DK0733628T3 - 5-substituerede 3-(1,2,3,6-tetrahydropyridin-4-yl)- og 3-(piperidin-4-yl)-1H-indoler: 5HT1F-agonister - Google Patents
5-substituerede 3-(1,2,3,6-tetrahydropyridin-4-yl)- og 3-(piperidin-4-yl)-1H-indoler: 5HT1F-agonisterInfo
- Publication number
- DK0733628T3 DK0733628T3 DK96301845T DK96301845T DK0733628T3 DK 0733628 T3 DK0733628 T3 DK 0733628T3 DK 96301845 T DK96301845 T DK 96301845T DK 96301845 T DK96301845 T DK 96301845T DK 0733628 T3 DK0733628 T3 DK 0733628T3
- Authority
- DK
- Denmark
- Prior art keywords
- 5ht1f
- tetrahydropyridin
- indoles
- piperidin
- agonists
- Prior art date
Links
- -1 1,2,3,6-tetrahydropyridin-4-yl Chemical group 0.000 title 1
- KAIRZPVWWIMPFT-UHFFFAOYSA-N 3-piperidin-4-yl-1h-indole Chemical class C1CNCCC1C1=CNC2=CC=CC=C12 KAIRZPVWWIMPFT-UHFFFAOYSA-N 0.000 title 1
- 239000000556 agonist Substances 0.000 title 1
Classifications
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US40755395A | 1995-03-20 | 1995-03-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DK0733628T3 true DK0733628T3 (da) | 2001-02-05 |
Family
ID=23612560
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK96301845T DK0733628T3 (da) | 1995-03-20 | 1996-03-19 | 5-substituerede 3-(1,2,3,6-tetrahydropyridin-4-yl)- og 3-(piperidin-4-yl)-1H-indoler: 5HT1F-agonister |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US5708008A (fr) |
| EP (1) | EP0733628B9 (fr) |
| JP (1) | JPH11502816A (fr) |
| KR (1) | KR19980703048A (fr) |
| CN (1) | CN1184425A (fr) |
| AR (1) | AR002971A1 (fr) |
| AT (1) | ATE198332T1 (fr) |
| AU (1) | AU702322B2 (fr) |
| BR (1) | BR9601061A (fr) |
| CA (1) | CA2215322A1 (fr) |
| CZ (1) | CZ288897A3 (fr) |
| DE (1) | DE69611315T2 (fr) |
| DK (1) | DK0733628T3 (fr) |
| EA (1) | EA001113B1 (fr) |
| ES (1) | ES2153078T3 (fr) |
| GR (1) | GR3035487T3 (fr) |
| HU (1) | HUP9800417A3 (fr) |
| MX (1) | MX9706969A (fr) |
| NO (1) | NO974220L (fr) |
| NZ (1) | NZ305166A (fr) |
| PL (1) | PL322843A1 (fr) |
| PT (1) | PT733628E (fr) |
| SI (1) | SI0733628T1 (fr) |
| TR (1) | TR199700993T1 (fr) |
| WO (1) | WO1996029075A1 (fr) |
Families Citing this family (68)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9615658D0 (en) * | 1996-07-25 | 1996-09-04 | Merck Sharp & Dohme | Therapeutic agents |
| US5962473A (en) * | 1996-08-16 | 1999-10-05 | Eli Lilly And Company | Methods of treating or ameliorating the symptoms of common cold or allergic rhinitis with serotonin 5-HT1F |
| WO1998011895A1 (fr) * | 1996-09-18 | 1998-03-26 | Eli Lilly And Company | Methode de prevention de migraine |
| CA2268164A1 (fr) * | 1996-10-08 | 1998-04-16 | Yao-Chang Xu | Nouveaux agonistes de la serotonine 5-ht1f |
| ZA979961B (en) * | 1996-11-15 | 1999-05-05 | Lilly Co Eli | 5-HT1F agonists |
| EP1082958A3 (fr) * | 1996-11-15 | 2002-12-11 | Eli Lilly And Company | Agonistes 5-HT1F dans la douleur chronique |
