ES2194844T3 - Antagonistas del receptor de aminoacidos excitadores. - Google Patents

Antagonistas del receptor de aminoacidos excitadores.

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Publication number
ES2194844T3
ES2194844T3 ES93306745T ES93306745T ES2194844T3 ES 2194844 T3 ES2194844 T3 ES 2194844T3 ES 93306745 T ES93306745 T ES 93306745T ES 93306745 T ES93306745 T ES 93306745T ES 2194844 T3 ES2194844 T3 ES 2194844T3
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Prior art keywords
alkilo
chr7
hydrogen
equivale
acilo
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Expired - Lifetime
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ES93306745T
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English (en)
Inventor
Macklin Brian Arnold
Nancy Kay Augenstein
Carl Franklin Bertsch
Marvin Martin Hansen
Allen Robert Harkness
Bret Eugene Huff
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Eli Lilly and Co
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Eli Lilly and Co
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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
    • A—HUMAN NECESSITIES
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    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
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    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
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    • A61P25/06—Antimigraine agents
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    • A61P25/08—Antiepileptics; Anticonvulsants
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/20—Hypnotics; Sedatives
    • A—HUMAN NECESSITIES
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/36—Opioid-abuse
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
    • C07D217/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • 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
    • C07D401/12—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 chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • 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
    • C07D413/02—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
    • 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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    • 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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    • 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
    • C07D417/12—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 chain containing hetero atoms as chain links
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    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6524—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having four or more nitrogen atoms as the only ring hetero atoms

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  • Organic Chemistry (AREA)
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  • Life Sciences & Earth Sciences (AREA)
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  • Pharmacology & Pharmacy (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurosurgery (AREA)
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  • Biomedical Technology (AREA)
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  • Ophthalmology & Optometry (AREA)
  • Vascular Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Otolaryngology (AREA)
  • Anesthesiology (AREA)
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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
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Abstract

EN ESTA INVENCION SE PRESENTAN NUEVOS COMPUESTOS DE DECAHIDROISOQUINOLINAS QUE CON UTILES COMO ANTAGONISTAS DE RECEPTORES DE AMINOACIDOS EXCITADORES EN EL TRATAMIENTO DE TRASTORNOS NEUROLOGICOS. EN ESTA INVENCION SE PRESENTAN TAMBIEN METODO SINTETICOS PARA LA PREPARACION DE LAS DECAHIDROISOQUINOLINAS ASI COMO NUEVOS INTERMEDIOS PARA LA SINTESIS DE LAS MISMAS. LOS NUEVOS COMPUESTOS FARMACEUTICOS TIENEN LA FORMULA EN DONDE: R1 ES HIDROGENO, ALKILO C1-C10, ARILALKILO, ALCOXICARBONILO O ACILO; R2 ES HIDROGENO, ALKILO C1-C6, ALKILO SUSTITUIDO, CICLOALKILO O ARILALKILO; R2 ES CO2H, SO3H, CONHSO2R8 O UN GRUPO DE LA FORMULA W ES (CH2)N, S, SO, SO2; Z ES NR6, CHR7 O CH; O W E Y JUNTOS SON HC=CH O C (EQUIVALE) C O Y Y Z JUNTOS SON HC=CH O C (EQUIVALE) C; R4 ES HIDROGENO, ALKILO C1-C4, FENILO O ACILO; R5 ES HIDROGENO, ALKILO C1-C4, CF3, FENILO, HIDROXI, AMINO, BROMO, YODO O CLORO; R6 ES ACILO; R7 ES INDEPENDIENTEMENTE HIDROGENO, ALKILO C1-C4, FENILO O FENILO SUSTITUIDO; R8 ES ALKILO C1-C4 O TETRAZOL-5-ILO; Y N ES 0, 1 O 2; SIEMPRE Y CUANDO SI Y ES NR4, O, S, SO O SO2, W SEA (CH2)N Y Z SEA CHR7 O CH; Y ADEMAS, SI W ES S, SO O SO2, Y SEA CHR7, Z SEA CHR7 O CH O Y Y Z JUNTOS SEAN HC=CH O C (EQUIVALE) C; Y QUE ADEMAS SI W Y Z SON CH2, Y NO SEA S; Y QUE ADEMAS W E Y JUNTOS SON HC=CH O C (EQUIVALE) C, Z SEA CHR7; O UNA SAL FARMACEUTICAMENTE ACEPTABLE DE LOS MISMOS.
ES93306745T 1992-09-03 1993-08-25 Antagonistas del receptor de aminoacidos excitadores. Expired - Lifetime ES2194844T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/939,780 US5284957A (en) 1992-09-03 1992-09-03 Excitatory amino acid receptor antagonists

