JP2005530722A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2005530722A5 JP2005530722A5 JP2003582146A JP2003582146A JP2005530722A5 JP 2005530722 A5 JP2005530722 A5 JP 2005530722A5 JP 2003582146 A JP2003582146 A JP 2003582146A JP 2003582146 A JP2003582146 A JP 2003582146A JP 2005530722 A5 JP2005530722 A5 JP 2005530722A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- substituted
- hydrogen
- halo
- compound
- 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.)
- Granted
Links
- -1 phenyloxy, benzyloxy, phenylthio, benzylthio Chemical group 0.000 claims description 9
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 claims description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 6
- 229910052744 lithium Inorganic materials 0.000 claims description 4
- FEYDZHNIIMENOB-UHFFFAOYSA-N 2,6-dibromopyridine Chemical compound BrC1=CC=CC(Br)=N1 FEYDZHNIIMENOB-UHFFFAOYSA-N 0.000 claims description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
- 125000006239 protecting group Chemical group 0.000 claims description 3
- XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 claims description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 9
- 229910052739 hydrogen Inorganic materials 0.000 claims 9
- 239000001257 hydrogen Substances 0.000 claims 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 7
- 125000000623 heterocyclic group Chemical group 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 125000005843 halogen group Chemical group 0.000 claims 5
- 125000001424 substituent group Chemical group 0.000 claims 5
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- 241000124008 Mammalia Species 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- XEDHVZKDSYZQBF-UHFFFAOYSA-N lasmiditan Chemical compound C1CN(C)CCC1C(=O)C1=CC=CC(NC(=O)C=2C(=CC(F)=CC=2F)F)=N1 XEDHVZKDSYZQBF-UHFFFAOYSA-N 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- YBTPRLDGGGYWIP-UHFFFAOYSA-N 2,4,6-trifluoro-n-[6-(1-methylpiperidine-4-carbonyl)pyridin-2-yl]benzamide;hydrochloride Chemical compound Cl.C1CN(C)CCC1C(=O)C1=CC=CC(NC(=O)C=2C(=CC(F)=CC=2F)F)=N1 YBTPRLDGGGYWIP-UHFFFAOYSA-N 0.000 claims 1
- FILKGCRCWDMBKA-UHFFFAOYSA-N 2,6-dichloropyridine Chemical compound ClC1=CC=CC(Cl)=N1 FILKGCRCWDMBKA-UHFFFAOYSA-N 0.000 claims 1
- 206010015866 Extravasation Diseases 0.000 claims 1
- 208000019695 Migraine disease Diseases 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 125000002393 azetidinyl group Chemical group 0.000 claims 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000036251 extravasation Effects 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000001041 indolyl group Chemical group 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 206010027599 migraine Diseases 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 239000008024 pharmaceutical diluent Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 125000001984 thiazolidinyl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36908802P | 2002-03-29 | 2002-03-29 | |
