JP5121716B2 - ピリジン誘導体および精神異常の処置におけるそれらの使用 - Google Patents
ピリジン誘導体および精神異常の処置におけるそれらの使用 Download PDFInfo
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- JP5121716B2 JP5121716B2 JP2008529564A JP2008529564A JP5121716B2 JP 5121716 B2 JP5121716 B2 JP 5121716B2 JP 2008529564 A JP2008529564 A JP 2008529564A JP 2008529564 A JP2008529564 A JP 2008529564A JP 5121716 B2 JP5121716 B2 JP 5121716B2
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- 0 CC1(C)N(C)*1 Chemical compound CC1(C)N(C)*1 0.000 description 11
- OTHDLFYZJORVOS-IKOFQBKESA-N CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N(C1)[C@@H](CO)CN(CC2)C1CS2(=O)=O)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N(C1)[C@@H](CO)CN(CC2)C1CS2(=O)=O)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 OTHDLFYZJORVOS-IKOFQBKESA-N 0.000 description 1
- ASMGFAOELMIEIG-UHFFFAOYSA-N CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N(CC1)CC(C2)N1CCN2S(C)(=O)=O)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N(CC1)CC(C2)N1CCN2S(C)(=O)=O)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 ASMGFAOELMIEIG-UHFFFAOYSA-N 0.000 description 1
- PDGMNJVKRYIVDR-UHFFFAOYSA-N CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N(CC1)CC(C2)N1CCS2(=O)=O)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N(CC1)CC(C2)N1CCS2(=O)=O)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 PDGMNJVKRYIVDR-UHFFFAOYSA-N 0.000 description 1
- KUSZSPBKPWFIEH-UHFFFAOYSA-N CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N1CC(CN(C)CC2)N2CC1)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N1CC(CN(C)CC2)N2CC1)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 KUSZSPBKPWFIEH-UHFFFAOYSA-N 0.000 description 1
- UXCBTZDZHHGJKO-SKCDSABHSA-N CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N1CC(CO)N(CCC2)[C@@H]2C1)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N1CC(CO)N(CCC2)[C@@H]2C1)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 UXCBTZDZHHGJKO-SKCDSABHSA-N 0.000 description 1
- JTJGSFNAJYBRDX-SSYAZFEXSA-N CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N1[C@@H](CO)CN(CCN(C2)C(C)=O)C2C1)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N1[C@@H](CO)CN(CCN(C2)C(C)=O)C2C1)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 JTJGSFNAJYBRDX-SSYAZFEXSA-N 0.000 description 1
- YFMZALAUALIBHT-UHFFFAOYSA-N CC(C)(C(N(C)c(c(-c1ccccc1C)c1)cnc1N(CC1)CC2N1CCOC2)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound CC(C)(C(N(C)c(c(-c1ccccc1C)c1)cnc1N(CC1)CC2N1CCOC2)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 YFMZALAUALIBHT-UHFFFAOYSA-N 0.000 description 1
- PXRKWLBROJKTLG-YHMJZVADSA-N CC(C)(C)OC(N(CCOC1)C1C(N[C@H](CO)C(OC)=O)=O)=O Chemical compound CC(C)(C)OC(N(CCOC1)C1C(N[C@H](CO)C(OC)=O)=O)=O PXRKWLBROJKTLG-YHMJZVADSA-N 0.000 description 1
- KVXXEKIGMOEPSA-UHFFFAOYSA-N CC(C)(C)OC(N(CCOC1)C1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CCOC1)C1C(O)=O)=O KVXXEKIGMOEPSA-UHFFFAOYSA-N 0.000 description 1
- FLJOPEJWNWDBDV-IAGOWNOFSA-N CC(C)(C)OC(N(CCOC1)[C@H]1C(N(Cc1ccccc1)[C@H](CO)C(OC)=O)=O)=O Chemical compound CC(C)(C)OC(N(CCOC1)[C@H]1C(N(Cc1ccccc1)[C@H](CO)C(OC)=O)=O)=O FLJOPEJWNWDBDV-IAGOWNOFSA-N 0.000 description 1
- UTLQTFKREASFAN-PVSHWOEXSA-N CCC(COCC1)(C(N[C@@H]2CO)=O)N1C2=O Chemical compound CCC(COCC1)(C(N[C@@H]2CO)=O)N1C2=O UTLQTFKREASFAN-PVSHWOEXSA-N 0.000 description 1
- IFNMXZXVWHQYLE-VUWPPUDQSA-N CCCC1(COCC2)N2C[C@@H](CO)NC1 Chemical compound CCCC1(COCC2)N2C[C@@H](CO)NC1 IFNMXZXVWHQYLE-VUWPPUDQSA-N 0.000 description 1
- NSCHICSLDIFHER-ULUSZKPHSA-N COS(CC1)(CC(C(N[C@@H]2CO)=O)N1C2=O)=O Chemical compound COS(CC1)(CC(C(N[C@@H]2CO)=O)N1C2=O)=O NSCHICSLDIFHER-ULUSZKPHSA-N 0.000 description 1
- JGXKGDZTGHHJMH-XJQHNOHDSA-N C[C@H](CN(CCN(C1)C(C)=O)C1C1)N1c(cc1-c(cc2)c(C)cc2F)ncc1N(C)C(C(C)(C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1)=O Chemical compound C[C@H](CN(CCN(C1)C(C)=O)C1C1)N1c(cc1-c(cc2)c(C)cc2F)ncc1N(C)C(C(C)(C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1)=O JGXKGDZTGHHJMH-XJQHNOHDSA-N 0.000 description 1
