JP2020531526A5 - - Google Patents

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Publication number
JP2020531526A5
JP2020531526A5 JP2020511322A JP2020511322A JP2020531526A5 JP 2020531526 A5 JP2020531526 A5 JP 2020531526A5 JP 2020511322 A JP2020511322 A JP 2020511322A JP 2020511322 A JP2020511322 A JP 2020511322A JP 2020531526 A5 JP2020531526 A5 JP 2020531526A5
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JP
Japan
Prior art keywords
carbon atoms
trisubstituted
disubstituted
unsubstituted
replaced
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
Application number
JP2020511322A
Other languages
English (en)
Japanese (ja)
Other versions
JP2020531526A (ja
JP7287951B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2018/072397 external-priority patent/WO2019038214A1/en
Publication of JP2020531526A publication Critical patent/JP2020531526A/ja
Publication of JP2020531526A5 publication Critical patent/JP2020531526A5/ja
Application granted granted Critical
Publication of JP7287951B2 publication Critical patent/JP7287951B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2020511322A 2017-08-21 2018-08-20 アデノシン受容体アンタゴニストとしてのキノキサリン誘導体 Active JP7287951B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP17187100 2017-08-21
EP17187100.7 2017-08-21
PCT/EP2018/072397 WO2019038214A1 (en) 2017-08-21 2018-08-20 QUINOXALINE DERIVATIVES AS ADENOSINE RECEPTOR ANTAGONISTS

Publications (3)

Publication Number Publication Date
JP2020531526A JP2020531526A (ja) 2020-11-05
JP2020531526A5 true JP2020531526A5 (enExample) 2023-02-02
JP7287951B2 JP7287951B2 (ja) 2023-06-06

Family

ID=59677147

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2020511322A Active JP7287951B2 (ja) 2017-08-21 2018-08-20 アデノシン受容体アンタゴニストとしてのキノキサリン誘導体

Country Status (14)

Country Link
US (1) US11192899B2 (enExample)
EP (1) EP3672951B1 (enExample)
JP (1) JP7287951B2 (enExample)
KR (1) KR20200043434A (enExample)
CN (1) CN110944994B (enExample)
AU (1) AU2018320672B2 (enExample)
BR (1) BR112020003283A2 (enExample)
CA (1) CA3073343A1 (enExample)
DK (1) DK3672951T3 (enExample)
ES (1) ES2964026T3 (enExample)
IL (1) IL272638B2 (enExample)
SG (1) SG11202001340VA (enExample)
TW (1) TW201920123A (enExample)
WO (1) WO2019038214A1 (enExample)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020182929A1 (en) 2019-03-13 2020-09-17 Bayer Aktiengesellschaft Substituted ureas and derivatives as new antifungal agents
JP7536036B2 (ja) * 2019-03-28 2024-08-19 シーストーン・ファーマスーティカルズ・(スージョウ)・カンパニー・リミテッド A2a受容体アンタゴニストの塩形態、結晶形態及びその製造方法
CN118955502A (zh) * 2020-07-23 2024-11-15 上海赛岚生物科技有限公司 一类具有激酶抑制活性的化合物
WO2022058327A1 (en) 2020-09-15 2022-03-24 Bayer Aktiengesellschaft Substituted ureas and derivatives as new antifungal agents
US20220127231A1 (en) * 2020-10-27 2022-04-28 Shilpa Medicare Ltd Process for the prepartion of amifampridine phosphate
EP4059498A1 (en) * 2021-03-16 2022-09-21 Centre Hospitalier Universitaire Vaudois (CHUV) Methods and compositions for treating conditions associated with hypermineralization
EP4351640A1 (en) 2021-06-07 2024-04-17 Ares Trading S.A. Combination treatment of cancer
CN116514803A (zh) * 2022-01-21 2023-08-01 上海赛岚生物科技有限公司 一种激酶抑制剂的盐晶型和自由碱晶型
CN121270522B (zh) * 2025-12-10 2026-03-17 四川大学华西医院 吲唑-苯并三唑-吡唑结构衍生物及其制备方法和应用

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US4207554A (en) 1972-08-04 1980-06-10 Med-El Inc. Method and apparatus for automated classification and analysis of cells
US4125828A (en) 1972-08-04 1978-11-14 Med-El Inc. Method and apparatus for automated classification and analysis of cells
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
CA2242425C (en) 1996-02-13 2006-07-18 Zeneca Limited Quinazoline derivatives as vegf inhibitors
NZ331191A (en) 1996-03-05 2000-03-27 Zeneca Ltd 4-anilinoquinazoline derivatives and pharmaceutical compositions thereof
GB9718972D0 (en) 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
GB9714249D0 (en) 1997-07-08 1997-09-10 Angiogene Pharm Ltd Vascular damaging agents
US6579868B1 (en) 1998-01-05 2003-06-17 Eisai Co., Ltd. Purine derivatives and adenosine A2 receptor antagonists serving as preventives/remedies for diabetes
GB9900334D0 (en) 1999-01-07 1999-02-24 Angiogene Pharm Ltd Tricylic vascular damaging agents
GB9900752D0 (en) 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
WO2001002400A1 (en) 1999-07-02 2001-01-11 Eisai Co., Ltd. Fused imidazole compounds and remedies for diabetes mellitus
BR0111230A (pt) 2000-05-31 2003-06-10 Astrazeneca Ab Composto, e, uso e processo para a preparação do mesmo
KR20030014425A (ko) 2000-07-07 2003-02-17 앤지오젠 파마슈티칼스 리미티드 혈관 손상제인 콜치놀 유도체
EE200300015A (et) 2000-07-07 2004-10-15 Angiogene Pharmaceuticals Limited Kolhinooli derivaadid kui angiogeneesi inhibiitorid
WO2004089942A2 (en) 2001-10-02 2004-10-21 Acadia Pharmaceuticals Inc. Benzimidazolidinone derivatives as muscarinic agents
JP2005516917A (ja) 2001-12-12 2005-06-09 アメリカ合衆国 細胞外アデノシン阻害剤およびアデノシン受容体阻害剤を用いて免疫応答および炎症を増強するための方法
WO2004092171A2 (en) 2003-04-09 2004-10-28 Biogen Idec Ma Inc. Triazolo[1,5-a]pyrimidines and pyrazolo[1,5-a]pyrimidines useful as a2a adenosin e receptor antagonists
ATE389652T1 (de) 2003-05-19 2008-04-15 Hoffmann La Roche Benzothiazol-derivate als liganden des adenosinrezeptors
WO2005028484A1 (en) 2003-09-19 2005-03-31 F. Hoffmann-La Roche Ag Thiazolopyridine derivatives as adenosine receptor ligands
JP2005154434A (ja) 2003-11-05 2005-06-16 Kyowa Hakko Kogyo Co Ltd 2−アミノキナゾリン誘導体
AU2005247567B2 (en) 2004-05-24 2010-09-02 F. Hoffmann-La Roche Ag 4-hydroxy-4-methyl-piperidine-1-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-amide
AU2005263500B2 (en) 2004-07-22 2011-02-24 F. Hoffmann-La Roche Ag Benzothiazole derivatives
WO2009111442A1 (en) 2008-03-04 2009-09-11 Schering Corporation AMINO-QUINOXALINE AND AMINO-QUINOLINE COMPOUNDS FOR USE AS ADENOSINE A2a RECEPTOR ANTAGONISTS

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