| EP0875513A1 (fr) * | 1997-04-14 | 1998-11-04 | Eli Lilly And Company | Composés hétéroaromatiques substitués agonistes du récepteur 5-HT1F |
| US6221884B1 (en) | 1997-06-04 | 2001-04-24 | Eli Lilly And Company | Carboxamides useful as 5-HT1F agonists |
| ID23053A (id) * | 1997-06-04 | 2000-01-20 | Lilly Co Eli | Karboksamida yang digunakan sebagai agonis 5-ht <if> |
| US6380201B1 (en) | 1997-08-05 | 2002-04-30 | Eli Lilly And Company | Methods of treating or ameliorating the symptoms of common cold or allergic rhinitis with serotonin 5-HT1F agonists |
| US6391891B1 (en) | 1997-08-09 | 2002-05-21 | Smithkline Beecham Plc | Bicyclic compounds as ligands for 5-HT1 receptors |
| US7189753B1 (en) | 1997-11-06 | 2007-03-13 | Cady Roger K | Preemptive prophylaxis of migraine |
| US5905084A (en) * | 1997-11-14 | 1999-05-18 | Eli Lilly And Company | 5-HTIF -agonists effective in treating migraine |
| ZA989389B (en) * | 1997-11-14 | 2000-04-14 | Lilly Co Eli | Pyrrolo [3,2-b] pyridine processes and intermediates. |
| US6861448B2 (en) * | 1998-01-14 | 2005-03-01 | Virtual Drug Development, Inc. | NAD synthetase inhibitors and uses thereof |
| US6673827B1 (en) | 1999-06-29 | 2004-01-06 | The Uab Research Foundation | Methods of treating fungal infections with inhibitors of NAD synthetase enzyme |
| WO1999036422A1 (fr) | 1998-01-14 | 1999-07-22 | The Uab Research Foundation | Procede de synthese et de criblage d'inhibiteurs d'enzyme synthetase nad bacterienne, composes a base de cette enzyme et procedes de traitement des infections bacteriennes et microbiennes au moyen d'inhibiteurs de ladite enzyme |
| CA2383983C (fr) * | 1998-03-31 | 2009-09-29 | The Institutes For Pharmaceutical Discovery, Llc | Acides indolalcanoiques substitues |
| CA2327360A1 (fr) * | 1998-04-08 | 1999-10-14 | Richard Eric Mewshaw | Derives d'amine indol-3-yl-cyclhexyle utilises dans le traitement de la depression (antagonistes du recepteur 5-ht1) |
| US6310066B1 (en) | 1998-04-29 | 2001-10-30 | American Home Products Corp. | Antipsychotic indolyl derivatives |
| US6204274B1 (en) | 1998-04-29 | 2001-03-20 | American Home Products Corporation | Indolyl derivatives as serotonergic agents |
| US6066637A (en) * | 1998-06-19 | 2000-05-23 | American Home Products Corporation | Indolyl derivatives as serotonergic agents |
| AU4961499A (en) * | 1998-06-26 | 2000-01-17 | Eli Lilly And Company | 5-HT1f agonists |
| US6133290A (en) * | 1998-07-31 | 2000-10-17 | Eli Lilly And Company | 5-HT1F agonists |
| US6608079B1 (en) | 1998-12-11 | 2003-08-19 | Eli Lilly And Company | Indole derivatives and their use as 5-HT1F agonists |
| PT1140919E (pt) * | 1999-01-07 | 2002-12-31 | Wyeth Corp | Novos derivados de ciclohexano 1,4-dissubstituido para o tratamento da depressao |
| US6200994B1 (en) | 1999-01-07 | 2001-03-13 | American Home Products Corp | 1,4-Disubstituted cyclohexane derivatives for the treatment of depression |
