HUP0402510A2 - Nociceptin analógok és ezeket tartalmazó gyógyszerkészítmények - Google Patents
Nociceptin analógok és ezeket tartalmazó gyógyszerkészítményekInfo
- Publication number
- HUP0402510A2 HUP0402510A2 HU0402510A HUP0402510A HUP0402510A2 HU P0402510 A2 HUP0402510 A2 HU P0402510A2 HU 0402510 A HU0402510 A HU 0402510A HU P0402510 A HUP0402510 A HU P0402510A HU P0402510 A2 HUP0402510 A2 HU P0402510A2
- Authority
- HU
- Hungary
- Prior art keywords
- alkyl
- carbon atom
- group
- cycloalkyl
- membered
- Prior art date
Links
- PULGYDLMFSFVBL-SMFNREODSA-N nociceptin Chemical class C([C@@H](C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O)[C@@H](C)O)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 PULGYDLMFSFVBL-SMFNREODSA-N 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 229910052799 carbon Inorganic materials 0.000 abstract 20
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000001072 heteroaryl group Chemical group 0.000 abstract 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 4
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 abstract 4
- 150000001721 carbon Chemical group 0.000 abstract 4
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 abstract 2
- 125000004442 acylamino group Chemical group 0.000 abstract 2
- -1 amino- Chemical class 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 125000003368 amide group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000004149 thio group Chemical group *S* 0.000 abstract 1
Classifications
-
- 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
- C07D417/02—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
- C07D417/04—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 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
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- 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
- 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
Abstract
A találmány az (I) általános képletű vegyületekre és azokgyógyászatilag elfogadható sóira és szolvátjaira vonatkozik, ahol aképletben W jelentése hidrogénatom, 1-10 szénatomos alkil-, 3-12szénatomos cikloalkil-, (3-12 szénatomos cikloalkil)-(1-4 szénatomosalkil)-, 1-10 szénatomos alkoxi-, 3-12 szénatomos cikloalkoxi-, 1-3halogénatommal szubsztituált 1-10 szénatomos alkil-, 1-3halogénatommal szubsztituált 3-12 szénatomos cikloalkil-, 1-3halogénatommal szubsztituált (3-12 szénatomos cikloalkil)-(1-4szénatomos alkil)-, 1-3 halogénatommal szubsztituált 1-10 szénatomosalkoxi-, 1-3 halogénatommal szubsztituált 3-12 szénatomoscikloalkoxicsoport, -COOV1, -C1-4COOV1, -CH2OH, -SO2N(V1)2, hidroxi-(1-10 szénatomos alkil)-, hidroxi-(3-10 szénatomos cikloalkil)-,ciano(1-10 szénatomos alkil)-, ciano(3-10 szénatomoscikloalkil)csoport, -CON(V1)2, NH2SO2-(1-4 szénatomos alkil)-, NH2SO-(1-4 szénatomos alkil)-, szulfonilamino(1-10 szénatomos alkil)-,diaminoalkil-, -szulfonil(1-4 szénatomos alkil)csoport, hattagúheterociklusos gyűrű, hattagú heteroaromás gyűrű, hattagúheterociklusos gyűrű(1-4 szénatomos alkil)-, hattagú heteroaromásgyűrű(1-4 szénatomos alkil)-csoport, hattagú aromás gyűrű, hattagúaromás gyűrű(1-4 szénatomos alkilcsoport), öttagú heterociklusosgyűrű, amely adott esetben oxo- vagy tiocsoporttal szubsztituált,öttagú heteroaromás gyűrű, öttagú heterociklusos gyűrű(1-4 szénatomosalkil)csoport, amely adott esetben egy oxo- vagy tiocsoporttalszubsztituált, öttagú heteroaromás gyűrű(1-4 szénatomos alkil)csoport,-C1-5(=O)W1, -C1-5(=NH)W1, -C1-5NHC(=O)W1, -C1-5NHS(=O)2W1, -C1-5NHS(=O)W1, ahol W1 jelentése hidrogénatom, 1-10 szénatomos alkil-, 3-12 szénatomos cikloalkil-, 1-10 szénatomos alkoxi-, 3-12 szénatomoscikloalkoxicsoport, -CH2OH, amino-, (1-4 szénatomos alkil)amino-,di(1-4 szénatomos alkil)amino-csoport, vagy egy öttagú heteroaromásgyűrű, amely adott esetben 1-3 rövid szénláncú alkilcsoporttalszubsztituált; ahol mindegyik V1 csoport jelentése egymástólfüggetlenül