JP6306053B2 - 2,3−ジヒドロイミダゾール[1,2−c]ピリミジン−5(1H)−オンに基づくリポタンパク質関連ホスホリパーゼA2(Lp−PLA2)阻害剤 - Google Patents
2,3−ジヒドロイミダゾール[1,2−c]ピリミジン−5(1H)−オンに基づくリポタンパク質関連ホスホリパーゼA2(Lp−PLA2)阻害剤 Download PDFInfo
- Publication number
- JP6306053B2 JP6306053B2 JP2015554138A JP2015554138A JP6306053B2 JP 6306053 B2 JP6306053 B2 JP 6306053B2 JP 2015554138 A JP2015554138 A JP 2015554138A JP 2015554138 A JP2015554138 A JP 2015554138A JP 6306053 B2 JP6306053 B2 JP 6306053B2
- Authority
- JP
- Japan
- Prior art keywords
- oxy
- dihydroimidazo
- pyrimidin
- esi
- retention time
- 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.)
- Expired - Fee Related
Links
- 0 CC(*)(C(*)(*)*)Nc1nc(Cl)nc(Cl)c1 Chemical compound CC(*)(C(*)(*)*)Nc1nc(Cl)nc(Cl)c1 0.000 description 15
- JAHVMNLMQSLVNQ-UHFFFAOYSA-N CC(CO)N(C)C(N1)=CC(Cl)=NC1=O Chemical compound CC(CO)N(C)C(N1)=CC(Cl)=NC1=O JAHVMNLMQSLVNQ-UHFFFAOYSA-N 0.000 description 2
- BBWXYZPXQLFFNE-UHFFFAOYSA-N CC(C)(CC12)N(C)C1=CC(OCCC1CCCC1)=NC2=O Chemical compound CC(C)(CC12)N(C)C1=CC(OCCC1CCCC1)=NC2=O BBWXYZPXQLFFNE-UHFFFAOYSA-N 0.000 description 1
- GRSRUOZGFVEQJU-UHFFFAOYSA-N CC(C)(CN12)N(C)C1=CC(OCC(C=C(C1Oc3cncc(Cl)c3)F)=CC1F)=NC2=O Chemical compound CC(C)(CN12)N(C)C1=CC(OCC(C=C(C1Oc3cncc(Cl)c3)F)=CC1F)=NC2=O GRSRUOZGFVEQJU-UHFFFAOYSA-N 0.000 description 1
- WQHMNFAOWSYMMI-UHFFFAOYSA-N CC(C)(CN12)N(C)C1=CC(OCc(cc1)cc(C(F)(F)F)c1F)=NC2=O Chemical compound CC(C)(CN12)N(C)C1=CC(OCc(cc1)cc(C(F)(F)F)c1F)=NC2=O WQHMNFAOWSYMMI-UHFFFAOYSA-N 0.000 description 1
- GNPLFGPCVRBTGK-UHFFFAOYSA-N CC(C)N(C(C)(C)CN12)C1=CC(OCc(cccc1F)c1F)=NC2=O Chemical compound CC(C)N(C(C)(C)CN12)C1=CC(OCc(cccc1F)c1F)=NC2=O GNPLFGPCVRBTGK-UHFFFAOYSA-N 0.000 description 1
- HWETYUFGGOHKCA-LURJTMIESA-N CCN([C@@H](C)CN12)C1=CC(Cl)=NC2=O Chemical compound CCN([C@@H](C)CN12)C1=CC(Cl)=NC2=O HWETYUFGGOHKCA-LURJTMIESA-N 0.000 description 1
- IBVIZIVOVLRMQP-VIFPVBQESA-N C[C@@H](CN12)N(C)C1=CC(OCc(cc1F)ccc1F)=NC2=O Chemical compound C[C@@H](CN12)N(C)C1=CC(OCc(cc1F)ccc1F)=NC2=O IBVIZIVOVLRMQP-VIFPVBQESA-N 0.000 description 1
- PYYIRLBSHVDFMO-SCSAIBSYSA-N C[C@H](CN12)NC1=CC(Cl)=NC2=O Chemical compound C[C@H](CN12)NC1=CC(Cl)=NC2=O PYYIRLBSHVDFMO-SCSAIBSYSA-N 0.000 description 1
- CISBGUWMXXOYSV-SCSAIBSYSA-N C[C@H](CO)Nc1nc(Cl)nc(Cl)c1 Chemical compound C[C@H](CO)Nc1nc(Cl)nc(Cl)c1 CISBGUWMXXOYSV-SCSAIBSYSA-N 0.000 description 1
- INOCZFXHGQXFAL-UHFFFAOYSA-N O=Cc(cc1)cc(F)c1Oc(cn1)ccc1F Chemical compound O=Cc(cc1)cc(F)c1Oc(cn1)ccc1F INOCZFXHGQXFAL-UHFFFAOYSA-N 0.000 description 1
- JIQOINAUAHCPOM-UHFFFAOYSA-N O=Cc(cc1F)ccc1Oc1cncc(C(F)(F)F)c1 Chemical compound O=Cc(cc1F)ccc1Oc1cncc(C(F)(F)F)c1 JIQOINAUAHCPOM-UHFFFAOYSA-N 0.000 description 1
- LDAFTDZWNFRXGG-UHFFFAOYSA-N OC1CN=C(C(F)(F)F)NC1 Chemical compound OC1CN=C(C(F)(F)F)NC1 LDAFTDZWNFRXGG-UHFFFAOYSA-N 0.000 description 1
- YENXWOZBZJDKNJ-UHFFFAOYSA-N OCc(cc1)cc(F)c1Oc(cc1)cnc1Cl Chemical compound OCc(cc1)cc(F)c1Oc(cc1)cnc1Cl YENXWOZBZJDKNJ-UHFFFAOYSA-N 0.000 description 1
