ES2194844T3 - Antagonistas del receptor de aminoacidos excitadores. - Google Patents
Antagonistas del receptor de aminoacidos excitadores.Info
- 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
- Authority
- ES
- Spain
- Prior art keywords
- alkilo
- chr7
- hydrogen
- equivale
- acilo
- 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
Links
Classifications
-
- 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
- C07D401/06—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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
-
- 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
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P25/06—Antimigraine agents
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P25/22—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
- A61P25/00—Drugs for disorders of the nervous system
- 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
- A61P25/00—Drugs for disorders of the nervous system
- 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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
-
- C—CHEMISTRY; METALLURGY
- 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
-
- C—CHEMISTRY; METALLURGY
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Pain & Pain Management (AREA)
- Molecular Biology (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Urology & Nephrology (AREA)
- Biochemistry (AREA)
- Epidemiology (AREA)
- Anesthesiology (AREA)
- Ophthalmology & Optometry (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Otolaryngology (AREA)
- Heart & Thoracic Surgery (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)
- Plural Heterocyclic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Control Of El Displays (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
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.
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)
| Publication Number | Publication Date |
|---|---|
| ES2194844T3 true ES2194844T3 (es) | 2003-12-01 |
Family
ID=25473721
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES93306745T Expired - Lifetime ES2194844T3 (es) | 1992-09-03 | 1993-08-25 | Antagonistas del receptor de aminoacidos excitadores. |
Country Status (26)
| Country | Link |
|---|---|
| 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) | CA2484248A1 (es) |
| CZ (1) | CZ285049B6 (es) |
| DE (1) | DE69332754T2 (es) |
| DK (1) | DK0590789T3 (es) |
| ES (1) | ES2194844T3 (es) |
| FI (1) | FI933810A7 (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)
| 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 |
| PT861236E (pt) * | 1995-11-13 | 2002-07-31 | Hoechst Ag | Acidos alfa-iminohidoxamicos e carboxilicos n-substituidos ciclicos e heterociclicos |
| US5723414A (en) * | 1996-01-24 | 1998-03-03 | Rohm And Haas Company | 5-aryl-isoxazolinones and herbicidal use thereof |
| PT901487E (pt) | 1996-05-15 | 2003-08-29 | Pfizer | 4(3h)-quinazolinonas 2,3,6-trissubstituidas |
| EP0807633B1 (en) * | 1996-05-15 | 2002-11-06 | Pfizer Inc. | Novel 2,3-disubstituted-(5,6)- heteroarylfused-pyrimidine-4-ones |
| WO1998045270A1 (en) * | 1997-04-07 | 1998-10-15 | Eli Lilly And Company | Pharmacological agents |
| US6627755B1 (en) | 1997-06-09 | 2003-09-30 | Pfizer Inc | Quinazolin-4-one AMPA antagonists |
| US6323208B1 (en) | 1997-09-05 | 2001-11-27 | Pfizer Inc | Atropisomers of 2,3-disubstituted-(5.6)-heteroaryl fused-pyrimidin-4-ones |
| 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 |
| WO1999044612A1 (en) | 1998-03-02 | 1999-09-10 | Cocensys, Inc. | Substituted quinazolines and analogs and the use thereof |
| TW513301B (en) * | 1999-03-01 | 2002-12-11 | Novartis Ag | Pharmaceutical composition for treatment of neuropathic pain and affective and attention disorders |
| ATE240299T1 (de) * | 1999-07-06 | 2003-05-15 | Lilly Co Eli | Diester prodrugs von decahydroischinoline-3- carbonsäure |
