WO1992012151A1 - Sels de n-alkyle quinuclidinium utilises comme antagonistes de substance p - Google Patents
Sels de n-alkyle quinuclidinium utilises comme antagonistes de substance p Download PDFInfo
- Publication number
- WO1992012151A1 WO1992012151A1 PCT/US1991/008836 US9108836W WO9212151A1 WO 1992012151 A1 WO1992012151 A1 WO 1992012151A1 US 9108836 W US9108836 W US 9108836W WO 9212151 A1 WO9212151 A1 WO 9212151A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compound
- substance
- mammal
- alkyl
- pharmaceutically acceptable
- 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.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
Definitions
- fibrositis in a mammal, including a human, comprising an amount of a compound of the formula I, or a pharmaceutically acceptable salt thereof, effective in treating or preventing such condition, and a pharmaceutically acceptable carrier.
- Formula I above includes compounds identical to those depicted but for the fact that one or more hydrogen or carbon atoms are replaced by radioactive isotopes thereof, (e.g., tritium, carbon-14 or n ' rtrogen-15 isotopes thereof).
- radioactive isotopes thereof e.g., tritium, carbon-14 or n ' rtrogen-15 isotopes thereof.
- Such radiolabelled compounds are useful as research and diagnostic tools in metabolism pharmacokinetic studies and in binding assays. Specific applications in research include radioligand binding assays, autoradiography studies and in vivo binding studies, while specific applications in the diagnostic area include studies of the substance P receptor in humans in in vivo binding in the relevant tissues for inflammation, e.g. immune-type cells or cells that are directly involved in inflammatory bowel disorders and the like.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU90947/91A AU652407B2 (en) | 1991-01-10 | 1991-12-04 | N-alkyl quinuclidinium salts as substance P antagonists |
| FI933167A FI933167A0 (fi) | 1991-01-10 | 1991-12-04 | N-alkylkinuklidiniumsalter som substans-p antagonister |
| JP4501342A JPH0733385B2 (ja) | 1991-01-10 | 1991-12-04 | 物質pの拮抗薬としてのn−アルキルキヌクリジニウム塩 |
| KR1019930701985A KR930703311A (ko) | 1991-01-10 | 1993-06-30 | 물질 p의 길항제인 n-알킬 퀴누클리디늄염 |
| NO93932513A NO932513L (no) | 1991-01-10 | 1993-07-09 | N-alkyl-kinuklidinium-salter |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US63964491A | 1991-01-10 | 1991-01-10 | |
| US639,644 | 1991-01-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1992012151A1 true WO1992012151A1 (fr) | 1992-07-23 |
Family
ID=24564973
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US1991/008836 Ceased WO1992012151A1 (fr) | 1991-01-10 | 1991-12-04 | Sels de n-alkyle quinuclidinium utilises comme antagonistes de substance p |
Country Status (14)
| Country | Link |
|---|---|
| EP (1) | EP0566589A1 (fr) |
| JP (1) | JPH0733385B2 (fr) |
| KR (1) | KR930703311A (fr) |
| AU (1) | AU652407B2 (fr) |
| CA (1) | CA2100163A1 (fr) |
| FI (1) | FI933167A0 (fr) |
| HU (1) | HUT65612A (fr) |
| IE (1) | IE920071A1 (fr) |
| IL (1) | IL100584A (fr) |
| MX (1) | MX9200057A (fr) |
| NZ (1) | NZ241261A (fr) |
| PT (1) | PT100003A (fr) |
| WO (1) | WO1992012151A1 (fr) |
| ZA (1) | ZA92148B (fr) |
Cited By (61)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5364943A (en) * | 1991-11-27 | 1994-11-15 | Pfizer Inc. | Preparation of substituted piperidines |
| US5387595A (en) * | 1992-08-26 | 1995-02-07 | Merck & Co., Inc. | Alicyclic compounds as tachykinin receptor antagonists |
