ES2397862T3 - Derivados de 1-aminociclohexano y de 1-ciclohexeno 4-heteroaril-sustituidos que tienen efecto sobre el sistema receptor opioide - Google Patents
Derivados de 1-aminociclohexano y de 1-ciclohexeno 4-heteroaril-sustituidos que tienen efecto sobre el sistema receptor opioide Download PDFInfo
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- ES2397862T3 ES2397862T3 ES07801431T ES07801431T ES2397862T3 ES 2397862 T3 ES2397862 T3 ES 2397862T3 ES 07801431 T ES07801431 T ES 07801431T ES 07801431 T ES07801431 T ES 07801431T ES 2397862 T3 ES2397862 T3 ES 2397862T3
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- heteroaryl
- substituted
- aminocyclohexane
- effect
- polysubstituted
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- 102000003840 Opioid Receptors Human genes 0.000 title 1
- 108090000137 Opioid Receptors Proteins 0.000 title 1
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical class C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 title 1
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 title 1
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
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- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
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- C07D257/12—Six-membered rings having four nitrogen atoms
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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Abstract
Derivados heteroarilo sustituidos de fórmula general I donde A representa N o CR7-10, donde A es N dos veces como máximo; W representa O, S o NR4, con la condición de que, cuando W es O oS, A significa CR7-10; uno de los grupos B o C denota H, alquilo(C1-8), en cada caso saturado oinsaturado, lineal o ramificado, mono o polisustituido o no sustituido,COR12, SO2R12, arilo, cicloalquilo(C3-8) o heteroarilo unido mediante unalquilo(C1-3), en cada caso mono o polisustituido o no sustituido; arilo oheteroarilo, en cada caso mono o polisustituido o no sustituido; cicloalquilo(C3-8), en cada caso mono o polisustituido o no sustituido; y elotro grupo B o C representa **Fórmula**
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006033109 | 2006-07-18 | ||
| DE102006033109A DE102006033109A1 (de) | 2006-07-18 | 2006-07-18 | Substituierte Heteroaryl-Derivate |
| PCT/EP2007/006325 WO2008009415A2 (de) | 2006-07-18 | 2007-07-17 | 4-heteroaryl-substituierte 1-aminocyclohexan-1- und cyclohexen-1-derivate mit wirkung auf das opiod rezeptor system |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2397862T3 true ES2397862T3 (es) | 2013-03-11 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES07801431T Active ES2397862T3 (es) | 2006-07-18 | 2007-07-17 | Derivados de 1-aminociclohexano y de 1-ciclohexeno 4-heteroaril-sustituidos que tienen efecto sobre el sistema receptor opioide |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US8138187B2 (es) |
| EP (1) | EP2044016B1 (es) |
| JP (1) | JP5271903B2 (es) |
| KR (1) | KR101455621B1 (es) |
| CN (1) | CN101516844B (es) |
| AU (1) | AU2007276413B2 (es) |
| BR (1) | BRPI0714041A2 (es) |
| CA (1) | CA2658376C (es) |
| CL (1) | CL2007001918A1 (es) |
| CO (1) | CO6140025A2 (es) |
| DE (1) | DE102006033109A1 (es) |
| ES (1) | ES2397862T3 (es) |
| IL (1) | IL196527A (es) |
| MX (1) | MX2009000608A (es) |
| NO (1) | NO20090295L (es) |
| NZ (1) | NZ573965A (es) |
| PE (1) | PE20080559A1 (es) |
| PL (1) | PL2044016T3 (es) |
| RU (1) | RU2459806C2 (es) |