- OYQQBKFKXHCTNG-UHFFFAOYSA-N OCc(cc1)cc(F)c1Oc1cc(F)ncc1 Chemical compound OCc(cc1)cc(F)c1Oc1cc(F)ncc1 OYQQBKFKXHCTNG-UHFFFAOYSA-N 0.000 description 1
- QPAXXIOBBIIATH-UHFFFAOYSA-N Oc1cnc(C(F)(F)F)nc1 Chemical compound Oc1cnc(C(F)(F)F)nc1 QPAXXIOBBIIATH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Epidemiology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2013070976 | 2013-01-25 | ||
| CNPCT/CN2013/070976 | 2013-01-25 | ||
| CN2013001556 | 2013-12-12 | ||
| CNPCT/CN2013/001556 | 2013-12-21 | ||
| PCT/EP2014/051286 WO2014114694A1 (en) | 2013-01-25 | 2014-01-23 | 2,3-dihydroimidazol[1,2-c]pyrimidin-5(1h)-one based lipoprotein-associated phospholipase a2 (lp-pla2) inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016505058A JP2016505058A (ja) | 2016-02-18 |
| JP2016505058A5 JP2016505058A5 (enExample) | 2017-02-23 |
| JP6306053B2 true JP6306053B2 (ja) | 2018-04-04 |
Family
ID=50002724
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015554138A Expired - Fee Related JP6306053B2 (ja) | 2013-01-25 | 2014-01-23 | 2,3−ジヒドロイミダゾール[1,2−c]ピリミジン−5(1H)−オンに基づくリポタンパク質関連ホスホリパーゼA2(Lp−PLA2)阻害剤 |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US9708330B2 (enExample) |
| EP (1) | EP2948452B1 (enExample) |
| JP (1) | JP6306053B2 (enExample) |
| KR (1) | KR20150108897A (enExample) |
| CN (1) | CN105008368B (enExample) |
| AU (1) | AU2014209949B2 (enExample) |
| BR (1) | BR112015017759B1 (enExample) |
| CA (1) | CA2899091A1 (enExample) |
| CL (1) | CL2015002060A1 (enExample) |
| CR (1) | CR20150390A (enExample) |
| EA (1) | EA025885B1 (enExample) |
| ES (1) | ES2642762T3 (enExample) |
| HK (1) | HK1216425A1 (enExample) |
| IL (1) | IL240046A0 (enExample) |
| MA (1) | MA38284B1 (enExample) |
| MX (1) | MX2015009633A (enExample) |
| PE (1) | PE20151251A1 (enExample) |
| PH (1) | PH12015501586A1 (enExample) |
| SG (1) | SG11201505520WA (enExample) |
| TW (1) | TW201443054A (enExample) |
| UY (1) | UY35276A (enExample) |
| WO (1) | WO2014114694A1 (enExample) |
| ZA (1) | ZA201505025B (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014114694A1 (en) | 2013-01-25 | 2014-07-31 | Glaxosmithkline Intellectual Property Development Limited | 2,3-dihydroimidazol[1,2-c]pyrimidin-5(1h)-one based lipoprotein-associated phospholipase a2 (lp-pla2) inhibitors |
| 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 |
| 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 |
| EP3172211B1 (en) | 2014-07-22 | 2019-07-03 | GlaxoSmithKline Intellectual Property Development Limited | Tricyclic imidazo-pyrimidinone derivatives for the treatment of diseases mediated by lp-pla2 |
| CN104892459A (zh) * | 2015-06-16 | 2015-09-09 | 苏州明锐医药科技有限公司 | 利奥西呱中间体及其制备方法 |
| 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 |
| CN114805389B (zh) * | 2019-11-09 | 2023-08-29 | 上海赛默罗生物科技有限公司 | 三环二氢咪唑并嘧啶酮衍生物、其制备方法、药物组合物和用途 |
| 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 |
| 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 |