Publications (1)

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ES2194844T3 true ES2194844T3 (es) 2003-12-01

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ID=25473721

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ES93306745T Expired - Lifetime ES2194844T3 (es) 1992-09-03 1993-08-25 Antagonistas del receptor de aminoacidos excitadores.

Country Status (26)

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US (7) US5284957A (es)
EP (1) EP0590789B9 (es)
JP (1) JP3601840B2 (es)
KR (1) KR100274367B1 (es)
CN (1) CN1043762C (es)
AT (1) ATE234287T1 (es)
AU (1) AU656482B2 (es)
BR (1) BR9303495A (es)
CA (2) CA2104909C (es)
CZ (1) CZ285049B6 (es)
DE (1) DE69332754T2 (es)
DK (1) DK0590789T3 (es)
ES (1) ES2194844T3 (es)
FI (1) FI933810L (es)
HU (2) HU224015B1 (es)
IL (1) IL106809A (es)
MX (1) MX9305294A (es)
MY (1) MY131442A (es)
NO (1) NO304072B1 (es)
NZ (1) NZ248513A (es)
PH (1) PH31250A (es)
PL (1) PL173809B1 (es)
PT (1) PT590789E (es)
RU (1) RU2117661C1 (es)
SG (1) SG45319A1 (es)
ZA (1) ZA936231B (es)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2087812B1 (es) * 1993-07-02 1997-03-16 Lilly Co Eli Derivados de decahidroisoquinolina utiles como antagonistas de los receptrores de los aminoacidos excitadores.
US5580877A (en) * 1994-04-25 1996-12-03 Merck Sharp & Dohme Ltd. Pyrazolo-quinoline derivatives for treating cerebral ischemia
US5446051A (en) * 1994-05-31 1995-08-29 Eli Lilly And Company Aryl-spaced decahydroisoquinoline-3-carboxylic acids as excitatory amino acid receptor antagonists
US6207672B1 (en) * 1995-11-13 2001-03-27 Aventis Pharma Deutschland Gmbh Cyclic and heterocyclic N-substituted α-iminohydroxamic and carboxyclic acids
US5723414A (en) * 1996-01-24 1998-03-03 Rohm And Haas Company 5-aryl-isoxazolinones and herbicidal use thereof
CN1103772C (zh) 1996-05-15 2003-03-26 辉瑞大药厂 新的2,3－二取代－4(3h)－喹唑啉酮类化合物
EP0807633B1 (en) * 1996-05-15 2002-11-06 Pfizer Inc. Novel 2,3-disubstituted-(5,6)- heteroarylfused-pyrimidine-4-ones
EA199900912A1 (ru) * 1997-04-07 2000-04-24 Эли Лилли Энд Компани Фармацевтические средства
US6627755B1 (en) 1997-06-09 2003-09-30 Pfizer Inc Quinazolin-4-one AMPA antagonists
IL125950A0 (en) * 1997-09-05 1999-04-11 Pfizer Prod Inc Methods of administering ampa receptor antagonists to treat dyskinesias associated with dopamine agonist therapy
US6323208B1 (en) 1997-09-05 2001-11-27 Pfizer Inc Atropisomers of 2,3-disubstituted-(5.6)-heteroaryl fused-pyrimidin-4-ones
JP2002505288A (ja) 1998-03-02 2002-02-19 コセンシス，インコーポレイテッド 置換キナゾリンおよびアナログならびにそれらの使用
TW513301B (en) * 1999-03-01 2002-12-11 Novartis Ag Pharmaceutical composition for treatment of neuropathic pain and affective and attention disorders
PT1200073E (pt) 1999-07-06 2007-03-30 Lilly Co Eli Antagonistas selectivos do receptor de iglur5 para o tratamento de enxaqueca
ATE240299T1 (de) * 1999-07-06 2003-05-15 Lilly Co Eli Diester prodrugs von decahydroischinoline-3- carbonsäure
US6313159B1 (en) 1999-08-20 2001-11-06 Guilford Pharmaceuticals Inc. Metabotropic glutamate receptor ligand derivatives as naaladase inhibitors
AU2574801A (en) * 1999-12-22 2001-07-03 Eli Lilly And Company Selective iGLUR5 receptor antagonists
