JP5921576B2 - ピリドン誘導体を含む医薬組成物 - Google Patents
ピリドン誘導体を含む医薬組成物 Download PDFInfo
- Publication number
- JP5921576B2 JP5921576B2 JP2013551904A JP2013551904A JP5921576B2 JP 5921576 B2 JP5921576 B2 JP 5921576B2 JP 2013551904 A JP2013551904 A JP 2013551904A JP 2013551904 A JP2013551904 A JP 2013551904A JP 5921576 B2 JP5921576 B2 JP 5921576B2
- Authority
- JP
- Japan
- Prior art keywords
- oxo
- octane
- azabicyclo
- pyridinecarboxamide
- phenyl
- 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.)
- Expired - Fee Related
Links
- 0 *N(C=C(C=C1)C(BC2C(CC3)CCN3C2)=O)C1=O Chemical compound *N(C=C(C=C1)C(BC2C(CC3)CCN3C2)=O)C1=O 0.000 description 2
- ZBZCELKOORGVAP-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1N(C=CC=C1C(NC2C(CC3)CCN3C2)=O)C1=O Chemical compound CC(C)(C)c(cc1)ccc1N(C=CC=C1C(NC2C(CC3)CCN3C2)=O)C1=O ZBZCELKOORGVAP-UHFFFAOYSA-N 0.000 description 1
- NNSOSLKULOMVRL-UHFFFAOYSA-N CC(C)SC(CC(C=C1)Cl)=C1N(C=C(C=C1)C(NC2C(CC3)CCN3C2)=O)C1=O Chemical compound CC(C)SC(CC(C=C1)Cl)=C1N(C=C(C=C1)C(NC2C(CC3)CCN3C2)=O)C1=O NNSOSLKULOMVRL-UHFFFAOYSA-N 0.000 description 1
- KAPVOTHIIOYSRN-UHFFFAOYSA-N CC(C)c(cc1)ccc1N(C(C=C1)O)C=C1C(NC1C(CC2)CCN2C1)=O Chemical compound CC(C)c(cc1)ccc1N(C(C=C1)O)C=C1C(NC1C(CC2)CCN2C1)=O KAPVOTHIIOYSRN-UHFFFAOYSA-N 0.000 description 1
- WLYRENPORUCODT-UHFFFAOYSA-N CN(C)c(cc1)ccc1N(C=C(C=C1)C(NC2C(CC3)CCN3C2)=O)C1=O Chemical compound CN(C)c(cc1)ccc1N(C=C(C=C1)C(NC2C(CC3)CCN3C2)=O)C1=O WLYRENPORUCODT-UHFFFAOYSA-N 0.000 description 1
- JVILKGXFLOUTEE-UHFFFAOYSA-N CN(C1C(CC2)CCN2C1)C(C(C=C1)=CN(c2cc(OC)cc(OC)c2)C1=O)=O Chemical compound CN(C1C(CC2)CCN2C1)C(C(C=C1)=CN(c2cc(OC)cc(OC)c2)C1=O)=O JVILKGXFLOUTEE-UHFFFAOYSA-N 0.000 description 1
- DDUVDNHSVDLAJU-UHFFFAOYSA-N COc(cc1)cc(OC)c1N(C=C(C=C1)C(NC2C(CC3)CCN3C2)=O)C1=O Chemical compound COc(cc1)cc(OC)c1N(C=C(C=C1)C(NC2C(CC3)CCN3C2)=O)C1=O DDUVDNHSVDLAJU-UHFFFAOYSA-N 0.000 description 1
- IEKXKNVHFFMSKD-UHFFFAOYSA-N COc(cc1)cc(SC)c1N(C=C(C=C1)C(NC2C(CC3)CCN3C2)=O)C1=O Chemical compound COc(cc1)cc(SC)c1N(C=C(C=C1)C(NC2C(CC3)CCN3C2)=O)C1=O IEKXKNVHFFMSKD-UHFFFAOYSA-N 0.000 description 1
- YHVILVMWVRHWDD-FXFXYLOPSA-N CSc(cc(cc1)Cl)c1N(/C=C(\C=C=C)/C(N[C@H]1C(CC2)CCN2C1)=O)C=O Chemical compound CSc(cc(cc1)Cl)c1N(/C=C(\C=C=C)/C(N[C@H]1C(CC2)CCN2C1)=O)C=O YHVILVMWVRHWDD-FXFXYLOPSA-N 0.000 description 1
- LZKFXJQNYZJALF-UHFFFAOYSA-N O=C(C(C=C1)=CN(c(cc2)ccc2Br)C1=O)NC1C(CC2)CCN2C1 Chemical compound O=C(C(C=C1)=CN(c(cc2)ccc2Br)C1=O)NC1C(CC2)CCN2C1 LZKFXJQNYZJALF-UHFFFAOYSA-N 0.000 description 1
- WSAWESCAPBKHKD-UHFFFAOYSA-N O=C(C(C=C1)=CN(c(cc2)ccc2Cl)C1=O)NC1C(CC2)CCN2C1 Chemical compound O=C(C(C=C1)=CN(c(cc2)ccc2Cl)C1=O)NC1C(CC2)CCN2C1 WSAWESCAPBKHKD-UHFFFAOYSA-N 0.000 description 1
- WSAWESCAPBKHKD-QGZVFWFLSA-N O=C(C(C=C1)=CN(c(cc2)ccc2Cl)C1=O)N[C@H]1C(CC2)CCN2C1 Chemical compound O=C(C(C=C1)=CN(c(cc2)ccc2Cl)C1=O)N[C@H]1C(CC2)CCN2C1 WSAWESCAPBKHKD-QGZVFWFLSA-N 0.000 description 1
- UGOCSOXBRVAYPJ-UHFFFAOYSA-N O=C(C(C=C1)=CN(c(cc2)ccc2F)C1=O)NC1C(CC2)CCN2C1 Chemical compound O=C(C(C=C1)=CN(c(cc2)ccc2F)C1=O)NC1C(CC2)CCN2C1 UGOCSOXBRVAYPJ-UHFFFAOYSA-N 0.000 description 1
- MXJQFCSEUVCJKU-UHFFFAOYSA-N O=C(C(C=C1)=CN(c(cc2C(F)(F)F)ccc2Cl)C1=O)NC1C(CC2)CCN2C1 Chemical compound O=C(C(C=C1)=CN(c(cc2C(F)(F)F)ccc2Cl)C1=O)NC1C(CC2)CCN2C1 MXJQFCSEUVCJKU-UHFFFAOYSA-N 0.000 description 1
- HAIGHIYUARLXHE-UHFFFAOYSA-N O=C(C(C=C1)=CN(c(ccc(Cl)c2)c2Cl)C1=O)OC1C(CC2)CCN2C1 Chemical compound O=C(C(C=C1)=CN(c(ccc(Cl)c2)c2Cl)C1=O)OC1C(CC2)CCN2C1 HAIGHIYUARLXHE-UHFFFAOYSA-N 0.000 description 1
- COOCSHZCYNAHLV-UHFFFAOYSA-N O=C(C(C=C1)=CN(c(ccc(OC(F)(F)F)c2)c2Cl)C1=O)NC1C(CC2)CCN2C1 Chemical compound O=C(C(C=C1)=CN(c(ccc(OC(F)(F)F)c2)c2Cl)C1=O)NC1C(CC2)CCN2C1 COOCSHZCYNAHLV-UHFFFAOYSA-N 0.000 description 1
- JLIXVVBMBCSKFY-UHFFFAOYSA-N O=C(C(C=C1)=CN(c(cccc2)c2Cl)C1=O)NC1C(CC2)CCN2C1 Chemical compound O=C(C(C=C1)=CN(c(cccc2)c2Cl)C1=O)NC1C(CC2)CCN2C1 JLIXVVBMBCSKFY-UHFFFAOYSA-N 0.000 description 1
- YSTZZRIXMLWIOJ-UHFFFAOYSA-N O=C(C(C=C1)=CN(c(cccc2)c2OC(F)(F)F)C1=O)NC1C(CC2)CCN2C1 Chemical compound O=C(C(C=C1)=CN(c(cccc2)c2OC(F)(F)F)C1=O)NC1C(CC2)CCN2C1 YSTZZRIXMLWIOJ-UHFFFAOYSA-N 0.000 description 1
- DQJKEDSOHAWSPK-UHFFFAOYSA-N O=C(C(C=C1)=CN(c2cccc3c2cccc3)C1=O)NC1C(CC2)CCN2C1 Chemical compound O=C(C(C=C1)=CN(c2cccc3c2cccc3)C1=O)NC1C(CC2)CCN2C1 DQJKEDSOHAWSPK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
- C07D453/04—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems having a quinolyl-4, a substituted quinolyl-4 or a alkylenedioxy-quinolyl-4 radical linked through only one carbon atom, attached in position 2, e.g. quinine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
-
- 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
- A61K31/439—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 the ring forming part of a bridged ring system, e.g. quinuclidine
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR10-2011-0008960 | 2011-01-28 | ||
| KR20110008960 | 2011-01-28 | ||
| PCT/KR2012/000648 WO2012102580A1 (en) | 2011-01-28 | 2012-01-30 | Pharmaceutical composition comprising pyridone derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014503599A JP2014503599A (ja) | 2014-02-13 |
| JP2014503599A5 JP2014503599A5 (https=) | 2014-12-25 |
| JP5921576B2 true JP5921576B2 (ja) | 2016-05-24 |
Family
ID=46581019
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013551904A Expired - Fee Related JP5921576B2 (ja) | 2011-01-28 | 2012-01-30 | ピリドン誘導体を含む医薬組成物 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8716309B2 (https=) |
| EP (1) | EP2668186B1 (https=) |
| JP (1) | JP5921576B2 (https=) |
| KR (1) | KR101925971B1 (https=) |
| CN (1) | CN103328477B (https=) |
| CA (1) | CA2824467C (https=) |
| ES (1) | ES2634204T3 (https=) |
| WO (1) | WO2012102580A1 (https=) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101928505B1 (ko) | 2011-01-28 | 2018-12-12 | 에스케이바이오팜 주식회사 | 피리돈 유도체 및 이를 포함하는 약학적 조성물 |
| AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
| MX382781B (es) | 2014-04-02 | 2025-03-13 | Intermune Inc | Piridinonas anti-fibroticas. |
| EP3259262A4 (en) * | 2015-02-17 | 2018-08-01 | Mapi Pharma Limited | Process and intermediates for the preparation of perampanel |
