ES2109516T3 - Derivados de quinoxalinodiona como antagonistas de aminoacidos excitadores. - Google Patents

Derivados de quinoxalinodiona como antagonistas de aminoacidos excitadores.

Info

Publication number
ES2109516T3
ES2109516T3 ES93922849T ES93922849T ES2109516T3 ES 2109516 T3 ES2109516 T3 ES 2109516T3 ES 93922849 T ES93922849 T ES 93922849T ES 93922849 T ES93922849 T ES 93922849T ES 2109516 T3 ES2109516 T3 ES 2109516T3
Authority
ES
Spain
Prior art keywords
hydrogen
alkyl
chr13
chr14
independently
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
ES93922849T
Other languages
English (en)
Inventor
Christopher Franklin Bigge
Thomas Charles Malone
Frank Watjen
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.)
Warner Lambert Co LLC
Original Assignee
Warner Lambert Co LLC
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 Warner Lambert Co LLC filed Critical Warner Lambert Co LLC
Application granted granted Critical
Publication of ES2109516T3 publication Critical patent/ES2109516T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • 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
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/02Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
    • C07D217/04Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Biochemistry (AREA)
  • Cardiology (AREA)
  • Molecular Biology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Psychiatry (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

UN COMPUESTO QUE TIENE LA FORMULA (I) O UNA SAL FARMACEUTICAMENTE ACEPTABLE DEL MISMO, EN LA QUE R ES HIDROGENO O HIDROXI; R1 ES HIDROGENO, ALQUILO, ARILALQUILO, (CH2)NOH O (CH2)NR7R8; R5 Y R6 SON CADA UNO, INDEPENDIENTEMENTE, HIDROGENO, HALOGENO, NO2, CN, CF3, SO2NR7R8, PO3R9R10, ALQUILO, ALQUENILO, ALQUINILO, (CH2)NCONR7R8, (CH2)NCO2R10, NHCOR11, EN DONDE R7 Y R8 SON CADA UNO, INDEPENDIENTEMENTE, HIDROGENO O ALQUILO O R7 Y R8 JUNTOS FORMAN UN ANILLO DE TRES A SIETE ATOMOS, R9 ES HIDROGENO O ALQUILO, R10 ES HIDROGENO O ALQUILO, R11 ES HIDROGENO O ALQUILO Y N ES UN ENTERO DE CERO A CUATRO; A ES UN ANILLO DE CINCO A SIETE ATOMOS FUSIONADO CON EL ANILLO BENZO EN LAS POSICIONES MARCADAS A Y B Y ESTA FORMADO POR LOS SIGUIENTES RADICALES BIVALENTES: A-NR12-CHR13-CHR14-B, A-CHR13CHR14-NR12-B, A-CHR13-NR12-CHR14-B, A-CHR14-CH2-NR12-CHR13-B, ACHR13-NR12-CH2-CHR14-B, A-CH2-CH2-CHR13-NR12-B, A-NR12-CHR13-CH2-CH2B, A-CH2-CH2-NR12-CH2-CH2-B, A-CH2-CH2-CH2-NR12-CH2-B, A-CH2-NR12CH2-CH2-CH2-B, A-CH2-CH2-CH2-CH2-NR12-B, A-NR12-CH2-CH2-CH2-CH2-B, EN DONDE R12 ES HIDROGENO, CH2CH2OH O ALQUILO Y R13 Y R14 SON CADA UNO, INDEPENDIENTEMENTE, HIDROGENO, CN, CONH2, CH2NH2, CH2OH, ALQUILO, ARILALQUILO, ALQUENILO O CO2R15, EN DONDE R15 ES HIDROGENO O ALQUILO. LOS COMPUESTOS SON UTILES PARA EL TRATAMIENTO DE TRASTORNOS DE MAMIFEROS Y RESPONDEN AL BLOQUEO DE RECEPTORES DE ACIDO GLUTAMICO Y ASPARTICO. TAMBIEN SE PRESENTAN LOS PROCESOS PARA LA PREPARACION DE LOS COMPUESTOS Y NUEVOS INTERMEDIOS UTILES EN LOS PROCESOS.
ES93922849T 1992-10-13 1993-10-08 Derivados de quinoxalinodiona como antagonistas de aminoacidos excitadores. Expired - Lifetime ES2109516T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US96015792A 1992-10-13 1992-10-13
US3433293A 1993-03-22 1993-03-22
US12477093A 1993-09-24 1993-09-24

Publications (1)

Publication Number Publication Date
ES2109516T3 true ES2109516T3 (es) 1998-01-16

Family

ID=27364627

Family Applications (1)

Application Number Title Priority Date Filing Date
ES93922849T Expired - Lifetime ES2109516T3 (es) 1992-10-13 1993-10-08 Derivados de quinoxalinodiona como antagonistas de aminoacidos excitadores.