| WO (1) | WO2008009415A2 (es) |
| ZA (1) | ZA200901129B (es) |
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| DE102007009235A1 (de) * | 2007-02-22 | 2008-09-18 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
| CN102046591B (zh) | 2008-03-27 | 2014-12-03 | 格吕伦塔尔有限公司 | 羟甲基环己胺 |
| EP2280941B1 (de) | 2008-03-27 | 2015-05-06 | Grünenthal GmbH | (hetero-)aryl-cyclohexan-derivate |
| ES2375543T3 (es) | 2008-03-27 | 2012-03-01 | Grünenthal GmbH | Derivados de espiro(5.5)undecano. |
| AU2009228647B2 (en) | 2008-03-27 | 2013-07-04 | Grunenthal Gmbh | Substituted spirocyclic cyclohexane derivatives |
| JP5529843B2 (ja) | 2008-03-27 | 2014-06-25 | グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | 置換シクロヘキシルジアミン |
| ES2464102T3 (es) | 2008-03-27 | 2014-05-30 | Grünenthal GmbH | Derivados de 4-aminociclohexano sustituidos |
| WO2011136285A1 (ja) * | 2010-04-27 | 2011-11-03 | 日本製紙株式会社 | 細胞分化促進剤およびその用途 |
| PL2649044T3 (pl) * | 2010-12-08 | 2018-02-28 | Grünenthal GmbH | Sposób syntezy podstawionych pochodnych aminocykloheksanonu |
| MY161170A (en) * | 2011-03-18 | 2017-04-14 | Corcept Therapeutics Inc | Pyrimidine cyclohexyl glucocorticoid receptor modulators |
| CN106939005A (zh) * | 2011-07-08 | 2017-07-11 | 格吕伦塔尔有限公司 | 晶态的(1r,4r)‑6’‑氟‑N,N‑二甲基‑4‑苯基‑4’,9’‑二氢‑3’H‑螺[环己烷‑1,1’‑吡喃并[3,4,b]吲哚]‑4‑胺 |
| KR20140058543A (ko) | 2011-07-08 | 2014-05-14 | 노파르티스 아게 | 신규 피롤로 피리미딘 유도체 |
| US8614245B2 (en) | 2011-07-08 | 2013-12-24 | Gruenenthal Gmbh | Crystalline (1r,4r)-6′-fluoro-N,N-dimethyl-4-phenyl-4′,9′-dihydro-3′H-spiro[cyclohexane-1,1′-pyrano[3,4,b]indol]-4-amine |
| CN102659662A (zh) * | 2012-03-28 | 2012-09-12 | 华东师范大学 | 3-r-3-羟基-2-氧化吲哚类化合物的合成方法 |
| US10093640B2 (en) | 2012-09-21 | 2018-10-09 | Vanderbilt University | Substituted benzofuran, benzothiophene and indole MCL-1 inhibitors |
| US10005728B2 (en) | 2013-08-28 | 2018-06-26 | Vanderbilt University | Substituted indole Mcl-1 inhibitors |
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| WO2015148854A1 (en) | 2014-03-27 | 2015-10-01 | Vanderbilt University | Substituted indole mcl-1 inhibitors |
| TW201607923A (zh) | 2014-07-15 | 2016-03-01 | 歌林達有限公司 | 被取代之氮螺環(4.5)癸烷衍生物 |
| BR112017000762A2 (pt) | 2014-07-15 | 2017-11-21 | Gruenenthal Gmbh | derivados de azaspiro(4.5)decano substituído. |
| WO2016040764A1 (en) * | 2014-09-12 | 2016-03-17 | Spero Therapeutics, Inc. | Carbonyl linked bicyclic heteroaryl n-benzimidazoles and analogs as antibiotic tolerance inhibitors |
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| BR112018067775B1 (pt) | 2016-03-04 | 2024-02-15 | Vanderbilt University | Compostos inibidores de mcl-1 indol substituídos, composição farmacêutica compreendendo ditos compostos e usos terapêuticos dos mesmos |
| TN2018000355A1 (en) * | 2016-05-20 | 2020-06-15 | Esteve Pharmaceuticals Sa | Tetrahydropyran and thiopyran derivatives having multimodal activity against pain. |
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| CN106220547A (zh) * | 2016-07-11 | 2016-12-14 | 孙剑 | 一种含氟化合物麻醉剂的半衰期控制剂 |
| CN106187850A (zh) * | 2016-07-11 | 2016-12-07 | 孙剑 | 一种可用作麻醉剂的化合物 |
| CN106565580A (zh) * | 2016-07-11 | 2017-04-19 | 孙剑 | 一种麻醉剂用稳定剂 |
| BR112019001270A2 (pt) | 2016-07-30 | 2019-04-30 | Bristol-Myers Squibb Company | compostos indol substituídos com dimetoxifenila como inibidores de tlr7, tlr8 ou tlr9 |
| JP7028861B2 (ja) | 2016-09-09 | 2022-03-02 | ブリストル-マイヤーズ スクイブ カンパニー | ピリジル置換のインドール化合物 |
