ES2150417T3 - Derivados de pirazina fusionados. - Google Patents

Derivados de pirazina fusionados.

Info

Publication number
ES2150417T3
ES2150417T3 ES91918943T ES91918943T ES2150417T3 ES 2150417 T3 ES2150417 T3 ES 2150417T3 ES 91918943 T ES91918943 T ES 91918943T ES 91918943 T ES91918943 T ES 91918943T ES 2150417 T3 ES2150417 T3 ES 2150417T3
Authority
ES
Spain
Prior art keywords
represent
alkyl
nitro
cycloalkyl
alternatively
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
ES91918943T
Other languages
English (en)
Inventor
Shuichi Sakamoto
Jun-Ya Ohmori
Hirokazu Kubota
Masao Sasamata
Masamichi Okada
Kazuyuki Hidaka
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Yamanouchi Pharmaceutical Co Ltd
Original Assignee
Yamanouchi Pharmaceutical Co Ltd
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 Yamanouchi Pharmaceutical Co Ltd filed Critical Yamanouchi Pharmaceutical Co Ltd
Application granted granted Critical
Publication of ES2150417T3 publication Critical patent/ES2150417T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Liquid Crystal Substances (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

UN DERIVADO DE PIRAZINA QUE INHIBE EL RECEPTOR DE GLUTAMATO, REPRESENTADO POR LA FORMULA GENERAL (IA) DONDE Z REPRESENTA C O N, SIEMPRE QUE DOS Z NO SEAN ATOMOS DE N AL MISMO TIEMPO; R1 REPRESENTA (1A) DONDE X REPRESENTA N O R8C, R6 REPRESENTA H O ALQUILO, Y R7 Y R8 REPRESENTAN CADA UNO H,ALQUILO, NITRO O FENILO, O ALTERNATIVAMENTE R7 Y R8 ESTAN COMBINADOS CONJUNTAMENTE PARA REPRESENTAR BUTADIENILENO O 1,4 PRESENTAN CADA UNO H, F, CIANO, ACILO, NITRO, ALQUILO, MORFOLINA O R1; R4 Y R5 REPRESENTAN CADA UNO H, HIDROXI, ALQUILO, CICLOALQUILO, HETEROCICLO, FERRILO O ALQUILO Y SUSTITUIDO; Y REPRESENTA HIDROXI, ACILOXI, METILO F SUSTITUIDO, CICLOALQUILO, TETRAHIDROFURILO, CARBOXILO, ALCOXICARBONILO O NR9R10; Y R9 Y R10 REPRESENTAN H O ALQUILO, O ALTERNATIVAMENTE R9 Y R10 ESTAN COMBINADOS CONJUNTAMENTE PARA REPRESENTAR UN GRUPO CICLICO DE 5 O 6 MIEMBROS QUE PUEDE CONTENER ATOMO(S) DE OXIGENO.
ES91918943T 1990-11-06 1991-11-01 Derivados de pirazina fusionados. Expired - Lifetime ES2150417T3 (es)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP30087990 1990-11-06
JP6959291 1991-01-11
JP13382891 1991-03-29
JP18324891 1991-06-27

Publications (1)

Publication Number Publication Date
ES2150417T3 true ES2150417T3 (es) 2000-12-01

Family

ID=27465151

Family Applications (1)

Application Number Title Priority Date Filing Date
ES91918943T Expired - Lifetime ES2150417T3 (es) 1990-11-06 1991-11-01 Derivados de pirazina fusionados.

Country Status (14)

Country Link
US (1) US5283244A (es)
EP (1) EP0556393B1 (es)
JP (1) JP2550456B2 (es)
KR (1) KR0132903B1 (es)
AT (1) ATE194985T1 (es)
AU (1) AU656154B2 (es)
CA (1) CA2095444C (es)
DE (1) DE69132340T2 (es)
DK (1) DK0556393T3 (es)
ES (1) ES2150417T3 (es)
GR (1) GR3034629T3 (es)
HU (2) HU221425B (es)
RU (1) RU2095352C1 (es)
WO (1) WO1992007847A1 (es)

Families Citing this family (44)