| AR107928A1 (es) | 2016-03-22 | 2018-06-28 | Merck Sharp & Dohme | Moduladores alostéricos de receptores de acetilcolina nicotínicos |
| WO2019028062A1 (en) * | 2017-07-31 | 2019-02-07 | Washington University | PIRFENIDONE DERIVATIVES FOR MODULATION OF B-LYMPHOCYTE ACTIVITY AND PROTECTION OF ORGANS |
| RS66290B1 (sr) | 2018-05-01 | 2025-01-31 | Merck Sharp & Dohme Llc | Spiropiperidin alosterični modulatori nikotinskih acetiholinskih receptora |
| CN109293507B (zh) * | 2018-10-12 | 2020-12-18 | 河北科技大学 | 4-甲氧基甲烯基-2-烯戊二酸二甲酯的合成方法及其应用 |
| EP4054569A4 (en) | 2019-11-05 | 2023-10-25 | Merck Sharp & Dohme LLC | ALLOSTERIC SPIROPIPERIDINE MODULATORS OF NICOTINIC ACETYLCHOLINE RECEPTORS |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4404138A (en) * | 1982-06-22 | 1983-09-13 | Warner-Lambert Company | 3-[2-(Azabicyclo) ethyl]-1,2,3,4-tetrahydro-5H-[1]benzopyrano[3,4-c]pyridin-5-ones |
| TR200102162T2 (tr) * | 1999-01-29 | 2001-12-21 | Abbott Laboratories | Nikotinik asetilkolin reseptör ligandları olarak diazabisiklik türevler. |
| SE0000540D0 (sv) * | 2000-02-18 | 2000-02-18 | Astrazeneca Ab | New compounds |
| US6569865B2 (en) * | 2001-06-01 | 2003-05-27 | Astrazeneca Ab | Spiro 1-azabicyclo[2.2.2]octane-3,2′(3′h)-furo[2,3-b]pyridine |
| AU2002339810A1 (en) * | 2001-10-16 | 2003-04-28 | Astrazeneca Ab | Azabicyclic compounds for the treatment of fibromyalgia syndrome |
| FR2834511B1 (fr) * | 2002-01-07 | 2004-02-13 | Sanofi Synthelabo | Derives de 5-(pyridin-3-yl)-1-azabicyclo[3.2.1]octane, leur preparation et leur application en therapeutique |
| EP2344636B1 (en) * | 2008-10-09 | 2017-12-06 | Howard Hughes Medical Institute | Novel chimeric ligand-gated ion channels and methods of use thereof |
| US20110262407A1 (en) * | 2008-11-11 | 2011-10-27 | Targacept, Inc. | Treatment with alpha7 selective ligands |
| KR101928505B1 (ko) * | 2011-01-28 | 2018-12-12 | 에스케이바이오팜 주식회사 | 피리돈 유도체 및 이를 포함하는 약학적 조성물 |
-
2012
- 2012-01-27 KR KR1020120008536A patent/KR101925971B1/ko active Active
- 2012-01-30 WO PCT/KR2012/000648 patent/WO2012102580A1/en not_active Ceased
- 2012-01-30 CN CN201280006741.XA patent/CN103328477B/zh active Active
- 2012-01-30 EP EP12740018.2A patent/EP2668186B1/en active Active
- 2012-01-30 ES ES12740018.2T patent/ES2634204T3/es active Active
- 2012-01-30 JP JP2013551904A patent/JP5921576B2/ja not_active Expired - Fee Related
- 2012-01-30 CA CA2824467A patent/CA2824467C/en active Active
- 2012-01-30 US US13/980,819 patent/US8716309B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| EP2668186B1 (en) | 2017-05-03 |
| ES2634204T3 (es) | 2017-09-27 |
| KR101925971B1 (ko) | 2018-12-06 |
| EP2668186A1 (en) | 2013-12-04 |
| US20130317059A1 (en) | 2013-11-28 |
| JP2014503599A (ja) | 2014-02-13 |
| CN103328477B (zh) | 2016-01-20 |
| CA2824467C (en) | 2019-07-02 |
| US8716309B2 (en) | 2014-05-06 |
| KR20120087852A (ko) | 2012-08-07 |
| CN103328477A (zh) | 2013-09-25 |
| EP2668186A4 (en) | 2014-03-19 |
| CA2824467A1 (en) | 2012-08-02 |
| WO2012102580A1 (en) | 2012-08-02 |
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