| EP3630109A4 (en) * | 2017-05-26 | 2021-03-17 | Rutgers, the State University of New Jersey | BACTERIAL EFFLUX PUMP INHIBITORS |
| KR102688509B1 (ko) | 2017-08-04 | 2024-07-24 | 브리스톨-마이어스 스큅 컴퍼니 | [1,2,4]트리아졸로[4,3-a]피리디닐 치환된 인돌 화합물 |
| WO2019028302A1 (en) | 2017-08-04 | 2019-02-07 | Bristol-Myers Squibb Company | SUBSTITUTED INDOLE COMPOUNDS USEFUL AS TLR7 / 8/9 INHIBITORS |
| JP7265554B2 (ja) | 2017-11-14 | 2023-04-26 | ブリストル-マイヤーズ スクイブ カンパニー | 置換インドール化合物 |
| KR102781141B1 (ko) | 2017-12-15 | 2025-03-13 | 브리스톨-마이어스 스큅 컴퍼니 | 치환된 인돌 에테르 화합물 |
| EA202091484A1 (ru) | 2017-12-18 | 2021-03-25 | Бристол-Маерс Сквибб Компани | 4-азаиндольные соединения |
| WO2019126081A1 (en) | 2017-12-19 | 2019-06-27 | Bristol-Myers Squibb Company | Amide substituted indole compounds useful as tlr inhibitors |
| JP7304352B2 (ja) | 2017-12-19 | 2023-07-06 | ブリストル-マイヤーズ スクイブ カンパニー | 6-アザインドール化合物 |
| MX2020005462A (es) | 2017-12-19 | 2020-09-07 | Bristol Myers Squibb Co | Compuestos de indol sustituidos utiles como inhibidores de receptores tipo toll (tlr). |
| EP3728218B1 (en) | 2017-12-20 | 2021-12-01 | Bristol-Myers Squibb Company | Amino indole compounds useful as tlr inhibitors |
| SG11202005733QA (en) | 2017-12-20 | 2020-07-29 | Bristol Myers Squibb Co | Diazaindole compounds |
| KR102730859B1 (ko) | 2017-12-20 | 2024-11-15 | 브리스톨-마이어스 스큅 컴퍼니 | 아릴 및 헤테로아릴 치환된 인돌 화합물 |
| CN112955450A (zh) | 2018-10-24 | 2021-06-11 | 百时美施贵宝公司 | 经取代的吲哚和吲唑化合物 |
| ES2963696T3 (es) | 2018-10-24 | 2024-04-01 | Bristol Myers Squibb Co | Compuestos diméricos de indol sustituidos |
| CN109678860A (zh) * | 2018-12-14 | 2019-04-26 | 温州大学 | 一种手性色胺酮β羟基酸酯类化合物的不对称合成方法 |
| KR102904576B1 (ko) | 2019-05-09 | 2025-12-24 | 브리스톨-마이어스 스큅 컴퍼니 | 치환된 벤즈이미다졸론 화합물 |
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| ES2819309B2 (es) * | 2019-10-14 | 2021-11-17 | Fundacion Para La Investigacion Biomedica Del Hospital Univ De La Princesa | Compuestos agonistas nicotínicos y antioxidantes para el tratamiento de enfermedades neurodegenerativas |
| KR102847070B1 (ko) | 2020-01-17 | 2025-08-14 | 상하이 하이옌 파마슈티컬 테크놀로지 컴퍼니, 리미티드 | 아자비시클릭 치환된 옥사스피로 유도체, 이의 제조 방법 및 의학적 용도 |
| CN118221680A (zh) | 2020-01-17 | 2024-06-21 | 上海海雁医药科技有限公司 | 光学纯的氧杂螺环取代的吡咯并吡唑衍生物、其制法与医药上的用途 |
| CN112194609B (zh) * | 2020-10-22 | 2022-11-04 | 西北农林科技大学 | 3,3-二取代氧化吲哚类化合物及其制备方法与用途 |
| CN114230507B (zh) * | 2021-12-31 | 2024-11-12 | 阜阳欣奕华制药科技有限公司 | 一种5-甲氧基色胺的制备方法 |
| AU2023215456A1 (en) * | 2022-02-01 | 2024-08-01 | Caamtech, Inc. | Psychedelic compounds and their therapeutic uses |
| CN116162644B (zh) * | 2022-07-07 | 2024-04-05 | 昆明理工大学 | 一种苯丙氨酸解氨酶基因pal的新用途 |
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| US5468768A (en) * | 1994-01-06 | 1995-11-21 | Bristol-Myers Squibb Company | Antimigraine derivatives of indolylcycloalkanylamines |
| IT1275433B (it) * | 1995-05-19 | 1997-08-07 | Smithkline Beecham Farma | Derivati di diarildiammine |
| JP2002510676A (ja) * | 1998-04-08 | 2002-04-09 | アメリカン・ホーム・プロダクツ・コーポレイション | うつ病治療用のn−アリールオキシエチルアミン誘導体 |
| DE19963178A1 (de) * | 1999-12-27 | 2001-07-05 | Gruenenthal Gmbh | Substituierte Indol-Mannichbasen |
| DE10123163A1 (de) * | 2001-05-09 | 2003-01-16 | Gruenenthal Gmbh | Substituierte Cyclohexan-1,4-diaminderivate |
| DE10135636A1 (de) * | 2001-07-17 | 2003-02-06 | Gruenenthal Gmbh | Substituierte 4-Aminocyclohexanole |
| DE10135637A1 (de) * | 2001-07-17 | 2003-02-06 | Gruenenthal Gmbh | Substituierte 4-Aminocyclohexanolderivate |
| PE20030320A1 (es) * | 2001-07-17 | 2003-04-03 | Gruenenthal Chemie | Derivados sustituidos de 4-aminociclohexanol |
