MA31800B1 - Dérivés de tétrahydroquinoléine pour traiter des troubles de stress post-traumatique - Google Patents
Dérivés de tétrahydroquinoléine pour traiter des troubles de stress post-traumatiqueInfo
- Publication number
- MA31800B1 MA31800B1 MA32806A MA32806A MA31800B1 MA 31800 B1 MA31800 B1 MA 31800B1 MA 32806 A MA32806 A MA 32806A MA 32806 A MA32806 A MA 32806A MA 31800 B1 MA31800 B1 MA 31800B1
- Authority
- MA
- Morocco
- Prior art keywords
- ptsd
- treatment
- tetrahydroquinoline derivatives
- derivatives
- group
- Prior art date
Links
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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (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)
- Other In-Based Heterocyclic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
L'invention concerne l'utilisation de dérivés de tétrahydroquinoléine représentés par la formule (i), r1 et r2 représentant chacun indépendamment un groupe alcoxy en c1-c4, r3 représentant un groupe arylalkyle en c1-c4 ou hétéroarylalkyle en c1-c4, et r4 représentant un atome d'hydrogène ou un groupe alkyle en c1-c4, ou de sels pharmaceutiquement acceptables de ces dérivés, pour la préparation d'un médicament destiné à prévenir ou traiter des troubles de stress post-traumatique.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IB2007054130 | 2007-10-10 | ||
| PCT/IB2008/054138 WO2009047723A2 (fr) | 2007-10-10 | 2008-10-09 | Dérivés de tétrahydroquinoléine pour traiter des troubles de stress post-traumatique |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA31800B1 true MA31800B1 (fr) | 2010-10-01 |
Family
ID=40467356
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA32806A MA31800B1 (fr) | 2007-10-10 | 2010-04-30 | Dérivés de tétrahydroquinoléine pour traiter des troubles de stress post-traumatique |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US9532985B2 (fr) |
| EP (1) | EP2207550B1 (fr) |
| JP (1) | JP5883222B2 (fr) |
| KR (1) | KR101733247B1 (fr) |
| CN (1) | CN101820878B (fr) |
| AR (1) | AR068768A1 (fr) |
| AU (1) | AU2008309194B2 (fr) |
| BR (1) | BRPI0818617A2 (fr) |
| CA (1) | CA2699504C (fr) |
| CY (1) | CY1114799T1 (fr) |
| DK (1) | DK2207550T3 (fr) |
| EA (1) | EA017443B1 (fr) |
| ES (1) | ES2444418T3 (fr) |
| HK (1) | HK1145440A1 (fr) |
| HR (1) | HRP20140214T1 (fr) |
| IL (1) | IL204838A (fr) |
| MA (1) | MA31800B1 (fr) |
| MX (1) | MX2010003711A (fr) |
| MY (1) | MY153044A (fr) |
| NZ (1) | NZ585086A (fr) |
| PE (1) | PE20091010A1 (fr) |
| PL (1) | PL2207550T3 (fr) |
| PT (1) | PT2207550E (fr) |
| SI (1) | SI2207550T1 (fr) |
| TW (1) | TWI428129B (fr) |
| UA (1) | UA99150C2 (fr) |
| WO (1) | WO2009047723A2 (fr) |
| ZA (1) | ZA201003251B (fr) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2007337659A1 (en) | 2006-12-22 | 2008-07-03 | Actelion Pharmaceuticals Ltd. | 5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine derivatives |