| PCT/US2003/008455 WO2003084949A1 (en) | 2002-03-29 | 2003-03-27 | Pyridinoylpiperidines as 5-ht1f agonists |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010044032A Division JP2010159272A (ja) | 2002-03-29 | 2010-03-01 | ５−ｈｔ１ｆアゴニストとしてのピリジノイルピペリジン |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005530722A JP2005530722A (ja) | 2005-10-13 |
| JP2005530722A5 true JP2005530722A5 (https=) | 2006-05-25 |
| JP4493345B2 JP4493345B2 (ja) | 2010-06-30 |
Family
ID=28791923
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003582146A Expired - Lifetime JP4493345B2 (ja) | 2002-03-29 | 2003-03-27 | ５−ｈｔ１ｆアゴニストとしてのピリジノイルピペリジン |
| JP2010044032A Pending JP2010159272A (ja) | 2002-03-29 | 2010-03-01 | ５−ｈｔ１ｆアゴニストとしてのピリジノイルピペリジン |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010044032A Pending JP2010159272A (ja) | 2002-03-29 | 2010-03-01 | ５−ｈｔ１ｆアゴニストとしてのピリジノイルピペリジン |
Country Status (31)
| Country | Link |
|---|---|
| US (6) | US7423050B2 (https=) |
| EP (1) | EP1492786B1 (https=) |
| JP (2) | JP4493345B2 (https=) |
| KR (1) | KR100985995B1 (https=) |
| CN (1) | CN100352817C (https=) |
| AR (1) | AR039150A1 (https=) |
| AT (1) | ATE341543T1 (https=) |
| AU (1) | AU2003224719B2 (https=) |
| BR (1) | BRPI0308495B8 (https=) |
| CA (2) | CA2694410C (https=) |
| CR (1) | CR7496A (https=) |
| CY (1) | CY1105899T1 (https=) |
| DE (1) | DE60308850T2 (https=) |
| DK (1) | DK1492786T3 (https=) |
| EA (1) | EA007966B1 (https=) |
| EC (1) | ECSP045317A (https=) |
| EG (1) | EG25226A (https=) |
| ES (1) | ES2277074T3 (https=) |
| HR (1) | HRP20040883B1 (https=) |
| IL (1) | IL163928A0 (https=) |
| MX (1) | MXPA04009497A (https=) |
| MY (1) | MY134666A (https=) |
| NO (1) | NO330394B1 (https=) |
| NZ (1) | NZ534952A (https=) |
| PE (1) | PE20030976A1 (https=) |
| PL (1) | PL210019B1 (https=) |
| PT (1) | PT1492786E (https=) |
| TW (1) | TWI263497B (https=) |
| UA (1) | UA77504C2 (https=) |
| WO (1) | WO2003084949A1 (https=) |
| ZA (1) | ZA200407666B (https=) |
Families Citing this family (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI263497B (en) | 2002-03-29 | 2006-10-11 | Lilly Co Eli | Pyridinoylpiperidines as 5-HT1F agonists |
| MXPA05011223A (es) | 2003-04-18 | 2006-01-26 | Lilly Co Eli | Compuestos de (piperidiniloxi)fenilo, (piperidiniloxi)piridinilo, (piperidinilsulfanil)fenilo y (piperidinilsulfanil)piridinilo como agonistas 5-htif. |
| AU2003903597A0 (en) * | 2003-07-11 | 2003-07-24 | Jakov Vaisman | Treatment of premature ejaculation |
| 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 |
| WO2006022442A1 (ja) * | 2004-08-24 | 2006-03-02 | Santen Pharmaceutical Co., Ltd. | ジヒドロオロテートデヒドロゲナーゼ阻害活性を有する新規複素環アミド誘導体 |
| WO2006032852A1 (en) * | 2004-09-20 | 2006-03-30 | Biolipox Ab | Pyrazole compounds useful uin the treatment of inflammation |
| WO2006032851A1 (en) * | 2004-09-20 | 2006-03-30 | Biolipox Ab | Pyrazole compounds useful in the treatment of inflammation |
| US20060178349A1 (en) * | 2005-01-24 | 2006-08-10 | Pozen Inc. | Compositions and therapeutic methods utilizing a combination of a 5-HT1F inhibitor and an NSAID |
| TW200800911A (en) * | 2005-10-20 | 2008-01-01 | Biolipox Ab | Pyrazoles useful in the treatment of inflammation |
| EP1943234A1 (en) * | 2005-10-31 | 2008-07-16 | Biolipox AB | Triazole compounds as lipoxygenase inhibitors |
