ATE510839T1 - Benzofuropyrimidinone als proteinkinase-hemmer - Google Patents
Benzofuropyrimidinone als proteinkinase-hemmerInfo
- Publication number
- ATE510839T1 ATE510839T1 AT08832770T AT08832770T ATE510839T1 AT E510839 T1 ATE510839 T1 AT E510839T1 AT 08832770 T AT08832770 T AT 08832770T AT 08832770 T AT08832770 T AT 08832770T AT E510839 T1 ATE510839 T1 AT E510839T1
- Authority
- AT
- Austria
- Prior art keywords
- benzofuropyrimidinone
- protein kinase
- kinase inhibitor
- inhibitor
- protein
- Prior art date
Links
- LPJFETZUCIPKPG-UHFFFAOYSA-N 1h-[1]benzofuro[3,2-d]pyrimidin-2-one Chemical compound C1=CC=C2C3=NC(=O)NC=C3OC2=C1 LPJFETZUCIPKPG-UHFFFAOYSA-N 0.000 title 1
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003909 protein kinase inhibitor Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US890707P | 2007-12-21 | 2007-12-21 | |
| US7097108P | 2008-03-25 | 2008-03-25 | |
| PCT/US2008/087939 WO2009086264A1 (en) | 2007-12-21 | 2008-12-22 | Benzofuropyrimidinones as protein kinase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE510839T1 true ATE510839T1 (de) | 2011-06-15 |
Family
ID=40383673
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT08832770T ATE510839T1 (de) | 2007-12-21 | 2008-12-22 | Benzofuropyrimidinone als proteinkinase-hemmer |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US20090247559A1 (de) |
| EP (1) | EP2097419B1 (de) |
| JP (1) | JP2011507908A (de) |
| KR (1) | KR20100098714A (de) |
| CN (1) | CN101965351A (de) |
| AR (1) | AR069869A1 (de) |
| AT (1) | ATE510839T1 (de) |
| AU (1) | AU2008345560A1 (de) |
| BR (1) | BRPI0821573A2 (de) |
| CA (1) | CA2712358A1 (de) |
| CL (1) | CL2008003873A1 (de) |
| CO (1) | CO6321258A2 (de) |
| EA (1) | EA019785B1 (de) |
| IL (1) | IL206416A0 (de) |
| MX (1) | MX2010006799A (de) |
| NZ (1) | NZ586936A (de) |
| PE (1) | PE20091669A1 (de) |
| TW (1) | TW200930375A (de) |
| WO (1) | WO2009086264A1 (de) |
| ZA (1) | ZA201004243B (de) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102007026341A1 (de) | 2007-06-06 | 2008-12-11 | Merck Patent Gmbh | Benzoxazolonderivate |
| DE102007032507A1 (de) | 2007-07-12 | 2009-04-02 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102007061963A1 (de) | 2007-12-21 | 2009-06-25 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102008019907A1 (de) | 2008-04-21 | 2009-10-22 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102008028905A1 (de) | 2008-06-18 | 2009-12-24 | Merck Patent Gmbh | 3-(3-Pyrimidin-2-yl-benzyl)-[1,2,4]triazolo[4,3-b]pyridazinderivate |
| CN102282155B (zh) | 2008-12-02 | 2017-06-09 | 日本波涛生命科学公司 | 磷原子修饰的核酸的合成方法 |
| SI2361250T1 (sl) | 2008-12-22 | 2013-12-31 | Merck Patent Gmbh | Nove polimorfne oblike 6-(1-metil-1h-pirazol-4-il)-2-(3-(5-(2-morfolin-4-il-etoksi)-pirimidin- 2-il)-benzil)-2h-piridazin-3-on dihidrogenfosfata in postopki za proizvodnjo le-tega |
| RU2612521C2 (ru) | 2009-07-06 | 2017-03-09 | Онтории, Инк. | Новые пролекарства нуклеиновых кислот и способы их применения |
| JP5868324B2 (ja) * | 2010-09-24 | 2016-02-24 | 株式会社Wave Life Sciences Japan | 不斉補助基 |
| CN103796657B (zh) | 2011-07-19 | 2017-07-11 | 波涛生命科学有限公司 | 合成官能化核酸的方法 |
