EA200800660A1 - TETRAHYDROCHINOLINONES AND THEIR APPLICATION AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS - Google Patents

TETRAHYDROCHINOLINONES AND THEIR APPLICATION AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS

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Publication number
EA200800660A1
EA200800660A1 EA200800660A EA200800660A EA200800660A1 EA 200800660 A1 EA200800660 A1 EA 200800660A1 EA 200800660 A EA200800660 A EA 200800660A EA 200800660 A EA200800660 A EA 200800660A EA 200800660 A1 EA200800660 A1 EA 200800660A1
Authority
EA
Eurasian Patent Office
Prior art keywords
modulators
tetrahydrochinolinones
application
metabotropic glutamate
glutamate receptors
Prior art date
Application number
EA200800660A
Other languages
Russian (ru)
Inventor
Кристофер Грахам Рафаэль Парсонс
Айгарс Йиргенсонс
Иева Яунземе
Иварс Калвиньш
Маркус Хенрих
Максимс Ванейевс
Таня Вайль
Валерьянс Каусс
Войцех Даныш
Клаудиа Ятцке
Original Assignee
Мерц Фарма Гмбх Унд Ко. Кгаа
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 Мерц Фарма Гмбх Унд Ко. Кгаа filed Critical Мерц Фарма Гмбх Унд Ко. Кгаа
Publication of EA200800660A1 publication Critical patent/EA200800660A1/en

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic 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
    • C07D215/16Heterocyclic 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
    • C07D215/20Oxygen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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    • C07D401/02Heterocyclic 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
    • C07D401/06Heterocyclic 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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    • C07ORGANIC CHEMISTRY
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    • C07D401/02Heterocyclic 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
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    • 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
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    • 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
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    • 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
    • C07D417/02Heterocyclic 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
    • C07D417/06Heterocyclic 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

Abstract

Настоящее изобретение относится к этинилзамещенным производным тетрагидрохинолинона, а также к их фармацевтически приемлемым солям. Настоящее изобретение далее относится к способу получения таких соединений. Соединения по настоящему изобретению являются модуляторами mGluR группы I, а потому применимы для лечения и предотвращения острых и/или хронических неврологических нарушений.The present invention relates to ethynyl substituted tetrahydroquinolinone derivatives, as well as pharmaceutically acceptable salts thereof. The present invention further relates to a method for producing such compounds. The compounds of the present invention are modulators of group I mGluR, and therefore are useful for the treatment and prevention of acute and / or chronic neurological disorders.

EA200800660A 2005-08-24 2006-08-24 TETRAHYDROCHINOLINONES AND THEIR APPLICATION AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS EA200800660A1 (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
EA200800660A1 true EA200800660A1 (en) 2008-06-30

Family

ID=36273537

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200800660A EA200800660A1 (en) 2005-08-24 2006-08-24 TETRAHYDROCHINOLINONES AND THEIR APPLICATION 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)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8349852B2 (en) 2009-01-13 2013-01-08 Novartis Ag Quinazolinone derivatives useful as vanilloid antagonists
AU2010332819B2 (en) * 2009-12-18 2014-02-27 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
NZ600605A (en) * 2009-12-18 2013-08-30 Janssen Pharmaceutica Nv Bicyclic thiazoles as allosteric modulators of mglur5 receptors
EP2531510B1 (en) 2010-02-01 2014-07-23 Novartis AG Pyrazolo[5,1b]oxazole derivatives as crf-1 receptor antagonists
AR080056A1 (en) 2010-02-01 2012-03-07 Novartis Ag CICLOHEXIL-AMIDA DERIVATIVES AS ANTAGONISTS OF CRF RECEIVERS
JP5748777B2 (en) 2010-02-02 2015-07-15 ノバルティス アーゲー Cyclohexylamide derivatives as CRF receptor antagonists
WO2012052451A1 (en) 2010-10-18 2012-04-26 Merz Pharma Gmbh & Co. Kgaa Metabotropic glutamate receptor 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
BR112016011079A2 (en) * 2013-11-15 2017-12-05 Wistar Inst ? ebna1 inhibitors and their method of use?
KR101579496B1 (en) * 2014-07-03 2015-12-23 한국과학기술연구원 mGluR5 Radiotracer composition
WO2016154527A1 (en) * 2015-03-26 2016-09-29 Merck Sharp & Dohme Corp. Phosphate-substituted quinolizine derivatives useful as hiv integrase inhibitors
US10442763B2 (en) 2015-05-14 2019-10-15 The Wistar Institute Of Anatomy And Biology EBNA1 inhibitors and methods using same
MY189453A (en) 2015-06-03 2022-02-14 Bristol Myers 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
WO2019222470A1 (en) 2018-05-17 2019-11-21 The Wistar Institute Ebna1 inhibitor crystalline forms, and methods of preparing and using same
US20220387429A1 (en) * 2019-10-21 2022-12-08 Sk Biopharmaceuticals Co., Ltd. Use of imidazopyrimidine or imidazotriazine compound for prevention, alleviation, or treatment of developmental disability
CA3155209A1 (en) * 2019-10-21 2021-04-29 Chan Mi Joung Use of imidazopyrimidine or imidazotriazine compounds for prevention, alleviation, or treatment of cognitive disorders, or for improving cognitive function

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002028837A1 (en) * 2000-10-02 2002-04-11 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
BRPI0615059A2 (en) 2011-04-26
CA2610873A1 (en) 2007-03-01
CA2610873C (en) 2010-08-03
JP2009506018A (en) 2009-02-12
KR20080031972A (en) 2008-04-11
WO2007023242A1 (en) 2007-03-01
CN101223142A (en) 2008-07-16
AU2006283359A1 (en) 2007-03-01
IL189617A0 (en) 2008-06-05
WO2007023290A1 (en) 2007-03-01
AU2006283359B2 (en) 2010-05-27
IL189617A (en) 2012-08-30
NO20081428L (en) 2008-03-18
ZA200710668B (en) 2009-08-26
AR056044A1 (en) 2007-09-12
TWI329635B (en) 2010-09-01
MX2008001871A (en) 2008-04-09
TW200728283A (en) 2007-08-01
EP1931635A1 (en) 2008-06-18

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