JP2009538358A - 脂肪酸アミド加水分解酵素のオキサゾリルピペリジン・モジュレーター - Google Patents
脂肪酸アミド加水分解酵素のオキサゾリルピペリジン・モジュレーター Download PDFInfo
- Publication number
- JP2009538358A JP2009538358A JP2009513231A JP2009513231A JP2009538358A JP 2009538358 A JP2009538358 A JP 2009538358A JP 2009513231 A JP2009513231 A JP 2009513231A JP 2009513231 A JP2009513231 A JP 2009513231A JP 2009538358 A JP2009538358 A JP 2009538358A
- Authority
- JP
- Japan
- Prior art keywords
- piperidin
- oxazol
- methanone
- benzyl
- ylmethyl
- 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.)
- Withdrawn
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- 0 C1CC*CC1 Chemical compound C1CC*CC1 0.000 description 10
- VQSBOUWGBQUCOL-FZRSOTFLSA-N C/C=C\C(\O/C(/C)=C/C=C(\C)/CN(CC1)CCC1C(C1OC=CN1C)=O)=C/C Chemical compound C/C=C\C(\O/C(/C)=C/C=C(\C)/CN(CC1)CCC1C(C1OC=CN1C)=O)=C/C VQSBOUWGBQUCOL-FZRSOTFLSA-N 0.000 description 1
- FPMGNKDHCPZZTI-UHFFFAOYSA-N CCC/N=C(/C(C1CCN(Cc(cc2)ccc2OCCC(C)C)CC1)=O)\O Chemical compound CCC/N=C(/C(C1CCN(Cc(cc2)ccc2OCCC(C)C)CC1)=O)\O FPMGNKDHCPZZTI-UHFFFAOYSA-N 0.000 description 1
- NAEHFIDFYYDMEB-UHFFFAOYSA-N COc1ccccc1C(N(CC1)CCC1C(c1ncc[o]1)=O)=O Chemical compound COc1ccccc1C(N(CC1)CCC1C(c1ncc[o]1)=O)=O NAEHFIDFYYDMEB-UHFFFAOYSA-N 0.000 description 1
- LHBSLCLDTRLNEL-UHFFFAOYSA-N C[n]1c2cc(CN(CC3)CCC3C(c3ncc[o]3)=O)ccc2cc1 Chemical compound C[n]1c2cc(CN(CC3)CCC3C(c3ncc[o]3)=O)ccc2cc1 LHBSLCLDTRLNEL-UHFFFAOYSA-N 0.000 description 1
- REBOCMHUMHZZMT-UHFFFAOYSA-N OC(C1CCN(Cc2ccc3[nH]ccc3c2)CC1)c1ncc[o]1 Chemical compound OC(C1CCN(Cc2ccc3[nH]ccc3c2)CC1)c1ncc[o]1 REBOCMHUMHZZMT-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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-
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-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Ophthalmology & Optometry (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Endocrinology (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Reproductive Health (AREA)
- Gynecology & Obstetrics (AREA)
- Virology (AREA)
- Pulmonology (AREA)
- Obesity (AREA)
- Molecular Biology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Emergency Medicine (AREA)
- Transplantation (AREA)
- Vascular Medicine (AREA)
- Addiction (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US80872306P | 2006-05-26 | 2006-05-26 | |
| PCT/US2007/012631 WO2007140005A2 (en) | 2006-05-26 | 2007-05-25 | Oxazolyl piperidine modulators of fatty acid amide hydrolase |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009538358A true JP2009538358A (ja) | 2009-11-05 |
| JP2009538358A5 JP2009538358A5 (https=) | 2010-07-01 |
Family
ID=38779275
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009513231A Withdrawn JP2009538358A (ja) | 2006-05-26 | 2007-05-25 | 脂肪酸アミド加水分解酵素のオキサゾリルピペリジン・モジュレーター |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20100292266A1 (https=) |
| EP (1) | EP2023728A4 (https=) |
| JP (1) | JP2009538358A (https=) |
| WO (1) | WO2007140005A2 (https=) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013523814A (ja) * | 2010-04-08 | 2013-06-17 | メルク・シャープ・エンド・ドーム・コーポレイション | Faahの調節薬として有用なオキサゾール誘導体 |
| JP2017529401A (ja) * | 2014-09-26 | 2017-10-05 | チャーンジョウ インシュヨン ファーマシューティカル カンパニー,リミティド | Ns4b阻害剤としてのベンゾフラン類似体 |
| JP2024518000A (ja) * | 2021-04-30 | 2024-04-23 | ヴァンキア バイオ,インコーポレイテッド | グルコセレブロシダーゼ活性の小分子モジュレータ及びその使用 |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| CA2714743C (en) | 2008-02-19 | 2017-01-17 | Janssen Pharmaceutica N.V. | Aryl-hydroxyethylamino-pyrimidines and triazines as modulators of fatty acid amide hydrolase |