| US5393762A (en) * | 1993-06-04 | 1995-02-28 | Pfizer Inc. | Pharmaceutical agents for treatment of emesis |
| US5461063A (en) * | 1992-08-10 | 1995-10-24 | Merck Sharp & Dohme Limited | Azabicyclic compounds |
| US5498614A (en) * | 1992-05-18 | 1996-03-12 | Pfizer Inc. | Bridged aza-bicyclic derivatives as substance P antagonist |
| US5512570A (en) * | 1994-03-04 | 1996-04-30 | Merck & Co., Inc. | Treatment of emesis with morpholine tachykinin receptor antagonists |
| US5521220A (en) * | 1991-11-12 | 1996-05-28 | Pfizer Inc. | Acyclic ethylenediamine derivatives |
| EP0717998A1 (fr) | 1994-12-19 | 1996-06-26 | L'oreal | Utilisation d'un antagoniste de substance P pour le traitement des prurits, des algies oculaires et/ou palpébrales et des dysesthésies oculaires ou palpébrales |
| EP0722722A1 (fr) | 1994-12-19 | 1996-07-24 | L'oreal | Utilisation d'un antagoniste de substance P pour le traitement des rougeurs cutanées d'origine neurogène |
| EP0722736A1 (fr) | 1994-12-19 | 1996-07-24 | L'oreal | Composition topique contenant un antagoniste de substance P |
| EP0769300A2 (fr) | 1995-10-20 | 1997-04-23 | Pfizer Inc. | Médicament antiémétique contenant des Antagonistes des récepteurs NK-1 |
| EP0774250A1 (fr) | 1995-11-20 | 1997-05-21 | L'oreal | Utilisation d'un antagoniste de TNF-alpha pour le traitement des rougeurs cutanées d'origine neurogène |
| US5637699A (en) * | 1992-06-29 | 1997-06-10 | Merck & Co., Inc. | Process for preparing morpholine tachykinin receptor antagonists |
| US5688804A (en) * | 1992-08-04 | 1997-11-18 | Pfizer Inc. | 3-Benzylamino-2-phenyl-piperidine derivatives as substance P receptor antagonists |
| US5719147A (en) * | 1992-06-29 | 1998-02-17 | Merck & Co., Inc. | Morpholine and thiomorpholine tachykinin receptor antagonists |
| US6048859A (en) * | 1992-06-29 | 2000-04-11 | Merck & Co., Inc. | Morpholine and thiomorpholine tachykinin receptor antagonists |
| US6376507B1 (en) * | 1994-12-12 | 2002-04-23 | Pfizer Inc. | NK-1 receptor antagonists for the treatment of neuronal injury and stroke |
| US6579885B2 (en) | 1999-11-03 | 2003-06-17 | Albany Molecular Research, Inc. | Aryl and heteroaryl substituted tetrahydroisoquinolines and use thereof |
| US7084152B2 (en) | 2000-07-11 | 2006-08-01 | Amr Technology, Inc. | 4-phenyl substituted tetrahydroisoquinolines therapeutic use thereof |
| WO2006123182A2 (fr) | 2005-05-17 | 2006-11-23 | Merck Sharp & Dohme Limited | Sulfones de cyclohexyle pour le traitement du cancer |
| US7163949B1 (en) | 1999-11-03 | 2007-01-16 | Amr Technology, Inc. | 4-phenyl substituted tetrahydroisoquinolines and use thereof |
| WO2007011820A2 (fr) | 2005-07-15 | 2007-01-25 | Amr Technology, Inc. | Tetrahydrobenzazepines substituees par aryle et heteroaryle, et leur utilisation pour bloquer la reabsorption de la noradrenaline, de la dopamine, et de la serotonine |
| WO2007041052A2 (fr) | 2005-09-29 | 2007-04-12 | Merck & Co., Inc. | Derives spiropiperidines acyles convenant comme modulateurs des recepteurs de la melanocortine-4 |
| WO2007093827A1 (fr) | 2006-02-15 | 2007-08-23 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa | Dérivés de trifluoroéthanone substitués par thiophène et thiazole en tant qu'inhibiteurs d'histone désacétylase (hdac) |
| WO2008120653A1 (fr) | 2007-04-02 | 2008-10-09 | Banyu Pharmaceutical Co., Ltd. | Dérivé d'indoledione |