| CN118221687B (zh) | 2023-07-17 | 2024-12-31 | 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 |
| CN116925023B (zh) * | 2023-07-18 | 2025-11-21 | 江苏桐孚高新材料有限公司 | 2-全氟烷基-4h-吡喃-4-酮衍生物的改进合成方法 |
Family Cites Families (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1993018035A1 (en) | 1992-03-04 | 1993-09-16 | Abbott Laboratories | Angiotensin ii receptor antagonists |
| GB9421816D0 (en) | 1994-10-29 | 1994-12-14 | Smithkline Beecham Plc | Novel compounds |
| WO1996019451A1 (en) | 1994-12-22 | 1996-06-27 | Smithkline Beecham Plc | Substituted azetidin-2-ones for treatment of atherosclerosis |
| 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. |
| HUP9901153A3 (en) | 1995-07-01 | 1999-11-29 | Smithkline Beecham Plc | Azetidinone derivatives for the treatment of atherosclerosis, their production and pharmaceutical compositions containing them |
| WO1997012963A2 (en) | 1995-09-29 | 1997-04-10 | Smithkline Beecham Plc | A paf-acetylhydrolase and use in therapy |
| EP0869943A1 (en) | 1995-12-08 | 1998-10-14 | Smithkline Beecham Plc | Monocyclic beta-lactame derivatives for treatment of atherosclerosis |
| EP0865429A1 (en) | 1995-12-08 | 1998-09-23 | Smithkline Beecham Plc | Azetidinone compounds for the treatment of atherosclerosis |
| CZ341098A3 (cs) | 1996-04-26 | 1999-03-17 | Smithkline Beecham Plc | Azetidinonové deriváty pro ošetřování aterosklerózy |
| GB9608649D0 (en) | 1996-04-26 | 1996-07-03 | Smithkline Beecham Plc | Novel compounds |
| GB9626615D0 (en) | 1996-12-20 | 1997-02-05 | Symphar Sa | 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 |
| 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 |
| DE60042286D1 (de) | 1999-05-01 | 2009-07-09 | 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 |
| DE60139429D1 (de) | 2000-02-16 | 2009-09-10 | Smithkline Beecham Plc | Pyrimidin-5-Onderivate als LDL-PLA2 Inhibitoren |
| GB0024807D0 (en) | 2000-10-10 | 2000-11-22 | Smithkline Beecham Plc | Novel compounds |
| GB0024808D0 (en) | 2000-10-10 | 2000-11-22 | Smithkline Beecham Plc | Novel compounds |
| GB0119793D0 (en) | 2001-08-14 | 2001-10-03 | Smithkline Beecham Plc | Novel compounds |
| GB0119795D0 (en) | 2001-08-14 | 2001-10-03 | Smithkline Beecham Plc | Novel process |
| GB0127143D0 (en) * | 2001-11-10 | 2002-01-02 | Smithkline Beecham | Novel compounds |
| GB0127141D0 (en) | 2001-11-10 | 2002-01-02 | Smithkline Beecham Plc | Novel compounds |
| GB0127139D0 (en) | 2001-11-10 | 2002-01-02 | Smithkline Beecham | Novel compounds |
| GB0127140D0 (en) | 2001-11-10 | 2002-01-02 | Smithkline Beecham | Novel compounds |
| GB0208280D0 (en) | 2002-04-10 | 2002-05-22 | Glaxo Group Ltd | Novel compounds |
| GB0208279D0 (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 |
| DE102004061008A1 (de) | 2004-12-18 | 2006-06-22 | Bayer Healthcare Ag | 3-Arylalkyl- und 3-Heteroarylalkyl-substituierte 1,2,4-Triazin-5(2H)-one |
| DE102004061009A1 (de) | 2004-12-18 | 2006-06-22 | Bayer Healthcare Ag | Substituierte 1,2,4-Triazin-5(2H)-one |
