AR009374A1 - Compuestos novedosos antagonistas de nmda (n-metil-d-aspartato), composicion farmaceutica y usos para fabricar medicamentos. - Google Patents

Compuestos novedosos antagonistas de nmda (n-metil-d-aspartato), composicion farmaceutica y usos para fabricar medicamentos.

Info

Publication number
AR009374A1
AR009374A1 ARP970104462A ARP970104462A AR009374A1 AR 009374 A1 AR009374 A1 AR 009374A1 AR P970104462 A ARP970104462 A AR P970104462A AR P970104462 A ARP970104462 A AR P970104462A AR 009374 A1 AR009374 A1 AR 009374A1
Authority
AR
Argentina
Prior art keywords
group
alkyl
hydrogen
physiologically acceptable
manufacture
Prior art date
Application number
ARP970104462A
Other languages
English (en)
Original Assignee
Hoechst Marion Roussel Inc
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 Hoechst Marion Roussel Inc filed Critical Hoechst Marion Roussel Inc
Publication of AR009374A1 publication Critical patent/AR009374A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/42Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • 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
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Indole Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Se describen compuestos de formula (1) donde: X se elige del grupo formado por hidroxi, un éster fisiologicamente aceptable y una amida fisiologicamenteaceptable; Y se elige del grupo formado por hidroxi, un éster fisiologicamente aceptable, y unaamida fisiologicamente aceptable; R es de 1 a 3 sustituyenteselegidos independientemente del grupo formado por hidrogeno, alquilo C1-C4, alcoxi C1-C4, halogeno, -CF3, y -OCF3; R1 se elige del grupo formado porhidrogeno y alquilo C1-C4; R2 es un radical elegido del grupo formado por la formula (2) donde: R3 se elige del grupo formado por hidrogeno y alquilo C1-C4;R4 es de 1 a 2 sustituyentes elegidos independientemente del grupo formado por hidrogeno, alquilo C1-C4, halogeno, y -CF3, R5 es alquilo C1-C4; R6 es alquiloC1-C4; R7 es de 1 a 2 sustituyentes elegidos independientemente del grupo formado por hidrogeno, alquilo C1-C4, alcoxi C1-C4, halogeno y -CF3; y lassales de adicion de ácido farmacéuticamente aceptables del mismo.También se describe una composicion farmacéutica que incluye dicho compuesto y los usos dedichos compuestos para la fabricacion de medicamentos para el tratamiento de enfermedades neurovegetativas, para prevenir el deterioro isquémico/hipoxico/hipoglicémico del tejido cerebral para el tratamiento de la ansiedad y los con efecto analgésico.
ARP970104462A 1996-09-30 1997-09-29 Compuestos novedosos antagonistas de nmda (n-metil-d-aspartato), composicion farmaceutica y usos para fabricar medicamentos. AR009374A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US72317596A 1996-09-30 1996-09-30

Publications (1)

Publication Number Publication Date
AR009374A1 true AR009374A1 (es) 2000-04-12

Family

ID=24905175

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP970104462A AR009374A1 (es) 1996-09-30 1997-09-29 Compuestos novedosos antagonistas de nmda (n-metil-d-aspartato), composicion farmaceutica y usos para fabricar medicamentos.

Country Status (18)