| US6777428B1 (en) | 1999-02-10 | 2004-08-17 | Eli Lilly And Company | 5-HT1f agonist |
| WO2000047559A2 (fr) * | 1999-02-10 | 2000-08-17 | Eli Lilly And Company | Agonistes 5-ht1f |
| PL350864A1 (en) * | 1999-02-26 | 2003-02-10 | Lilly Co Eli | 5-ht1f |
| US6696439B1 (en) | 1999-02-26 | 2004-02-24 | Eli Lilly And Company | 5-HT1F agonists |
| WO2001021614A1 (fr) * | 1999-09-09 | 2001-03-29 | H. Lundbeck A/S | Indoles substitues 5-aminoalkyle et 5-aminocarbonyle |
| CN1275967C (zh) * | 2001-01-30 | 2006-09-20 | 伊莱利利公司 | 用作5－ht6受体拮抗剂的苯磺酸吲哚－5－基酯 |
| ES2187300B1 (es) * | 2001-11-14 | 2004-06-16 | Laboratorios Del Dr. Esteve, S.A. | Derivados de sulfonamidas, su preparacion y su aplicacion como medicamentos. |
| TWI263497B (en) | 2002-03-29 | 2006-10-11 | Lilly Co Eli | Pyridinoylpiperidines as 5-HT1F agonists |
| WO2003087087A2 (fr) * | 2002-04-09 | 2003-10-23 | Astex Technology Limited | Composes pharmaceutiques |
| EP1554271A1 (fr) * | 2002-10-15 | 2005-07-20 | Rigel Pharmaceuticals, Inc. | Indoles substitues et leur utilisation en tant qu'inhibiteurs du virus de l'hepatite c (vhc) |
| ES2388547T3 (es) | 2003-04-18 | 2012-10-16 | Eli Lilly And Company | Compuestos de (piperidiniloxi)fenilo, (piperidiniloxi)piridinilo, (piperidinilsulfanil)fenilo y (piperidinilsulfanil)piridinilo como agonistas de 5-HT 1F |
| DE602004016491D1 (de) * | 2003-05-09 | 2008-10-23 | Esteve Labor Dr | Verwendung von sulfonamid-derivate zur herstellung eines medikaments für die vorbeugung oder behandlung von essstörungen |
| ES2219181B1 (es) * | 2003-05-09 | 2005-12-16 | Laboratorios Del Dr. Esteve, S.A. | Uso de derivados de sulfonamidas para la fabricacion de un medicamento para la profilaxis y/o tratamiento de las disfunciones alimentarias. |
| ES2222829B1 (es) | 2003-07-30 | 2006-03-01 | Laboratorios Del Dr. Esteve, S.A. | Derivados de 4-indolilsulfonamidas, su preparacion y su aplicacion como medicamentos. |
| ES2222832B1 (es) | 2003-07-30 | 2006-02-16 | Laboratorios Del Dr. Esteve, S.A. | Derivados de 6-indolilsulfonamidas, su preparacion y su aplicacion como medicamentos. |
| UA82711C2 (en) | 2003-09-12 | 2008-05-12 | Эли Лилли Энд Компани | Substituted 2-carbonylamino-6-piperidinaminopyridines and substituted 1-carbonylamino-3-piperidinaminobenzenes as 5-ht1f agonists |
| DE602004008338T2 (de) | 2003-12-17 | 2008-05-29 | Eli Lilly And Co., Indianapolis | Substituierte (4-aminocyclohexen-1-yl) phenyl and (4-aminocyclohexen-1-yl) pyridinyl verbindungen als 5-ht1f agonisten |
| US7550499B2 (en) * | 2004-05-12 | 2009-06-23 | Bristol-Myers Squibb Company | Urea antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
| ATE499370T1 (de) * | 2005-01-19 | 2011-03-15 | Bristol Myers Squibb Co | 2-phenoxy-n-(1,3,4-thiadizol-2-yl)pyridin-3- aminderivate und verwandte verbindungen als p2y1- rezeptor-hemmer zur behandlung thromboembolischer erkrankungen |