| US20080090852A1 (en) | 2006-10-13 | 2008-04-17 | Colin Andrew Leach | Bicyclic Heteroaromatic Compounds |
| US7705005B2 (en) | 2006-10-13 | 2010-04-27 | Glaxo Group Limited | Bicyclic heteroaromatic compounds |
| WO2008048867A2 (en) | 2006-10-13 | 2008-04-24 | Glaxo Group Limited | Bicyclic heteroaromatic compounds |
| US20080090851A1 (en) | 2006-10-13 | 2008-04-17 | Colin Andrew Leach | Bicyclic Heteroaromatic Compounds |
| US8338437B2 (en) | 2007-02-28 | 2012-12-25 | Methylgene Inc. | Amines as small molecule inhibitors |
| US20080279846A1 (en) | 2007-05-11 | 2008-11-13 | Thomas Jefferson University | Methods of treatment and prevention of neurodegenerative diseases and disorders |
| US9029383B2 (en) | 2007-05-11 | 2015-05-12 | The Trustees Of The University Of Pennsylvania | Methods of treatment of skin ulcers |
| US8962633B2 (en) | 2007-05-11 | 2015-02-24 | Thomas Jefferson University | Methods of treatment and prevention of metabolic bone diseases and disorders |
| JP2011088847A (ja) | 2009-10-21 | 2011-05-06 | Takeda Chem Ind Ltd | 三環性化合物およびその用途 |
| EP2619203A4 (en) * | 2010-09-20 | 2014-04-16 | Glaxo Group Ltd | TRICYCLIC COMPOUNDS, PROCESS FOR THEIR PREPARATION AND APPLICATIONS THEREOF |
| WO2012075917A1 (en) * | 2010-12-06 | 2012-06-14 | Glaxo Group Limited | Compounds |
| EP2651403B1 (en) | 2010-12-17 | 2020-12-02 | Glaxo Group Limited | Use of lp-pla2 inhibitors in the treatment and prevention of eye diseases |
| EP2739627A4 (en) * | 2011-07-27 | 2015-01-21 | Glaxo Group Ltd | 2,3-DIHYDROIMIDAZO- [1,2-C-] PYRIMIDIN-5 (1H) -ONE COMPOUNDS AS LP-PLA² INHIBITORS |
| WO2014114694A1 (en) | 2013-01-25 | 2014-07-31 | Glaxosmithkline Intellectual Property Development Limited | 2,3-dihydroimidazol[1,2-c]pyrimidin-5(1h)-one based lipoprotein-associated phospholipase a2 (lp-pla2) inhibitors |
-
2014
- 2014-01-23 WO PCT/EP2014/051286 patent/WO2014114694A1/en not_active Ceased
- 2014-01-23 PE PE2015001537A patent/PE20151251A1/es not_active Application Discontinuation
- 2014-01-23 CN CN201480013675.8A patent/CN105008368B/zh not_active Expired - Fee Related
- 2014-01-23 ES ES14701355.1T patent/ES2642762T3/es active Active
- 2014-01-23 EA EA201591379A patent/EA025885B1/ru not_active IP Right Cessation
- 2014-01-23 HK HK16104389.3A patent/HK1216425A1/zh unknown
- 2014-01-23 MA MA38284A patent/MA38284B1/fr unknown
- 2014-01-23 US US14/761,636 patent/US9708330B2/en not_active Expired - Fee Related
- 2014-01-23 TW TW103102388A patent/TW201443054A/zh unknown
- 2014-01-23 BR BR112015017759-0A patent/BR112015017759B1/pt not_active IP Right Cessation
- 2014-01-23 UY UY0001035276A patent/UY35276A/es not_active Application Discontinuation
- 2014-01-23 CA CA2899091A patent/CA2899091A1/en not_active Abandoned
- 2014-01-23 KR KR1020157022396A patent/KR20150108897A/ko not_active Ceased
- 2014-01-23 SG SG11201505520WA patent/SG11201505520WA/en unknown
- 2014-01-23 JP JP2015554138A patent/JP6306053B2/ja not_active Expired - Fee Related