| US20110105514A1 (en) | 2008-06-25 | 2011-05-05 | Hamed Aissaoui | 5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine compounds |
| EP2402322A1 (fr) | 2010-07-02 | 2012-01-04 | Actelion Pharmaceuticals Ltd. | Dérivé de 1,2,3,4-tétrahydroisoquinoline et son utilisation comme antagoniste du récepteur de l'orexine |
| TW201209037A (en) | 2010-08-24 | 2012-03-01 | Actelion Pharmaceuticals Ltd | Proline sulfonamide derivatives as orexin receptor antagonists |
| PE20131162A1 (es) | 2010-09-22 | 2013-10-19 | Eisai Randd Man Co Ltd | Compuestos de ciclopropano como antagonistas del receptor de orexina |
| US9242970B2 (en) | 2010-11-10 | 2016-01-26 | Actelion Pharmaceuticals Ltd. | Lactam derivatives useful as orexin receptor antagonists |
| WO2012085857A1 (fr) | 2010-12-22 | 2012-06-28 | Actelion Pharmaceuticals Ltd | 3,8-diaza-bicyclo[4.2.0]oct-3-ylamides |
| EP2675801B1 (fr) | 2011-02-18 | 2015-04-08 | Actelion Pharmaceuticals Ltd. | Nouveaux dérivés de pyrazole et d'imidazole utiles à titre d'antagonistes d'orexine |
| WO2012114252A1 (fr) | 2011-02-21 | 2012-08-30 | Actelion Pharmaceuticals Ltd | Nouveaux amides d'indole et de pyrrolopyridine |
| WO2013050938A1 (fr) | 2011-10-04 | 2013-04-11 | Actelion Pharmaceuticals Ltd | Dérivés de 3,7-diazabicyclo[3.3.1]nonane et de 9-oxa-3,7- diazabicyclo[3.3.1]nonane |
| IN2014CN04127A (fr) | 2011-11-08 | 2015-07-10 | Actelion Pharmaceuticals Ltd | |
| KR101689093B1 (ko) | 2012-06-04 | 2016-12-22 | 액테리온 파마슈티칼 리미티드 | 벤즈이미다졸-프롤린 유도체 |
| SG11201502493XA (en) | 2012-10-10 | 2015-04-29 | Actelion Pharmaceuticals Ltd | Orexin receptor antagonists which are [ortho bi (hetero )aryl]-[2-(meta bi (hetero )aryl)-pyrrolidin-1-yl]-methanone derivatives |
| JP2016510810A (ja) | 2013-03-12 | 2016-04-11 | 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 | オレキシン受容体アンタゴニストとしてのアゼチジンアミド誘導体 |
| HUE035731T2 (hu) | 2013-12-03 | 2018-05-28 | Idorsia Pharmaceuticals Ltd | (S)-(2-(6-klór-7-metil-1H-benzo[d]imidazol-2-il)-2-metilpirrolidin-1-il)(5-metoxi-2- (2H-l,2,3-triazol-2-il)fenil)metanon kristályos formája és alkalmazása orexin receptor antagonistaként |
| 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 |
| TR201815342T4 (tr) | 2013-12-04 | 2018-11-21 | Idorsia Pharmaceuticals Ltd | Benzimidazol-prolin türevlerinin kullanımı. |
| ES2843952T3 (es) | 2014-10-23 | 2021-07-21 | Eisai R&D Man Co Ltd | Composiciones para tratar el insomnio |
| WO2019024845A1 (fr) * | 2017-08-01 | 2019-02-07 | 苏州科睿思制药有限公司 | Forme cristalline d'antagoniste du récepteur de l'orexine, procédé de préparation associé et utilisation correspondante |
| WO2020007964A1 (fr) | 2018-07-05 | 2020-01-09 | Idorsia Pharmaceuticals Ltd | Dérivés de 2-(2-azabicyclo [3.1.0] hexan-1-yl)-1h-benzimidazole |
| WO2020007977A1 (fr) | 2018-07-06 | 2020-01-09 | Idorsia Pharmaceuticals Ltd | Dérivés de 7-trifluorométhyl-[1,4]diazépane |
| WO2020099511A1 (fr) | 2018-11-14 | 2020-05-22 | Idorsia Pharmaceuticals Ltd | Dérivés de benzimidazole-2-méthyl-morpholine |
