JP2017520613A5 - - Google Patents

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Publication number
JP2017520613A5
JP2017520613A5 JP2017503504A JP2017503504A JP2017520613A5 JP 2017520613 A5 JP2017520613 A5 JP 2017520613A5 JP 2017503504 A JP2017503504 A JP 2017503504A JP 2017503504 A JP2017503504 A JP 2017503504A JP 2017520613 A5 JP2017520613 A5 JP 2017520613A5
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JP
Japan
Prior art keywords
oxy
compound
pharmaceutically acceptable
acceptable salt
tetrahydropyrrolo
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JP2017503504A
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English (en)
Japanese (ja)
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JP6625603B2 (ja
JP2017520613A (ja
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Priority claimed from PCT/CN2015/084607 external-priority patent/WO2016011931A1/en
Publication of JP2017520613A publication Critical patent/JP2017520613A/ja
Publication of JP2017520613A5 publication Critical patent/JP2017520613A5/ja
Application granted granted Critical
Publication of JP6625603B2 publication Critical patent/JP6625603B2/ja
Active legal-status Critical Current
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JP2017503504A 2014-07-22 2015-07-21 化合物 Active JP6625603B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN2014000695 2014-07-22
CNPCT/CN2014/000695 2014-07-22
PCT/CN2015/084607 WO2016011931A1 (en) 2014-07-22 2015-07-21 Compounds

Publications (3)

Publication Number Publication Date
JP2017520613A JP2017520613A (ja) 2017-07-27
JP2017520613A5 true JP2017520613A5 (enExample) 2018-08-23
JP6625603B2 JP6625603B2 (ja) 2019-12-25

Family

ID=55162512

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2017503504A Active JP6625603B2 (ja) 2014-07-22 2015-07-21 化合物
JP2017503553A Active JP6625604B2 (ja) 2014-07-22 2015-07-21 化合物

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2017503553A Active JP6625604B2 (ja) 2014-07-22 2015-07-21 化合物

Country Status (14)

Country Link
US (5) US10125141B2 (enExample)
EP (2) EP3172208B1 (enExample)
JP (2) JP6625603B2 (enExample)
KR (2) KR20170029516A (enExample)
CN (2) CN106536521B (enExample)
AR (1) AR101261A1 (enExample)
AU (2) AU2015292048B2 (enExample)
BR (1) BR112016030939B1 (enExample)
CA (2) CA2955910C (enExample)
ES (2) ES2747636T3 (enExample)
RU (2) RU2690190C2 (enExample)
TW (1) TW201617348A (enExample)
UY (1) UY36224A (enExample)
WO (2) WO2016011931A1 (enExample)

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AR101261A1 (es) 2014-07-22 2016-12-07 Glaxosmithkline Ip Dev Ltd Compuesto de tetrahidropirrolo[1,2:3,4]imidazo[1,2-c]pirimidin-1(6h)-ona y composición farmacéutica que lo comprende
US11273176B2 (en) 2016-03-02 2022-03-15 The Brigham And Women's Hospital, Inc. Use of PLA2G5-deficient suppressive macrophages in suppression of inflammation
WO2019063634A1 (en) * 2017-09-26 2019-04-04 INSERM (Institut National de la Santé et de la Recherche Médicale) DARAPLADIB RADIOMARQUÉ, ITS ANALOGUES AND THEIR USE AS IMAGING COMPOUNDS
CN109988126B (zh) * 2017-12-29 2023-05-16 南京富润凯德生物医药有限公司 一种3-氨基-氧杂环丁烷衍生物及其制备方法和应用
CN109134523A (zh) * 2018-09-30 2019-01-04 中昊(大连)化工研究设计院有限公司 一种3,6-二氢-2h-吡喃-4-硼酸频哪醇酯的合成新工艺
JP2022116370A (ja) * 2019-06-13 2022-08-10 アグロカネショウ株式会社 新規な1-ベンジルアミン誘導体及びこれを有効成分とする農園芸用薬剤
CN112574221B (zh) * 2019-09-30 2022-03-04 上海纽思克生物科技有限公司 四环嘧啶酮类化合物、其制备方法、其组合物和用途
EP4056571A4 (en) * 2019-11-09 2024-01-24 Shanghai Simr Biotechnology Co., Ltd. Tricyclic dihydroimidazopyrimidone derivative, preparation method therefor, pharmaceutical composition and use thereof
WO2021228159A1 (zh) * 2020-05-13 2021-11-18 上海纽思克生物科技有限公司 桥环嘧啶酮类化合物、其制备方法、其组合物和用途
CN113666930B (zh) * 2020-05-13 2022-10-25 上海纽思克生物科技有限公司 桥环嘧啶酮类化合物、其制备方法、其组合物和用途
CN113861220B (zh) * 2020-06-30 2023-06-16 上海纽思克生物科技有限公司 三环嘧啶酮类化合物、其制备方法、其组合物和用途
CN113912622B (zh) * 2020-07-10 2023-12-01 上海纽思克生物科技有限公司 三环嘧啶酮类化合物、其制备方法、其组合物和用途
CN115304620A (zh) 2021-05-07 2022-11-08 上海赛默罗生物科技有限公司 嘧啶酮衍生物、其制备方法、药物组合物和用途
CN114057740B (zh) * 2021-12-15 2024-04-02 上海赛默罗生物科技有限公司 螺环嘧啶酮衍生物、其制备方法、药物组合物和用途
JP2025527291A (ja) * 2022-08-04 2025-08-20 4ビー テクノロジーズ (ベイジン) カンパニー リミテッド Lp-PLA2阻害剤としてのジヒドロイミダゾピリミジノン化合物およびその使用
CN121311231A (zh) * 2023-04-18 2026-01-09 赛神医药有限公司 Lp-PLA2抑制剂和第二药剂的联合治疗
WO2025015951A1 (zh) * 2023-07-17 2025-01-23 上海枢境生物科技有限公司 双环[5,6]咪唑嘧啶酮类衍生物、其制备方法和应用
WO2025217646A1 (en) * 2024-04-12 2025-10-16 Scineuro Therapeutics Inc. Method of treating neurodegenerative and ocular neovascular diseases

