AU1816901A - Benzimidazole compounds having nociceptin receptor affinity - Google Patents
Benzimidazole compounds having nociceptin receptor affinityInfo
- Publication number
- AU1816901A AU1816901A AU18169/01A AU1816901A AU1816901A AU 1816901 A AU1816901 A AU 1816901A AU 18169/01 A AU18169/01 A AU 18169/01A AU 1816901 A AU1816901 A AU 1816901A AU 1816901 A AU1816901 A AU 1816901A
- Authority
- AU
- Australia
- Prior art keywords
- receptor affinity
- benzimidazole compounds
- nociceptin receptor
- compounds
- affinity
- 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.)
- Abandoned
Links
- 108010020615 nociceptin receptor Proteins 0.000 title abstract 2
- 102100028646 Nociceptin receptor Human genes 0.000 title 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 title 1
- 208000002193 Pain Diseases 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000000094 Chronic Pain Diseases 0.000 abstract 1
- 208000005298 acute pain Diseases 0.000 abstract 1
- 230000001684 chronic effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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]
- A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
-
- 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)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16939499P | 1999-12-06 | 1999-12-06 | |
| US60169394 | 1999-12-06 | ||
| PCT/US2000/033019 WO2001039775A1 (en) | 1999-12-06 | 2000-12-06 | Benzimidazole compounds having nociceptin receptor affinity |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU1816901A true AU1816901A (en) | 2001-06-12 |
Family
ID=22615490
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU18169/01A Abandoned AU1816901A (en) | 1999-12-06 | 2000-12-06 | Benzimidazole compounds having nociceptin receptor affinity |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US7456198B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1242085B1 (cg-RX-API-DMAC7.html) |
| JP (2) | JP2003524634A (cg-RX-API-DMAC7.html) |
| AT (1) | ATE302770T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU1816901A (cg-RX-API-DMAC7.html) |
| DE (1) | DE60022226D1 (cg-RX-API-DMAC7.html) |
| HK (1) | HK1049284B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2001039775A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU1816901A (en) * | 1999-12-06 | 2001-06-12 | Euro-Celtique S.A. | Benzimidazole compounds having nociceptin receptor affinity |
| IL158484A0 (en) * | 2001-04-18 | 2004-05-12 | Euro Celtique Sa | Nociceptin analogs |
| CA2465328C (en) * | 2001-11-01 | 2011-06-14 | Michael Francis Gross | Piperidines |
| JP4056977B2 (ja) | 2002-03-29 | 2008-03-05 | 田辺三菱製薬株式会社 | 睡眠障害治療薬 |
| JP2005289816A (ja) * | 2002-05-14 | 2005-10-20 | Banyu Pharmaceut Co Ltd | ベンズイミダゾール誘導体 |
| DE10252666A1 (de) * | 2002-11-11 | 2004-08-05 | Grünenthal GmbH | N-Piperidyl-cyclohexan-Derivate |
| US7202259B2 (en) * | 2002-11-18 | 2007-04-10 | Euro-Celtique S.A. | Therapeutic agents useful for treating pain |
| AR045939A1 (es) | 2003-09-25 | 2005-11-16 | Solvay Pharm Bv | Derivados de bencimidazolona y quinazolinona como agonistas de los receptores orl 1 humanos |
| AR045843A1 (es) | 2003-10-03 | 2005-11-16 | Solvay Pharm Bv | Derivados de bencimidazolonas y quinazolinonas sustituidas con hidronopol como agonistas en receptores orl 1 humanos |
| KR100886002B1 (ko) | 2004-01-30 | 2009-03-03 | 유로-셀띠끄 소시에떼 아노님 | 4-테트라졸릴-4-페닐피페리딘 화합물의 제조방법 |
| UA83919C2 (en) * | 2004-04-20 | 2008-08-26 | Санофи Авентис | Polymorphic forms of methyl(+)-(s)-alpha-(2-chlorophenyl)-6,7-dihydrothieno[3,2-c]pyridine-5(4h) acetate hydrobromide, clopidrogel hydrobromide |
