JP2010522711A5 - - Google Patents

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Publication number
JP2010522711A5
JP2010522711A5 JP2010500240A JP2010500240A JP2010522711A5 JP 2010522711 A5 JP2010522711 A5 JP 2010522711A5 JP 2010500240 A JP2010500240 A JP 2010500240A JP 2010500240 A JP2010500240 A JP 2010500240A JP 2010522711 A5 JP2010522711 A5 JP 2010522711A5
Authority
JP
Japan
Prior art keywords
methyl
compound
hydrogen
pharmaceutically acceptable
salt
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Withdrawn
Application number
JP2010500240A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010522711A (ja
Filing date
Publication date
Priority claimed from GBGB0706030.4A external-priority patent/GB0706030D0/en
Priority claimed from GB0805047A external-priority patent/GB0805047D0/en
Application filed filed Critical
Priority claimed from PCT/EP2008/053433 external-priority patent/WO2008116845A1/en
Publication of JP2010522711A publication Critical patent/JP2010522711A/ja
Publication of JP2010522711A5 publication Critical patent/JP2010522711A5/ja
Withdrawn legal-status Critical Current

Links

JP2010500240A 2007-03-28 2008-03-20 P2x7調節因子としてのピペリジノンカルボキサミド誘導体 Withdrawn JP2010522711A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB0706030.4A GB0706030D0 (en) 2007-03-28 2007-03-28 Novel compounds
GB0805047A GB0805047D0 (en) 2008-03-18 2008-03-18 Novel compounds
PCT/EP2008/053433 WO2008116845A1 (en) 2007-03-28 2008-03-20 Piperidinone carboxamide derivatives as p2x7 modulators

Publications (2)

Publication Number Publication Date
JP2010522711A JP2010522711A (ja) 2010-07-08
JP2010522711A5 true JP2010522711A5 (enExample) 2011-05-12

Family

ID=39788062

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010500240A Withdrawn JP2010522711A (ja) 2007-03-28 2008-03-20 P2x7調節因子としてのピペリジノンカルボキサミド誘導体

Country Status (4)

Country Link
US (1) US20100168171A1 (enExample)
EP (1) EP2139858A1 (enExample)
JP (1) JP2010522711A (enExample)
WO (1) WO2008116845A1 (enExample)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2007271182B2 (en) * 2006-07-06 2012-03-15 Glaxo Group Limited Substituted N-phenylmethyl -5-oxo-proline-2-amides as P2X7-receptor antagonists and their methods of use
JP5478637B2 (ja) * 2008-12-23 2014-04-23 エフ.ホフマン−ラ ロシュ アーゲー P2x7モジュレーターとしてのジヒドロピリドンアミド
DK2509609T3 (da) * 2009-12-08 2014-11-10 Univ Vanderbilt Forbedrede fremgangsmåder og sammensætninger for venehøst og autotransplantation
MX2014000894A (es) 2011-07-22 2014-02-27 Actelion Pharmaceuticals Ltd Derivados de amidas heterociclicas como antagonistas de receptores p2x7.
TWI576347B (zh) 2012-01-20 2017-04-01 艾克泰聯製藥有限公司 作為p2x受體拮抗劑之雜環醯胺衍生物
KR102232742B1 (ko) 2012-12-12 2021-03-26 이도르시아 파마슈티컬스 리미티드 P2x7 수용체 길항제로서의 인돌 카르복사미드 유도체
WO2014097140A1 (en) 2012-12-18 2014-06-26 Actelion Pharmaceuticals Ltd Indole carboxamide derivatives as p2x7 receptor antagonists
JP6282016B2 (ja) * 2013-01-22 2018-02-21 イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd P2x7受容体アンタゴニストとしての複素環アミド誘導体
JP6282017B2 (ja) 2013-01-22 2018-02-21 イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd P2x7受容体アンタゴニストとしての複素環アミド誘導体
EP3773557A1 (en) 2018-03-29 2021-02-17 Centre national de la recherche scientifique P2rx7 modulators in therapy
TW202229235A (zh) * 2021-01-28 2022-08-01 大陸商深圳晶泰科技有限公司 環胺衍生物及其製備方法和應用

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6054579A (en) * 1997-06-26 2000-04-25 Leukosite, Inc. Synthesis of substituted lactams
SE9704546D0 (sv) * 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
SE9704544D0 (sv) * 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
AU2007271182B2 (en) * 2006-07-06 2012-03-15 Glaxo Group Limited Substituted N-phenylmethyl -5-oxo-proline-2-amides as P2X7-receptor antagonists and their methods of use

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