MA38284B1 - Inhibiteurs de la phospholipase associée aux lipoprotéines a2 (lp-pla2) à base de 2,3-dihydro-imidazol[1,2-c]pyrimidin-5(1 h)-one - Google Patents
Inhibiteurs de la phospholipase associée aux lipoprotéines a2 (lp-pla2) à base de 2,3-dihydro-imidazol[1,2-c]pyrimidin-5(1 h)-oneInfo
- Publication number
- MA38284B1 MA38284B1 MA38284A MA38284A MA38284B1 MA 38284 B1 MA38284 B1 MA 38284B1 MA 38284 A MA38284 A MA 38284A MA 38284 A MA38284 A MA 38284A MA 38284 B1 MA38284 B1 MA 38284B1
- Authority
- MA
- Morocco
- Prior art keywords
- dihydroimidazol
- pla2
- lipoprotein
- pyrimidin
- inhibitors
- Prior art date
Links
- LWTIGYSPAXKMDG-UHFFFAOYSA-N 2,3-dihydro-1h-imidazole Chemical compound C1NC=CN1 LWTIGYSPAXKMDG-UHFFFAOYSA-N 0.000 title 1
- ZIIUUSVHCHPIQD-UHFFFAOYSA-N 2,4,6-trimethyl-N-[3-(trifluoromethyl)phenyl]benzenesulfonamide Chemical compound CC1=CC(C)=CC(C)=C1S(=O)(=O)NC1=CC=CC(C(F)(F)F)=C1 ZIIUUSVHCHPIQD-UHFFFAOYSA-N 0.000 title 1
- 102000015439 Phospholipases Human genes 0.000 title 1
- 108010064785 Phospholipases Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 208000024827 Alzheimer disease Diseases 0.000 abstract 1
- 201000001320 Atherosclerosis Diseases 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 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)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (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)
Abstract
La présente invention concerne de nouveaux composés qui inhibent l'activité de la lp-pla2, des procédés pour leur préparation, des compositions les contenant et leur utilisation pour le traitement de maladies associées à l'activité de la lp-pla2, par exemple l'athérosclérose et la maladie d'alzheimer.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2013070976 | 2013-01-25 | ||
| CN2013001556 | 2013-12-12 | ||
| PCT/EP2014/051286 WO2014114694A1 (fr) | 2013-01-25 | 2014-01-23 | Inhibiteurs de la phospholipase associée aux lipoprotéines a2 (lp-pla2) à base de 2,3-dihydro-imidazol[1,2-c]pyrimidin-5(1 h)-one |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MA38284A1 MA38284A1 (fr) | 2017-12-29 |
| MA38284B1 true MA38284B1 (fr) | 2018-05-31 |
Family
ID=50002724
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA38284A MA38284B1 (fr) | 2013-01-25 | 2014-01-23 | Inhibiteurs de la phospholipase associée aux lipoprotéines a2 (lp-pla2) à base de 2,3-dihydro-imidazol[1,2-c]pyrimidin-5(1 h)-one |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US9708330B2 (fr) |
| EP (1) | EP2948452B1 (fr) |
| JP (1) | JP6306053B2 (fr) |
| KR (1) | KR20150108897A (fr) |
| CN (1) | CN105008368B (fr) |
| AU (1) | AU2014209949B2 (fr) |
| BR (1) | BR112015017759B1 (fr) |
| CA (1) | CA2899091A1 (fr) |
| CL (1) | CL2015002060A1 (fr) |
| CR (1) | CR20150390A (fr) |
| EA (1) | EA025885B1 (fr) |
| ES (1) | ES2642762T3 (fr) |
| HK (1) | HK1216425A1 (fr) |
| IL (1) | IL240046A0 (fr) |
| MA (1) | MA38284B1 (fr) |
| MX (1) | MX2015009633A (fr) |
| PE (1) | PE20151251A1 (fr) |
| PH (1) | PH12015501586A1 (fr) |
| SG (1) | SG11201505520WA (fr) |
| TW (1) | TW201443054A (fr) |
| UY (1) | UY35276A (fr) |
| WO (1) | WO2014114694A1 (fr) |
| ZA (1) | ZA201505025B (fr) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2948452B1 (fr) | 2013-01-25 | 2017-08-09 | GlaxoSmithKline Intellectual Property Development Limited | Inhibiteurs de la phospholipase associée aux lipoprotéines a2 (lp-pla2) à base de 2,3-dihydro-imidazol[1,2-c]pyrimidin-5(1 h)-one |
| CN106536521B (zh) * | 2014-07-22 | 2018-08-03 | 葛兰素史密斯克莱知识产权发展有限公司 | 化合物 |
| WO2016012916A1 (fr) * | 2014-07-22 | 2016-01-28 | Glaxosmithkline Intellectual Property Development Limited | Dérivés 1,2,3,5-tétrahydro-imidazo [1,2-c]pyrimidine utiles pour le traitement de maladies et de troubles médiés par la lp-pla2 |
