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
Links
- 150000001875 compounds Chemical class 0.000 claims 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 8
- 125000005843 halogen group Chemical group 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 7
- 125000001424 substituent group Chemical group 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 6
- 125000001072 heteroaryl group Chemical group 0.000 claims 5
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- 201000001320 Atherosclerosis Diseases 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000002950 monocyclic group Chemical group 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims 1
- -1 pyrimidinyl compound Chemical class 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2010079465 | 2010-12-06 | ||
| CNPCT/CN2010/079465 | 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) | US20130252963A1 (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) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8349577B2 (en) * | 2009-04-23 | 2013-01-08 | Research Foundation For Mental Hygiene, Inc. | Method for evaluating blood-neural barrier permeability |
| EP2649050A4 (en) * | 2010-12-06 | 2014-04-23 | Glaxo Group Ltd | LINKS |
| EA023796B1 (ru) * | 2010-12-06 | 2016-07-29 | Глэксо Груп Лимитед | ПИРИМИДИНОНОВЫЕ СОЕДИНЕНИЯ ДЛЯ ПРИМЕНЕНИЯ В ЛЕЧЕНИИ ЗАБОЛЕВАНИЙ ИЛИ СОСТОЯНИЙ, ОПОСРЕДОВАННЫХ Lp-PLA |
| SI2751094T1 (sl) | 2011-09-01 | 2018-10-30 | Glaxo Group Limited | Nova kristalinična oblika |
| 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 |
| AU2014210259B2 (en) * | 2013-01-25 | 2016-11-03 | Glaxosmithkline Intellectual Property Development Limited | Compounds |
| EP2764866A1 (en) | 2013-02-07 | 2014-08-13 | IP Gesellschaft für Management mbH | Inhibitors of nedd8-activating enzyme |
| EP3816155A1 (en) * | 2013-08-23 | 2021-05-05 | 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 |
| JP6596417B2 (ja) * | 2014-07-04 | 2019-10-23 | 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 |
| CN110129298B (zh) * | 2016-06-02 | 2021-08-03 | 天津科技大学 | 一种磷脂酶d突变体及其应用 |
| US11364240B2 (en) | 2017-08-15 | 2022-06-21 | Agios Pharmaceuticals, Inc. | Pyruvate kinase activators for use in treating blood disorders |
| EP4081511B1 (en) * | 2019-12-23 | 2024-07-31 | Sitryx Therapeutics Limited | Carboxy derivatives with antiinflammatory properties |
| 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 |
| EP4565587A1 (en) * | 2022-08-04 | 2025-06-11 | 4B Technologies (Beijing) Co., Limited | Dihydroimidazo-pyrimidinone compounds as lp-pla2 inhibitors and use thereof |
Family Cites Families (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9421816D0 (en) | 1994-10-29 | 1994-12-14 | Smithkline Beecham Plc | Novel compounds |
| AR002012A1 (es) | 1994-12-22 | 1998-01-07 | Smithkline Beecham Plc | Un compuesto, una composicion farmaceutica que lo comprende, su uso, metodo de tratamiento terapeutico, metodo para la preparacion del compuesto. |
| 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. |
| CZ422197A3 (cs) | 1995-07-01 | 1998-06-17 | Smithkline Beecham Plc | Azetidinonové deriváty, způsob jejich přípravy, meziprodukty tohoto postupu, farmaceutický prostředek obsahující tyto sloučeniny a použití těchto sloučenin jako léčiv |
| EP0859834A2 (en) | 1995-09-29 | 1998-08-26 | Smithkline Beecham Plc | A paf-acetylhydrolase and use in therapy |
| WO1997021676A1 (en) | 1995-12-08 | 1997-06-19 | Smithkline Beecham Plc | Azetidinone compounds for the treatment of atherosclerosis |
| WO1997021675A1 (en) | 1995-12-08 | 1997-06-19 | Smithkline Beecham Plc | Monocyclic beta-lactame derivatives for treatment of atherosclerosis |
| GB9608649D0 (en) | 1996-04-26 | 1996-07-03 | Smithkline Beecham Plc | Novel compounds |
| TR199802160T2 (xx) | 1996-04-26 | 1999-04-21 | Smithkline Beecham Plc | Ateroskleroz tedavisi i�in azetidinon t�revleri. |
| GB9626616D0 (en) | 1996-12-20 | 1997-02-05 | Symphar Sa | Novel compounds |
| GB9626536D0 (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 |
| DE69816471T2 (de) | 1997-11-06 | 2004-05-27 | Smithkline Beecham P.L.C., Brentford | Pyrimidinon verbindungen und diese enthaltende pharmazeutische zusammenstellungen |
| EP1105377B1 (en) * | 1998-08-21 | 2003-10-08 | SmithKline Beecham plc | Pyrimidinone derivatives for the treatment of atherosclerosis |
| GB9910079D0 (en) | 1999-05-01 | 1999-06-30 | Smithkline Beecham Plc | Novel compounds |
| ES2233361T3 (es) * | 1999-05-01 | 2005-06-16 | Smithkline Beecham Plc | Compuestos de piridinona. |
| 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 |
| ES2330552T3 (es) | 2000-02-16 | 2009-12-11 | Smithkline Beecham Plc | Derivados de pirimidin-5-ona como inhibidores de 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 |
| EP1351691A4 (en) * | 2000-12-12 | 2005-06-22 | Cytovia Inc | SUBSTITUTED 2-ARYL-4-ARYLAMINOPYRIMIDINES AND ANALOGUES AS ACTIVATORS OF CASPASES AND APOPTOSIS INDUCERS, AND USE THEREOF |
| GEP20053619B (en) * | 2001-04-10 | 2005-09-26 | Pfizer | Pyrazole Derivatives for Treating HIV |
| 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 |
| 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 |
| GB0127141D0 (en) | 2001-11-10 | 2002-01-02 | Smithkline Beecham Plc | Novel compounds |
| GB0127140D0 (en) | 2001-11-10 | 2002-01-02 | Smithkline Beecham | Novel compounds |
| GB0127143D0 (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 |
| WO2005003118A1 (de) | 2003-07-02 | 2005-01-13 | 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 |
| 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 |
| US20080090851A1 (en) | 2006-10-13 | 2008-04-17 | Colin Andrew Leach | Bicyclic Heteroaromatic Compounds |
| US8962633B2 (en) | 2007-05-11 | 2015-02-24 | Thomas Jefferson University | Methods of treatment and prevention of metabolic bone diseases and disorders |
| BRPI0810336A2 (pt) | 2007-05-11 | 2019-03-19 | The Trustees Of The University Of Pennsylvania | "método para tratar e/ou prevenir úlceras de pele em um indivíduo" |
| US20080279846A1 (en) | 2007-05-11 | 2008-11-13 | Thomas Jefferson University | Methods of treatment and prevention of neurodegenerative diseases and disorders |
| EA023796B1 (ru) * | 2010-12-06 | 2016-07-29 | Глэксо Груп Лимитед | ПИРИМИДИНОНОВЫЕ СОЕДИНЕНИЯ ДЛЯ ПРИМЕНЕНИЯ В ЛЕЧЕНИИ ЗАБОЛЕВАНИЙ ИЛИ СОСТОЯНИЙ, ОПОСРЕДОВАННЫХ Lp-PLA |
| EP2649050A4 (en) * | 2010-12-06 | 2014-04-23 | Glaxo Group Ltd | LINKS |
-
2011
- 2011-12-05 EA EA201390826A patent/EA023796B1/ru not_active IP Right Cessation
- 2011-12-05 EP EP11802872.9A patent/EP2649053B1/en active Active
- 2011-12-05 CA CA2820408A patent/CA2820408C/en active Active
- 2011-12-05 AU AU2011340690A patent/AU2011340690C1/en not_active Ceased
- 2011-12-05 MX MX2013006342A patent/MX2013006342A/es unknown
- 2011-12-05 JP JP2013542482A patent/JP5886310B2/ja not_active Expired - Fee Related
- 2011-12-05 BR BR112013013898-0A patent/BR112013013898B1/pt not_active IP Right Cessation
- 2011-12-05 AR ARP110104535A patent/AR084153A1/es unknown
- 2011-12-05 PH PH1/2013/501089A patent/PH12013501089A1/en unknown
- 2011-12-05 US US13/991,955 patent/US20130252963A1/en not_active Abandoned
- 2011-12-05 UY UY0001033766A patent/UY33766A/es unknown
- 2011-12-05 WO PCT/EP2011/071690 patent/WO2012076435A1/en not_active Ceased
- 2011-12-05 US US13/310,818 patent/US8637536B2/en active Active
- 2011-12-05 SG SG2013038427A patent/SG190830A1/en unknown
- 2011-12-05 ES ES11802872.9T patent/ES2559224T3/es active Active
- 2011-12-05 PE PE2013001234A patent/PE20140421A1/es not_active Application Discontinuation
- 2011-12-05 CN CN201180066903.4A patent/CN103347864B/zh not_active Expired - Fee Related
- 2011-12-05 KR KR1020137017621A patent/KR101861883B1/ko not_active Expired - Fee Related
- 2011-12-05 TW TW100144556A patent/TW201307324A/zh unknown
-
2012
- 2012-10-17 DO DO2013000130A patent/DOP2013000130A/es unknown
-
2013
- 2013-05-16 ZA ZA2013/03560A patent/ZA201303560B/en unknown
- 2013-05-20 IL IL226473A patent/IL226473A0/en unknown
- 2013-06-05 CL CL2013001604A patent/CL2013001604A1/es unknown
- 2013-06-07 CO CO13138754A patent/CO6801726A2/es active IP Right Grant
- 2013-09-06 CR CR20130264A patent/CR20130264A/es unknown
- 2013-12-19 US US14/133,720 patent/US20140113922A1/en not_active Abandoned
-
2014
- 2014-12-15 US US14/569,970 patent/US9174968B2/en not_active Expired - Fee Related