| WO2009002495A1 (fr) | 2007-06-27 | 2008-12-31 | Merck & Co., Inc. | Dérivés de 4-carboxybenzylamino utilisés en tant qu'inhibiteurs de l'histone désacétylase |
| US7541357B2 (en) | 2004-07-15 | 2009-06-02 | Amr Technology, Inc. | Aryl- and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
| WO2009111354A2 (fr) | 2008-03-03 | 2009-09-11 | Tiger Pharmatech | Inhibiteurs de la tyrosine kinase |
| WO2010000073A1 (fr) | 2008-07-03 | 2010-01-07 | Neuraxon, Inc. | Benzoxazines, benzothiazines et composés apparentés ayant une activité d'inhibition de nos |
| WO2010114780A1 (fr) | 2009-04-01 | 2010-10-07 | Merck Sharp & Dohme Corp. | Inhibiteurs de l'activité akt |
| WO2010132442A1 (fr) | 2009-05-12 | 2010-11-18 | Albany Molecular Reserch, Inc. | 7-([1,2, 4,]triazolo[1,5,-a]pyridine-6-yl)-4-(3,4-dichlorophényl)-1,2,3,4- tétrahydroisoquinoline et son utilisation |
| WO2010132487A1 (fr) | 2009-05-12 | 2010-11-18 | Bristol-Myers Squibb Company | Formes cristallines de (s)-7-([1,2,4]triazolo[1,5-a] pyridin -6-yl)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydroisoquinoline et leurs utilisations |
| WO2011046771A1 (fr) | 2009-10-14 | 2011-04-21 | Schering Corporation | Pipéridines substituées qui accroissent l'activité de p53, et utilisations de ces composés |
| EP2336120A1 (fr) | 2007-01-10 | 2011-06-22 | Istituto di ricerche di Biologia Molecolare P. Angeletti S.R.L. | Combinaisons contenant indazoles à substitution amide utilisés comme inhibiteurs de la poly(ADP-ribose)polymérase (PARP) |
| WO2011163330A1 (fr) | 2010-06-24 | 2011-12-29 | Merck Sharp & Dohme Corp. | Nouveaux composés hétérocycliques utilisés comme inhibiteurs de erk |
| WO2012018754A2 (fr) | 2010-08-02 | 2012-02-09 | Merck Sharp & Dohme Corp. | Inhibition à médiation par interférence arn de caténine (protéine associée à cadhérine), expression du gène bêta 1 (ctnnb1) à l'aide de petit acide nucléique interférent (sian) |
| WO2012027236A1 (fr) | 2010-08-23 | 2012-03-01 | Schering Corporation | Nouveaux dérivés de pyrazolo[1,5-a]pyrimidine utilisés comme inhibiteurs de mtor |
| WO2012030685A2 (fr) | 2010-09-01 | 2012-03-08 | Schering Corporation | Dérivés d'indazole utilisables en tant qu'inhibiteurs de la voie erk |
| WO2012036997A1 (fr) | 2010-09-16 | 2012-03-22 | Schering Corporation | Dérivés condensés de pyrazole utilisés comme nouveaux inhibiteurs erk |
| WO2012087772A1 (fr) | 2010-12-21 | 2012-06-28 | Schering Corporation | Dérivés d'indazole utiles en tant qu'inhibiteurs de erk |
| WO2012145471A1 (fr) | 2011-04-21 | 2012-10-26 | Merck Sharp & Dohme Corp. | Inhibiteurs du récepteur du facteur de croissance 1 analogue à l'insuline |
| US8420811B2 (en) | 2008-06-04 | 2013-04-16 | Bristol-Myers Squibb Company | Tetrahydroisoquinolines and intermediates therefor |
| WO2013063214A1 (fr) | 2011-10-27 | 2013-05-02 | Merck Sharp & Dohme Corp. | Nouveaux composés qui sont des inhibiteurs d'erk |
| WO2013165816A2 (fr) | 2012-05-02 | 2013-11-07 | Merck Sharp & Dohme Corp. | Compositions de petit acide nucléique interférent (sina) |
| EP2698157A1 (fr) | 2006-09-22 | 2014-02-19 | Merck Sharp & Dohme Corp. | Procédé de traitement utilisant des inhibiteurs de synthèse d'acide gras |
| WO2014052563A2 (fr) | 2012-09-28 | 2014-04-03 | Merck Sharp & Dohme Corp. | Nouveaux composés inhibiteurs de erk |
| WO2014085216A1 (fr) | 2012-11-28 | 2014-06-05 | Merck Sharp & Dohme Corp. | Compositions et procédés pour traiter le cancer |