hidrogénatom, 1-6 szénatomos alkil-, 3-6 szénatomoscikloalkil-, benzil- vagy fenilcsoport; Q jelentése 5-8 tagúcikloalkilcsoport, 5-8 tagú heterociklusos csoport vagy hattagú aromásvagy heteroaromás csoport; mindegyik n értéke egymástól függetlenül 0,1, 2 vagy 3; A, B és C jelentése egymástól függetlenül hidrogénatom,1-10 szénatomos alkil-, 3-12 szénatomos cikloalkil-, 1-10 szénatomosalkoxi-, 3-12 szénatomos cikloalkoxicsoport, -CH2OH, -NHSO2, hidroxi-(1-10 szénatomos alkil)-, aminokarbonil-, (1-4 szénatomosalkil)aminokarbonil-, di(1-4 szénatomos alkil)aminokarbonil-,acilamino-, (acilamino)alkil-, amid-, szulfonilamino(1-10 szénatomosalkil)-, vagy A-B együtt egy 2-6 szénatomos hidat, vagy B-C együtt egy3-7 szénatomos hidat, vagy A-C együtt egy 1-5 széna
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28467601P | 2001-04-18 | 2001-04-18 | |
| US28467401P | 2001-04-18 | 2001-04-18 | |
| PCT/US2002/012356 WO2002085291A2 (en) | 2001-04-18 | 2002-04-18 | Nociceptin analogs |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| HUP0402510A2 true HUP0402510A2 (hu) | 2005-04-28 |
| HUP0402510A3 HUP0402510A3 (en) | 2012-08-28 |
Family
ID=26962736
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU0402510A HUP0402510A3 (en) | 2001-04-18 | 2002-04-18 | Nociceptin analogs and pharmaceutical compositions containing them |
Country Status (14)
| Country | Link |
|---|---|
| US (3) | US6861421B2 (hu) |
| EP (2) | EP1379252A4 (hu) |
| JP (2) | JP4380992B2 (hu) |
| KR (3) | KR100855204B1 (hu) |
| CN (1) | CN100441182C (hu) |
| AU (2) | AU2002303406B2 (hu) |
| BR (1) | BR0209128A (hu) |
| CA (1) | CA2444108C (hu) |
| HK (1) | HK1070573A1 (hu) |
| HU (1) | HUP0402510A3 (hu) |
| IL (2) | IL158486A0 (hu) |
| MX (1) | MXPA03009602A (hu) |
| RU (1) | RU2268883C2 (hu) |
| WO (1) | WO2002085291A2 (hu) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| OA12790A (en) * | 2002-03-13 | 2006-07-10 | Janssen Pharmaceutica Nv | New inhibitors of histone deacetylase. |
| DK1491212T3 (da) | 2002-03-29 | 2012-10-29 | Mitsubishi Tanabe Pharma Corp | Middel til behandling af søvnforstyrrelser |
| WO2008073958A2 (en) | 2006-12-12 | 2008-06-19 | Wyeth | Substituted benzothiadiazinedioxide derivatives and methods of their use |
| CL2007003590A1 (es) * | 2006-12-12 | 2008-02-29 | Wyeth Corp | Compuestos derivados de aril sulfamida; procedimiento de preparacion; composicion farmaceutica que comprende a dichos compuestos; y su uso en prevencion y tratamiento de sintomas vasomotrices, disfuncion sexual, transtornos gastrointestinales, transt |
| CN101595100B (zh) * | 2007-01-16 | 2014-06-11 | 普渡制药公司 | 作为orl-1配体的杂环取代的哌啶 |
| EP3564240B1 (en) * | 2007-08-31 | 2022-04-06 | Purdue Pharma L.P. | Piperidine intermediates |
| AU2009275218C1 (en) | 2008-07-21 | 2015-02-05 | Purdue Pharma L.P. | Substituted-Quinoxaline-Type Bridged-Piperidine Compounds and the uses thereof |
| AU2011346749A1 (en) | 2010-12-22 | 2013-05-02 | Purdue Pharma L.P. | Phosphorus-substituted quinoxaline-type piperidine compounds and uses thereof |
| WO2014102589A1 (en) | 2012-12-27 | 2014-07-03 | Purdue Pharma L.P. | Quinazolin-4(3h)-one-type piperidine compounds and uses thereof |
| US9090618B2 (en) | 2012-12-27 | 2015-07-28 | Purdue Pharma L.P. | Substituted benzimidazole-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 |
| WO2014102588A2 (en) | 2012-12-27 | 2014-07-03 | Purdue Pharma L.P. | Indole and indoline-type piperidine compounds and uses thereof |
| US9884844B2 (en) | 2012-12-31 | 2018-02-06 | Sunovion Pharmaceuticals, Inc. | Heterocyclic compounds and methods of use thereof |
| JP6854823B2 (ja) | 2016-01-13 | 2021-04-07 | 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 | ３−（カルボキシメチル）−８−アミノ−２−オキソ−１，３−ジアザ−スピロ−［４．５］−デカン誘導体 |
| PL3402781T3 (pl) | 2016-01-13 | 2020-09-21 | Grünenthal GmbH | Pochodne 3-((hetero-)arylo)-8-amino-2-okso-1,3-diazaspiro-[4.5]-dekanu |