| DE10252666A1 (de) * | 2002-11-11 | 2004-08-05 | Grünenthal GmbH | N-Piperidyl-cyclohexan-Derivate |
| DE10252667A1 (de) * | 2002-11-11 | 2004-05-27 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
| DE10252874A1 (de) * | 2002-11-12 | 2004-09-16 | Grünenthal GmbH | 4-Alkyl-1-Aryl-Cyclohexylamin-Derivate |
| DE10253054B4 (de) * | 2002-11-14 | 2007-01-18 | Keiper Gmbh & Co.Kg | Beschlag für einen Fahrzeugsitz |
| EP1575586A1 (en) * | 2002-12-17 | 2005-09-21 | Pfizer Japan Inc. | 2-pyridyl and 2-pyrimidyl cycloalkylene amide compounds as nr2b receptor antagonists |
| DE10360793A1 (de) * | 2003-12-23 | 2005-07-28 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
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2006
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2007
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- 2007-07-16 PE PE2007000916A patent/PE20080559A1/es not_active Application Discontinuation
- 2007-07-17 PL PL07801431T patent/PL2044016T3/pl unknown
- 2007-07-17 CN CN2007800344498A patent/CN101516844B/zh not_active Expired - Fee Related
- 2007-07-17 KR KR1020097003316A patent/KR101455621B1/ko not_active Expired - Fee Related
- 2007-07-17 MX MX2009000608A patent/MX2009000608A/es active IP Right Grant
- 2007-07-17 ES ES07801431T patent/ES2397862T3/es active Active
- 2007-07-17 WO PCT/EP2007/006325 patent/WO2008009415A2/de not_active Ceased
- 2007-07-17 NZ NZ573965A patent/NZ573965A/en not_active IP Right Cessation
- 2007-07-17 BR BRPI0714041-0A patent/BRPI0714041A2/pt not_active IP Right Cessation
- 2007-07-17 JP JP2009519860A patent/JP5271903B2/ja not_active Expired - Fee Related
- 2007-07-17 RU RU2009105398/04A patent/RU2459806C2/ru not_active IP Right Cessation
- 2007-07-17 US US12/373,947 patent/US8138187B2/en not_active Expired - Fee Related
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- 2007-07-17 AU AU2007276413A patent/AU2007276413B2/en not_active Ceased
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2009
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- 2009-01-16 CO CO09003208A patent/CO6140025A2/es unknown
- 2009-01-19 NO NO20090295A patent/NO20090295L/no not_active Application Discontinuation
- 2009-02-17 ZA ZA200901129A patent/ZA200901129B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2007276413B2 (en) | 2012-09-06 |
| CO6140025A2 (es) | 2010-03-19 |
| EP2044016A2 (de) | 2009-04-08 |
| JP2009543824A (ja) | 2009-12-10 |
| JP5271903B2 (ja) | 2013-08-21 |
| NO20090295L (no) | 2009-01-20 |
| US20100009986A1 (en) | 2010-01-14 |
| KR20090031631A (ko) | 2009-03-26 |
| CN101516844A (zh) | 2009-08-26 |
| NZ573965A (en) | 2011-12-22 |
| RU2459806C2 (ru) | 2012-08-27 |
| MX2009000608A (es) | 2009-03-06 |
| WO2008009415A2 (de) | 2008-01-24 |
| HK1126479A1 (en) | 2009-09-04 |
| EP2044016B1 (de) | 2012-12-05 |
| ZA200901129B (en) | 2010-07-28 |
| PL2044016T3 (pl) | 2013-03-29 |
| DE102006033109A1 (de) | 2008-01-31 |
| CL2007001918A1 (es) | 2008-03-28 |
| IL196527A0 (en) | 2009-11-18 |
| BRPI0714041A2 (pt) | 2012-12-18 |
| AU2007276413A1 (en) | 2008-01-24 |
| RU2009105398A (ru) | 2010-08-27 |
| CN101516844B (zh) | 2013-12-11 |
| KR101455621B1 (ko) | 2014-10-28 |
| US8138187B2 (en) | 2012-03-20 |
| CA2658376C (en) | 2015-03-24 |
| PE20080559A1 (es) | 2008-05-16 |
| WO2008009415A3 (de) | 2008-04-24 |
| CA2658376A1 (en) | 2008-01-24 |
| IL196527A (en) | 2014-01-30 |
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