Country Link
EP (1) EP0929521B1 (es)
JP (1) JP2001501221A (es)
KR (1) KR20000048715A (es)
CN (1) CN1139572C (es)
AR (1) AR009374A1 (es)
AT (1) ATE309215T1 (es)
AU (1) AU732997B2 (es)
BR (1) BR9712144A (es)
CA (1) CA2266556C (es)
DE (1) DE69734594T2 (es)
DK (1) DK0929521T3 (es)
HU (1) HUP0000882A3 (es)
IL (1) IL129187A0 (es)
NO (1) NO314080B1 (es)
NZ (1) NZ334343A (es)
TW (1) TW492958B (es)
WO (1) WO1998014427A1 (es)
ZA (1) ZA978602B (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20010053849A1 (en) * 1999-06-16 2001-12-20 Mary Jeanne Kreek Plural biological sample arrays, and preparation and uses thereof
WO2001082914A2 (en) 2000-04-28 2001-11-08 Memorial Sloan-Kettering Cancer Center Topical anesthetic/opioid formulations and uses thereof
HU227197B1 (en) 2000-10-24 2010-10-28 Richter Gedeon Nyrt Nmda receptor antagonist carboxylic acid amide derivatives and pharmaceutical compositions containing them
US7820688B2 (en) 2001-04-27 2010-10-26 Memorial Sloan-Kettering Cancer Center Topical anesthetic/opioid formulations and uses thereof
WO2003039540A2 (en) * 2001-11-09 2003-05-15 Sepracor Inc. D-amino acid oxidase inhibitors for learning and memory
DE10306202A1 (de) 2003-02-13 2004-08-26 Grünenthal GmbH Arzneimittel enthaltend substituierte 2-Aryl-Aminoessigsäure-Verbindungen und/oder substituierte 2-Heteroaryl-Aminoessigsäure-Verbindungen
US7884124B2 (en) 2006-06-30 2011-02-08 Sepracor Inc. Fluoro-substituted inhibitors of D-amino acid oxidase
US8450525B2 (en) * 2007-10-22 2013-05-28 Orchid Chemicals & Pharmaceuticals Limited Histone deacetylase inhibitors
CN102762554A (zh) 2010-02-16 2012-10-31 辉瑞大药厂 5-ht4受体的部分激动剂(r)-4-((4-((4-(四氢呋喃-3-基氧基)苯并[d]异*唑-3-基氧基)甲基)哌啶-1-基)甲基)四氢-2h-吡喃-4-醇
WO2021007366A1 (en) 2019-07-08 2021-01-14 St. Louis College Of Pharmacy G-protein biased opioid receptor agonist/analgesics with reduced arrestin recruitment

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR0178469B1 (ko) * 1990-07-16 1999-03-20 메이나드 알. 존슨 흥분성 아미노산 길항제
GB9208492D0 (en) * 1992-04-16 1992-06-03 Glaxo Spa Heterocyclic compounds
ATE151750T1 (de) * 1993-05-27 1997-05-15 Merrell Pharma Inc 3-(indol-3-yl) propensäurderivate, die als nmda- antagonisten nützlich sind
US5519048A (en) * 1993-05-27 1996-05-21 Merrell Pharmaceuticals Inc. 3-(indol-3-yl)-propenoic acid derivatives and pharmaceutical compositions thereof
GB9319243D0 (en) * 1993-09-17 1993-11-03 Glaxo Spa Heterocyclic compounds

Also Published As

Publication number Publication date
CN1139572C (zh) 2004-02-25
DE69734594T2 (de) 2006-07-06
HUP0000882A3 (en) 2001-04-28
ZA978602B (en) 1998-03-30
IL129187A0 (en) 2000-02-17
DE69734594D1 (en) 2005-12-15
NO991533L (no) 1999-05-28
TW492958B (en) 2002-07-01
AU4071897A (en) 1998-04-24
NZ334343A (en) 2001-01-26
KR20000048715A (ko) 2000-07-25
CA2266556C (en) 2007-11-06
CA2266556A1 (en) 1998-04-09
CN1232452A (zh) 1999-10-20
NO314080B1 (no) 2003-01-27
BR9712144A (pt) 1999-08-31
EP0929521A1 (en) 1999-07-21
EP0929521B1 (en) 2005-11-09
NO991533D0 (no) 1999-03-29
DK0929521T3 (da) 2006-03-27
WO1998014427A1 (en) 1998-04-09
HUP0000882A2 (hu) 2000-09-28
ATE309215T1 (de) 2005-11-15
JP2001501221A (ja) 2001-01-30
AU732997B2 (en) 2001-05-03

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