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Publication number Priority date Publication date Assignee Title
DK162491D0 (da) * 1991-09-20 1991-09-20 Novo Nordisk As Heterocycliske forbindelser, deres fremstilling og farmaceutiske praeparater indeholdende forbindelserne
US6057304A (en) 1992-10-26 2000-05-02 Schering Aktiengesellschaft Quinoxaline-phosphonic acid derivatives
DE4217952A1 (de) * 1992-05-30 1993-12-02 Basf Ag Chinoxalin-2,3(1H,4H)-dione
ES2313714T3 (es) * 1992-06-22 2009-03-01 The Regents Of The University Of California Antagonistas de receptores de glicina y uso de los mismos.
EP0664807B1 (en) 1992-10-13 1997-09-10 Warner-Lambert Company Quinoxalinedione derivatives as eaa antagonists
PH31122A (en) * 1993-03-31 1998-02-23 Eisai Co Ltd Nitrogen-containing fused-heterocycle compounds.
IL109397A0 (en) * 1993-04-28 1994-07-31 Schering Ag Quinoxalinedione derivatives, processes for the preparation thereof and pharmaceutical compositions containing the same
US5631373A (en) * 1993-11-05 1997-05-20 State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University And The University Of Oregon, Eugene Oregon Alkyl, azido, alkoxy, and fluoro-substituted and fused quinoxalinediones
DE4340045A1 (de) * 1993-11-24 1995-06-01 Basf Ag Neue Chinoxaline und Arzneimittel daraus
AU1599395A (en) * 1994-01-03 1995-08-01 Cocensys, Inc. 8-aza, 6-aza and 6,8-diaza-1,4-dihydroquinoxaline-2,3-diones and the use thereof as antagonists for the glycine/nmda receptor
AU688459B2 (en) * 1994-04-08 1998-03-12 Shionogi & Co., Ltd. Oxopyridinylquinoxaline derivative
DE4428152A1 (de) * 1994-06-22 1996-01-04 Basf Ag Neue Amido-chinoxalindione, ihrer Herstellung und Verwendung
GB9419318D0 (en) * 1994-09-24 1994-11-09 Pfizer Ltd Therapeutic agents
DK0784054T3 (da) * 1994-09-27 2002-03-25 Yamanouchi Pharma Co Ltd 1,2,3,4-tetrahydroquinoxalinderivater og deres anvendelse som glutamatreceptorantagonister
DE4436852A1 (de) * 1994-10-14 1996-04-18 Basf Ag Pyrrolyl-tetrahydrobenzochinoxalindione, ihre Herstellung und Verwendung
US5801183A (en) * 1995-01-27 1998-09-01 State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University And The University Of Oregon Aza and aza (N-oxy) analogs of glycine/NMDA receptor antagonists
US6110911A (en) * 1995-06-07 2000-08-29 Warner-Lambert Company Cyclic amine derivatives of substituted quinoxaline 2,3-diones as glutamate receptor antagonists
DE19521058A1 (de) * 1995-06-09 1996-12-12 Basf Ag Verfahren zur Herstellung von Aromaten enthaltenden Polyetherpolyolen
DE19532050A1 (de) * 1995-08-31 1997-03-06 Basf Ag Pyrrolyl-tetrahydrochinoxalindione, ihre Herstellung und Verwendung zur Bekämpfung von Krankheiten
GB9605027D0 (en) * 1996-03-09 1996-05-08 Pfizer Ltd Quinoxalinediones
ZA973884B (en) 1996-05-23 1998-11-06 Du Pont Merck Pharma Tetrahydropteridines and pyridylpiperazines for treatment of neurological disorders
TW448171B (en) * 1996-06-06 2001-08-01 Yamanouchi Pharma Co Ltd Imidazole-substituted quinoxalinedione derivatives
US6017903A (en) 1996-09-27 2000-01-25 Guilford Pharmaceuticals Inc. Pharmaceutical compositions and methods of treating a glutamate abnormality and effecting a neuronal activity in an animal using NAALADase inhibitors
US5824662A (en) * 1996-09-27 1998-10-20 Guilford Pharmaceuticals Inc. Treatment of global and focal ischemia using naaladase inhibitors
DE19624808A1 (de) 1996-06-21 1998-01-02 Basf Ag Pyrrolylchinoxalindione, ihre Herstellung und Verwendung
KR20000036227A (ko) 1996-09-27 2000-06-26 토마스 씨. 서 날라다아제조성물, 글루탐산염 이상 치료법 및 동물내의 뉴우런활성법
WO1998017672A1 (de) * 1996-10-24 1998-04-30 Novartis Ag Substituierte aminoalkanphosphonsäuren
AP982A (en) * 1997-02-27 2001-07-16 Pfizer Quinoxalinediones.
ATE282608T1 (de) * 1997-02-27 2004-12-15 Pfizer Chinoxalindionen
TW403740B (en) 1997-06-10 2000-09-01 Novartis Ag Novel crystal modifications of the compound 1-(2,6-difluorobenzyl)-1H-1,2,3-triazole-4-carboxamide
US6015800A (en) * 1997-09-03 2000-01-18 Warner-Lambert Company Substituted quinoxaline-2-ones as glutamate receptor antagonists
KR20010031983A (ko) 1997-11-11 2001-04-16 우에노 도시오 축합 피라진 화합물
WO2001055110A1 (en) 2000-01-24 2001-08-02 Neurosearch A/S Isatine derivatives with neurotrophic activity
EP1904481B1 (en) 2005-06-23 2016-02-17 Array Biopharma, Inc. Process for preparing benzimidazole compounds
ES2366239T3 (es) * 2006-04-21 2011-10-18 Pfizer Products Inc. Piridin[3,4-b]pirazinonas.
US7601716B2 (en) * 2006-05-01 2009-10-13 Cephalon, Inc. Pyridopyrazines and derivatives thereof as ALK and c-Met inhibitors
NZ578078A (en) 2007-01-16 2011-11-25 Purdue Pharma Lp Heterocyclic-substituted piperidine as orl-1 ligands
CA2686816A1 (en) 2007-01-16 2008-07-24 The Johns Hopkins University Use of various glutamate receptor antagonists for delaying or preventing platelet activity or for treating or preventing a thrombotic disease or disorder
JP5554709B2 (ja) 2007-08-31 2014-07-23 パーデュー、ファーマ、リミテッド、パートナーシップ 置換キノキサリンタイプピペリジン化合物とその使用
WO2010053757A1 (en) * 2008-10-29 2010-05-14 Gilead Palo Alto, Inc. 2 -oxoquinoxalin blockers of the late sodium channel
US20100113514A1 (en) 2008-10-30 2010-05-06 Gilead Palo Alto, Inc. Fused heterocyclic compounds as ion channel modulators
EP2338492A1 (en) 2009-12-24 2011-06-29 Universidad del Pais Vasco Methods and compositions for the treatment of alzheimer
JPWO2023042887A1 (es) 2021-09-15 2023-03-23
EP4403185A1 (en) 2021-09-15 2024-07-24 University of The Ryukyus Pharmaceutical composition for treating cognitive decline or for treating overweightness or obesity