| PL2872485T3 (pl) | 2012-07-13 | 2021-05-31 | Wave Life Sciences Ltd. | Asymetryczna grupa pomocnicza |
| CA2879066C (en) | 2012-07-13 | 2019-08-13 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant |
| KR102213609B1 (ko) | 2012-07-13 | 2021-02-08 | 웨이브 라이프 사이언시스 리미티드 | 키랄 제어 |
| CN102875558A (zh) * | 2012-11-05 | 2013-01-16 | 贵州大学 | 2-氯-4-取代-8-硝基苯并呋喃[3,2-d]嘧啶类化合物及其制备方法和用途 |
| CN103044370A (zh) * | 2012-12-28 | 2013-04-17 | 山东邹平大展新材料有限公司 | 一种5-(哌嗪-1-基)苯并呋喃-2-甲酰胺的制备方法 |
| CN104045642B (zh) * | 2013-03-14 | 2016-08-24 | 上海医药工业研究院 | 含嘧啶或吡啶的稠环化合物及其作为抗肿瘤药物的应用 |
| US10322173B2 (en) | 2014-01-15 | 2019-06-18 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant having anti-allergic activity, and anti-allergic agent |
| JPWO2015108047A1 (ja) | 2014-01-15 | 2017-03-23 | 株式会社新日本科学 | 免疫誘導活性を有するキラル核酸アジュバンド及び免疫誘導活性剤 |
| JPWO2015108048A1 (ja) | 2014-01-15 | 2017-03-23 | 株式会社新日本科学 | 抗腫瘍作用を有するキラル核酸アジュバンド及び抗腫瘍剤 |
| BR112016016400A2 (pt) | 2014-01-16 | 2017-10-03 | Wave Life Sciences Ltd | Composições de oligonucleotídeos quiralmente controlados, seu uso, sua composição farmacêutica, e métodos |
| JP6569908B2 (ja) | 2014-01-31 | 2019-09-04 | カルナバイオサイエンス株式会社 | 抗がん剤組成物 |
| CA2936886A1 (en) | 2014-02-27 | 2015-08-03 | Merck Patent Gmbh | Heterocyclic compounds as nav channel inhibitors and uses thereof |
| WO2015152319A1 (ja) * | 2014-04-02 | 2015-10-08 | 株式会社 三和化学研究所 | 5,7-無置換-ピラゾロ[1,5-a]ピリミジン-6-カルボン酸の製造方法 |
| KR101837565B1 (ko) | 2014-08-06 | 2018-03-12 | 삼성에스디아이 주식회사 | 유기 화합물, 유기 광전자 소자 및 표시 장치 |
| JP6840931B2 (ja) * | 2015-03-09 | 2021-03-10 | 東ソー株式会社 | 縮環芳香族化合物の製造方法 |
| EP3538523B1 (de) | 2016-11-08 | 2021-05-19 | Cancer Research Technology Limited | Pyrimidinonderivate als cdc7-inhibitoren |
| NL2021185B1 (en) | 2018-06-26 | 2020-01-06 | Stichting Het Nederlands Kanker Inst Antoni Van Leeuwenhoek Ziekenhuis | Combination Therapy and Use Thereof for Treating Cancer |
| AU2019350581B2 (en) | 2018-09-24 | 2025-07-10 | Carna Biosciences, Inc. | Methods of treatment of cancer comprising Cdc7 inhibitors |
| WO2020068729A1 (en) | 2018-09-25 | 2020-04-02 | Incyte Corporation | Pyrazolo[4,3-d]pyrimidine compounds as alk2 abd/or fgfr modulators |
| CN111689947B (zh) * | 2019-03-13 | 2023-07-14 | 鲁南制药集团股份有限公司 | 替加氟-l-脯氨酸共晶体及其制备方法 |
| JP2023512281A (ja) * | 2020-02-03 | 2023-03-24 | ゲイン セラピューティクス エスアー | Mps1を処置するための併用療法 |
| WO2021198191A1 (en) | 2020-03-30 | 2021-10-07 | Enyo Pharma | Quinazolinone derivatives and uses thereof for treating a cancer |
| CA3196024A1 (en) * | 2020-10-05 | 2022-04-14 | Japan Tobacco Inc. | Tetrahydrobenzofurodiazepinone compounds and pharmaceutical applications thereof |
| CN117043302A (zh) | 2021-03-18 | 2023-11-10 | 默克专利有限公司 | 用于有机电致发光器件的杂芳族化合物 |
| CN117120447A (zh) * | 2021-03-18 | 2023-11-24 | 薛定谔公司 | 环状化合物和其使用方法 |
| IL314895A (en) * | 2022-02-16 | 2024-10-01 | Duke Street Bio Ltd | Pharmaceutical compound |
| CN116731025B (zh) * | 2023-05-24 | 2025-06-24 | 曲阜师范大学 | 一种具有2-芳基苯并呋喃并[2,3-d]嘧啶酮类结构的荧光材料及其制备方法和应用 |