Family Cites Families (16)

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Publication number Priority date Publication date Assignee Title
GB0127143D0 (en) * 2001-11-10 2002-01-02 Smithkline Beecham Novel compounds
WO2004014923A1 (en) * 2002-08-13 2004-02-19 Warner-Lambert Company Llc Pyrimidinone fused bicyclic metalloproteinase inhibitors
GB0320522D0 (en) 2003-09-02 2003-10-01 Glaxo Group Ltd Formulation
WO2009147476A1 (en) 2008-06-02 2009-12-10 Matrix Laboratories Ltd. Novel pde inhibitors, pharmaceutical compositions containing them and processes for their preparation
JP2013537203A (ja) * 2010-09-20 2013-09-30 グラクソ グループ リミテッド 三環式化合物、製造方法、およびそれらの使用
ES2847883T3 (es) * 2010-12-17 2021-08-04 Glaxo Group Ltd Uso de inhibidores de LP-PLA2 en el tratamiento y prevención de enfermedades oculares
CN103842362B (zh) * 2011-05-09 2017-05-24 爱普制药有限责任公司 用于治疗阿尔茨海默氏病的组合物和方法
CN103827118B (zh) * 2011-07-27 2016-03-09 葛兰素集团有限公司 双环嘧啶酮化合物
AR087309A1 (es) * 2011-07-27 2014-03-12 Glaxo Group Ltd Compuesto heterociclico de anillos condensados sustituido, composicion farmaceutica que lo comprende y su uso para la fabricacion de un medicamento para el tratamiento de enfermedades neurogenerativas y aterosclerosis
CA2842965A1 (en) * 2011-07-27 2013-01-31 Glaxo Group Limited 2,3-dihydroimidazo[1,2-c] pyrimidin-5(1h)-one compounds use as lp-pla2 inhibitors
CN104024249A (zh) 2011-10-17 2014-09-03 埃南塔制药公司 丙型肝炎病毒抑制剂
JP6065786B2 (ja) 2012-09-14 2017-01-25 信越化学工業株式会社 化学増幅レジスト材料及びパターン形成方法
MX2015009633A (es) * 2013-01-25 2015-11-30 Glaxosmithkline Ip Dev Ltd Inhibidores de fosfolipasa a2 asociada con lipoproteinas basados en 2,3-dihidroimidazol[1,2-c] pirimidin-5(1h)-ona.
EP2948456A4 (en) 2013-01-25 2016-09-14 Glaxosmithkline Ip Dev Ltd BICYCLIC PYRIMIDONE COMPOUNDS AS LP-PLA2 INHIBITORS
CN103927116A (zh) * 2014-03-18 2014-07-16 兴唐通信科技有限公司 基于触屏设备的手势输入汉字的键盘和方法
AR101261A1 (es) * 2014-07-22 2016-12-07 Glaxosmithkline Ip Dev Ltd Compuesto de tetrahidropirrolo[1,2:3,4]imidazo[1,2-c]pirimidin-1(6h)-ona y composición farmacéutica que lo comprende

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