| AU2017207467B2 (en) | 2016-01-13 | 2020-07-16 | Grünenthal GmbH | 3-(carboxyethyl)-8-amino-2-oxo-1,3-diaza-spiro-[4.5]-decane derivatives |
| TWI654181B (zh) | 2016-01-13 | 2019-03-21 | 歌林達有限公司 | ８－胺基－２－側氧基－１，３－二氮－螺－［４．５］－癸烷衍生物 |
| ES2797904T3 (es) | 2016-01-13 | 2020-12-04 | Gruenenthal Gmbh | Derivados de 3-((hetero)aril)alquil-8-amino-2-oxo-1,3-diazaespiro-[4.5]-decano |
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| US3318900A (en) | 1964-05-06 | 1967-05-09 | Janssen Pharmaceutica Nv | Derivatives of benzimidazolinyl piperidine |
| US3325499A (en) | 1964-11-02 | 1967-06-13 | Mcneilab Inc | 1-(1-hydrocarbyl-4-piperdyl)-2-indolinone |
| DE2609645A1 (de) | 1976-03-09 | 1977-09-15 | Boehringer Sohn Ingelheim | Aminoalkylheterocyclen |
| EP0029707B1 (en) * | 1979-11-21 | 1984-02-01 | Kyowa Hakko Kogyo Co., Ltd | Novel piperidine derivatives, method for the preparation thereof and pharmaceutical compositions containing them |
| US4344945A (en) * | 1980-03-10 | 1982-08-17 | Kyowa Hakko Kogyo Co., Ltd. | Piperidine derivatives |
| 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 |
| US4410528A (en) | 1980-05-16 | 1983-10-18 | Kyowa Hakko Kogyo Co., Ltd. | Hypotensive piperidine derivatives |
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| US6262066B1 (en) | 1998-07-27 | 2001-07-17 | Schering Corporation | High affinity ligands for nociceptin receptor ORL-1 |
| MA26659A1 (fr) | 1998-08-06 | 2004-12-20 | Pfizer | Dérivés de benzimidazole nouveaux, compositions pharmaceutiques les contenant et procédé pour leur préparation. |
| JP2001044213A (ja) * | 1999-07-30 | 2001-02-16 | Hitachi Cable Ltd | ヘテロバイポーラトランジスタ用エピタキシャルウエハ |
| SE9904652D0 (sv) | 1999-12-17 | 1999-12-17 | Astra Pharma Prod | Novel Compounds |
| ES2248281T3 (es) | 2000-02-18 | 2006-03-16 | Meiji Seika Kaisha, Ltd. | Derivados de fenoxialquilamina utiles como agonistas del receptor opioide delta. |
| JP5049447B2 (ja) * | 2000-08-14 | 2012-10-17 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | 置換ピラゾール |
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| JP2007009500A (ja) * | 2005-06-30 | 2007-01-18 | Nissei Ltd | パズル循環式駐車設備の運転方法 |
-
2002
- 2002-04-18 MX MXPA03009602A patent/MXPA03009602A/es active IP Right Grant
- 2002-04-18 EP EP02731427A patent/EP1379252A4/en not_active Withdrawn
- 2002-04-18 HU HU0402510A patent/HUP0402510A3/hu unknown
- 2002-04-18 KR KR1020067024260A patent/KR100855204B1/ko not_active IP Right Cessation
- 2002-04-18 RU RU2003133454/04A patent/RU2268883C2/ru not_active IP Right Cessation
- 2002-04-18 KR KR1020057022594A patent/KR100722207B1/ko not_active IP Right Cessation
- 2002-04-18 AU AU2002303406A patent/AU2002303406B2/en not_active Ceased
- 2002-04-18 CA CA2444108A patent/CA2444108C/en not_active Expired - Fee Related
- 2002-04-18 US US10/126,507 patent/US6861421B2/en not_active Expired - Lifetime
- 2002-04-18 BR BR0209128-3A patent/BR0209128A/pt not_active Application Discontinuation
- 2002-04-18 JP JP2002582867A patent/JP4380992B2/ja not_active Expired - Fee Related
- 2002-04-18 CN CNB028121686A patent/CN100441182C/zh not_active Expired - Fee Related
- 2002-04-18 EP EP08015057A patent/EP1997818A3/en not_active Withdrawn
- 2002-04-18 WO PCT/US2002/012356 patent/WO2002085291A2/en active Application Filing
- 2002-04-18 IL IL15848602A patent/IL158486A0/xx unknown
- 2002-04-18 KR KR1020037013695A patent/KR100729242B1/ko not_active IP Right Cessation
-
2003
- 2003-10-19 IL IL158486A patent/IL158486A/en not_active IP Right Cessation
-
2005
- 2005-03-01 US US11/069,728 patent/US7563809B2/en not_active Expired - Fee Related
- 2005-04-15 HK HK05103227.4A patent/HK1070573A1/xx not_active IP Right Cessation
-
2006
- 2006-06-30 AU AU2006202794A patent/AU2006202794A1/en not_active Abandoned
-
2009
- 2009-06-16 US US12/485,612 patent/US20090253727A1/en not_active Abandoned
- 2009-07-24 JP JP2009173441A patent/JP2009280603A/ja active Pending
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