| CN120114459B (zh) * | 2025-05-14 | 2025-07-29 | 南京工业大学 | 苯并呋喃嘧啶酮或苯并噻吩嘧啶酮类化合物的应用 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL112248A0 (en) * | 1994-01-25 | 1995-03-30 | Warner Lambert Co | Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them |
| WO2002051849A1 (en) | 2000-12-26 | 2002-07-04 | Daiichi Pharmaceutical Co., Ltd. | Cdk4 inhibitors |
| CA2444598A1 (en) * | 2001-04-20 | 2003-10-31 | Vertex Pharmaceuticals Incorporated | Compositions useful as inhibitors of gsk-3 |
| US7345046B2 (en) * | 2003-05-30 | 2008-03-18 | Chiron Corporation | Heteroaryl-fused pyrimidinyl compounds as anticancer agents |
| WO2006023381A1 (en) * | 2004-08-16 | 2006-03-02 | Taigen Biotechnology | Pyrimidinone compounds |
| EP1776982A1 (de) * | 2005-10-18 | 2007-04-25 | Argenta Discovery Limited | Pyrimidine Derivate als Modulator der Histamine Rezeptor |
| EP1812113A1 (de) | 2004-11-11 | 2007-08-01 | Argenta Discovery Limited | Pyrimidin-verbindungen als histaminmodulatoren |
-
2008
- 2008-12-19 AR ARP080105615A patent/AR069869A1/es unknown
- 2008-12-19 PE PE2008002147A patent/PE20091669A1/es not_active Application Discontinuation
- 2008-12-19 TW TW097149655A patent/TW200930375A/zh unknown
- 2008-12-22 NZ NZ586936A patent/NZ586936A/en not_active IP Right Cessation
- 2008-12-22 BR BRPI0821573A patent/BRPI0821573A2/pt not_active IP Right Cessation
- 2008-12-22 MX MX2010006799A patent/MX2010006799A/es active IP Right Grant
- 2008-12-22 CL CL2008003873A patent/CL2008003873A1/es unknown
- 2008-12-22 AU AU2008345560A patent/AU2008345560A1/en not_active Abandoned
- 2008-12-22 KR KR1020107016179A patent/KR20100098714A/ko not_active Ceased
- 2008-12-22 EP EP08832770A patent/EP2097419B1/de active Active
- 2008-12-22 US US12/341,210 patent/US20090247559A1/en not_active Abandoned
- 2008-12-22 WO PCT/US2008/087939 patent/WO2009086264A1/en not_active Ceased
- 2008-12-22 AT AT08832770T patent/ATE510839T1/de not_active IP Right Cessation
- 2008-12-22 EA EA201070786A patent/EA019785B1/ru not_active IP Right Cessation
- 2008-12-22 CA CA2712358A patent/CA2712358A1/en not_active Abandoned
- 2008-12-22 CN CN2008801272275A patent/CN101965351A/zh active Pending
- 2008-12-22 JP JP2010539930A patent/JP2011507908A/ja not_active Ceased
-
2010
- 2010-06-15 ZA ZA2010/04243A patent/ZA201004243B/en unknown
- 2010-06-16 IL IL206416A patent/IL206416A0/en unknown
- 2010-07-21 CO CO10088575A patent/CO6321258A2/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| JP2011507908A (ja) | 2011-03-10 |
| PE20091669A1 (es) | 2009-12-06 |
| TW200930375A (en) | 2009-07-16 |
| EP2097419B1 (de) | 2011-05-25 |
| US20090247559A1 (en) | 2009-10-01 |
| MX2010006799A (es) | 2010-10-05 |
| AU2008345560A1 (en) | 2009-07-09 |
| AR069869A1 (es) | 2010-02-24 |
| WO2009086264A1 (en) | 2009-07-09 |
| KR20100098714A (ko) | 2010-09-08 |
| EA201070786A1 (ru) | 2011-02-28 |
| ZA201004243B (en) | 2011-03-30 |
| NZ586936A (en) | 2012-07-27 |
| EP2097419A1 (de) | 2009-09-09 |
| CA2712358A1 (en) | 2009-07-09 |
| EA019785B1 (ru) | 2014-06-30 |
| CN101965351A (zh) | 2011-02-02 |
| CO6321258A2 (es) | 2011-09-20 |
| IL206416A0 (en) | 2010-12-30 |
| BRPI0821573A2 (pt) | 2016-08-09 |
| CL2008003873A1 (es) | 2009-06-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |