JP2013544860A5 - - Google Patents

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Publication number
JP2013544860A5
JP2013544860A5 JP2013542482A JP2013542482A JP2013544860A5 JP 2013544860 A5 JP2013544860 A5 JP 2013544860A5 JP 2013542482 A JP2013542482 A JP 2013542482A JP 2013542482 A JP2013542482 A JP 2013542482A JP 2013544860 A5 JP2013544860 A5 JP 2013544860A5
Authority
JP
Japan
Prior art keywords
alkyl
compound
phenyl
haloalkyl
heteroaryl
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.)
Granted
Application number
JP2013542482A
Other languages
English (en)
Japanese (ja)
Other versions
JP5886310B2 (ja
JP2013544860A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2011/071690 external-priority patent/WO2012076435A1/en
Publication of JP2013544860A publication Critical patent/JP2013544860A/ja
Publication of JP2013544860A5 publication Critical patent/JP2013544860A5/ja
Application granted granted Critical
Publication of JP5886310B2 publication Critical patent/JP5886310B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2013542482A 2010-12-06 2011-12-05 Lp−PLA2により媒介される疾患または状態の処置における使用のためのピリミジノン化合物 Expired - Fee Related JP5886310B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CNPCT/CN2010/079465 2010-12-06
CN2010079465 2010-12-06
PCT/EP2011/071690 WO2012076435A1 (en) 2010-12-06 2011-12-05 Pyrimidinone compounds for use in the treatment of diseases or conditions mediated by lp - pla2

Publications (3)

Publication Number Publication Date
JP2013544860A JP2013544860A (ja) 2013-12-19
JP2013544860A5 true JP2013544860A5 (enExample) 2015-01-29
JP5886310B2 JP5886310B2 (ja) 2016-03-16

Family

ID=45440490

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013542482A Expired - Fee Related JP5886310B2 (ja) 2010-12-06 2011-12-05 Lp−PLA2により媒介される疾患または状態の処置における使用のためのピリミジノン化合物

Country Status (24)

Country Link
US (4) US8637536B2 (enExample)
EP (1) EP2649053B1 (enExample)
JP (1) JP5886310B2 (enExample)
KR (1) KR101861883B1 (enExample)
CN (1) CN103347864B (enExample)
AR (1) AR084153A1 (enExample)
AU (1) AU2011340690C1 (enExample)
BR (1) BR112013013898B1 (enExample)
CA (1) CA2820408C (enExample)
CL (1) CL2013001604A1 (enExample)
CO (1) CO6801726A2 (enExample)
CR (1) CR20130264A (enExample)
DO (1) DOP2013000130A (enExample)
EA (1) EA023796B1 (enExample)
ES (1) ES2559224T3 (enExample)
IL (1) IL226473A0 (enExample)
MX (1) MX2013006342A (enExample)
PE (1) PE20140421A1 (enExample)
PH (1) PH12013501089A1 (enExample)
SG (1) SG190830A1 (enExample)
TW (1) TW201307324A (enExample)
UY (1) UY33766A (enExample)
WO (1) WO2012076435A1 (enExample)
ZA (1) ZA201303560B (enExample)