| WO2014100065A1 (fr) | 2012-12-20 | 2014-06-26 | Merck Sharp & Dohme Corp. | Imidazopyridines substituées en tant qu'inhibiteurs de hdm2 |
| WO2014120748A1 (fr) | 2013-01-30 | 2014-08-07 | Merck Sharp & Dohme Corp. | Purines 2,6,7,8-substituées utilisées en tant qu'inhibiteurs de hdm2 |
| WO2015034925A1 (fr) | 2013-09-03 | 2015-03-12 | Moderna Therapeutics, Inc. | Polynucléotides circulaires |
| US9034899B2 (en) | 2009-05-12 | 2015-05-19 | Albany Molecular Research, Inc. | Aryl, heteroaryl, and heterocycle substituted tetrahydroisoquinolines and use thereof |
| US9156812B2 (en) | 2008-06-04 | 2015-10-13 | Bristol-Myers Squibb Company | Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine |
| WO2018071283A1 (fr) | 2016-10-12 | 2018-04-19 | Merck Sharp & Dohme Corp. | Inhibiteurs de kdm5 |
| EP3327125A1 (fr) | 2010-10-29 | 2018-05-30 | Sirna Therapeutics, Inc. | Inhibition au moyen d'interférence arn d'une expression de gène utilisant des acides nucléiques à petit interférent (sina) |
| WO2019094312A1 (fr) | 2017-11-08 | 2019-05-16 | Merck Sharp & Dohme Corp. | Inhibiteurs de prmt5 |
| WO2019094311A1 (fr) | 2017-11-08 | 2019-05-16 | Merck Sharp & Dohme Corp. | Inhibiteurs de prmt5 |
| WO2020033288A1 (fr) | 2018-08-07 | 2020-02-13 | Merck Sharp & Dohme Corp. | Inhibiteurs de prmt5 |
| WO2020033282A1 (fr) | 2018-08-07 | 2020-02-13 | Merck Sharp & Dohme Corp. | Inhibiteurs de prmt5 |
| WO2020033284A1 (fr) | 2018-08-07 | 2020-02-13 | Merck Sharp & Dohme Corp. | Inhibiteurs de prmt5 |
| US11096950B2 (en) | 2006-11-01 | 2021-08-24 | Barbara Brooke Jennings | Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development |
| EP4079856A1 (fr) | 2010-08-17 | 2022-10-26 | Sirna Therapeutics, Inc. | Inhibition médiée par des arn interférents de l'expression génique du virus de l'hépatite b (vhb) à l'aide de petits acides nucléiques interférents (pani) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0532527B1 (fr) * | 1990-06-01 | 1994-11-09 | Pfizer Inc. | Quinuclidines de 3-amino-2-aryle, procede relatif a leur preparation et compositions pharmaceutiques les contenant |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0159059A1 (fr) * | 1984-03-16 | 1985-10-23 | Laboratori Guidotti S.p.A. | Composés ayant une activité anti-bronchospastique et compositions pharmaceutiques qui les contiennent |
| WO1990005729A1 (fr) * | 1988-11-23 | 1990-05-31 | Pfizer Inc. | Agents therapeutiques de quinuclidine |
| EP0404737A2 (fr) * | 1989-06-20 | 1990-12-27 | BOEHRINGER INGELHEIM ITALIA S.p.A. | Dérivés R(-)3-quinuclidinol |
-
1991
- 1991-12-04 WO PCT/US1991/008836 patent/WO1992012151A1/fr not_active Ceased
- 1991-12-04 EP EP92901108A patent/EP0566589A1/fr not_active Withdrawn
- 1991-12-04 FI FI933167A patent/FI933167A0/fi not_active Application Discontinuation
- 1991-12-04 CA CA002100163A patent/CA2100163A1/fr not_active Abandoned
- 1991-12-04 JP JP4501342A patent/JPH0733385B2/ja not_active Expired - Lifetime
- 1991-12-04 AU AU90947/91A patent/AU652407B2/en not_active Ceased
- 1991-12-04 HU HU9301988A patent/HUT65612A/hu unknown
-
1992
- 1992-01-08 MX MX9200057A patent/MX9200057A/es unknown
- 1992-01-09 ZA ZA92148A patent/ZA92148B/xx unknown
- 1992-01-09 PT PT100003A patent/PT100003A/pt not_active Application Discontinuation
- 1992-01-09 NZ NZ241261A patent/NZ241261A/en unknown
- 1992-01-09 IE IE007192A patent/IE920071A1/en not_active Application Discontinuation
- 1992-10-05 IL IL10058492A patent/IL100584A/en not_active IP Right Cessation