| TW200732320A (en) * | 2005-10-31 | 2007-09-01 | Biolipox Ab | Pyrazoles useful in the treatment of inflammation |
| JP2009513692A (ja) * | 2005-11-01 | 2009-04-02 | バイオリポックス エービー | 炎症の治療に有用なピラゾール化合物 |
| ES2399447T3 (es) * | 2006-02-17 | 2013-04-01 | F. Hoffmann-La Roche Ag | Derivados benzoil-piperidina como moduladores de 5HT2/D3 |
| CN102753171A (zh) * | 2009-04-02 | 2012-10-24 | 科鲁西德制药公司 | 2,4,6-三氟-n-[6-(1-甲基-哌啶-4-羰基)-吡啶-2-基]-苯甲酰胺的组合物 |
| US8429652B2 (en) | 2009-06-22 | 2013-04-23 | Citrix Systems, Inc. | Systems and methods for spillover in a multi-core system |
| US8697876B2 (en) | 2010-04-02 | 2014-04-15 | Colucid Pharmaceuticals, Inc. | Compositions and methods of synthesis of pyridinolypiperidine 5-HT1F agonists |
| WO2012068209A2 (en) | 2010-11-18 | 2012-05-24 | Janssen Pharmaceutica Nv | Bisthiazole inhibitors of pro-matrix metalloproteinase activation |
| CN102993086A (zh) * | 2012-10-11 | 2013-03-27 | 南通市华峰化工有限责任公司 | 一种2，6-二溴吡啶的合成方法 |
| US10669256B2 (en) * | 2016-07-15 | 2020-06-02 | Hangzhou Solipharma Co., Ltd. | Crystalline forms of lasmiditan, preparation methods, pharmaceutical compositions and uses thereof |
| CN109952314A (zh) | 2016-09-23 | 2019-06-28 | 泰瓦制药国际有限公司 | 治疗难治性偏头痛 |
| US10899767B2 (en) | 2016-10-05 | 2021-01-26 | Hangzhou Solipharma Co., Ltd. | Crystal form of ACP-196, preparation method therefor and pharmaceutical composition thereof |
| WO2018085491A1 (en) * | 2016-11-02 | 2018-05-11 | Musc Foundation For Research Development | 5ht1f receptor agonists and mitochondrial biogenesis |
| KR20230008257A (ko) * | 2016-12-06 | 2023-01-13 | 코루시드 파마슈티컬즈 인코포레이티드 | 피리디노일피페리딘 5-ht1f 작용제에 관한 조성물 및 방법 |
| EP3569233A4 (en) | 2017-01-13 | 2020-09-30 | Sumitomo Dainippon Pharma Co., Ltd. | THERAPEUTIC AGENT FOR NON-MOTOR SYMPTOMS ASSOCIATED WITH PARKINSON'S DISEASE |
| WO2018148961A1 (zh) | 2017-02-20 | 2018-08-23 | 杭州领业医药科技有限公司 | Acp-196盐的晶型、其制备方法、药物组合物和用途 |
| MA49014A (fr) * | 2017-03-21 | 2020-02-05 | Arbutus Biopharma Corp | Dihydroindène-4-carboxamides substitués, leurs analogues et procédés d'utilisation correspondant |
| TWI754772B (zh) | 2017-09-06 | 2022-02-11 | 美商美國禮來大藥廠 | 用於治療偏頭痛之拉米迪坦(lasmiditan)與cgrp拮抗劑之組合療法 |
| CN110386918B (zh) * | 2018-04-23 | 2020-06-09 | 新发药业有限公司 | 一种5-ht1f激动剂化合物的制备方法 |
| WO2020038435A1 (en) * | 2018-08-24 | 2020-02-27 | Sunshine Lake Pharma Co., Ltd. | Pyridinylmethylenepiperidine derivatives and uses thereof |
| 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 |
| WO2020095171A1 (en) * | 2018-11-05 | 2020-05-14 | Glenmark Life Sciences Limited, Glenmark Pharmaceuticals Limited | Process for preparation of lasmiditan |
| ES2801774B2 (es) | 2019-07-01 | 2022-03-30 | Moehs Iberica Sl | 2,2-dimetil-n-[6-(1-metil-piperidin-4-carbonil)-piridin-2-il]-propionamida, procedimiento para la preparacion de (6-amino-piridin-2-il)-(1-metil-piperidin-4-il)-metanona usando dicho compuesto y uso de dicho compuesto en la preparacion de lasmiditan |
| TWI829107B (zh) * | 2019-07-09 | 2024-01-11 | 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 |
| CN110981854B (zh) * | 2019-09-10 | 2023-03-28 | 南京三元阳普医药科技有限公司 | 2-氨基-6-(1-烷基哌啶-4-羰基)吡啶类化合物的合成方法 |