| CN101247853B (zh) | 2005-04-13 | 2014-11-12 | 轴突公司 | 具有nos抑制活性的取代的吲哚化合物 |
| KR20080027890A (ko) * | 2005-06-27 | 2008-03-28 | 브리스톨-마이어스 스큅 컴퍼니 | 혈전성 증상의 치료에 유용한 ｐ2ｙ1 수용체의 ｎ-연결헤테로시클릭 길항제 |
| US7714002B2 (en) * | 2005-06-27 | 2010-05-11 | Bristol-Myers Squibb Company | Carbocycle and heterocycle antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
| ATE502924T1 (de) | 2005-06-27 | 2011-04-15 | Bristol Myers Squibb Co | Lineare harnstoffmimetika-antagonisten des p2y1- rezeptors zur behandlung von thromboseleiden |
| DE602006017694D1 (de) * | 2005-06-27 | 2010-12-02 | Bristol Myers Squibb Co | C-verknüpfte zyklische antagonisten des p2y1-rezeptors mit eignung bei der behandlung thrombotischer leiden |
| ZA200809659B (en) * | 2006-04-13 | 2010-03-31 | Neuraxon Inc | 1,5 and 3,6-substituted indole compounds having NOS inhibitory activity |
| US7960569B2 (en) * | 2006-10-17 | 2011-06-14 | Bristol-Myers Squibb Company | Indole antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
| EP2220074A4 (fr) * | 2007-11-16 | 2012-01-04 | Neuraxon Inc | Composés d'indole 3,5-substitués ayant une activité d'inhibition de la réabsorption de la nos et de la noradrénaline |
| EA201000808A1 (ru) * | 2007-11-16 | 2011-04-29 | Ньюраксон, Инк. | Индольные соединения и способы лечения висцеральной боли |
| WO2009064505A1 (fr) * | 2007-11-16 | 2009-05-22 | The Arizona Board Of Regents On Behalf Of The University Of Arizona | Procédés de traitement de la douleur viscérale |
| EP2413933B2 (fr) * | 2009-04-02 | 2021-06-09 | Colucid Pharmaceuticals, Inc. | 2,4,6-trifluoro-n-ý6-(l-méthyl-pipéridin-4- carbonyl)-pyridin-2-yl]-benzamide destiné au traitement de la migraine par la voie orale ou intraveineuse |
| US8697876B2 (en) | 2010-04-02 | 2014-04-15 | Colucid Pharmaceuticals, Inc. | Compositions and methods of synthesis of pyridinolypiperidine 5-HT1F agonists |
| WO2014055142A1 (fr) * | 2012-06-20 | 2014-04-10 | Cocrystal Discovery, Inc. | Inhibiteurs de la polymérase du virus de l'hépatite c |
| ES2685839T3 (es) * | 2013-08-02 | 2018-10-11 | Pfizer Inc. | Inhibidores de RORC2 heterobicicloarilo y procedimientos de uso de los mismos |
| MA40759A (fr) | 2014-09-26 | 2017-08-01 | Pfizer | Modulateurs de rorc2 de type pyrrolopyridine substitué par un méthyle et trifluorométhyle et leurs procédés d'utilisation |
| TWI731854B (zh) | 2015-03-23 | 2021-07-01 | 美商共結晶製藥公司 | Ｃ型肝炎病毒聚合酶之抑制劑 |
| US11014892B2 (en) | 2016-11-02 | 2021-05-25 | Musc Foundation For Research Development | 5HT1F receptor agonists and mitochondrial biogenesis |
| TWI826514B (zh) | 2018-09-04 | 2023-12-21 | 美商美國禮來大藥廠 | 用於預防偏頭痛之拉米迪坦(lasmiditan)長期夜間投藥 |
| TWI776175B (zh) | 2019-07-09 | 2022-09-01 | 美商美國禮來大藥廠 | 大規模製備2,4,6-三氟-n-[6-(1-甲基-哌啶-4-羰基)-吡啶-2-基]-苯甲醯胺半琥珀酸鹽的方法及中間體，以及2,4,6-三氟-n-[6-(1-甲基-哌啶-4-羰基)-吡啶-2-基]-苯甲醯胺醋酸鹽之製備 |
| CN113233964A (zh) * | 2021-05-14 | 2021-08-10 | 武汉工程大学 | 一种5-甲氧基-2-萘满酮的合成方法 |