-
1993
- 1993-06-30 KR KR1019930701985A patent/KR930703311A/ko not_active Withdrawn
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0159059A1 (fr) * | 1984-03-16 | 1985-10-23 | Laboratori Guidotti S.p.A. | Composés ayant une activité anti-bronchospastique et compositions pharmaceutiques qui les contiennent |
| WO1990005729A1 (fr) * | 1988-11-23 | 1990-05-31 | Pfizer Inc. | Agents therapeutiques de quinuclidine |
| WO1990005525A1 (fr) * | 1988-11-23 | 1990-05-31 | Pfizer Inc. | Derives de quinuclidine en tant qu'antagonsites de substance p |
| EP0404737A2 (fr) * | 1989-06-20 | 1990-12-27 | BOEHRINGER INGELHEIM ITALIA S.p.A. | Dérivés R(-)3-quinuclidinol |
Cited By (86)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5663349A (en) * | 1990-05-31 | 1997-09-02 | Pfizer Inc | Preparation of substituted piperidenes |
| US5521220A (en) * | 1991-11-12 | 1996-05-28 | Pfizer Inc. | Acyclic ethylenediamine derivatives |
| US5364943A (en) * | 1991-11-27 | 1994-11-15 | Pfizer Inc. | Preparation of substituted piperidines |
| US5498614A (en) * | 1992-05-18 | 1996-03-12 | Pfizer Inc. | Bridged aza-bicyclic derivatives as substance P antagonist |
| US5637699A (en) * | 1992-06-29 | 1997-06-10 | Merck & Co., Inc. | Process for preparing morpholine tachykinin receptor antagonists |
| US6638930B2 (en) | 1992-06-29 | 2003-10-28 | Merck & Co. Inc. | Morpholine and thiomorpholine tachykinin receptor antagonists |
| US6235735B1 (en) | 1992-06-29 | 2001-05-22 | Merck & Co., Inc. | Morpholine and thiomorpholine tachykinin receptor antagonists |
| US6048859A (en) * | 1992-06-29 | 2000-04-11 | Merck & Co., Inc. | Morpholine and thiomorpholine tachykinin receptor antagonists |
| US5922706A (en) * | 1992-06-29 | 1999-07-13 | Merck & Co., Inc. | Morpholine and thiomorpholine tachykinin receptor antagonists |
| US5872116A (en) * | 1992-06-29 | 1999-02-16 | Merck & Co., Inc. | Morpholine and thiomorpholine tachykinin receptor antagonists |
| US5719147A (en) * | 1992-06-29 | 1998-02-17 | Merck & Co., Inc. | Morpholine and thiomorpholine tachykinin receptor antagonists |
| US5688804A (en) * | 1992-08-04 | 1997-11-18 | Pfizer Inc. | 3-Benzylamino-2-phenyl-piperidine derivatives as substance P receptor antagonists |
| US5461063A (en) * | 1992-08-10 | 1995-10-24 | Merck Sharp & Dohme Limited | Azabicyclic compounds |
| US5387595A (en) * | 1992-08-26 | 1995-02-07 | Merck & Co., Inc. | Alicyclic compounds as tachykinin receptor antagonists |
| US5393762A (en) * | 1993-06-04 | 1995-02-28 | Pfizer Inc. | Pharmaceutical agents for treatment of emesis |
| US5512570A (en) * | 1994-03-04 | 1996-04-30 | Merck & Co., Inc. | Treatment of emesis with morpholine tachykinin receptor antagonists |
| US5691336A (en) * | 1994-03-04 | 1997-11-25 | Merck & Co., Inc. | Morpholine compounds are prodrugs useful as tachykinin receptor antagonists |
| US5716942A (en) * | 1994-03-04 | 1998-02-10 | Merck & Co., Inc. | Treatment of migraine with morpholine tachykinin receptor antagonists |
| US5780467A (en) * | 1994-03-04 | 1998-07-14 | Merck & Co., Inc. | Morpholine compounds are prodrugs useful as tachykinin receptor antagonists |
| US6376507B1 (en) * | 1994-12-12 | 2002-04-23 | Pfizer Inc. | NK-1 receptor antagonists for the treatment of neuronal injury and stroke |
| EP0717998A1 (fr) | 1994-12-19 | 1996-06-26 | L'oreal | Utilisation d'un antagoniste de substance P pour le traitement des prurits, des algies oculaires et/ou palpébrales et des dysesthésies oculaires ou palpébrales |
