NO20080750L - (Indol-3-YL)-heterocykelderivater som agonister av cannabinoid CB1 reseptor - Google Patents
(Indol-3-YL)-heterocykelderivater som agonister av cannabinoid CB1 reseptorInfo
- Publication number
- NO20080750L NO20080750L NO20080750A NO20080750A NO20080750L NO 20080750 L NO20080750 L NO 20080750L NO 20080750 A NO20080750 A NO 20080750A NO 20080750 A NO20080750 A NO 20080750A NO 20080750 L NO20080750 L NO 20080750L
- Authority
- NO
- Norway
- Prior art keywords
- cannabinoid
- indol
- agonists
- receptor
- heterocycle derivatives
- Prior art date
Links
- 102000009132 CB1 Cannabinoid Receptor Human genes 0.000 title 1
- 108010073366 CB1 Cannabinoid Receptor Proteins 0.000 title 1
- -1 Indol-3-YL Chemical class 0.000 title 1
- 239000000556 agonist Substances 0.000 title 1
- 229930003827 cannabinoid Natural products 0.000 title 1
- 239000003557 cannabinoid Substances 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 title 1
- 229940054051 antipsychotic indole derivative Drugs 0.000 abstract 2
- 150000002475 indoles Chemical class 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4245—Oxadiazoles
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- C07D417/00—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
- C07D417/14—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 three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Abstract
Oppfinnelsen angår indolderivat som har den generelle formel I Formel I hvor A, X1, X2 ,X3 ,Y, R1 ,R2 ,R3 og R4 er som definert i kravene, eller et farmasøytisk akseptabelt salt derav, farmasøytiske preparater omfattende disse og anvendelse av nevnte indolderivater ved behandling av smerte.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05107725 | 2005-08-23 | ||
| PCT/EP2006/065496 WO2007023143A1 (en) | 2005-08-23 | 2006-08-21 | (indol-3-yl)-heterocycle derivatives as agonists of the cannabinoid cb1 receptor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20080750L true NO20080750L (no) | 2008-05-14 |
Family
ID=35539284
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20080750A NO20080750L (no) | 2005-08-23 | 2008-02-12 | (Indol-3-YL)-heterocykelderivater som agonister av cannabinoid CB1 reseptor |
Country Status (18)
| Country | Link |
|---|---|
| EP (1) | EP1919471B1 (no) |
| JP (1) | JP5283505B2 (no) |
| KR (1) | KR20080038239A (no) |
| CN (1) | CN101272783B (no) |
| AR (1) | AR055384A1 (no) |
| AU (1) | AU2006283884B2 (no) |
| BR (1) | BRPI0615201A2 (no) |
| CA (1) | CA2619038A1 (no) |
| EC (1) | ECSP088270A (no) |
| IL (1) | IL189390A0 (no) |
| MX (1) | MX2008002539A (no) |
| NO (1) | NO20080750L (no) |
| NZ (1) | NZ566007A (no) |
| PE (1) | PE20070236A1 (no) |
| RU (1) | RU2008110961A (no) |
| TW (1) | TW200745096A (no) |
| WO (1) | WO2007023143A1 (no) |
| ZA (1) | ZA200801519B (no) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI330635B (en) | 2004-03-05 | 2010-09-21 | Organon Nv | (indol-3-yl)-heterocycle derivatives |
| US7763732B2 (en) | 2005-08-24 | 2010-07-27 | N.V. Organon | Indole derivatives |
| TW200848417A (en) | 2007-02-22 | 2008-12-16 | Organon Nv | Indole derivatives |
| ES2548764T3 (es) * | 2007-03-30 | 2015-10-20 | Janssen Pharmaceutica N.V. | Agonistas de cannabinoides de bencimidazol |
| EP2388252B1 (en) | 2009-01-16 | 2013-07-24 | Daiso Co., Ltd. | Process for producing 2-hydroxymethylmorpholine salt |