| CN114728929A (zh) * | 2019-11-22 | 2022-07-08 | 广东东阳光药业有限公司 | 吡啶亚甲基哌啶衍生物及其用途 |
| CN110845402B (zh) * | 2019-11-22 | 2023-05-09 | 广东东阳光药业有限公司 | 吡啶亚甲基哌嗪衍生物及其用途 |
| CN111187251B (zh) * | 2019-11-22 | 2023-06-09 | 广东东阳光药业有限公司 | 吡啶酰基哌啶衍生物及其用途 |
| CN111187252B (zh) * | 2019-11-22 | 2023-06-09 | 广东东阳光药业有限公司 | 吡啶酰基氮杂螺庚烷衍生物及其用途 |
| IT201900023937A1 (it) | 2019-12-13 | 2021-06-13 | Olon Spa | Procedimento per la preparazione di Lasmiditan e di un intermedio di sintesi |
| CN113045540B (zh) * | 2019-12-27 | 2024-02-13 | 上海天慈国际药业有限公司 | 一种拉司米地坦的制备方法 |
| WO2021152462A1 (en) | 2020-01-31 | 2021-08-05 | Glenmark Life Sciences Limited | Process for preparation of lasmiditan |
| CN113637003B (zh) * | 2020-05-11 | 2024-03-19 | 鲁南制药集团股份有限公司 | 一种制备2-氨基-6-（哌啶-4-酰基）吡啶衍生物的方法 |
| CN111943930B (zh) * | 2020-08-25 | 2022-11-01 | 南京三元阳普医药科技有限公司 | Lasmiditan的合成工艺 |
| WO2022079591A1 (en) * | 2020-10-14 | 2022-04-21 | Alembic Pharmaceuticals Limited | Pharmaceutical composition of lasmiditan and process of preparation thereof |
| CN114573555B (zh) * | 2020-11-30 | 2026-02-17 | 上海天慈国际药业有限公司 | 一种用于治疗偏头痛的化合物的制备方法 |
| CN114685439B (zh) * | 2020-12-30 | 2025-07-22 | 鲁南制药集团股份有限公司 | 一种拉司米地坦的制备方法 |
| WO2022236004A1 (en) | 2021-05-07 | 2022-11-10 | Eli Lilly And Company | Taste masked compostions of 2,4,6-trifluoro- n-[6-(1-methyl-piperidine-4-carbonyl)-pyridin-2- ylj-benzamide hemisuccinate, and orally disentegrating tablet comprising the same |
| CN115594665A (zh) * | 2021-07-08 | 2023-01-13 | 北京万全德众医药生物技术有限公司（Cn） | 拉司米地坦的新制备方法 |
| IT202100023861A1 (it) | 2021-09-16 | 2023-03-16 | Procos Spa | Processo per la preparazione di (6-alopiridin-2-il)(1-metilpiperidin-4-il)metanone |
| CN113866318B (zh) * | 2021-10-21 | 2023-07-04 | 佛山奕安赛医药科技有限公司 | 一种(6-氨基吡啶-2-基)(1-甲基哌啶-4-基)甲酮双盐酸盐的检测方法 |
| CN116239569B (zh) * | 2021-12-07 | 2025-11-21 | 山东新时代药业有限公司 | 一种半琥珀酸拉司米地坦晶型及其制备方法 |
| CN116239570B (zh) * | 2021-12-08 | 2025-11-25 | 山东新时代药业有限公司 | 一种半琥珀酸拉司米地坦新晶型 |
| WO2023152081A1 (en) | 2022-02-09 | 2023-08-17 | Inke, S.A. | Process for preparing pyridinoylpiperidines 5-ht1f agonists and salts thereof |
| CN116925037B (zh) * | 2022-04-02 | 2026-04-07 | 山东新时代药业有限公司 | 一种2-氨基-6-(1-甲基哌啶-4-基羰基)吡啶的制备方法 |
| WO2025240390A1 (en) * | 2024-05-13 | 2025-11-20 | Arizona Board Of Regents On Behalf Of The University Of Arizona | Mary1 and derivatives thereof for the treatment of mitochondrial dysfunction, vascular injury, kidney diseases, and organ aging |
Family Cites Families (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US677428A (en) * | 1900-04-28 | 1901-07-02 | Chicago Handle Bar Co | Steering device for bicycles. |
| US5023252A (en) | 1985-12-04 | 1991-06-11 | Conrex Pharmaceutical Corporation | Transdermal and trans-membrane delivery of drugs |
| US5011472A (en) | 1988-09-06 | 1991-04-30 | Brown University Research Foundation | Implantable delivery system for biological factors |
| JPH03255426A (ja) | 1990-03-06 | 1991-11-14 | Toshiba Corp | 有機非線形光学材料 |
| US5385912A (en) * | 1991-03-08 | 1995-01-31 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Multicyclic tertiary amine polyaromatic squalene synthase inhibitors |