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US8349577B2 (en) * 2009-04-23 2013-01-08 Research Foundation For Mental Hygiene, Inc. Method for evaluating blood-neural barrier permeability
TW201307324A (zh) * 2010-12-06 2013-02-16 Glaxo Group Ltd 化合物
JP2013544854A (ja) * 2010-12-06 2013-12-19 グラクソ グループ リミテッド 化合物
PH12014500382A1 (en) 2011-09-01 2021-07-12 Glaxo Group Ltd Novel crystal form
JP6037277B2 (ja) * 2012-12-19 2016-12-07 国立研究開発法人農業・食品産業技術総合研究機構 オーキシン生合成阻害剤
EP2948457A4 (en) * 2013-01-25 2016-09-07 Glaxosmithkline Ip Dev Ltd COMPOUNDS
EP2764866A1 (en) 2013-02-07 2014-08-13 IP Gesellschaft für Management mbH Inhibitors of nedd8-activating enzyme
WO2015027067A2 (en) * 2013-08-23 2015-02-26 Virginia Commonwealth University Ester nitrates derivatives of aromatic aldehydes with multiple pharmalogic properties to treat sickle cell disease
GB201322602D0 (en) * 2013-12-19 2014-02-05 Almac Discovery Ltd Pharmaceutical compounds
CN103896906A (zh) * 2014-02-28 2014-07-02 苏州维泰生物技术有限公司 一种农药咯菌腈中间体的新合成方法
WO2016002918A1 (ja) * 2014-07-04 2016-01-07 日本たばこ産業株式会社 インドール化合物の製造方法
WO2016012916A1 (en) 2014-07-22 2016-01-28 Glaxosmithkline Intellectual Property Development Limited 1,2,3,5-tetrahydroimidazo[1,2-c]pyrimidine derivatives useful in the treatment of diseases and disorders mediated by lp-pla2
WO2016012917A1 (en) 2014-07-22 2016-01-28 Glaxosmithkline Intellectual Property Development Limited 1,2,3,5-tetrahydroimidazo[1,2-c]pyrimidine derivatives useful in the treatment of diseases and disorders mediated by lp-pla2
CN106188063A (zh) * 2015-05-08 2016-12-07 中国科学院上海药物研究所 用作Lp-PLA2抑制剂的双环类化合物、其制备方法及医药用途
CN110129300B (zh) * 2016-06-02 2021-08-03 天津科技大学 一种磷脂酶d
SG11202001353PA (en) 2017-08-15 2020-03-30 Agios Pharmaceuticals Inc Pyruvate kinase modulators and use thereof
MD4081511T2 (ro) * 2019-12-23 2025-01-31 Sitryx Therapeutics Ltd Derivați carboxilici cu proprietăți antiinflamatorii
CN111533699B (zh) * 2020-05-27 2023-12-01 龙曦宁(上海)医药科技有限公司 一种2-(三氟甲基)嘧啶-5-醇的合成方法
WO2024027116A1 (en) * 2022-08-04 2024-02-08 4B Technologies (Beijing) Co., Limited Dihydroimidazo-pyrimidinone compounds as lp-pla2 inhibitors and use thereof

Family Cites Families (45)

