Biopharmaceuticals Co., Ltd. Use of imidazopyrimidine or imidazotriazine compound for prevention, alleviation, or treatment of developmental disability

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7115630B2 (en) * 2000-10-02 2006-10-03 Janssen Pharmaceutica N.V. Metabotropic glutamate receptor antagonists
TWI301760B (en) * 2004-02-27 2008-10-11 Merz Pharma Gmbh & Co Kgaa Tetrahydroquinolinones and their use as antagonists of metabotropic glutamate receptors

Also Published As

Publication number Publication date
CN101223142A (en) 2008-07-16
KR20080031972A (en) 2008-04-11
CA2610873C (en) 2010-08-03
AU2006283359B2 (en) 2010-05-27
JP2009506018A (en) 2009-02-12
MX2008001871A (en) 2008-04-09
BRPI0615059A2 (en) 2011-04-26
WO2007023242A1 (en) 2007-03-01
EA200800660A1 (en) 2008-06-30
WO2007023290A1 (en) 2007-03-01
AR056044A1 (en) 2007-09-12
CA2610873A1 (en) 2007-03-01
IL189617A0 (en) 2008-06-05
ZA200710668B (en) 2009-08-26
AU2006283359A1 (en) 2007-03-01
TW200728283A (en) 2007-08-01
TWI329635B (en) 2010-09-01
IL189617A (en) 2012-08-30
EP1931635A1 (en) 2008-06-18

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