| EP0722722A1 (fr) | 1994-12-19 | 1996-07-24 | L'oreal | Utilisation d'un antagoniste de substance P pour le traitement des rougeurs cutanées d'origine neurogène |
| EP0722736A1 (fr) | 1994-12-19 | 1996-07-24 | L'oreal | Composition topique contenant un antagoniste de substance P |
| EP0769300A2 (fr) | 1995-10-20 | 1997-04-23 | Pfizer Inc. | Médicament antiémétique contenant des Antagonistes des récepteurs NK-1 |
| EP0774250A1 (fr) | 1995-11-20 | 1997-05-21 | L'oreal | Utilisation d'un antagoniste de TNF-alpha pour le traitement des rougeurs cutanées d'origine neurogène |
| US6579885B2 (en) | 1999-11-03 | 2003-06-17 | Albany Molecular Research, Inc. | Aryl and heteroaryl substituted tetrahydroisoquinolines and use thereof |
| US7265116B2 (en) | 1999-11-03 | 2007-09-04 | Arm Technology, Inc. | Aryl and heteroaryl substituted tetrahydroisoquinolines and use thereof |
| US7612090B2 (en) | 1999-11-03 | 2009-11-03 | Albany Molecular Research, Inc. | Aryl and heteroaryl substituted tetrahydroisoquinolines and use thereof |
| US7163949B1 (en) | 1999-11-03 | 2007-01-16 | Amr Technology, Inc. | 4-phenyl substituted tetrahydroisoquinolines and use thereof |
| US7084152B2 (en) | 2000-07-11 | 2006-08-01 | Amr Technology, Inc. | 4-phenyl substituted tetrahydroisoquinolines therapeutic use thereof |
| US7309789B2 (en) | 2000-07-11 | 2007-12-18 | Amr Technology, Inc. | 4-phenyl substituted tetrahydroisoquinolines and therapeutic use thereof |
| US7419985B2 (en) | 2000-07-11 | 2008-09-02 | Amr Technology, Inc. | 4-Phenyl substituted tetrahydroisoquinolines and therapeutic use thereof |
| US9085531B2 (en) | 2004-07-15 | 2015-07-21 | Albany Molecular Research, Inc. | Aryl- and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
| US7541357B2 (en) | 2004-07-15 | 2009-06-02 | Amr Technology, Inc. | Aryl- and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
| US9499531B2 (en) | 2004-07-15 | 2016-11-22 | Albany Molecular Research, Inc. | Aryl- and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
| WO2006123182A2 (fr) | 2005-05-17 | 2006-11-23 | Merck Sharp & Dohme Limited | Sulfones de cyclohexyle pour le traitement du cancer |
| WO2007011820A2 (fr) | 2005-07-15 | 2007-01-25 | Amr Technology, Inc. | Tetrahydrobenzazepines substituees par aryle et heteroaryle, et leur utilisation pour bloquer la reabsorption de la noradrenaline, de la dopamine, et de la serotonine |
| US9403776B2 (en) | 2005-07-15 | 2016-08-02 | Albany Molecular Research, Inc. | Aryl- and heteroaryl-substituted tetrahydrobenzazepines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
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Also Published As
| Publication number | Publication date |
|---|---|
| HUT65612A (en) | 1994-07-28 |
| IL100584A (en) | 1995-10-31 |
| MX9200057A (es) | 1992-07-01 |
| IL100584A0 (en) | 1992-09-06 |
| EP0566589A1 (fr) | 1993-10-27 |
| KR930703311A (ko) | 1993-11-29 |
| IE920071A1 (en) | 1992-07-15 |
| FI933167A7 (fi) | 1993-07-09 |
| JPH0733385B2 (ja) | 1995-04-12 |
| AU652407B2 (en) | 1994-08-25 |
| HU9301988D0 (en) | 1993-12-28 |
| CA2100163A1 (fr) | 1992-07-11 |
| FI933167L (fi) | 1993-07-09 |
| JPH05508866A (ja) | 1993-12-09 |
| PT100003A (pt) | 1993-02-26 |
| AU9094791A (en) | 1992-08-17 |
| ZA92148B (en) | 1993-07-09 |
| NZ241261A (en) | 1994-05-26 |
| FI933167A0 (fi) | 1993-07-09 |
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