| CN113336633B (zh) * | 2021-05-14 | 2022-12-06 | 武汉工程大学 | 一种5-羟基-2-萘满酮的合成方法 |
| CN114539120A (zh) * | 2022-03-09 | 2022-05-27 | 台州学院 | 一种吲哚类钾离子通道激动剂的制备方法 |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2193584B1 (fr) * | 1972-07-28 | 1975-08-08 | Roussel Uclaf | |
| FR2421899A1 (fr) * | 1978-01-16 | 1979-11-02 | Roussel Uclaf | Nouveaux derives du tetrahydropyridinyl-indole et leurs sels, le procede de preparation et l'application a titre de medicaments de ces nouveaux produits |
| US4359468A (en) * | 1981-02-25 | 1982-11-16 | Boehringer Ingelheim Ltd. | Antiallergic N-[4-(indolyl)-piperidino-alkyl]-benzimidazolones |
| FR2533924A1 (fr) * | 1982-10-05 | 1984-04-06 | Roussel Uclaf | Nouveaux derives du 4-(1h-indol-3-yl)a-methyl piperidine-1-ethanol, leurs sels, le procede de preparation, l'application a titre de medicaments et les compositions les renfermant |
| IE58370B1 (en) * | 1985-04-10 | 1993-09-08 | Lundbeck & Co As H | Indole derivatives |
| US4742057A (en) * | 1985-12-05 | 1988-05-03 | Fujisawa Pharmaceutical Co., Ltd. | Antiallergic thiazole compounds |
| DE3882614T2 (de) * | 1987-08-13 | 1993-11-18 | Glaxo Group Ltd | Indol-Derivate. |
| GB8719167D0 (en) * | 1987-08-13 | 1987-09-23 | Glaxo Group Ltd | Chemical compounds |
| DK733788A (da) * | 1988-01-14 | 1989-07-15 | Fujisawa Pharmaceutical Co | Indolylpiperidinderivater og fremgangsmaade til fremstilling deraf |
| GB8819024D0 (en) * | 1988-08-10 | 1988-09-14 | Glaxo Group Ltd | Chemical compounds |
| GB8900382D0 (en) * | 1989-01-09 | 1989-03-08 | Janssen Pharmaceutica Nv | 2-aminopyrimidinone derivatives |
| GB8903036D0 (en) * | 1989-02-10 | 1989-03-30 | Glaxo Group Ltd | Chemical compounds |
| IL96891A0 (en) * | 1990-01-17 | 1992-03-29 | Merck Sharp & Dohme | Indole-substituted five-membered heteroaromatic compounds,their preparation and pharmaceutical compositions containing them |
| EP0636623B1 (fr) * | 1990-06-07 | 2001-08-16 | AstraZeneca AB | Dérivés d'indole comme 5-HT1-like agonistes |
| DK158590D0 (da) * | 1990-07-02 | 1990-07-02 | Lundbeck & Co As H | Indolderivater |
| US5322851A (en) * | 1990-07-02 | 1994-06-21 | H. Lundbeck A/S | Indole derivatives |
| US5118691A (en) * | 1990-09-20 | 1992-06-02 | Warner-Lambert Co. | Substituted tetrahydropyridines as central nervous system agents |
| US5187280A (en) * | 1990-09-20 | 1993-02-16 | Warner-Lambert Company | Substituted tetrahydropyridines and their use as central nervous system agents |
| US5545644A (en) * | 1990-10-15 | 1996-08-13 | Pfizer Inc. | Indole derivatives |
| DE9190141U1 (de) * | 1990-10-15 | 1993-07-15 | Pfizer Inc., New York, N.Y. | Indolderivate |
| SK278998B6 (sk) * | 1991-02-01 | 1998-05-06 | Merck Sharp & Dohme Limited | Deriváty imidazolu, triazolu a tetrazolu, spôsob i |
| TW263508B (fr) * | 1991-02-12 | 1995-11-21 | Pfizer | |
| US5639752A (en) * | 1991-11-25 | 1997-06-17 | Pfizer Inc | Indole derivatives |