| US7300947B2 (en) * | 2005-07-13 | 2007-11-27 | Banyu Pharmaceutical Co., Ltd. | N-dihydroxyalkyl-substituted 2-oxo-imidazole derivatives |
| AR054816A1 (es) * | 2005-07-13 | 2007-07-18 | Banyu Pharma Co Ltd | Derivados de n-dihidroxialquil 2-oxo- imidazol sustituidos |
| WO2007037513A1 (ja) * | 2005-09-30 | 2007-04-05 | Banyu Pharmaceutical Co., Ltd. | アリール置換含窒素複素環化合物 |
| US20080015214A1 (en) * | 2005-10-24 | 2008-01-17 | Bignan Gilles C | 3-piperidin-4-yl-indole orl-1 receptor modulators |
| JP2009525269A (ja) * | 2006-01-30 | 2009-07-09 | ユーロ−セルティーク エス.エイ. | カルシウムチャネルブロッカーとしての環状尿素化合物 |
| GB0605784D0 (en) * | 2006-03-22 | 2006-05-03 | Glaxo Group Ltd | Compounds |
| GB0605786D0 (en) * | 2006-03-22 | 2006-05-03 | Glaxo Group Ltd | Compounds |
| US8775704B2 (en) * | 2006-04-05 | 2014-07-08 | Nvidia Corporation | Method and system for communication between a secondary processor and an auxiliary display subsystem of a notebook |
| DE102006046745A1 (de) * | 2006-09-29 | 2008-04-03 | Grünenthal GmbH | Gemischte ORL1/µ-Agonisten zur Behandlung von Schmerz |
| EP2397477B1 (en) * | 2007-01-16 | 2014-03-05 | Purdue Pharma LP | Heterocyclic-substituted piperidine compounds and the uses thereof |
| BRPI0808025A2 (pt) * | 2007-03-01 | 2014-06-24 | Mitsubishi Tanabe Pharma Corp | Composto de benzimidazol e uso farmacêutico do mesmo |
| RU2451017C2 (ru) * | 2007-03-01 | 2012-05-20 | Мицубиси Танабе Фарма Корпорейшн | Бензимидазольное соединение и его фармацевтическое применение |
| MY150602A (en) | 2007-08-31 | 2014-01-30 | Purdue Pharma Lp | Subtituted-quinoxaline-type piperidine compounds and the uses thereof |
| WO2009124883A1 (en) * | 2008-04-09 | 2009-10-15 | H. Lundbeck A/S | Novel 1,3-dihydro-benzoimidazol-2-ones as m1 agonists |
| KR101333660B1 (ko) | 2008-07-21 | 2013-11-27 | 시오노기세이야쿠가부시키가이샤 | 치환-퀴녹살린-형 가교-피페리딘 화합물 및 그의 용도 |
| US8736617B2 (en) * | 2008-08-04 | 2014-05-27 | Nvidia Corporation | Hybrid graphic display |
| TW201016675A (en) | 2008-09-16 | 2010-05-01 | Mitsubishi Tanabe Pharma Corp | Crystalline benzoimidazole compound and salt thereof |
| US9075559B2 (en) * | 2009-02-27 | 2015-07-07 | Nvidia Corporation | Multiple graphics processing unit system and method |
| US9135675B2 (en) * | 2009-06-15 | 2015-09-15 | Nvidia Corporation | Multiple graphics processing unit display synchronization system and method |
| US8766989B2 (en) * | 2009-07-29 | 2014-07-01 | Nvidia Corporation | Method and system for dynamically adding and removing display modes coordinated across multiple graphics processing units |
| US8780122B2 (en) * | 2009-09-16 | 2014-07-15 | Nvidia Corporation | Techniques for transferring graphics data from system memory to a discrete GPU |
| US9111325B2 (en) * | 2009-12-31 | 2015-08-18 | Nvidia Corporation | Shared buffer techniques for heterogeneous hybrid graphics |
| US9951038B2 (en) | 2012-12-27 | 2018-04-24 | Purdue Pharma L.P. | Quinazolin-4(3H)-one-type piperidine compounds and uses thereof |
| US10118927B2 (en) | 2012-12-27 | 2018-11-06 | Purdue Pharma L.P. | Substituted piperidin-4-amino-type compounds and uses thereof |
| WO2014102594A2 (en) | 2012-12-27 | 2014-07-03 | Purdue Pharma L.P. | Substituted benzimidazole-type piperidine compounds and uses thereof |
| WO2014102588A2 (en) | 2012-12-27 | 2014-07-03 | Purdue Pharma L.P. | Indole and indoline-type piperidine compounds and uses thereof |
| US9818379B2 (en) | 2013-08-08 | 2017-11-14 | Nvidia Corporation | Pixel data transmission over multiple pixel interfaces |
| US20240287019A1 (en) * | 2021-06-07 | 2024-08-29 | Kinki University | T-type calcium channel blocker |