| US5360735A (en) | 1992-01-08 | 1994-11-01 | Synaptic Pharmaceutical Corporation | DNA encoding a human 5-HT1F receptor, vectors, and host cells |
| US5698571A (en) * | 1994-10-05 | 1997-12-16 | Eli Lilly And Company | 5-HT1F mediated inhibition of neurogenic meningeal extravasation: a method for the treatment of migraine |
| US5521196A (en) * | 1994-10-05 | 1996-05-28 | Eli Lilly And Company | 5-HT1F agonists for the treatment of migraine |
| 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 |
| WO1996029075A1 (en) | 1995-03-20 | 1996-09-26 | Eli Lilly And Company | 5-substituted-3-(1,2,3,6-tetrahydropyridin-4-yl)- and 3-(piperidin-4-yl)-1h-indoles: new 5-ht1f agonists |
| WO1997013512A1 (en) | 1995-10-10 | 1997-04-17 | Eli Lilly And Company | N-[2-substituted-3-(2-aminoethyl)-1h-indol-5-yl]-amides: new 5-ht1f agonists |
| US6153754A (en) * | 1995-12-21 | 2000-11-28 | Albany Molecular Research, Inc. | Process for production of piperidine derivatives |
| EA001485B1 (ru) * | 1996-03-29 | 2001-04-23 | Пфайзер Инк. | Производные бензил(иден)-лактамов, их получение и применение в качестве селективных (ант)агонистов рецепторов 5-htи/или 5-ht |
| US5708187A (en) * | 1996-06-27 | 1998-01-13 | Eli Lilly And Company | 6-substituted-1,2,3,4-tetrahydro-9H-carbazoles and 7-substituted-10H-cyclohepta 7,6-B!indoles: New 5-HT1F agonists |
| TR199900430T2 (xx) | 1996-08-28 | 1999-06-21 | Eli Lilly And Company | �kameli 1,2,3,4-tetrahidro-2-dibenzofuranaminler ve 2-aminosiklohepta$b] benzofuranlar. |
| AU4074897A (en) * | 1996-09-18 | 1998-04-14 | Eli Lilly And Company | A method for the prevention of migraine |
| CA2268164A1 (en) | 1996-10-08 | 1998-04-16 | Yao-Chang Xu | New serotonin 5-ht1f agonists |
| ZA979961B (en) * | 1996-11-15 | 1999-05-05 | Lilly Co Eli | 5-HT1F agonists |
| EP0875513A1 (en) | 1997-04-14 | 1998-11-04 | Eli Lilly And Company | Substituted heteroaromatic 5-HT 1F agonists |
| ID23053A (id) | 1997-06-04 | 2000-01-20 | Lilly Co Eli | Karboksamida yang digunakan sebagai agonis 5-ht <if> |
| US5905084A (en) | 1997-11-14 | 1999-05-18 | Eli Lilly And Company | 5-HTIF -agonists effective in treating migraine |
| US6528529B1 (en) * | 1998-03-31 | 2003-03-04 | Acadia Pharmaceuticals Inc. | Compounds with activity on muscarinic receptors |
| US6303627B1 (en) * | 1998-06-19 | 2001-10-16 | Eli Lilly And Company | Inhibitors of serotonin reuptake |
| WO2000000490A2 (en) | 1998-06-26 | 2000-01-06 | Eli Lilly And Company | 5-ht1f agonists |
| ATE252572T1 (de) * | 1998-06-30 | 2003-11-15 | Lilly Co Eli | 5-ht1f agonisten |
| AU1937300A (en) | 1998-12-11 | 2000-06-26 | Eli Lilly And Company | Indole derivatives and their use as 5-HT1F agonists |
| US6777428B1 (en) * | 1999-02-10 | 2004-08-17 | Eli Lilly And Company | 5-HT1f agonist |
| CA2360164A1 (en) * | 1999-02-10 | 2000-08-17 | Eli Lilly And Company | 5-ht1f agonists |
| KR20010102355A (ko) | 1999-02-26 | 2001-11-15 | 피터 지. 스트링거 | 5-ｈｔ1ｆ 효능제 |
| DE60132456T2 (de) | 2000-07-13 | 2009-01-08 | Merck Patent Gmbh | Chirale verbindungen i |
| US6650463B2 (en) * | 2001-03-13 | 2003-11-18 | Seiko Epson Corporation | Electrophoretic display device |
| WO2003000245A1 (en) | 2001-06-22 | 2003-01-03 | Poseidon Pharmaceuticals A/S | Compounds for use in disorders associated with mast cell or basophil activity |