| US9310374B2 (en) | 2012-11-16 | 2016-04-12 | Redwood Bioscience, Inc. | Hydrazinyl-indole compounds and methods for producing a conjugate |
| KR102114323B1 (ko) * | 2013-12-09 | 2020-05-22 | 이니스트에스티 주식회사 | 광학활성 1-(인돌린-5-일)프로판-2-올 유도체의 제조방법 |
| JP6855496B2 (ja) | 2015-11-09 | 2021-04-07 | アール.ピー.シェーラー テクノロジーズ エルエルシー | 抗cd22抗体−メイタンシンコンジュゲートおよびその使用方法 |
| PE20181203A1 (es) * | 2015-12-09 | 2018-07-23 | Hoffmann La Roche | Derivados de fenilo como agonistas de receptor de cannabinoides 2 |
| CN115667212A (zh) * | 2020-05-29 | 2023-01-31 | 富士胶片富山化学株式会社 | 高纯度的n-(5-甲氧基-2-苯氧基苯基)甲磺酰胺及其制造方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AUPR118000A0 (en) * | 2000-11-02 | 2000-11-23 | Amrad Operations Pty. Limited | Therapeutic molecules and methods |
| TW200402417A (en) * | 2002-06-21 | 2004-02-16 | Akzo Nobel Nv | 1-[(Indol-3-yl)carbonyl]piperazine derivatives |
| EP1556373A1 (en) * | 2002-10-18 | 2005-07-27 | Pfizer Products Inc. | Cannabinoid receptor ligands and uses thereof |
| US7247628B2 (en) * | 2002-12-12 | 2007-07-24 | Pfizer, Inc. | Cannabinoid receptor ligands and uses thereof |
| TWI330635B (en) * | 2004-03-05 | 2010-09-21 | Organon Nv | (indol-3-yl)-heterocycle derivatives |
-
2006
- 2006-08-09 TW TW095129209A patent/TW200745096A/zh unknown
- 2006-08-21 JP JP2008527455A patent/JP5283505B2/ja not_active Expired - Fee Related
- 2006-08-21 EP EP06764335.3A patent/EP1919471B1/en active Active
- 2006-08-21 PE PE2006001011A patent/PE20070236A1/es not_active Application Discontinuation
- 2006-08-21 RU RU2008110961/04A patent/RU2008110961A/ru not_active Application Discontinuation
- 2006-08-21 KR KR1020087006920A patent/KR20080038239A/ko not_active Withdrawn
- 2006-08-21 WO PCT/EP2006/065496 patent/WO2007023143A1/en not_active Ceased
- 2006-08-21 CN CN2006800358250A patent/CN101272783B/zh not_active Expired - Fee Related
- 2006-08-21 MX MX2008002539A patent/MX2008002539A/es not_active Application Discontinuation
- 2006-08-21 BR BRPI0615201-5A patent/BRPI0615201A2/pt not_active IP Right Cessation
- 2006-08-21 CA CA002619038A patent/CA2619038A1/en not_active Abandoned
- 2006-08-21 NZ NZ566007A patent/NZ566007A/en not_active IP Right Cessation
- 2006-08-21 AU AU2006283884A patent/AU2006283884B2/en not_active Ceased
- 2006-08-23 AR ARP060103655A patent/AR055384A1/es unknown
-
2008
- 2008-02-07 IL IL189390A patent/IL189390A0/en unknown
- 2008-02-12 NO NO20080750A patent/NO20080750L/no not_active Application Discontinuation
- 2008-02-14 ZA ZA200801519A patent/ZA200801519B/xx unknown
- 2008-03-13 EC EC2008008270A patent/ECSP088270A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP1919471B1 (en) | 2014-01-08 |
| AU2006283884B2 (en) | 2011-06-02 |
| MX2008002539A (es) | 2008-03-14 |
| AU2006283884A1 (en) | 2007-03-01 |
| ZA200801519B (en) | 2008-12-31 |
| BRPI0615201A2 (pt) | 2011-05-10 |
| CN101272783B (zh) | 2011-05-25 |
| AR055384A1 (es) | 2007-08-22 |
| CA2619038A1 (en) | 2007-03-01 |
| NZ566007A (en) | 2009-12-24 |
| JP5283505B2 (ja) | 2013-09-04 |
| IL189390A0 (en) | 2008-06-05 |
| JP2009506010A (ja) | 2009-02-12 |
| PE20070236A1 (es) | 2007-04-16 |
| TW200745096A (en) | 2007-12-16 |
| EP1919471A1 (en) | 2008-05-14 |
| WO2007023143A1 (en) | 2007-03-01 |
| RU2008110961A (ru) | 2009-09-27 |
| KR20080038239A (ko) | 2008-05-02 |
| CN101272783A (zh) | 2008-09-24 |
| ECSP088270A (es) | 2008-04-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC2A | Withdrawal, rejection or dismissal of laid open patent application |