| CN1230174C (zh) * | 1999-07-06 | 2005-12-07 | 伊莱利利公司 | 治疗偏头痛的选择性iGluR5受体拮抗剂 |
| US6313159B1 (en) | 1999-08-20 | 2001-11-06 | Guilford Pharmaceuticals Inc. | Metabotropic glutamate receptor ligand derivatives as naaladase inhibitors |
| EP1257545A1 (en) * | 1999-12-22 | 2002-11-20 | Eli Lilly And Company | SELECTIVE iGLUR 5? RECEPTOR ANTAGONISTS |
| CZ20031856A3 (cs) * | 2001-01-05 | 2003-09-17 | Eli Lilly And Company | Antagonisté receptorů excitačních aminokyselin |
| US6924294B2 (en) | 2001-01-05 | 2005-08-02 | Eli Lilly And Company | Excitatory amino acid receptor antagonists |
| US6855725B2 (en) | 2001-01-05 | 2005-02-15 | Eli Lilly And Company | Excitatory amino acid receptor antagonists |
| US7205313B2 (en) | 2001-01-05 | 2007-04-17 | Eli Lilly And Company | Excitatory amino acid receptor antagonists |
| MXPA03005982A (es) * | 2001-01-05 | 2003-09-10 | Lilly Co Eli | Antagonistas de receptores de aminoacidos excitadores. |
| US6953805B2 (en) | 2001-01-05 | 2005-10-11 | 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 |
| DK1511741T3 (da) | 2002-04-26 | 2013-01-21 | Lilly Co Eli | Esterderivater af en decahydroisoquinolin-3-carboxylsyre som analgetika |
| US20050176068A1 (en) * | 2002-04-26 | 2005-08-11 | Emmert-Buck Michael R. | Direct cell target analysis |
| 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 |
| US20080108603A1 (en) * | 2006-10-19 | 2008-05-08 | Eisenach James C | Combination therapy for the treatment of pain |
| US20080108622A1 (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 |
| ES2660249T3 (es) | 2012-12-20 | 2018-03-21 | Inception 2, Inc. | Compuestos de tipo triazolona y sus usos |
| 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 |
| JP2016529311A (ja) | 2013-09-06 | 2016-09-23 | インセプション 2、 インコーポレイテッド | トリアゾロン化合物類及びそれらの使用 |
| 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 |
| AU2021299570A1 (en) * | 2020-07-02 | 2023-02-23 | 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)
| 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 |
-
1992
- 1992-09-03 US US07/939,780 patent/US5284957A/en not_active Expired - Lifetime
-
1993
- 1993-08-25 SG SG1996003438A patent/SG45319A1/en unknown
- 1993-08-25 EP EP93306745A patent/EP0590789B9/en not_active Expired - Lifetime
- 1993-08-25 ZA ZA936231A patent/ZA936231B/xx unknown
- 1993-08-25 DK DK93306745T patent/DK0590789T3/da active
- 1993-08-25 CZ CZ931745A patent/CZ285049B6/cs not_active IP Right Cessation
- 1993-08-25 AT AT93306745T patent/ATE234287T1/de active
- 1993-08-25 PT PT93306745T patent/PT590789E/pt unknown
- 1993-08-25 DE DE69332754T patent/DE69332754T2/de not_active Expired - Lifetime
- 1993-08-25 ES ES93306745T patent/ES2194844T3/es not_active Expired - Lifetime
- 1993-08-25 US US08/111,747 patent/US5399696A/en not_active Expired - Lifetime
- 1993-08-26 IL IL10680993A patent/IL106809A/en not_active IP Right Cessation
- 1993-08-26 BR BR9303495A patent/BR9303495A/pt not_active Application Discontinuation
- 1993-08-26 CA CA002484248A patent/CA2484248A1/en not_active Abandoned
- 1993-08-26 CA CA002104909A patent/CA2104909C/en not_active Expired - Lifetime
- 1993-08-27 PH PH46762A patent/PH31250A/en unknown
- 1993-08-27 NZ NZ248513A patent/NZ248513A/en unknown
- 1993-08-30 HU HU9302453A patent/HU224015B1/hu active IP Right Grant
- 1993-08-31 FI FI933810A patent/FI933810A7/fi unknown
- 1993-08-31 MX MX9305294A patent/MX9305294A/es unknown
- 1993-08-31 AU AU46003/93A patent/AU656482B2/en not_active Expired
- 1993-08-31 RU RU93049265A patent/RU2117661C1/ru active
- 1993-08-31 NO NO933100A patent/NO304072B1/no not_active IP Right Cessation
- 1993-09-01 MY MYPI93001753A patent/MY131442A/en unknown
- 1993-09-01 CN CN93117627A patent/CN1043762C/zh not_active Expired - Lifetime
- 1993-09-01 PL PL93300250A patent/PL173809B1/pl unknown