Country Status (10)

Country Link
US (1) US6703391B2 (es)
EP (1) EP0664807B1 (es)
JP (1) JPH08502483A (es)
AT (1) ATE157977T1 (es)
AU (1) AU680632B2 (es)
DE (1) DE69313866T2 (es)
DK (1) DK0664807T3 (es)
ES (1) ES2109516T3 (es)
GR (1) GR3025257T3 (es)
WO (1) WO1994009000A1 (es)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2161783C (en) * 1993-05-13 2006-08-15 Frank Watjen Ampa antagonists and a method of treatment therewith
US5843945A (en) * 1993-05-13 1998-12-01 Neurosearch A/S AMPA antagonists and a method of treatment
EP0705834A1 (de) * 1994-07-27 1996-04-10 Ciba-Geigy Ag Azaaliphatisch Überbrückte Chinoxalin-2,3-dione
EP0705835A1 (de) * 1994-09-01 1996-04-10 Ciba-Geigy Ag Oxa- oder thiaaliphatisch überbrückte Chinoxalin-2,3-dione
AU687255B2 (en) * 1994-09-14 1998-02-19 Neurosearch A/S Indole-2,3-dione-3-oxime derivatives, their preparation and use
US5801174A (en) * 1994-09-14 1998-09-01 Neurosearch A/S Fused indole and quinoxaline derivatives, their preparation and use
WO1996028445A1 (en) * 1995-03-14 1996-09-19 Warner-Lambert Company Novel glutamate (ampa/kainate) receptor antagonists: n-substituted fused azacycloalkylquinoxalinediones
WO1998005651A1 (en) * 1996-08-01 1998-02-12 Warner-Lambert Company Novel glutamate receptor antagonists: fused cycloalkyl quinoxalinediones
WO2002014277A1 (en) * 2000-08-10 2002-02-21 Tanabe Seiyaku Co., Ltd. Biphenylcarboxamidoisoindoline compounds, processes for the preparation of the same and intermediates for the synthesis thereof
WO2002014276A1 (en) * 2000-08-10 2002-02-21 Tanabe Seiyaku Co., Ltd. Benzoylaminoisoindoline compounds, processes for the preparation of the same and intermediates for the synthesis thereof
DE10121215A1 (de) * 2001-04-30 2002-10-31 Merck Patent Gmbh Dihydro-imidazo[4,5-e]indol- und 7H-Pyrrolo[3,2-f]chinoxalin Derivate als nikotinische Acetylcholinrezeptor Liganden und/oder serotonerge Liganden
WO2007059608A1 (en) 2005-11-23 2007-05-31 Painceptor Pharma Corporation Compositions and methods for modulating gated ion channels
WO2007115409A1 (en) * 2006-04-10 2007-10-18 Painceptor Pharma Corporation Compositions and methods for modulating gated ion channels
WO2012014910A1 (ja) * 2010-07-29 2012-02-02 日本ケミファ株式会社 P2x4受容体拮抗剤

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK146787A (da) * 1987-03-23 1988-09-24 Ferrosan Heterocykliske forbindelser, deres fremstilling og anvendelse
DK160941C (da) 1988-06-28 1991-10-21 Novo Nordisk As Kondenserede 2,3-dihydroxypyraziner, fremgangsmaade til deres fremstilling og farmaceutiske praeparater, hvori forbindelserne indgaar
DK716188D0 (da) * 1988-12-22 1988-12-22 Ferrosan As Quinoxalinforbindelser, deres fremstilling og anvendelse
DK101290D0 (da) 1990-04-24 1990-04-24 Novo Nordisk As Heterocykliske forbindelser, deres fremstilling og anvendelse
ATE194985T1 (de) 1990-11-06 2000-08-15 Yamanouchi Pharma Co Ltd Kondensiertes pyrazinderivat
CA2076948C (en) 1991-08-28 2002-04-16 Frank Watjen Isatineoxime derivatives, their preparation and use
WO1996028445A1 (en) * 1995-03-14 1996-09-19 Warner-Lambert Company Novel glutamate (ampa/kainate) receptor antagonists: n-substituted fused azacycloalkylquinoxalinediones

Also Published As

Publication number Publication date
EP0664807B1 (en) 1997-09-10
US6703391B2 (en) 2004-03-09
DE69313866T2 (de) 1998-03-05
DE69313866D1 (de) 1997-10-16
US20030114422A1 (en) 2003-06-19
GR3025257T3 (en) 1998-02-27
AU680632B2 (en) 1997-08-07
JPH08502483A (ja) 1996-03-19
EP0664807A1 (en) 1995-08-02
WO1994009000A1 (en) 1994-04-28
AU5171593A (en) 1994-05-09
DK0664807T3 (da) 1998-04-27
ATE157977T1 (de) 1997-09-15

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