| TWI263497B (en) | 2002-03-29 | 2006-10-11 | Lilly Co Eli | Pyridinoylpiperidines as 5-HT1F agonists |
| EP1581498A2 (en) | 2002-11-22 | 2005-10-05 | Bristol-Myers Squibb Company | Pyridinyl, pyrimidinyl and pyrazinyl amides as potassium channel openers |
| GB0308186D0 (en) | 2003-04-09 | 2003-05-14 | Smithkline Beecham Corp | Novel compounds |
| MXPA05011223A (es) * | 2003-04-18 | 2006-01-26 | Lilly Co Eli | Compuestos de (piperidiniloxi)fenilo, (piperidiniloxi)piridinilo, (piperidinilsulfanil)fenilo y (piperidinilsulfanil)piridinilo como agonistas 5-htif. |
| WO2004099127A1 (en) | 2003-05-07 | 2004-11-18 | Novo Nordisk A/S | Novel compounds as kinase inhibitors |
| EP1651595A2 (en) | 2003-05-30 | 2006-05-03 | Rigel Pharmaceuticals, Inc. | Ubiquitin ligase inhibitors |
| 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 |
| GB0325956D0 (en) | 2003-11-06 | 2003-12-10 | Addex Pharmaceuticals Sa | Novel compounds |
| WO2006048771A1 (en) | 2004-11-04 | 2006-05-11 | Addex Pharmaceuticals Sa | Novel tetrazole derivatives as positive allosteric modulators of metabotropic glutamate receptors |
| GB0510143D0 (en) | 2005-05-18 | 2005-06-22 | Addex Pharmaceuticals Sa | Novel compounds A1 |
| KR20070094754A (ko) | 2004-12-01 | 2007-09-21 | 데브젠 엔브이 | 이온 채널, 특히 Ｋｖ 패밀리로부터의 이온 채널과상호작용하는 5-카복사미도 치환된 티아졸 유도체 |
| KR20060067738A (ko) | 2004-12-15 | 2006-06-20 | 주식회사 대웅제약 | 바닐로이드 수용체의 길항제로서 강력한 진통효과를나타내는 신규한 ｎ-아릴아마이드 유도체 및 이를함유하는 약제학적 조성물 |
| US20060178349A1 (en) | 2005-01-24 | 2006-08-10 | Pozen Inc. | Compositions and therapeutic methods utilizing a combination of a 5-HT1F inhibitor and an NSAID |
| DE102005016634A1 (de) | 2005-04-12 | 2006-10-19 | Merck Patent Gmbh | Neuartige Aza-Hetercyclen als Kinase-Inhibitoren |
| KR100976063B1 (ko) | 2007-03-16 | 2010-08-17 | 동아제약주식회사 | 신규한 벤즈아미드 유도체 화합물 및 그의 제조방법 |
| CN102753171A (zh) | 2009-04-02 | 2012-10-24 | 科鲁西德制药公司 | 2,4,6-三氟-n-[6-(1-甲基-哌啶-4-羰基)-吡啶-2-基]-苯甲酰胺的组合物 |
| US8697876B2 (en) | 2010-04-02 | 2014-04-15 | Colucid Pharmaceuticals, Inc. | Compositions and methods of synthesis of pyridinolypiperidine 5-HT1F agonists |
-
2003
- 2003-03-21 TW TW092106334A patent/TWI263497B/zh not_active IP Right Cessation
- 2003-03-25 PE PE2003000301A patent/PE20030976A1/es active IP Right Grant
- 2003-03-26 MY MYPI20031097A patent/MY134666A/en unknown
- 2003-03-26 AR ARP030101055A patent/AR039150A1/es active IP Right Grant
- 2003-03-26 EG EG2003030289A patent/EG25226A/xx active
- 2003-03-27 PT PT03721402T patent/PT1492786E/pt unknown
- 2003-03-27 DK DK03721402T patent/DK1492786T3/da active
- 2003-03-27 UA UA20040907833A patent/UA77504C2/uk unknown
- 2003-03-27 CN CNB038073633A patent/CN100352817C/zh not_active Expired - Lifetime
- 2003-03-27 EP EP03721402A patent/EP1492786B1/en not_active Expired - Lifetime
- 2003-03-27 MX MXPA04009497A patent/MXPA04009497A/es active IP Right Grant
- 2003-03-27 ES ES03721402T patent/ES2277074T3/es not_active Expired - Lifetime
- 2003-03-27 US US10/509,770 patent/US7423050B2/en active Active
- 2003-03-27 IL IL16392803A patent/IL163928A0/xx unknown
- 2003-03-27 WO PCT/US2003/008455 patent/WO2003084949A1/en not_active Ceased
- 2003-03-27 CA CA2694410A patent/CA2694410C/en not_active Expired - Lifetime
- 2003-03-27 CA CA2478229A patent/CA2478229C/en not_active Expired - Lifetime
- 2003-03-27 NZ NZ534952A patent/NZ534952A/en not_active IP Right Cessation
- 2003-03-27 AU AU2003224719A patent/AU2003224719B2/en not_active Expired
- 2003-03-27 KR KR1020047015294A patent/KR100985995B1/ko not_active Expired - Lifetime
- 2003-03-27 EA EA200401282A patent/EA007966B1/ru unknown
- 2003-03-27 PL PL372845A patent/PL210019B1/pl unknown
- 2003-03-27 BR BRPI0308495A patent/BRPI0308495B8/pt not_active IP Right Cessation
- 2003-03-27 JP JP2003582146A patent/JP4493345B2/ja not_active Expired - Lifetime
- 2003-03-27 HR HRP20040883 patent/HRP20040883B1/xx not_active IP Right Cessation
- 2003-03-27 DE DE60308850T patent/DE60308850T2/de not_active Expired - Lifetime
- 2003-03-27 AT AT03721402T patent/ATE341543T1/de active
-
2004
- 2004-09-22 ZA ZA200407666A patent/ZA200407666B/xx unknown
- 2004-09-24 CR CR7496A patent/CR7496A/es unknown
- 2004-09-27 EC EC2004005317A patent/ECSP045317A/es unknown
- 2004-10-28 NO NO20044654A patent/NO330394B1/no not_active IP Right Cessation
-
2007
- 2007-01-03 CY CY20071100004T patent/CY1105899T1/el unknown
-
2008
- 2008-07-22 US US12/220,225 patent/US8044207B2/en not_active Expired - Lifetime
- 2008-08-07 US US12/221,919 patent/US20090209563A1/en not_active Abandoned
-
2010
- 2010-03-01 JP JP2010044032A patent/JP2010159272A/ja active Pending
-
2012
- 2012-02-01 US US13/363,895 patent/US8748459B2/en not_active Expired - Lifetime
-
2014
- 2014-06-05 US US14/296,911 patent/US20150376178A1/en not_active Abandoned
-
2016
- 2016-04-06 US US15/091,776 patent/US20170044136A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2005530722A5 (https=) | ||
| JP4326468B2 (ja) | ヒスタミンｈ３アンタゴニストとして有用なインドール誘導体 | |
| JP5432718B2 (ja) | ピロール化合物 | |
| JP2006524222A5 (https=) | ||
| JP2020512343A5 (https=) | ||
| CA2478229A1 (en) | Pyridinoylpiperidines as 5-ht1f agonists | |
| CN101001851A (zh) | 具有作为组蛋白脱乙酰酶(hdac)抑制剂的活性的羟基酰胺化合物 | |
| CA2551508A1 (en) | Novel quinoline derivatives | |
| CZ285370B6 (cs) | Aminoheterocyklické deriváty jako antitrombotická a antikoagulační činidla | |
| HUP0302153A2 (hu) | Kemokin receptor aktívitás modulátoraiként hatásos piperidinszármazékok, eljárás előállításukra és a vegyületeket tartalmazó gyógyszerkészítmények | |
| EP1571145A1 (en) | Substituted piperidine compounds for use as H3 histamine receptor antagonists | |
| JP2007524696A5 (https=) | ||
| AU2002215355A1 (en) | Piperidine compounds as anti-allergic | |
| TW201249823A (en) | Tetrasubstituted cyclohexyl compounds as kinase inhibitors | |
| CN112961104A (zh) | 用于治疗nk-1受体相关疾病的取代的4-苯基吡啶 | |
| JP2007516205A5 (https=) | ||
| JP2006525293A5 (https=) | ||
| WO2005063709A1 (ja) | アミド誘導体及び医薬 | |
| JP2005514420A5 (https=) | ||
| KR20110133049A (ko) | 항암 약물로서의 니코틴아미드 유도체, 그의 제조법 및 그의 치료 용도 | |
| JP2008513405A5 (https=) | ||
| KR100642231B1 (ko) | 2-티오-치환 이미다졸 유도체류 및 제약에서의 그 용도 | |
| JP2014521620A5 (https=) | ||
| EP3297991B1 (en) | Novel amidoheteroaryl aroyl hydrazide ethynes | |
| WO2013107285A1 (zh) | 氨基杂芳基化合物及其制备方法与应用 |