- UOXNNWQPOPHYLC-LWOQYNTDSA-N C[C@H]1NC(CN)CC1 Chemical compound C[C@H]1NC(CN)CC1 UOXNNWQPOPHYLC-LWOQYNTDSA-N 0.000 description 1
- WCRSYQVCIQHCHN-GVHYBUMESA-N C[C@H]1NCC(COCC2)N2C1 Chemical compound C[C@H]1NCC(COCC2)N2C1 WCRSYQVCIQHCHN-GVHYBUMESA-N 0.000 description 1
- NAGUWAAPRMPAPU-UHFFFAOYSA-N O=C(C(C1)(F)F)N(CC2)C1CN2P Chemical compound O=C(C(C1)(F)F)N(CC2)C1CN2P NAGUWAAPRMPAPU-UHFFFAOYSA-N 0.000 description 1
- QPLVLFGFWZWRGG-UHFFFAOYSA-N O=C(C(C1)(F)F)N2C1CNCC2 Chemical compound O=C(C(C1)(F)F)N2C1CNCC2 QPLVLFGFWZWRGG-UHFFFAOYSA-N 0.000 description 1
- HAFMRRQBQBMBMR-UHFFFAOYSA-N O=C(CC1)N(CC2)C1CN2P Chemical compound O=C(CC1)N(CC2)C1CN2P HAFMRRQBQBMBMR-UHFFFAOYSA-N 0.000 description 1
- VHNVKVILFAFJMN-UHFFFAOYSA-N OCC1(CCC2)N2CCNC1 Chemical compound OCC1(CCC2)N2CCNC1 VHNVKVILFAFJMN-UHFFFAOYSA-N 0.000 description 1
- YXMWPMAMMZJVEN-LWOQYNTDSA-N OC[C@H](C(N1C2CSCC1)=O)NC2=O Chemical compound OC[C@H](C(N1C2CSCC1)=O)NC2=O YXMWPMAMMZJVEN-LWOQYNTDSA-N 0.000 description 1
- YMWOLNFXRAZLKA-HUUCEWRRSA-N O[C@]1(COCC2)N2C[C@@H](CF)N(Cc2ccccc2)C1 Chemical compound O[C@]1(COCC2)N2C[C@@H](CF)N(Cc2ccccc2)C1 YMWOLNFXRAZLKA-HUUCEWRRSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
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- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5383—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
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- A61P25/36—Opioid-abuse
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Anesthesiology (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Child & Adolescent Psychology (AREA)
- Nutrition Science (AREA)
- Gynecology & Obstetrics (AREA)
- Rheumatology (AREA)
- Reproductive Health (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0518472.6 | 2005-09-09 | ||
| GB0518472A GB0518472D0 (en) | 2005-09-09 | 2005-09-09 | Novel compounds |
| GB0611153A GB0611153D0 (en) | 2006-06-06 | 2006-06-06 | Novel compounds |
| GB0611153.8 | 2006-06-06 | ||
| PCT/EP2006/008845 WO2007028654A1 (en) | 2005-09-09 | 2006-09-07 | Pyridine derivatives and their use in the treatment of psychotic disorders |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009507801A JP2009507801A (ja) | 2009-02-26 |
| JP2009507801A5 JP2009507801A5 (https=) | 2012-10-25 |
| JP5121716B2 true JP5121716B2 (ja) | 2013-01-16 |
Family
ID=37546936
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008529564A Active JP5121716B2 (ja) | 2005-09-09 | 2006-09-07 | ピリジン誘導体および精神異常の処置におけるそれらの使用 |
Country Status (28)
| Country | Link |
|---|---|
| US (3) | US7683056B2 (https=) |
| EP (2) | EP1928886B1 (https=) |
| JP (1) | JP5121716B2 (https=) |
| KR (1) | KR101292348B1 (https=) |
| CN (1) | CN101305011B (https=) |
| AR (1) | AR058805A1 (https=) |
| AT (1) | ATE505472T1 (https=) |
| AU (1) | AU2006289281B2 (https=) |
| BR (1) | BRPI0615787B8 (https=) |
| CA (1) | CA2621564C (https=) |
| CR (1) | CR9847A (https=) |
| CY (1) | CY1111907T1 (https=) |
| DE (1) | DE602006021323D1 (https=) |
| DK (1) | DK1928886T3 (https=) |
| EA (1) | EA013909B1 (https=) |
| HR (1) | HRP20110457T1 (https=) |
| IL (1) | IL189578A (https=) |
| JO (1) | JO2722B1 (https=) |
| MA (1) | MA29780B1 (https=) |
| MY (1) | MY145713A (https=) |
| NO (1) | NO340921B1 (https=) |
| NZ (1) | NZ565983A (https=) |
| PE (1) | PE20070614A1 (https=) |
| PL (1) | PL1928886T3 (https=) |
| PT (1) | PT1928886E (https=) |
| SI (1) | SI1928886T1 (https=) |
| TW (1) | TWI378101B (https=) |
| WO (1) | WO2007028654A1 (https=) |
Families Citing this family (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007039123A2 (en) * | 2005-09-22 | 2007-04-12 | Smithkline Beecham Corporation | Combination therapy comprising an nk-3 antagonist and an antipsychotic agent |
| ATE472529T1 (de) * | 2005-10-10 | 2010-07-15 | Glaxo Group Ltd | Prolinamidderivate als natriumkanalmodulatoren |
| TW200730494A (en) * | 2005-10-10 | 2007-08-16 | Glaxo Group Ltd | Novel compounds |
| CN102775396B (zh) | 2005-11-08 | 2014-10-08 | 沃泰克斯药物股份有限公司 | Atp-结合弹夹转运蛋白的杂环调控剂 |
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