| EP2299824B1 (en) * | 2008-06-11 | 2013-06-19 | Merck Sharp & Dohme Corp. | Pyrazole derivatives useful as inhibitors of faah |
| US8906914B2 (en) | 2009-08-18 | 2014-12-09 | Janssen Pharmaceutica Nv | Ethylene diamine modulators of fatty acid hydrolase |
| WO2011085216A2 (en) | 2010-01-08 | 2011-07-14 | Ironwood Pharmaceuticals, Inc. | Use of faah inhibitors for treating parkinson's disease and restless legs syndrome |
| WO2011123719A2 (en) | 2010-03-31 | 2011-10-06 | Ironwood Pharmaceuticals, Inc. | Use of faah inhibitors for treating abdominal, visceral and pelvic pain |
| EP2670245B1 (en) * | 2011-02-04 | 2015-09-09 | The Scripps Research Institute | Alpha-ketoheterocycles and methods of making and using |
| US8828995B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| EP2683705B1 (de) | 2011-03-08 | 2015-04-22 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| US8871758B2 (en) | 2011-03-08 | 2014-10-28 | Sanofi | Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof |
| WO2012120052A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| EP2683699B1 (de) | 2011-03-08 | 2015-06-24 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| CN108084130B (zh) * | 2017-12-15 | 2019-09-10 | 东南大学 | 一种降糖药达格列净的制备方法 |
| WO2020179859A1 (ja) | 2019-03-06 | 2020-09-10 | 第一三共株式会社 | ピロロピラゾール誘導体 |
| CN110804048A (zh) * | 2019-11-08 | 2020-02-18 | 暨南大学 | 恶唑酮类化合物及其应用、faah的正电子药物 |
| CN115850241B (zh) * | 2021-09-24 | 2025-01-14 | 中国药科大学 | 一种含α-酮骨架的取代杂环类化合物及其用途 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5856537A (en) * | 1996-06-26 | 1999-01-05 | The Scripps Research Institute | Inhibitors of oleamide hydrolase |
| US6462054B1 (en) * | 2000-03-27 | 2002-10-08 | The Scripps Research Institute | Inhibitors of fatty acid amide hydrolase |
| EP1558591B1 (en) * | 2002-10-07 | 2014-05-07 | The Regents of The University of California | Modulation of anxiety through blockade of anandamide hydrolysis |
| AU2004289303A1 (en) * | 2003-11-10 | 2005-05-26 | Synta Pharmaceuticals, Corp. | Fused heterocyclic compounds |
| US7351724B2 (en) * | 2004-10-15 | 2008-04-01 | The Scripps Research Institute | Oxadiazole ketone inhibitors of fatty acid amide hydrolase |
| AR055831A1 (es) * | 2004-12-30 | 2007-09-12 | Janssen Pharmaceutica Nv | Pepirazinilureas y piperidinilureas como moduladores de hidrolasa de amida de acidos grasos |
-
2007
- 2007-05-25 JP JP2009513231A patent/JP2009538358A/ja not_active Withdrawn
- 2007-05-25 EP EP07795432A patent/EP2023728A4/en not_active Withdrawn
- 2007-05-25 WO PCT/US2007/012631 patent/WO2007140005A2/en not_active Ceased
- 2007-05-25 US US12/227,756 patent/US20100292266A1/en not_active Abandoned
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013523814A (ja) * | 2010-04-08 | 2013-06-17 | メルク・シャープ・エンド・ドーム・コーポレイション | Faahの調節薬として有用なオキサゾール誘導体 |
| JP2017529401A (ja) * | 2014-09-26 | 2017-10-05 | チャーンジョウ インシュヨン ファーマシューティカル カンパニー,リミティド | Ns4b阻害剤としてのベンゾフラン類似体 |
| US10100027B2 (en) | 2014-09-26 | 2018-10-16 | Changzhou Yinsheng Pharmaceutical Co., Ltd. | Benzofuran analogue as NS4B inhibitor |
| JP2024518000A (ja) * | 2021-04-30 | 2024-04-23 | ヴァンキア バイオ,インコーポレイテッド | グルコセレブロシダーゼ活性の小分子モジュレータ及びその使用 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20100292266A1 (en) | 2010-11-18 |
| EP2023728A2 (en) | 2009-02-18 |
| EP2023728A4 (en) | 2010-11-24 |
| WO2007140005A2 (en) | 2007-12-06 |
| WO2007140005A3 (en) | 2008-01-31 |
Similar Documents
| Publication | Publication Date | Title |
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