- 2014-01-23 AU AU2014209949A patent/AU2014209949B2/en not_active Ceased
- 2014-01-23 EP EP14701355.1A patent/EP2948452B1/en active Active
- 2014-01-23 MX MX2015009633A patent/MX2015009633A/es unknown
-
2015
- 2015-07-13 ZA ZA2015/05025A patent/ZA201505025B/en unknown
- 2015-07-20 IL IL240046A patent/IL240046A0/en unknown
- 2015-07-20 PH PH12015501586A patent/PH12015501586A1/en unknown
- 2015-07-23 CL CL2015002060A patent/CL2015002060A1/es unknown
- 2015-07-24 CR CR20150390A patent/CR20150390A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2948452A1 (en) | 2015-12-02 |
| CR20150390A (es) | 2015-10-19 |
| CN105008368B (zh) | 2017-02-01 |
| US9708330B2 (en) | 2017-07-18 |
| WO2014114694A1 (en) | 2014-07-31 |
| CA2899091A1 (en) | 2014-07-31 |
| PE20151251A1 (es) | 2015-09-10 |
| PH12015501586A1 (en) | 2015-10-05 |
| IL240046A0 (en) | 2015-08-31 |
| EP2948452B1 (en) | 2017-08-09 |
| CN105008368A (zh) | 2015-10-28 |
| CL2015002060A1 (es) | 2015-11-27 |
| EA201591379A1 (ru) | 2016-01-29 |
| US20150361082A1 (en) | 2015-12-17 |
| ZA201505025B (en) | 2017-08-30 |
| ES2642762T3 (es) | 2017-11-20 |
| HK1216425A1 (zh) | 2016-11-11 |
| MX2015009633A (es) | 2015-11-30 |
| SG11201505520WA (en) | 2015-08-28 |
| JP2016505058A (ja) | 2016-02-18 |
| KR20150108897A (ko) | 2015-09-30 |
| AU2014209949B2 (en) | 2016-09-08 |
| EA025885B1 (ru) | 2017-02-28 |
| TW201443054A (zh) | 2014-11-16 |
| UY35276A (es) | 2014-08-29 |
| AU2014209949A1 (en) | 2015-07-30 |
| MA38284B1 (fr) | 2018-05-31 |
| BR112015017759A2 (pt) | 2017-07-11 |
| MA38284A1 (fr) | 2017-12-29 |
| BR112015017759B1 (pt) | 2022-05-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US9708330B2 (en) | 2,3-dihydroimidazol[1,2-C]pyrimidin-5(1-H)-one based ipoprotein-associated phospholipase A2 (Lp-PLA2) inhibitors | |
| AU2012288865B2 (en) | Bicyclic pyrimidone compounds | |
| AU2014210260B2 (en) | Bicyclic pyrimidone compounds as inhibitors of Lp-PLA2 | |
| JP6625603B2 (ja) | 化合物 | |
| JP2014521611A (ja) | Lp−PLA2阻害剤としての2,3−ジヒドロイミダゾ[1,2−c]ピリミジン−5(1H)−オン化合物の使用 | |
| AU2014210259B2 (en) | Compounds | |
| US9051325B2 (en) | Bicyclic [5,6] imidazo pyrimodone compounds for use in the treatment of diseases or conditions mediated by Lp-PLA2 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RD03 | Notification of appointment of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7423 Effective date: 20170106 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20170120 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20170120 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20171114 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20171116 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20180130 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20180209 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20180307 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 6306053 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| LAPS | Cancellation because of no payment of annual fees |