JP2013518110A5 - - Google Patents

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Publication number
JP2013518110A5
JP2013518110A5 JP2012551232A JP2012551232A JP2013518110A5 JP 2013518110 A5 JP2013518110 A5 JP 2013518110A5 JP 2012551232 A JP2012551232 A JP 2012551232A JP 2012551232 A JP2012551232 A JP 2012551232A JP 2013518110 A5 JP2013518110 A5 JP 2013518110A5
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JP
Japan
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mono
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JP2012551232A
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English (en)
Japanese (ja)
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JP2013518110A (ja
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Priority claimed from PCT/US2011/022412 external-priority patent/WO2011094209A1/en
Publication of JP2013518110A publication Critical patent/JP2013518110A/ja
Publication of JP2013518110A5 publication Critical patent/JP2013518110A5/ja
Withdrawn legal-status Critical Current

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JP2012551232A 2010-01-28 2011-01-25 疼痛および他の適応症の治療用の医薬組成物 Withdrawn JP2013518110A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US29908710P 2010-01-28 2010-01-28
US61/299,087 2010-01-28
PCT/US2011/022412 WO2011094209A1 (en) 2010-01-28 2011-01-25 Pharmaceutical compositions for the treatment of pain and other indicatons

Publications (2)

Publication Number Publication Date
JP2013518110A JP2013518110A (ja) 2013-05-20
JP2013518110A5 true JP2013518110A5 (https=) 2014-03-13

Family

ID=44319717

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012551232A Withdrawn JP2013518110A (ja) 2010-01-28 2011-01-25 疼痛および他の適応症の治療用の医薬組成物

Country Status (11)

Country Link
US (1) US20130030000A1 (https=)
EP (1) EP2528603A4 (https=)
JP (1) JP2013518110A (https=)
KR (1) KR20120123691A (https=)
CN (1) CN102858338A (https=)
AU (1) AU2011209754A1 (https=)
BR (1) BR112012018913A2 (https=)
CA (1) CA2786888A1 (https=)
MX (1) MX2012008801A (https=)
RU (1) RU2012136624A (https=)
WO (1) WO2011094209A1 (https=)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2321288B1 (en) * 2008-08-04 2014-03-19 Merck Sharp & Dohme Corp. Oxazole derivatives useful as inhibitors of faah
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
US9006433B2 (en) 2010-04-21 2015-04-14 Merck Sharp & Dohme Corp. Substituted pyrimidines
KR20130050952A (ko) 2010-06-16 2013-05-16 브루스 챈들러 메이 인플루엔자, 감기 및 염증의 치료에서 레보세티리진 및 몬테루카스트의 용도
JO3407B1 (ar) 2012-05-31 2019-10-20 Eisai R&D Man Co Ltd مركبات رباعي هيدرو بيرازولو بيريميدين
WO2014164285A2 (en) 2013-03-13 2014-10-09 Inflammatory Response Research, Inc. Use of levocetirizine and montelukast in the treatment of vasculitis
MX382776B (es) 2013-03-13 2025-03-13 Inflammatory Response Res Inc Uso de levocetirizina y montelukast en el tratamiento de lesion traumatica.
RU2015134423A (ru) 2013-03-13 2017-04-26 Инфламматори Респонс Ресёрч, Инк. Применение левоцитиризина и монтелукаста при лечении аутоиммуных расстройств
CN105636945B (zh) 2013-10-14 2017-11-17 卫材R&D管理有限公司 选择性取代的喹啉化合物
JP6223563B2 (ja) 2013-10-14 2017-11-01 エーザイ・アール・アンド・ディー・マネジメント株式会社 選択的に置換されたキノリン化合物
SI3077047T1 (sl) * 2013-12-04 2019-09-30 Galmed Research & Development Ltd. Soli aramchola
WO2016036588A1 (en) * 2014-09-03 2016-03-10 Merck Sharp & Dohme Corp. Pharmaceutical suspensions containing etoricoxib
WO2016044095A1 (en) 2014-09-15 2016-03-24 Inflammatory Response Research, Inc. Levocetirizine and montelukast in the treatment of inflammation mediated conditions
NZ797702A (en) * 2017-03-13 2026-03-27 Lundbeck La Jolla Research Center Inc Dual magl and faah inhibitors
WO2019008115A1 (en) 2017-07-07 2019-01-10 Syngenta Participations Ag HETEROCYCLIC DERIVATIVES HAVING PESTICIDE ACTIVITY HAVING SUBSTITUENTS CONTAINING SULFUR
KR102257685B1 (ko) 2018-09-20 2021-05-31 성균관대학교산학협력단 Cox-2 억제제를 유효성분으로 포함하는 소염진통 예방 또는 치료용 정제 조성물
CN110156710B (zh) * 2019-04-30 2022-10-28 贵州省中国科学院天然产物化学重点实验室(贵州医科大学天然产物化学重点实验室) 一种多取代噁唑类化合物的制备方法
JP7464955B2 (ja) 2020-02-27 2024-04-10 国立大学法人千葉大学 ヨードオキサゾール化合物の製造方法、オキサゾール化合物の製造方法
WO2021236518A1 (en) * 2020-05-19 2021-11-25 IRR, Inc. Levocetirizine and montelukast in the treatment of sepsis and symptoms thereof
US20240252519A1 (en) * 2021-05-28 2024-08-01 Ananda Scientific, Inc. Methods for the treatment of post-traumatic stress disorder and traumatic brain injury with cannabinoids

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR0314980A (pt) * 2002-10-08 2005-08-09 Scripps Research Inst Inibidores de hidrolase de amida de ácido graxo
AR055831A1 (es) * 2004-12-30 2007-09-12 Janssen Pharmaceutica Nv Pepirazinilureas y piperidinilureas como moduladores de hidrolasa de amida de acidos grasos
CA2602336A1 (en) * 2005-03-31 2006-10-05 Ucb Pharma S.A. Compounds comprising an oxazole or thiazole moiety, processes for making them, and their uses
AU2008257154B2 (en) * 2007-05-25 2014-03-06 The Scripps Research Institute Tetracyclic inhibitors of fatty acid amide hydrolase
CA2727245A1 (en) * 2008-06-11 2009-12-17 Merck Sharp & Dohme Corp. Imidazole derivatives useful as inhibitors of faah
EP2299824B1 (en) * 2008-06-11 2013-06-19 Merck Sharp & Dohme Corp. Pyrazole derivatives useful as inhibitors of faah
EP2321288B1 (en) * 2008-08-04 2014-03-19 Merck Sharp & Dohme Corp. Oxazole derivatives useful as inhibitors of faah

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