| GB9201089D0 (en) * | 1992-01-18 | 1992-03-11 | Scient Generics Ltd | A diagnostic article |
| IL106445A (en) * | 1992-07-30 | 1998-01-04 | Merck Sharp & Dohme | History of 1,2,4-Trans-Triazole 4-Transform, Preparation and Pharmaceutical Preparations Containing Them |
| TW251284B (fr) * | 1992-11-02 | 1995-07-11 | Pfizer | |
| GB9226532D0 (en) * | 1992-12-21 | 1993-02-17 | Smithkline Beecham Plc | Compounds |
| PL311204A1 (en) * | 1993-04-22 | 1996-02-05 | Pfizer Res & Dev | Indole derivatives as antagonists of 5-ht-like receptors for use in hemicrania |
| FR2705346B1 (fr) * | 1993-05-18 | 1995-08-11 | Union Pharma Scient Appl | Nouveaux dérivés de pipéridinyl thio indole, leurs procédés de préparation, compositions pharmaceutiques les contenant, utiles notamment comme antalgiques . |
| US5521197A (en) * | 1994-12-01 | 1996-05-28 | Eli Lilly And Company | 3-<1-alkylenearyl>-4-<1,2,3,6-tetrahydropyridinyl>-and 3-<1-alkylenearyl>-4-piperidinyl-1h-indoles: new 5-HT1F agonists |
-
1996
- 1996-03-15 NZ NZ305166A patent/NZ305166A/xx unknown
- 1996-03-15 WO PCT/US1996/003500 patent/WO1996029075A1/fr not_active Ceased
- 1996-03-15 TR TR97/00993T patent/TR199700993T1/xx unknown
- 1996-03-15 CZ CZ972888A patent/CZ288897A3/cs unknown
- 1996-03-15 MX MX9706969A patent/MX9706969A/es unknown
- 1996-03-15 HU HU9800417A patent/HUP9800417A3/hu unknown
- 1996-03-15 JP JP8528501A patent/JPH11502816A/ja not_active Ceased
- 1996-03-15 PL PL96322843A patent/PL322843A1/xx unknown
- 1996-03-15 EA EA199700251A patent/EA001113B1/ru not_active IP Right Cessation
- 1996-03-15 CA CA002215322A patent/CA2215322A1/fr not_active Abandoned
- 1996-03-15 KR KR1019970706457A patent/KR19980703048A/ko not_active Withdrawn
- 1996-03-15 CN CN96193881A patent/CN1184425A/zh active Pending
- 1996-03-15 AU AU53112/96A patent/AU702322B2/en not_active Ceased
- 1996-03-19 DK DK96301845T patent/DK0733628T3/da active
- 1996-03-19 AT AT96301845T patent/ATE198332T1/de not_active IP Right Cessation
- 1996-03-19 DE DE69611315T patent/DE69611315T2/de not_active Expired - Fee Related
- 1996-03-19 EP EP96301845A patent/EP0733628B9/fr not_active Expired - Lifetime
- 1996-03-19 SI SI9630288T patent/SI0733628T1/xx unknown
- 1996-03-19 ES ES96301845T patent/ES2153078T3/es not_active Expired - Lifetime
- 1996-03-19 PT PT96301845T patent/PT733628E/pt unknown
- 1996-03-20 BR BR9601061A patent/BR9601061A/pt active Search and Examination
- 1996-03-20 US US08/619,783 patent/US5708008A/en not_active Expired - Fee Related
- 1996-03-20 AR ARP960101828A patent/AR002971A1/es unknown
-
1997
- 1997-09-12 NO NO974220A patent/NO974220L/no not_active Application Discontinuation
- 1997-11-24 US US08/977,526 patent/US5962474A/en not_active Expired - Fee Related
-
2001
- 2001-02-28 GR GR20010400330T patent/GR3035487T3/el not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| ES2153078T3 (es) | 2001-02-16 |