| WO2016012917A1 (fr) * | 2014-07-22 | 2016-01-28 | Glaxosmithkline Intellectual Property Development Limited | Dérivés 1,2,3,5-tétrahydro-imidazo [1,2-c]pyrimidine utiles pour le traitement de maladies et de troubles médiés par la 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 |
| CN112778331B (zh) * | 2019-11-09 | 2022-07-05 | 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 |
| EP4565587A1 (fr) * | 2022-08-04 | 2025-06-11 | 4B Technologies (Beijing) Co., Limited | Composés de dihydroimidazo-pyrimidinone utiles en tant qu'inhibiteurs de lp-pla2 et leur utilisation |
| TWI896037B (zh) | 2023-07-17 | 2025-09-01 | 大陸商上海樞境生物科技有限公司 | 雙環[5,6]咪唑嘧啶酮類衍生物、其製備方法和應用 |
| 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 |
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| WO1993018035A1 (fr) | 1992-03-04 | 1993-09-16 | Abbott Laboratories | Antagonistes des recepteurs de l'angiotensine ii |
| GB9421816D0 (en) | 1994-10-29 | 1994-12-14 | Smithkline Beecham Plc | Novel compounds |
| CN1175246A (zh) | 1994-12-22 | 1998-03-04 | 史密丝克莱恩比彻姆有限公司 | 用于治疗动脉粥样硬化的取代的氮杂环丁-2-酮 |
| 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. |
| JP2002515852A (ja) | 1995-07-01 | 2002-05-28 | 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誘導体 |
| EP0859834A2 (fr) | 1995-09-29 | 1998-08-26 | Smithkline Beecham Plc | Paf-acetylhydrolase paf et son utilisation en therapie |
| WO1997021675A1 (fr) | 1995-12-08 | 1997-06-19 | Smithkline Beecham Plc | Derives de beta-lactame monocycliques utilises dans le traitement de l'atherosclerose |
| WO1997021676A1 (fr) | 1995-12-08 | 1997-06-19 | Smithkline Beecham Plc | Composes azetidinone destines au traitement de l'atherosclerose |
| NZ332476A (en) | 1996-04-26 | 2000-06-23 | Smithkline Beecham Plc | substituted 4-(carboxybenzylsulphinyl)-2-oxo-azetidine derivatives |
| GB9608649D0 (en) | 1996-04-26 | 1996-07-03 | Smithkline Beecham Plc | 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 |
| GB9626536D0 (en) | 1996-12-20 | 1997-02-05 | Symphar Sa | Novel compounds |
| WO1999024420A1 (fr) | 1997-11-06 | 1999-05-20 | Smithkline Beecham Plc | Composes de pyrimidinone et compositions pharmaceutiques les renfermant |
| US6559155B1 (en) | 1998-08-21 | 2003-05-06 | Smithkline Beecham P.L.C. | Pyrimidinone derivatives for the treatment of atherosclerosis |
| GB9910079D0 (en) | 1999-05-01 | 1999-06-30 | Smithkline Beecham Plc | Novel compounds |
| HUP0201122A3 (en) | 1999-05-01 | 2003-11-28 | Smithkline Beecham Plc | Pyrimidinone compounds, process for their preparation and pharmaceutical compositions containing them |
| 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 |
| EP1686119B1 (fr) | 2000-02-16 | 2009-07-29 | Smithkline Beecham Plc | Dérivés de Pyrimidine-5-one comme inhibiteurs LDL-PLA2 |
| GB0024808D0 (en) | 2000-10-10 | 2000-11-22 | Smithkline Beecham Plc | Novel compounds |
| GB0024807D0 (en) | 2000-10-10 | 2000-11-22 | Smithkline Beecham Plc | Novel compounds |
| 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 |
| GB0127139D0 (en) | 2001-11-10 | 2002-01-02 | Smithkline Beecham | Novel compounds |
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| CA2530816A1 (fr) | 2003-07-02 | 2005-01-13 | Bayer Healthcare Ag | 1,2,4-triazino-5(2h)-ones a substitution amide destinees au traitement de maladies inflammatoires chroniques |
| 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 |
| US20080090852A1 (en) | 2006-10-13 | 2008-04-17 | Colin Andrew Leach | Bicyclic Heteroaromatic Compounds |
| WO2008048867A2 (fr) * | 2006-10-13 | 2008-04-24 | Glaxo Group Limited | Composés hétoroaromatiques bicycliques |
| 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 |
| US8338437B2 (en) | 2007-02-28 | 2012-12-25 | Methylgene Inc. | Amines as small molecule inhibitors |