AU2002228736A1 (en) * 2001-01-05 2002-07-16 Eli Lilly And Company Pyrrolidinylmethyl substituted decahydroisoquinolines as excitatory amino acid receptor antagonists
US7205313B2 (en) 2001-01-05 2007-04-17 Eli Lilly And Company Excitatory amino acid receptor antagonists
EA200300770A1 (ru) * 2001-01-05 2003-10-30 Эли Лилли Энд Компани Антагонисты рецепторов возбуждающей аминокислоты
AU2002227020A1 (en) * 2001-01-05 2002-07-16 Eli Lilly And Company Pyrrolidinylmethyl- and piperidinyl substituted decahydroisoquinolines as excitatory amino acid receptor antagonists
CN100548299C (zh) * 2001-01-05 2009-10-14 伊莱利利公司 兴奋性氨基酸受体拮抗剂
US6924294B2 (en) 2001-01-05 2005-08-02 Eli Lilly And Company Excitatory amino acid receptor antagonists
GB0106858D0 (en) * 2001-03-20 2001-05-09 Perkins Engines Co Ltd An accessory drive for driving an engine accessory
GB0128996D0 (en) 2001-12-04 2002-01-23 Novartis Ag Organic compounds
US7091249B2 (en) * 2001-12-26 2006-08-15 University Of Iowa Research Foundation Drugs for spinal anesthesia
AU2003219955A1 (en) * 2002-03-22 2003-10-13 Eli Lilly And Company Isoquinoline-3-carboxylic acid derivatives as excitatory amino acid receptor antagonists
AU2003234210A1 (en) * 2002-04-26 2003-11-10 The Government Of The United States Of America, Represented By The Secretary, Department Of Health A Direct cell target analysis
EP1511741B1 (en) * 2002-04-26 2012-12-26 Eli Lilly And Company Ester derivatives of a decahydroisoquinoline-3-carboxylic acid as analgestics
GB0222056D0 (en) * 2002-09-23 2002-10-30 Novartis Ag Process for the manufacture of organic compounds
US20040152694A1 (en) * 2003-02-04 2004-08-05 Istvan Kurucz Methods and compositions for treating inflammatory disorders of the airways
US20060220794A1 (en) * 2005-04-04 2006-10-05 Jeffrey Zhu Phase modulation for backscatter transponders
WO2007101116A2 (en) * 2006-02-24 2007-09-07 The Trustees Of Columbia University In The City Of New York Glur2 receptor modulators
US20080108622A1 (en) * 2006-10-19 2008-05-08 Eisenach James C Combination therapy for the treatment of pain
US20080108603A1 (en) * 2006-10-19 2008-05-08 Eisenach James C Combination therapy for the treatment of pain
US20090270508A1 (en) * 2007-02-23 2009-10-29 James Eric Gouaux GluR2 receptor modulators
EP2338492A1 (en) 2009-12-24 2011-06-29 Universidad del Pais Vasco Methods and compositions for the treatment of alzheimer
CN101812031A (zh) * 2010-04-29 2010-08-25 南通市华峰化工有限责任公司 一种5-羟烷基四氮唑的高压生产方法
EP2822931B1 (en) 2012-03-09 2017-05-03 Inception 2, Inc. Triazolone compounds and uses thereof
SG11201504622PA (en) 2012-12-20 2015-07-30 Inception 2 Inc Triazolone compounds and uses thereof
TWI593692B (zh) * 2013-03-12 2017-08-01 美國禮來大藥廠 四氫吡咯并噻嗪化合物
CN105579440A (zh) 2013-09-06 2016-05-11 因森普深2公司 三唑酮化合物及其应用
EP3661500B1 (en) 2017-07-31 2026-01-07 Novartis AG Use of mavoglurant in the reduction of cocaine use or in preventing relapse into cocaine use
EP4175635B1 (en) 2020-07-02 2026-03-25 Sea Pharmaceuticals LLC Pharmaceutical compositions of 6-(2-(2h-tetrazol-5-yl)ethyl)-6-fluorodecahydroisoquinoline-3-carboxylic acid and ester derivatives thereof