| CN121843930A (zh) * | 2024-01-05 | 2026-04-10 | 宜昌人福药业有限责任公司 | 一种环己基取代哌啶衍生物、包含其的药物组合物及其用途 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE633495A (cg-RX-API-DMAC7.html) * | 1962-06-13 | |||
| US3161645A (en) | 1962-12-18 | 1964-12-15 | Res Lab Dr C Janssen N V | 1-(1-aroylpropyl-4-piperidyl)-2-benzimidazolinones and related compounds |
| US3318900A (en) | 1964-05-06 | 1967-05-09 | Janssen Pharmaceutica Nv | Derivatives of benzimidazolinyl piperidine |
| GR69650B (cg-RX-API-DMAC7.html) * | 1978-07-20 | 1982-07-07 | Science Union & Cie | |
| US4329353A (en) * | 1980-10-22 | 1982-05-11 | Janssen Pharmaceutica, N.V. | 1-(4-Aryl-cyclohexyl)piperidine derivatives, method of use thereof and pharmaceutical compositions thereof |
| JPS58180481A (ja) | 1982-04-15 | 1983-10-21 | Kyowa Hakko Kogyo Co Ltd | 新規なピペリジン誘導体 |
| EP0974583B1 (en) | 1995-09-13 | 2002-05-29 | Kyowa Hakko Kogyo Co., Ltd. | Phenylpiperidine derivatives |
| US6180649B1 (en) * | 1996-04-19 | 2001-01-30 | Nerosearch A/S | 1-(4-piperidyl)-benzimidazoles having neurotrophic activity |
| ES2226129T3 (es) | 1997-05-30 | 2005-03-16 | Banyu Pharmaceutical Co., Ltd. | Derivados de 2-0x0imidazol. |
| SI0921125T1 (en) | 1997-12-05 | 2002-04-30 | F. Hoffmann-La Roche Ag | 1,3,8-Triazaspiro(4,5)decan-4-on derivatives |
| US6166209A (en) | 1997-12-11 | 2000-12-26 | Hoffmann-La Roche Inc. | Piperidine derivatives |
| US6626939B1 (en) | 1997-12-18 | 2003-09-30 | Boston Scientific Scimed, Inc. | Stent-graft with bioabsorbable structural support |
| AU1679099A (en) * | 1998-01-19 | 1999-08-02 | Pfizer Inc. | 4-(2-keto-1-benzimidazolinyl)piperidine compounds as orl1-receptor agonists |
| NZ507760A (en) | 1998-03-26 | 2002-10-25 | Japan Tobacco Inc | Amide derivatives and nociceptin antagonists |
| AU3809999A (en) | 1998-05-18 | 1999-12-06 | Novo Nordisk A/S | Novel 1,3,8-triazaspiro[4.5]decanones with high affinity for opioid receptor subtypes |
| ID29137A (id) * | 1998-07-27 | 2001-08-02 | Schering Corp | Ligan-ligan afinitas tinggi untuk reseptor nosiseptin orl-1 |
| US6262066B1 (en) * | 1998-07-27 | 2001-07-17 | Schering Corporation | High affinity ligands for nociceptin receptor ORL-1 |
| AU1816901A (en) * | 1999-12-06 | 2001-06-12 | Euro-Celtique S.A. | Benzimidazole compounds having nociceptin receptor affinity |
-
2000
- 2000-12-06 AU AU18169/01A patent/AU1816901A/en not_active Abandoned
- 2000-12-06 JP JP2001541507A patent/JP2003524634A/ja active Pending
- 2000-12-06 US US09/730,934 patent/US7456198B2/en not_active Expired - Lifetime
- 2000-12-06 EP EP00980981A patent/EP1242085B1/en not_active Expired - Lifetime
- 2000-12-06 HK HK03101335.9A patent/HK1049284B/en not_active IP Right Cessation
- 2000-12-06 WO PCT/US2000/033019 patent/WO2001039775A1/en not_active Ceased
- 2000-12-06 AT AT00980981T patent/ATE302770T1/de not_active IP Right Cessation
- 2000-12-06 DE DE60022226T patent/DE60022226D1/de not_active Expired - Lifetime
-
2006
- 2006-07-28 US US11/494,826 patent/US7678809B2/en not_active Expired - Fee Related
-
2007
- 2007-06-15 JP JP2007158916A patent/JP2007277257A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| DE60022226D1 (de) | 2005-09-29 |
| EP1242085B1 (en) | 2005-08-24 |
| JP2007277257A (ja) | 2007-10-25 |
| ATE302770T1 (de) | 2005-09-15 |
| WO2001039775A1 (en) | 2001-06-07 |
| US7456198B2 (en) | 2008-11-25 |
| EP1242085A1 (en) | 2002-09-25 |
| US20060264638A1 (en) | 2006-11-23 |
| EP1242085A4 (en) | 2003-02-12 |
| HK1049284A1 (en) | 2003-05-09 |
| US20020128288A1 (en) | 2002-09-12 |
| HK1049284B (en) | 2006-02-24 |
| US7678809B2 (en) | 2010-03-16 |
| JP2003524634A (ja) | 2003-08-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK6 | Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase |