AR063081A1 - Derivados de 3- aza- biciclo [3.1.0] hexano y su uso para la preparacion de medicamentos - Google Patents
Derivados de 3- aza- biciclo [3.1.0] hexano y su uso para la preparacion de medicamentosInfo
- Publication number
- AR063081A1 AR063081A1 ARP070104342A ARP070104342A AR063081A1 AR 063081 A1 AR063081 A1 AR 063081A1 AR P070104342 A ARP070104342 A AR P070104342A AR P070104342 A ARP070104342 A AR P070104342A AR 063081 A1 AR063081 A1 AR 063081A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- substituted
- heterocyclyl
- alkyl
- nr2r3
- Prior art date
Links
- 239000003814 drug Substances 0.000 title abstract 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 title 3
- -1 trimethylsilyl ethynyl Chemical group 0.000 abstract 11
- 125000000623 heterocyclic group Chemical group 0.000 abstract 8
- 125000003118 aryl group Chemical group 0.000 abstract 7
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 6
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000001424 substituent group Chemical group 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- YQBBCPKSALSCAP-UHFFFAOYSA-N 2,3,6,7-tetrahydrofuro[2,3-f][1]benzofuran Chemical compound C1=C2OCCC2=CC2=C1CCO2 YQBBCPKSALSCAP-UHFFFAOYSA-N 0.000 abstract 1
- 125000000850 2H-chromenyl group Chemical group O1C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- HGWUUOXXAIISDB-UHFFFAOYSA-N 3-azabicyclo[3.1.0]hexane Chemical compound C1NCC2CC21 HGWUUOXXAIISDB-UHFFFAOYSA-N 0.000 abstract 1
- 208000012902 Nervous system disease Diseases 0.000 abstract 1
- 208000025966 Neurological disease Diseases 0.000 abstract 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000005605 benzo group Chemical group 0.000 abstract 1
- 125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 206010022437 insomnia Diseases 0.000 abstract 1
- 208000004296 neuralgia Diseases 0.000 abstract 1
- 230000000926 neurological effect Effects 0.000 abstract 1
- 208000021722 neuropathic pain Diseases 0.000 abstract 1
- 208000020016 psychiatric disease Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 208000019116 sleep disease Diseases 0.000 abstract 1
- 125000006168 tricyclic group Chemical group 0.000 abstract 1
Classifications
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- 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
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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Abstract
Compuestos de 3-aza-biciclo [3.1.0] hexano y su uso en la preparacion de medicamentos. Estos compuestos son utiles en trastornos del sueno, como insomnio, apicea del sueno, dolor neuropático y trastornos neurologicos y psiquiátricos. Reivindicacion 1: Un compuesto de formula (1) donde X representa C(O) o SO2; A representa arilo o heterociclilo, donde el arilo o heterociclilo no está sustituido o está independientemente mono- o di-sustituido, donde los sustituyentes se seleccionan independientemente del grupo que consiste en alquilo C1-4, cicloalquilo C3-6, alquinilo C2-6, hidroxi-alquilo C1-4, hidroxi-alquinilo C2-6, trimetilsilil-etinilo, cicloalquil C3-6-etinilo, alcoxi C1-4, trifluorometilo, trifluorometoxi, NR2R3, N(R2)C(O)R3, C(O)NR2R3 y halogeno; B representa un átomo de hidrogeno o un grupo arilo o heterociclilo, donde el arilo o heterociclilo no está sustituido o está independientemente mono-, di- o trisustituido, donde los sustituyentes se seleccionan independientemente del grupo que consiste en alquilo C1-4, cicloalquilo C3-6, alcoxi C1-4, rnetoxi-alcoxi C1-4, ciano, trifluorometilo, trifluorometoxi, NR2R3, N(R2)C(O)R3, C(O)NR2R3 y halogeno; o B representa un grupo 2,3-dihidro-benzo[1 ,4]dioxinilo; o A y B juntos representan un grupo tricíclico; n representa 0 o 1; R1 representa arilo o heterociclilo, donde el arilo o heterociclilo no está sustituido está independientemente mono-, di- o tri-sustituido, donde los sustituyentes se seleccionan independientemente del grupo que consiste en alquilo C1-4, alquinilo C2-6, cicloalquilo C3-6, alcoxi C1-4, alquil C1-4-tio, halogeno, hidroxi, ciano, trifluorometilo, trifluorometoxi, NR2R3, N(R2)C(O)R3, COOR2 y C(O)NR2R3, o R1 representa un grupo heterociclil-etenilo, heterociclil-alquilo C1-4 o ariloxialquilo C1-4, donde dichos grupos no están sustituidos o están independientemente mono- o di-sustituidos en la porcion arilo o heterociclilo, donde los sustituyentes se seleccionan independientemente del grupo que consiste en alquilo C1-4, alcoxi C1-4, halogeno, trifluorometilo, trifluorometoxi y NR2R3, o R1 representa un grupo 2,3-dihidro-benzofuranilo, benzo[1,3jdioxolilo, 2,3-dihidro-benzo[1,4]dioxinilo, 4-oxo- 4H-cromenilo, 2H-cromenilo, cromanilo, 4H-benzo[1,3]dioxinilo, 2,3-dihidro-tieno[3,4-b][1,4]dioxinilo, morfolin-4-il-fenilo, piperazin-1-il-fenilo, 3,4-dihidro-2H-benzo[1,4]oxazinilo, 3-oxo-3,4-dihidro-2H-benzo[1,4]oxazinilo o 2,3,6,7-tetrahidro- benzo[1,2-b;4,5-b']difuranilo, donde dichos grupos no están sustituidos o están independientemente mono- o di-sustituidos, donde los sustituyentes se seleccionan independientemente del grupo que consiste en alquilo C1-4, alcoxi C1-4 y halogeno; R2 representa hidrogeno o alquilo C1-4; y R3 representa hidrogeno o alquilo C1-4; o una sal farmacéuticamente aceptable de dicho compuesto.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IB2006053570 | 2006-09-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR063081A1 true AR063081A1 (es) | 2008-12-23 |
Family
ID=39106344
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070104342A AR063081A1 (es) | 2006-09-29 | 2007-10-01 | Derivados de 3- aza- biciclo [3.1.0] hexano y su uso para la preparacion de medicamentos |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US20100016401A1 (es) |
| EP (1) | EP2079690B1 (es) |
| JP (1) | JP2010504957A (es) |
| KR (1) | KR20090077051A (es) |
| CN (1) | CN101522618A (es) |
| AR (1) | AR063081A1 (es) |
| AT (1) | ATE481383T1 (es) |
| CA (1) | CA2662612A1 (es) |
| CL (1) | CL2007002809A1 (es) |
| DE (1) | DE602007009284D1 (es) |
| ES (1) | ES2350460T3 (es) |
| TW (1) | TW200823227A (es) |
| WO (1) | WO2008038251A2 (es) |
Families Citing this family (56)
| Publication number | Priority date | Publication date | Assignee | Title |
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| DE602007012142D1 (en) | 2006-12-01 | 2011-03-03 | Actelion Pharmaceuticals Ltd | 3-heteroaryl (amino bzw. amido)-1- (biphenyl bzw. phenylthiazolyl) carbonylpiperdinderivate als orexinrezeptor-inhibitoren |
| CL2007003827A1 (es) * | 2006-12-28 | 2008-09-26 | Actelion Pharmaceuticals Ltd | Compuestos derivados de n-(2-aza-biciclo(3.1.0)hex-3-ilmetil)amida; y su uso para prevenir o tratar la depresion, neurosis, esquizofrenia, ansiedad, adicciones, epilepsia, dolor, enfermedades cardiacas, entre otras. |
| CL2008000836A1 (es) * | 2007-03-26 | 2008-11-07 | Actelion Pharmaceuticals Ltd | Compuestos derivados de tiazolidina, antagonistas del receptor de orexina; composicion farmaceutica que los comprende; y su uso en el tratamiento de neurosis emocional, depresion grave, trastornos psicoticos, alzheimer, parkinson, dolor, entre otras. |
| AU2008260647A1 (en) * | 2007-05-23 | 2008-12-11 | Merck Sharp & Dohme Corp. | Cyclopropyl pyrrolidine orexin receptor antagonists |
| CN101679366B (zh) | 2007-05-23 | 2013-08-07 | 默沙东公司 | 吡啶基哌啶食欲素受体拮抗剂 |
| AU2008272449A1 (en) * | 2007-07-03 | 2009-01-08 | Actelion Pharmaceuticals Ltd | 3-aza-bicyclo[3.3.0]octane compounds |
| AR067665A1 (es) | 2007-07-27 | 2009-10-21 | Actelion Pharmaceuticals Ltd | Derivados de trans-3- aza-biciclo ( 3.1.0) hexano |
| WO2009016560A2 (en) * | 2007-07-27 | 2009-02-05 | Actelion Pharmaceuticals Ltd | Trans-3-aza-bicyclo[3.1.0]hexane derivatives |
| AU2008281399A1 (en) * | 2007-07-27 | 2009-02-05 | Actelion Pharmaceuticals Ltd | 2-aza-bicyclo[3.3.0]octane derivatives |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| WO2009040730A2 (en) * | 2007-09-24 | 2009-04-02 | Actelion Pharmaceuticals Ltd | Pyrrolidines and piperidines as orexin receptor antagonists |
| ATE555107T1 (de) * | 2008-02-21 | 2012-05-15 | Actelion Pharmaceuticals Ltd | 2-aza-bicyclo-ä2,2,1-üheptan-derivate |
| KR20100135962A (ko) * | 2008-04-30 | 2010-12-27 | 액테리온 파마슈티칼 리미티드 | 피페리딘 및 피롤리딘 화합물 |
| MX2011003191A (es) * | 2008-10-14 | 2011-04-27 | Actelion Pharmaceuticals Ltd | Derivados de fenetilamida y sus analogos heterociclicos. |
| WO2010063662A1 (en) | 2008-12-02 | 2010-06-10 | Glaxo Group Limited | N-{[(ir,4s,6r-3-(2-pyridinylcarbonyl)-3-azabicyclo [4.1.0] hept-4-yl] methyl}-2-heteroarylamine derivatives and uses thereof |
| EP2370426A1 (en) * | 2008-12-02 | 2011-10-05 | Glaxo Group Limited | N-{[(ir,4s,6r-3-(2-pyridinylcarbonyl)-3-azabicyclo [4.1.0]hept-4-yl]methyl}-2-heteroarylamine derivatives and uses thereof |
| GB0823467D0 (en) | 2008-12-23 | 2009-01-28 | Glaxo Group Ltd | Novel Compounds |
| MX2011006845A (es) * | 2008-12-29 | 2011-08-04 | Univ Vanderbilt | Inhibidores de glyt1 biciclicos 3.1.0 y metodos para elaboracion y utilizacion de los mismos. |
| EA201171293A1 (ru) | 2009-04-24 | 2012-05-30 | Глэксо Груп Лимитед | 3-азабицикло[4.1.0]гептаны, применяемые в качестве антагонистов орексина |
| EP2275421A1 (en) | 2009-07-15 | 2011-01-19 | Rottapharm S.p.A. | Spiro amino compounds suitable for the treatment of inter alia sleep disorders and drug addiction |
| WO2011023585A1 (en) | 2009-08-24 | 2011-03-03 | Glaxo Group Limited | Piperidine derivatives used as orexin antagonists |
| EP2470523A1 (en) | 2009-08-24 | 2012-07-04 | Glaxo Group Limited | 5-methyl-piperidine derivatives as orexin receptor antagonists for the treatment of sleep disorder |
| SI2491038T1 (sl) | 2009-10-23 | 2016-08-31 | Janssen Pharmaceutica N.V. | Disubstituirani oktahil-dropirolo(3,4-c)piroli kot modulatorji oreksinskega receptorja |
| CN102762556B (zh) * | 2009-11-05 | 2017-04-26 | 圣母大学 | 咪唑并[1,2‑a]吡啶类化合物及其合成及使用方法 |
| MX2012006909A (es) * | 2009-12-29 | 2012-07-10 | Suven Life Sciences Ltd | LIGANDOS DEL RECEPTOR NICOTINICO NEURONAL A4ß2 DE ACETILCOLINA. |
| UA108510C2 (xx) | 2010-09-22 | 2015-05-12 | Eisai R&D Man Co Ltd | Циклопропанова сполука |
| EP2638008B1 (en) * | 2010-11-10 | 2015-07-01 | Actelion Pharmaceuticals Ltd | Lactam derivatives useful as orexin receptor antagonists |
| WO2012089606A1 (en) | 2010-12-28 | 2012-07-05 | Glaxo Group Limited | Azabicyclo [4.1.0] hept - 4 - yl derivatives as human orexin receptor antagonists |
| WO2012089607A1 (en) | 2010-12-28 | 2012-07-05 | Glaxo Group Limited | Novel compounds with a 3a-azabicyclo [4.1.0] heptane core acting on orexin receptors |
| AR088352A1 (es) | 2011-10-19 | 2014-05-28 | Merck Sharp & Dohme | Antagonistas del receptor de 2-piridiloxi-4-nitrilo orexina |
| US9440982B2 (en) | 2012-02-07 | 2016-09-13 | Eolas Therapeutics, Inc. | Substituted prolines/piperidines as orexin receptor antagonists |
| HK1204955A1 (zh) | 2012-02-07 | 2015-12-11 | Eolas Therapeutics Inc. | 取代的脯氨酸/哌啶用作食慾素受體拮抗劑 |
| ITMI20120424A1 (it) | 2012-03-19 | 2013-09-20 | Rottapharm Spa | Composti chimici |
| KR101689093B1 (ko) | 2012-06-04 | 2016-12-22 | 액테리온 파마슈티칼 리미티드 | 벤즈이미다졸-프롤린 유도체 |
| RU2696278C2 (ru) | 2012-07-18 | 2019-08-01 | Юниверсити Оф Нотр Дам Дю Лак | 5,5-гетероароматические противоинфекционные соединения |
| JP6244365B2 (ja) | 2012-10-10 | 2017-12-06 | アクテリオン ファーマシューティカルズ リミテッドActelion Pharmaceuticals Ltd | [オルトビ−(ヘテロ−)アリール]−[2−(メタビ−(ヘテロ−)アリール)−ピロリジン−1−イル]−メタノン誘導体であるオレキシン受容体アンタゴニスト |
| CN105051040A (zh) | 2013-03-12 | 2015-11-11 | 埃科特莱茵药品有限公司 | 作为食欲素受体拮抗剂的氮杂环丁烷酰胺衍生物 |
| SG10201709565QA (en) | 2013-03-14 | 2017-12-28 | Janssen Pharmaceutica Nv | Benzo-fused heterocyclic derivatives useful as agonists of gpr120 |
| US20160279098A1 (en) * | 2013-11-11 | 2016-09-29 | Euthymics Bioscience, Inc. | Novel methods |
| UA119151C2 (uk) | 2013-12-03 | 2019-05-10 | Ідорсія Фармасьютікалз Лтд | КРИСТАЛІЧНА СОЛЬОВА ФОРМА (S)-(2-(6-ХЛОР-7-МЕТИЛ-1H-БЕНЗО[d]ІМІДАЗОЛ-2-ІЛ)-2-МЕТИЛПІРОЛІДИН-1-ІЛ)(5-МЕТОКСИ-2-(2H-1,2,3-ТРИАЗОЛ-2-ІЛ)ФЕНІЛ)МЕТАНОНУ ЯК АНТАГОНІСТ ОРЕКСИНОВОГО РЕЦЕПТОРА |
| WO2015083070A1 (en) | 2013-12-03 | 2015-06-11 | Actelion Pharmaceuticals Ltd | Crystalline form of (s)-(2-(6-chloro-7-methyl-1h-benzo[d]imidazol-2-yl)-2-methylpyrrolidin-1 -yl)(5-methoxy-2-(2h-1,2,3-triazol-2-yl)phenyl)methanone and its use as orexin receptor antagonists |
| MX366642B (es) | 2013-12-04 | 2019-07-17 | Idorsia Pharmaceuticals Ltd | Uso de derivados de bencimidazol-prolina. |
| US10221170B2 (en) | 2014-08-13 | 2019-03-05 | Eolas Therapeutics, Inc. | Difluoropyrrolidines as orexin receptor modulators |
| MX376164B (es) | 2014-10-23 | 2025-03-07 | Eisai R&D Man Co Ltd | Composiciones y metodos para tratar el insomnio. |
| IL257743B (en) | 2015-09-17 | 2022-08-01 | Marvin J Miller | Benzyl amine-containing heterocyclic compounds and compositions useful against mycobacterial infection |
| SMT202200323T1 (it) | 2016-02-12 | 2022-09-14 | Astrazeneca Ab | Piperidine alo-sostituite come modulatori del recettore di oressina |
| PH12018501903B1 (en) | 2016-03-10 | 2023-03-17 | Janssen Pharmaceutica Nv | Methods of treating depression using orexin-2 receptor antagonists |
| EP3454857A1 (en) | 2016-05-10 | 2019-03-20 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical compositions for the treatment of autoimmune inflammatory diseases |
| RS62357B1 (sr) | 2017-05-03 | 2021-10-29 | Idorsia Pharmaceuticals Ltd | Dobijanje derivata 2-([1,2,3]triazol-2-il)-benzojeve kiseline |
| WO2020007964A1 (en) | 2018-07-05 | 2020-01-09 | Idorsia Pharmaceuticals Ltd | 2-(2-azabicyclo[3.1.0]hexan-1-yl)-1h-benzimidazole derivatives |
| WO2020007977A1 (en) | 2018-07-06 | 2020-01-09 | Idorsia Pharmaceuticals Ltd | 7-trifluoromethyl-[1,4]diazepan derivatives |
| WO2020099511A1 (en) | 2018-11-14 | 2020-05-22 | Idorsia Pharmaceuticals Ltd | Benzimidazole-2-methyl-morpholine derivatives |
| WO2022166768A1 (zh) * | 2021-02-02 | 2022-08-11 | 南京明德新药研发有限公司 | 四氢吡咯并环化合物及其应用 |
| TW202400149A (zh) | 2022-05-13 | 2024-01-01 | 瑞士商愛杜西亞製藥有限公司 | 經噻唑并芳基-甲基取代之環狀肼-n-甲醯胺衍生物 |
| CN117126101A (zh) * | 2023-08-28 | 2023-11-28 | 瑞博(杭州)医药科技有限公司 | 一种脯氨酸结构的盐酸盐中间体的高效制备方法 |
| WO2025224168A1 (en) | 2024-04-24 | 2025-10-30 | Idorsia Pharmaceuticals Ltd | Aryl sulfone and sulfanone derivatives as orexin receptor modulators |
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| WO2001096302A1 (en) * | 2000-06-16 | 2001-12-20 | Smithkline Beecham P.L.C. | Piperidines for use as orexin receptor antagonists |
| AU2002224885A1 (en) * | 2000-11-28 | 2002-06-11 | Smithkline Beecham Plc | Morpholine derivatives as antagonists of orexin receptors |
| EP1435955A2 (en) * | 2001-05-05 | 2004-07-14 | SmithKline Beecham P.L.C. | N-aroyl cyclic amine derivatives as orexin receptor antagonists |
| AR033306A1 (es) * | 2001-05-05 | 2003-12-10 | Smithkline Beecham Plc | Compuestos |
| GB0115862D0 (en) * | 2001-06-28 | 2001-08-22 | Smithkline Beecham Plc | Compounds |
| MXPA03011706A (es) * | 2001-06-28 | 2004-03-19 | Smithkline Beecham Plc | Derivados de n-aroil-amina ciclica como antagonistas del receptor de orexina. |
| GB0124463D0 (en) * | 2001-10-11 | 2001-12-05 | Smithkline Beecham Plc | Compounds |
| GB0127145D0 (en) * | 2001-11-10 | 2002-01-02 | Smithkline Beecham | Compounds |
| GB0130335D0 (en) * | 2001-12-19 | 2002-02-06 | Smithkline Beecham Plc | Compounds |
| GB0130393D0 (en) * | 2001-12-19 | 2002-02-06 | Smithkline Beecham Plc | Compounds |
| EP1539747B1 (en) * | 2002-09-18 | 2006-11-02 | Glaxo Group Limited | N-aroyl cyclic amines as orexin receptor antagonists |
| GB0225938D0 (en) * | 2002-11-06 | 2002-12-11 | Glaxo Group Ltd | Novel compounds |
| GB0225944D0 (en) * | 2002-11-06 | 2002-12-11 | Glaxo Group Ltd | Novel compounds |
| GB0225884D0 (en) * | 2002-11-06 | 2002-12-11 | Glaxo Group Ltd | Novel compounds |
| US20060014733A1 (en) * | 2004-07-19 | 2006-01-19 | Pfizer Inc | Histamine-3 agonists and antagonists |
| US7994336B2 (en) * | 2006-08-15 | 2011-08-09 | Actelion Pharmaceuticals Ltd. | Azetidine compounds as orexin receptor antagonists |
| DE602007012142D1 (en) * | 2006-12-01 | 2011-03-03 | Actelion Pharmaceuticals Ltd | 3-heteroaryl (amino bzw. amido)-1- (biphenyl bzw. phenylthiazolyl) carbonylpiperdinderivate als orexinrezeptor-inhibitoren |
| CL2007003827A1 (es) * | 2006-12-28 | 2008-09-26 | Actelion Pharmaceuticals Ltd | Compuestos derivados de n-(2-aza-biciclo(3.1.0)hex-3-ilmetil)amida; y su uso para prevenir o tratar la depresion, neurosis, esquizofrenia, ansiedad, adicciones, epilepsia, dolor, enfermedades cardiacas, entre otras. |
| CL2008000836A1 (es) * | 2007-03-26 | 2008-11-07 | Actelion Pharmaceuticals Ltd | Compuestos derivados de tiazolidina, antagonistas del receptor de orexina; composicion farmaceutica que los comprende; y su uso en el tratamiento de neurosis emocional, depresion grave, trastornos psicoticos, alzheimer, parkinson, dolor, entre otras. |
| DE602008002934D1 (de) * | 2007-05-14 | 2010-11-18 | Actelion Pharmaceuticals Ltd | 2-cyclopropylthiazolderivate |
| CN101679366B (zh) * | 2007-05-23 | 2013-08-07 | 默沙东公司 | 吡啶基哌啶食欲素受体拮抗剂 |
| AU2008272449A1 (en) * | 2007-07-03 | 2009-01-08 | Actelion Pharmaceuticals Ltd | 3-aza-bicyclo[3.3.0]octane compounds |
| WO2009016560A2 (en) * | 2007-07-27 | 2009-02-05 | Actelion Pharmaceuticals Ltd | Trans-3-aza-bicyclo[3.1.0]hexane derivatives |
| AU2008281399A1 (en) * | 2007-07-27 | 2009-02-05 | Actelion Pharmaceuticals Ltd | 2-aza-bicyclo[3.3.0]octane derivatives |
| AR067665A1 (es) * | 2007-07-27 | 2009-10-21 | Actelion Pharmaceuticals Ltd | Derivados de trans-3- aza-biciclo ( 3.1.0) hexano |
| WO2009040730A2 (en) * | 2007-09-24 | 2009-04-02 | Actelion Pharmaceuticals Ltd | Pyrrolidines and piperidines as orexin receptor antagonists |
| ATE555107T1 (de) * | 2008-02-21 | 2012-05-15 | Actelion Pharmaceuticals Ltd | 2-aza-bicyclo-ä2,2,1-üheptan-derivate |
| KR20100135962A (ko) * | 2008-04-30 | 2010-12-27 | 액테리온 파마슈티칼 리미티드 | 피페리딘 및 피롤리딘 화합물 |
-
2007
- 2007-09-28 AT AT07826577T patent/ATE481383T1/de not_active IP Right Cessation
- 2007-09-28 TW TW096136490A patent/TW200823227A/zh unknown
- 2007-09-28 ES ES07826577T patent/ES2350460T3/es active Active
- 2007-09-28 DE DE602007009284T patent/DE602007009284D1/de active Active
- 2007-09-28 CL CL200702809A patent/CL2007002809A1/es unknown
- 2007-09-28 CN CNA2007800357375A patent/CN101522618A/zh active Pending
- 2007-09-28 WO PCT/IB2007/053947 patent/WO2008038251A2/en not_active Ceased
- 2007-09-28 JP JP2009529841A patent/JP2010504957A/ja not_active Ceased
- 2007-09-28 KR KR1020097008574A patent/KR20090077051A/ko not_active Ceased
- 2007-09-28 EP EP07826577A patent/EP2079690B1/en not_active Not-in-force
- 2007-09-28 US US12/311,451 patent/US20100016401A1/en not_active Abandoned
- 2007-09-28 CA CA002662612A patent/CA2662612A1/en not_active Abandoned
- 2007-10-01 AR ARP070104342A patent/AR063081A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TW200823227A (en) | 2008-06-01 |
| CN101522618A (zh) | 2009-09-02 |
| ATE481383T1 (de) | 2010-10-15 |
| DE602007009284D1 (de) | 2010-10-28 |
| KR20090077051A (ko) | 2009-07-14 |
| EP2079690A2 (en) | 2009-07-22 |
| ES2350460T3 (es) | 2011-01-24 |
| WO2008038251A3 (en) | 2008-06-26 |
| JP2010504957A (ja) | 2010-02-18 |
| CA2662612A1 (en) | 2008-04-03 |
| EP2079690B1 (en) | 2010-09-15 |
| US20100016401A1 (en) | 2010-01-21 |
| WO2008038251A2 (en) | 2008-04-03 |
| CL2007002809A1 (es) | 2008-04-18 |
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