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK704488D0 (da) * 1988-12-19 1988-12-19 Novo Industri As Nye n-substituerede azaheterocykliske carboxylsyrer
US4897490A (en) * 1987-02-25 1990-01-30 Bristol-Meyers Company Antihypercholesterolemic tetrazole compounds
US4824959A (en) * 1988-02-18 1989-04-25 Bristol-Myers Company Intermediates for antihypercholesterolemic tetrazole compounds
US4902695A (en) * 1989-02-13 1990-02-20 Eli Lilly And Company Excitatory amino acid receptor antagonists
US5192751A (en) * 1992-07-24 1993-03-09 Eli Lilly And Company Use of competitive NMDA receptor antagonists in the treatment of urinary incontinence

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AU656482B2 (en) 1995-02-02
PH31250A (en) 1998-06-18
US5675008A (en) 1997-10-07
CA2104909A1 (en) 1994-03-04
US5284957A (en) 1994-02-08
PL173809B1 (pl) 1998-05-29
US5399696A (en) 1995-03-21
ATE234287T1 (de) 2003-03-15
EP0590789A1 (en) 1994-04-06
US5606062A (en) 1997-02-25
HK1013989A1 (en) 1999-09-17
FI933810A7 (fi) 1994-03-04
NZ248513A (en) 1996-02-27
EP0590789B1 (en) 2003-03-12
US5648492A (en) 1997-07-15
NO933100D0 (no) 1993-08-31
BR9303495A (pt) 1994-03-22
HU211992A9 (en) 1996-01-29
NO933100L (no) 1994-03-04
HU224015B1 (hu) 2005-04-28
CZ174593A3 (en) 1994-03-16
JP3601840B2 (ja) 2004-12-15
CA2104909C (en) 2005-01-11
NO304072B1 (no) 1998-10-19
FI933810A0 (fi) 1993-08-31
CZ285049B6 (cs) 1999-05-12
MY131442A (en) 2007-08-30
EP0590789B9 (en) 2004-02-04
AU4600393A (en) 1994-03-10
KR100274367B1 (ko) 2000-12-15
IL106809A (en) 1999-03-12
DE69332754D1 (de) 2003-04-17
HU9302453D0 (en) 1993-11-29
PT590789E (pt) 2003-07-31
KR940007021A (ko) 1994-04-26
FI933810L (fi) 1994-03-04
HUT65228A (en) 1994-05-02
MX9305294A (es) 1994-06-30
JPH06199802A (ja) 1994-07-19
RU2117661C1 (ru) 1998-08-20
US5637712A (en) 1997-06-10
CN1043762C (zh) 1999-06-23
US5670516A (en) 1997-09-23
DE69332754T2 (de) 2004-06-17
SG45319A1 (en) 1998-01-16
CN1091129A (zh) 1994-08-24
ZA936231B (en) 1995-02-27
DK0590789T3 (da) 2004-03-22
CA2484248A1 (en) 1994-03-04

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