- 1993-09-01 JP JP21744193A patent/JP3601840B2/ja not_active Expired - Lifetime
- 1993-09-01 KR KR1019930017398A patent/KR100274367B1/ko not_active Expired - Lifetime
-
1994
- 1994-11-21 US US08/343,079 patent/US5637712A/en not_active Expired - Lifetime
-
1995
- 1995-06-01 US US08/456,439 patent/US5670516A/en not_active Expired - Lifetime
- 1995-06-01 US US08/456,577 patent/US5648492A/en not_active Expired - Lifetime
- 1995-06-01 US US08/457,556 patent/US5606062A/en not_active Expired - Lifetime
- 1995-06-01 US US08/457,766 patent/US5675008A/en not_active Expired - Lifetime
- 1995-06-22 HU HU95P/P00401P patent/HU211992A9/hu unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HU9302453D0 (en) | Antagonists of excitatoric amino acid receptors | |
| DK0640592T3 (da) | N-acylerede tricycliske azaheteroringe anvendelige som vasopressin-antagonister | |
| PA8431301A1 (es) | Inhibidores de metaloproteinasas, composiciones farmaceuticas que los contienen y sus usos farmaceuticos y los metodos e intermedios utiles para su preparacion | |
| PE46899A1 (es) | Derivados de n-fenil-sulfonamida | |
| ES2178038T3 (es) | Nuevos derivados de ciclosporina, su preparacion y las composiciones farmaceuticas que los contienen. | |
| ES2170859T3 (es) | Derivados de imidazol 1h-4(5)-sustituidos. | |
| CO4440627A1 (es) | Antagonistas de factor de liberacion de corticotropina | |
| DK0657428T3 (da) | Fremstilling af 3,4,4-trisubstituerede-piperidinyl-N-alkylcarboxylater og mellemprodukter, der er egnede som opioidantagonister | |
| ES542321A0 (es) | Un procedimiento para la preparacion de derivados de la 2 pirimidinil-1-piperazina | |
| DK188288A (da) | 1-phenyl-3-naphthalenyloxypropanaminer, fremgangsmaade til fremstilling af saadanne forbindelser og farmaceutiske midler indeholdende disse | |
| ES2161718T3 (es) | 2,5-dioxo-2,5-dihidro-1h-benzo(b)azepinas como antagonistas de los receptores de nmda. | |
| EA199900161A1 (ru) | Производные пиридазино [4,5-в]-хинолин-5-оксида, их получение и применение в качестве антагонистов глицина | |
| AR015446A1 (es) | Antagonistas de receptores de vitronectina, composicion farmaceutica que los contiene, procedimiento para su preparacion, su uso para la elaboracion de unmedicamento y compuestos intermediarios | |
| ES2090024T3 (es) | Compuestos de cefemo y procedimientos para su preparacion. | |
| ES2089255T3 (es) | N-(ariloxialquil)heteroaril-8-azabiciclo(3.2.1)octanos, compuestos intermedios y un procedimiento para su preparacion y su uso como medicamentos. | |
| GB8717374D0 (en) | Pharmaceutically active compounds | |
| DK136987A (da) | Selektive alfa-adrenerge receptorantagonister, fremgangsmaade til fremstilling heraf samt farmaceutiske midler indeholdende disse | |
| ES2111025T3 (es) | Piridinilamino-1h-indoles, 1h-indazoles, 2h-indazoles, benzo(b)tiofenos y 1,2-benzoisotiazoles sustituidos, un procedimiento para su preparacion y su utilizacion como medicamentos. | |
| ES2081834T3 (es) | Pirrolidin-2-onas 4-metil y 4-etil sustituidas. | |
| PE41896A1 (es) | Antagonista del receptor de aminoacido excitativo | |
| DK247784D0 (da) | Spiro(indolo(1,7-ab)(1,5)benzodiazepin-2,4'-piperidiner),fremgangsmaade til fremstilling deraf samt mellemprodukter til brug herved,og deres anvendelse som laegemidler | |
| RU93004405A (ru) | Производные хинолон- и нафтиридонкарбоновой кислоты в виде смеси изомеров или отдельных изомеров, их гидраты и соли, способ их получения и содержащее их лекарственное средство | |
| ES2135383T3 (es) | Pirido(3,4-b)pirrolo(1,2-e)(1,4,5)oxadiazepinas y compuestos analogos relacionados, un procedimiento para su preparacion y su uso como medicamentos. | |
| ES2058641T3 (es) | Un procedimiento para preparar un derivado de bifenilo. | |
| ATE41770T1 (de) | Derivate von n-(2-pyrrolidinylmethyl)benzamid, verfahren zu ihrer herstellung, zwischenprodukte und pharmazeutische zubereitung. |