| 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 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4009460B2 (ja) * | 2000-03-14 | 2007-11-14 | アクテリオン ファマシューティカルズ リミテッド | １，２，３，４−テトラヒドロイソキノリン誘導体 |
| CN100432056C (zh) * | 2003-03-26 | 2008-11-12 | 埃科特莱茵药品有限公司 | 四氢异喹啉基乙酰胺衍生物作为阿立新受体拮抗剂的应用 |
| WO2005118548A1 (fr) * | 2004-03-01 | 2005-12-15 | Actelion Pharmaceuticals Ltd | Derives de 1,2,3,4-tétrahydroisoquinoléine substitués |
| US7501395B2 (en) | 2005-04-25 | 2009-03-10 | Eisai R & D Management Co., Ltd. | Method of screening for antianxiety drugs |
| MX2008011647A (es) * | 2006-03-15 | 2008-09-22 | Actelion Pharmaceuticals Ltd | Derivados de tetrahidroisoquinolina para mejorar la funcion de la memoria. |
| EP2402322A1 (fr) | 2010-07-02 | 2012-01-04 | Actelion Pharmaceuticals Ltd. | Dérivé de 1,2,3,4-tétrahydroisoquinoline et son utilisation comme antagoniste du récepteur de l'orexine |
-
2008
- 2008-10-07 PE PE2008001739A patent/PE20091010A1/es not_active Application Discontinuation
- 2008-10-09 NZ NZ585086A patent/NZ585086A/en unknown
- 2008-10-09 EP EP08807937.1A patent/EP2207550B1/fr active Active
- 2008-10-09 DK DK08807937.1T patent/DK2207550T3/da active
- 2008-10-09 AU AU2008309194A patent/AU2008309194B2/en not_active Ceased
- 2008-10-09 US US12/681,802 patent/US9532985B2/en active Active
- 2008-10-09 PL PL08807937T patent/PL2207550T3/pl unknown
- 2008-10-09 BR BRPI0818617-0A patent/BRPI0818617A2/pt not_active Application Discontinuation
- 2008-10-09 EA EA201000557A patent/EA017443B1/ru not_active IP Right Cessation
- 2008-10-09 KR KR1020107010186A patent/KR101733247B1/ko active IP Right Grant
- 2008-10-09 ES ES08807937.1T patent/ES2444418T3/es active Active
- 2008-10-09 TW TW097139093A patent/TWI428129B/zh active
- 2008-10-09 WO PCT/IB2008/054138 patent/WO2009047723A2/fr active Application Filing
- 2008-10-09 CA CA2699504A patent/CA2699504C/fr active Active
- 2008-10-09 UA UAA201005122A patent/UA99150C2/ru unknown
- 2008-10-09 SI SI200831152T patent/SI2207550T1/sl unknown
- 2008-10-09 MX MX2010003711A patent/MX2010003711A/es active IP Right Grant
- 2008-10-09 CN CN2008801113334A patent/CN101820878B/zh active Active
- 2008-10-09 JP JP2010528515A patent/JP5883222B2/ja active Active
- 2008-10-09 AR ARP080104422A patent/AR068768A1/es unknown
- 2008-10-09 MY MYPI2010001561A patent/MY153044A/en unknown
- 2008-10-09 PT PT88079371T patent/PT2207550E/pt unknown
-
2010
- 2010-04-06 IL IL204838A patent/IL204838A/en active IP Right Grant
- 2010-04-30 MA MA32806A patent/MA31800B1/fr unknown
- 2010-05-07 ZA ZA2010/03251A patent/ZA201003251B/en unknown
- 2010-12-17 HK HK10111852.2A patent/HK1145440A1/xx not_active IP Right Cessation
-
2014
- 2014-02-04 CY CY20141100085T patent/CY1114799T1/el unknown
- 2014-03-10 HR HRP20140214AT patent/HRP20140214T1/hr unknown
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