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IE66149B1 (en) * 1986-09-16 1995-12-13 Novo Nordisk As Quinoxaline compounds and their preparation and use
NO179551C (no) * 1987-11-10 1996-10-30 Novo Nordisk As Analogifremgangsmåte for fremstilling av terapeutisk virksomme kinoxalinforbindelser
CA2002864C (en) * 1988-11-29 1999-11-16 Eddy J. E. Freyne (1h-azol-1-ylmethyl) substituted quinoline, quinazoline or quinoxaline derivatives
GB8827822D0 (en) * 1988-11-29 1988-12-29 Janssen Pharmaceutica Nv (1h-azol-1-ylmethyl)substituted quinoline derivatives
DK715888D0 (da) * 1988-12-22 1988-12-22 Ferrosan As Quinoxalinforbindelser, deres fremstilling og anvendelse

Also Published As

Publication number Publication date
WO1992007847A1 (en) 1992-05-14
KR0132903B1 (ko) 1998-04-17
GR3034629T3 (en) 2001-01-31
DE69132340D1 (de) 2000-08-31
AU8766691A (en) 1992-05-26
US5283244A (en) 1994-02-01
DK0556393T3 (da) 2000-10-16
EP0556393A1 (en) 1993-08-25
EP0556393A4 (en) 1994-04-13
JP2550456B2 (ja) 1996-11-06
AU656154B2 (en) 1995-01-27
HU221425B (en) 2002-10-28
HUT64324A (en) 1993-12-28
HU211310A9 (en) 1995-11-28
CA2095444A1 (en) 1992-05-07
EP0556393B1 (en) 2000-07-26
DE69132340T2 (de) 2001-02-08
RU2095352C1 (ru) 1997-11-10
CA2095444C (en) 2001-06-19
HU9301298D0 (en) 1993-09-28
ATE194985T1 (de) 2000-08-15

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