| EA199700251A1 (ru) | 1998-04-30 |
| MX9706969A (es) | 1997-11-29 |
| NO974220L (no) | 1997-11-04 |
| AU5311296A (en) | 1996-10-08 |
| BR9601061A (pt) | 1998-01-06 |
| AR002971A1 (es) | 1998-05-27 |
| DE69611315D1 (de) | 2001-02-01 |
| EP0733628A1 (fr) | 1996-09-25 |
| KR19980703048A (ko) | 1998-09-05 |
| AU702322B2 (en) | 1999-02-18 |
| CZ288897A3 (cs) | 1998-02-18 |
| WO1996029075A1 (fr) | 1996-09-26 |
| US5708008A (en) | 1998-01-13 |
| PL322843A1 (en) | 1998-02-16 |
| HUP9800417A3 (en) | 2001-04-28 |
| EA001113B1 (ru) | 2000-10-30 |
| CA2215322A1 (fr) | 1996-09-26 |
| HUP9800417A2 (hu) | 1999-06-28 |
| NZ305166A (en) | 1998-12-23 |
| SI0733628T1 (en) | 2001-06-30 |
| JPH11502816A (ja) | 1999-03-09 |
| TR199700993T1 (xx) | 1998-03-21 |
| EP0733628B1 (fr) | 2000-12-27 |
| EP0733628B9 (fr) | 2002-06-12 |
| ATE198332T1 (de) | 2001-01-15 |
| DE69611315T2 (de) | 2001-05-31 |
| NO974220D0 (no) | 1997-09-12 |
| CN1184425A (zh) | 1998-06-10 |
| US5962474A (en) | 1999-10-05 |
| GR3035487T3 (en) | 2001-05-31 |
| PT733628E (pt) | 2001-06-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DK0733628T3 (da) | 5-substituerede 3-(1,2,3,6-tetrahydropyridin-4-yl)- og 3-(piperidin-4-yl)-1H-indoler: 5HT1F-agonister | |
| DZ2026A1 (fr) | Compositions vaccinantes. | |
| DZ2055A1 (fr) | Compositions vaccinantes. | |
| IS1903B (is) | 2-methýl-thíenó-bensódíasepín, samsetning til inntöku | |
| PT915846E (pt) | Fenilcetoenois 2-substituidos e 2,5-substituidos | |
| TR199800077T1 (xx) | Kontroll� ��z�len paroksetin terkipleri. | |
| DE59608798D1 (de) | Endoparasitizide mittel | |
| TR199800783T2 (xx) | (-) C�s-6(S)-Fenil-5(R)$4-(2-Pirolidin-1-�letoksi) Fenil]-5,6,7,8-Tetrahidronaftalen-2-ol-d-tartrat | |
| ATE91139T1 (de) | Waermestabilisierte copolymerzusammensetzung. | |
| NO965084D0 (no) | N-[3(3-cyanopyrazol[1,5-aÅpyrimidin-7-yl)fenylÅ-N-etyl-acetamid | |
| DE59507222D1 (de) | Substituierte 1,2,3,4-tetrahydro-5-nitro-pyrimidine | |
| TR199501645A2 (tr) | Agiz bilesimleri. | |
| DE69007908D1 (de) | Shampoo-Zusammensetzung. | |
| DK0708105T3 (da) | 5-HT4-receptoragonister | |
| IT1302243B1 (it) | Sintesi dell'1,1,1,3,3-pentafluoropropano. | |
| TR199601012A2 (tr) | Sampuan terkibi. | |
| IT1293202B1 (it) | Dispositivo per l'agugliatura di ovatte prestabilizzate. | |
| ATE263165T1 (de) | 3-(4,5-dihydroisoxazol-5-yl)benzoylpyrazole | |
| IT238708Y1 (it) | Guarnitura per mobili. | |
| DE69101269D1 (de) | Feuerfeste Zusammensetzung. | |
| DK0866709T3 (da) | 1,2,4-benzotriazinoxidformuleringer | |
| FI906162L (fi) | Foerfarande foer framstaellning av 3-(n-metyl-n-alkyl)-amino-2-metoximetylenpropan-1-olderivat. | |
| FR2655400B1 (fr) | Masse d'equilibrage, en particulier pour ventilateur. | |
| ID24047A (id) | Turunan 5-tersubstitusi-3-oksaziazolil 1,6-naftiridin-2 1h-on | |
| DE69714019D1 (de) | 1,4-dihydropyridin-verbindungen als bradykinin-antagonisten |