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
EP17187100.7 2017-08-21
EP17187100 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)

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WO2020182929A1 (en) 2019-03-13 2020-09-17 Bayer Aktiengesellschaft Substituted ureas and derivatives as new antifungal agents
CN113646313B (zh) * 2019-03-28 2023-05-30 基石药业(苏州)有限公司 一种a2a受体拮抗剂的盐型、晶型及其制备方法
US20230339936A1 (en) * 2020-07-23 2023-10-26 Cytosinlab Therapeutics Co. Ltd. Compound having kinase inhibitory activity
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
DE69720965T2 (de) 1996-02-13 2004-02-05 Astrazeneca Ab Chinazolinderivate und deren verwendung als vegf hemmer
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
AU1688599A (en) 1998-01-05 1999-07-26 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
US6841549B1 (en) 1999-07-02 2005-01-11 Eisai Co., Ltd. Condensed imidazole compounds and a therapeutic agent for diabetes mellitus
AU2001258628A1 (en) 2000-05-31 2001-12-11 Astrazeneca Ab Indole derivatives with vascular damaging activity
MXPA02012903A (es) 2000-07-07 2004-07-30 Angiogene Pharm Ltd Derivados de colquinol como inhibidores de angiogenesis.
MXPA02012905A (es) 2000-07-07 2004-07-30 Angiogene Pharm Ltd Derivados de colquinol como agentes de dano vascular..
WO2004089942A2 (en) 2001-10-02 2004-10-21 Acadia Pharmaceuticals Inc. Benzimidazolidinone derivatives as muscarinic agents
EP1465634B1 (en) 2001-12-12 2014-10-22 The Government of the United States of America, as represented by the Secretary Department of Health and Human Services Methods for using adenosine receptor inhibitors to enhance immune response and inflammation
US20080070932A1 (en) 2003-04-09 2008-03-20 Chi Vu Triazolo[ 1,5-A] Pyrimidines And Pyrazolo[ 1,5-A] Pyrimidines And Methods Of Making And Using The Same
PT1636223E (pt) * 2003-05-19 2008-05-06 F Hoffmann-La Roche Ag Derivados de benzotiazole como ligandos de receptores da adenosina
RU2006112847A (ru) 2003-09-19 2007-11-10 Ф. Хоффманн-Ля Рош Аг (Ch) Производные тиазолопиридина в качестве лигандов аденозинового рецептора
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
RS50574B (sr) * 2004-05-24 2010-05-07 F. Hoffmann-La Roche Ag. (4-metoksi-7-morfolin-4-il-benzotiazol-2-il)-amid 4-hidroksi-4-metil-piperidin-1-karboksilne kiseline
JP5202946B2 (ja) 2004-07-22 2013-06-05 エフ.ホフマン−ラ ロシュ アーゲー ベンゾチアゾール誘導体
EP2282999B1 (en) 2008-03-04 2014-05-21 Merck Sharp & Dohme Corp. Amino-quinoxaline and amino-quinoline compounds for use as adenosine a2a receptor antagonists

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