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Publication number Priority date Publication date Assignee Title
GB9421816D0 (en) 1994-10-29 1994-12-14 Smithkline Beecham Plc Novel compounds
FI972584L (fi) 1994-12-22 1997-08-19 Smithkline Beecham Plc Substituoituja atsetidin-2-oneja ateroskleroosin hoitamiseksi
CH690264A5 (fr) 1995-06-30 2000-06-30 Symphar Sa Dérivés aminophosphonates substitués, leur procédé de préparation et leur utilisation pour la préparation de compositions pharmaceutiques.
WO1997002242A1 (en) 1995-07-01 1997-01-23 Smithkline Beecham Plc Azetidinone derivatives for the treatment of atherosclerosis
WO1997012963A2 (en) 1995-09-29 1997-04-10 Smithkline Beecham Plc A paf-acetylhydrolase and use in therapy
JP2000502079A (ja) 1995-12-08 2000-02-22 スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー アテローム性動脈硬化症の治療のための単環β―ラクタム誘導体
JP2000505063A (ja) 1995-12-08 2000-04-25 スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー アテローム性動脈硬化症の治療のためのアゼチジノン化合物
CA2252696A1 (en) 1996-04-26 1997-11-06 Deirdre Mary Bernadette Hickey Azetidinone derivatives for the treatment of atherosclerosis
GB9608649D0 (en) 1996-04-26 1996-07-03 Smithkline Beecham Plc Novel compounds
GB9626536D0 (en) 1996-12-20 1997-02-05 Symphar Sa Novel compounds
GB9626616D0 (en) 1996-12-20 1997-02-05 Symphar Sa Novel compounds
GB9626615D0 (en) 1996-12-20 1997-02-05 Symphar Sa Novel compounds
IL132522A0 (en) 1997-04-22 2001-03-19 Cocensys Inc Carbocyclic and heterocyclic substituted semicarbazones and thiosemicarbazones and pharmaceutical compositions containing the same
WO1999024420A1 (en) 1997-11-06 1999-05-20 Smithkline Beecham Plc Pyrimidinone compounds and pharmaceutical compositions containing them
DE69911980T2 (de) * 1998-08-21 2004-09-09 Smithkline Beecham P.L.C., Brentford Pyrimidinonderivate zur behandlung von atheroscleros
GB9910079D0 (en) 1999-05-01 1999-06-30 Smithkline Beecham Plc Novel compounds
ATE283845T1 (de) * 1999-05-01 2004-12-15 Smithkline Beecham Plc Pyrimidinon verbindungen
GB9910378D0 (en) * 1999-05-05 1999-06-30 Smithkline Beecham Plc Novel compounds
JP3757703B2 (ja) 1999-09-22 2006-03-22 凸版印刷株式会社 再封可能な開口維持部材付パウチ
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EE05400B1 (et) * 2001-04-10 2011-04-15 Pfizer Inc. Prasoolderivaadid, neid v?i nende farmatseutiliselt vastuv?etavaid sooli, solvaate v?i derivaate sisaldavad farmatseutilised kompositsioonid, nende kasutamine ning meetodid nende valmistamiseks
GB0119795D0 (en) 2001-08-14 2001-10-03 Smithkline Beecham Plc Novel process
GB0119793D0 (en) 2001-08-14 2001-10-03 Smithkline Beecham Plc Novel compounds
HN2002000317A (es) * 2001-11-02 2003-05-21 Pfizer Inhibidores de pde9 para tratamiento de trastornos cardiovasculares
GB0127139D0 (en) 2001-11-10 2002-01-02 Smithkline Beecham Novel compounds
GB0127140D0 (en) 2001-11-10 2002-01-02 Smithkline Beecham Novel compounds
GB0127141D0 (en) 2001-11-10 2002-01-02 Smithkline Beecham Plc Novel compounds
GB0127143D0 (en) 2001-11-10 2002-01-02 Smithkline Beecham Novel compounds
GB0208279D0 (en) 2002-04-10 2002-05-22 Glaxo Group Ltd Novel compounds
GB0208280D0 (en) 2002-04-10 2002-05-22 Glaxo Group Ltd Novel compounds
EP1644353A1 (de) 2003-07-02 2006-04-12 Bayer HealthCare AG Amid-substituierte 1, 2, 4-triazin-5 (2h) - one zur behandlung von chronisch inflammatorischen krankheiten
DE102004061009A1 (de) 2004-12-18 2006-06-22 Bayer Healthcare Ag Substituierte 1,2,4-Triazin-5(2H)-one
DE102004061008A1 (de) 2004-12-18 2006-06-22 Bayer Healthcare Ag 3-Arylalkyl- und 3-Heteroarylalkyl-substituierte 1,2,4-Triazin-5(2H)-one
US7705005B2 (en) 2006-10-13 2010-04-27 Glaxo Group Limited Bicyclic heteroaromatic compounds
US20080090851A1 (en) 2006-10-13 2008-04-17 Colin Andrew Leach Bicyclic Heteroaromatic Compounds
EP2083625A4 (en) 2006-10-13 2011-10-19 Glaxo Group Ltd BICYCLIC HETOROAROMATIC COMPOUNDS
US20080090852A1 (en) 2006-10-13 2008-04-17 Colin Andrew Leach Bicyclic Heteroaromatic Compounds
ES2548878T3 (es) 2007-05-11 2015-10-21 The Trustees Of The University Of Pennsylvania Métodos de tratamiento de úlceras de la piel
US8962633B2 (en) 2007-05-11 2015-02-24 Thomas Jefferson University Methods of treatment and prevention of metabolic bone diseases and disorders
US20080279846A1 (en) 2007-05-11 2008-11-13 Thomas Jefferson University Methods of treatment and prevention of neurodegenerative diseases and disorders
JP2013544854A (ja) * 2010-12-06 2013-12-19 グラクソ グループ リミテッド 化合物
TW201307324A (zh) * 2010-12-06 2013-02-16 Glaxo Group Ltd 化合物

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