| AU2008251467B2 (en) | 2007-05-11 | 2014-07-31 | The Trustees Of The University Of Pennsylvania | Methods of treatment of skin ulcers |
| US20080279846A1 (en) | 2007-05-11 | 2008-11-13 | Thomas Jefferson University | Methods of treatment and prevention of neurodegenerative diseases and disorders |
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| 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 |
| US8871928B2 (en) * | 2010-09-20 | 2014-10-28 | Glaxo Group Limited | Tricyclic compounds, preparation methods, and their uses |
| JP2013544854A (ja) * | 2010-12-06 | 2013-12-19 | グラクソ グループ リミテッド | 化合物 |
| EP2651403B1 (fr) | 2010-12-17 | 2020-12-02 | Glaxo Group Limited | Procédés de traitement et de prévention de maladies oculaires |
| EP2739627A4 (fr) * | 2011-07-27 | 2015-01-21 | Glaxo Group Ltd | Composés 2,3-dihydroimidazo[1,2-c]pyrimidin-5(1h)-one et utilisation en tant qu'inhibiteurs de lp-pla2 |
| CN103827116B (zh) * | 2011-07-27 | 2016-08-31 | 葛兰素集团有限公司 | 用作LP-PLA2抑制剂的2,3-二氢咪唑并[1,2-c]嘧啶-5(1H)-酮化合物 |
| EP2948452B1 (fr) | 2013-01-25 | 2017-08-09 | GlaxoSmithKline Intellectual Property Development Limited | Inhibiteurs de la phospholipase associée aux lipoprotéines a2 (lp-pla2) à base de 2,3-dihydro-imidazol[1,2-c]pyrimidin-5(1 h)-one |
-
2014
- 2014-01-23 EP EP14701355.1A patent/EP2948452B1/fr active Active
- 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 AU AU2014209949A patent/AU2014209949B2/en not_active Ceased
- 2014-01-23 CN CN201480013675.8A patent/CN105008368B/zh not_active Expired - Fee Related
- 2014-01-23 BR BR112015017759-0A patent/BR112015017759B1/pt not_active IP Right Cessation
- 2014-01-23 SG SG11201505520WA patent/SG11201505520WA/en 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 CA CA2899091A patent/CA2899091A1/fr not_active Abandoned
- 2014-01-23 JP JP2015554138A patent/JP6306053B2/ja not_active Expired - Fee Related
- 2014-01-23 UY UY0001035276A patent/UY35276A/es not_active Application Discontinuation
- 2014-01-23 KR KR1020157022396A patent/KR20150108897A/ko not_active Ceased
- 2014-01-23 TW TW103102388A patent/TW201443054A/zh unknown
- 2014-01-23 MX MX2015009633A patent/MX2015009633A/es unknown
- 2014-01-23 PE PE2015001537A patent/PE20151251A1/es not_active Application Discontinuation
- 2014-01-23 WO PCT/EP2014/051286 patent/WO2014114694A1/fr not_active Ceased
- 2014-01-23 HK HK16104389.3A patent/HK1216425A1/zh 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 |
|---|---|
| BR112015017759B1 (pt) | 2022-05-24 |
| EP2948452A1 (fr) | 2015-12-02 |
| JP2016505058A (ja) | 2016-02-18 |
| PH12015501586A1 (en) | 2015-10-05 |
| CN105008368A (zh) | 2015-10-28 |
| IL240046A0 (en) | 2015-08-31 |
| WO2014114694A1 (fr) | 2014-07-31 |
| TW201443054A (zh) | 2014-11-16 |
| MX2015009633A (es) | 2015-11-30 |
| US9708330B2 (en) | 2017-07-18 |
| EA025885B1 (ru) | 2017-02-28 |
| EP2948452B1 (fr) | 2017-08-09 |
| ZA201505025B (en) | 2017-08-30 |
| AU2014209949B2 (en) | 2016-09-08 |
| PE20151251A1 (es) | 2015-09-10 |
| EA201591379A1 (ru) | 2016-01-29 |
| MA38284A1 (fr) | 2017-12-29 |
| BR112015017759A2 (pt) | 2017-07-11 |
| HK1216425A1 (zh) | 2016-11-11 |
| SG11201505520WA (en) | 2015-08-28 |
| CA2899091A1 (fr) | 2014-07-31 |
| KR20150108897A (ko) | 2015-09-30 |
| JP6306053B2 (ja) | 2018-04-04 |
| CL2015002060A1 (es) | 2015-11-27 |
| UY35276A (es) | 2014-08-29 |
| CR20150390A (es) | 2015-10-19 |
| CN105008368B (zh) | 2017-02-01 |
| US20150361082A1 (en) | 2015-12-17 |
| AU2014209949A1 (en) | 2015-07-30 |
| ES2642762T3 (es) | 2017-11-20 |
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| MA38473B1 (fr) | (benzyl-cyano-méthyl)-amides substitués de l'acide 2-aza-bicyclo[2.2.1]heptane-3-carboxylique utilisés comme inhibiteurs de la cathépsine c |