JP2020531531A5 - - Google Patents

Info

Publication number
JP2020531531A5
JP2020531531A5 JP2020511371A JP2020511371A JP2020531531A5 JP 2020531531 A5 JP2020531531 A5 JP 2020531531A5 JP 2020511371 A JP2020511371 A JP 2020511371A JP 2020511371 A JP2020511371 A JP 2020511371A JP 2020531531 A5 JP2020531531 A5 JP 2020531531A5
Authority
JP
Japan
Prior art keywords
carbon atoms
alkyl
group
trisubstituted
disubstituted
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
JP2020511371A
Other languages
English (en)
Japanese (ja)
Other versions
JP7287952B2 (ja
JP2020531531A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2018/072398 external-priority patent/WO2019038215A1/en
Publication of JP2020531531A publication Critical patent/JP2020531531A/ja
Publication of JP2020531531A5 publication Critical patent/JP2020531531A5/ja
Application granted granted Critical
Publication of JP7287952B2 publication Critical patent/JP7287952B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2020511371A 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ベンズイミダゾール誘導体 Active JP7287952B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP17187101 2017-08-21
EP17187101.5 2017-08-21
PCT/EP2018/072398 WO2019038215A1 (en) 2017-08-21 2018-08-20 BENZIMIDAZOLE DERIVATIVES AS ADENOSINE RECEPTOR ANTAGONISTS

Publications (3)

Publication Number Publication Date
JP2020531531A JP2020531531A (ja) 2020-11-05
JP2020531531A5 true JP2020531531A5 (enExample) 2023-02-02
JP7287952B2 JP7287952B2 (ja) 2023-06-06

Family

ID=59677148

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2020511371A Active JP7287952B2 (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ベンズイミダゾール誘導体

Country Status (14)

Country Link
US (2) US11453647B2 (enExample)
EP (1) EP3672952B1 (enExample)
JP (1) JP7287952B2 (enExample)
KR (1) KR20200043433A (enExample)
CN (1) CN110997662B (enExample)
AU (1) AU2018320673B2 (enExample)
BR (1) BR112020003594A2 (enExample)
CA (1) CA3073333A1 (enExample)
ES (1) ES2940408T3 (enExample)
IL (1) IL272637B2 (enExample)
SG (1) SG11202001337XA (enExample)
TW (1) TWI791593B (enExample)
WO (1) WO2019038215A1 (enExample)
ZA (1) ZA202001780B (enExample)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3746124A4 (en) 2018-01-30 2021-10-27 Foghorn Therapeutics Inc. COMPOUNDS AND THEIR USES
US12509453B2 (en) 2019-01-29 2025-12-30 Foghorn Therapeutics Inc. BRM/BRG1 inhibitors and uses thereof
WO2021155264A1 (en) * 2020-01-29 2021-08-05 Foghorn Therapeutics Inc. Compounds and uses thereof
WO2021155262A1 (en) 2020-01-29 2021-08-05 Foghorn Therapeutics Inc. Compounds and uses thereof
US11618751B1 (en) 2022-03-25 2023-04-04 Ventus Therapeutics U.S., Inc. Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 derivatives
WO2022164135A1 (ko) * 2021-01-29 2022-08-04 한국화학연구원 벤조티아졸 및 벤즈이미다졸 유도체, 약제학적으로 허용 가능한 염, 이의 제조방법 및 이를 유효성분으로 함유하는 약제학적 조성물
US12606553B2 (en) 2021-03-09 2026-04-21 Foghorn Therapeutics Inc. Crystalline forms, compositions containing same, and methods of their use
US11319319B1 (en) 2021-04-07 2022-05-03 Ventus Therapeutics U.S., Inc. Compounds for inhibiting NLRP3 and uses thereof
EP4351640A1 (en) 2021-06-07 2024-04-17 Ares Trading S.A. Combination treatment of cancer
US12331048B2 (en) 2022-10-31 2025-06-17 Ventus Therapeutics U.S., Inc. Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 inhibitors
WO2024235218A1 (zh) * 2023-05-15 2024-11-21 微境生物医药科技(上海)有限公司 Hdac1/2选择性抑制剂及其用途

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
EE200300015A (et) 2000-07-07 2004-10-15 Angiogene Pharmaceuticals Limited Kolhinooli derivaadid kui angiogeneesi inhibiitorid
KR20030014425A (ko) 2000-07-07 2003-02-17 앤지오젠 파마슈티칼스 리미티드 혈관 손상제인 콜치놀 유도체
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
WO2004101558A1 (en) 2003-05-13 2004-11-25 F. Hoffmann-La Roche Ag 2-imidazo-benzothiazoles as adenosine receptor ligands
ATE389652T1 (de) * 2003-05-19 2008-04-15 Hoffmann La Roche Benzothiazol-derivate als liganden des adenosinrezeptors
EP1628662B1 (en) 2003-05-21 2007-02-14 F. Hoffmann-La Roche Ag Benzothiazole derivatives and use thereof in the treatment of diseases related to the adenosine a2a receptor
WO2005028484A1 (en) 2003-09-19 2005-03-31 F. Hoffmann-La Roche Ag Thiazolopyridine derivatives as adenosine receptor ligands
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
US20060223849A1 (en) * 2005-03-14 2006-10-05 Mjalli Adnan M Benzazole derivatives, compositions, and methods of use as beta-secretase inhibitors
CN102731488A (zh) * 2011-04-02 2012-10-17 中国医学科学院药物研究所 苯并咪唑类衍生物、及其制法和药物组合物与用途

Similar Documents

Publication Publication Date Title
JP2020531526A5 (enExample)
RU2506256C2 (ru) Лиганды для визуализации иннервации сердца
JP2022524914A5 (enExample)
JP2020528922A5 (enExample)
CA2324418A1 (en) Novel opiate compounds, methods of making and methods of use
JP2019104748A5 (enExample)
RU99128073A (ru) Замещенные 2-(2,6-диоксопиперидин-3-ил)-фталимиды и -1-оксоизоиндолины и способ снижения уровней фноа
KR830007624A (ko) 헤테로 사이클릭 화합물의 제조방법
JP2023504542A5 (enExample)
CA2457054A1 (en) Activator of peroxisome proliferator-activated receptor .delta.
RU2008152087A (ru) Макроциклические оксимильные ингибиторы протеазы гепатита
RU2012143212A (ru) Способ лечения артрита
ES436385A1 (es) Procedimiento para la preparacion de compuestos derivados deanilidas.
JP2004525117A5 (enExample)
RU2007131274A (ru) Замещенные пиразолопиридины, композиции, содержащие их, способ получения и применение
KR870011129A (ko) 디스타마이신 a 동족체 및 이의 제조방법
JP2009536221A5 (enExample)
JP2002531564A5 (enExample)
GB1046506A (en) Guanidine compounds and process for their manufacture
RU2009125439A (ru) Комбинация ингибитора гда и антиметаболита
EP0092158A3 (en) Thiazolidine compound and fungicidal composition containing it
JP2020504184A5 (enExample)
MX2024008480A (es) Compuesto heterociclico que contiene nitrogeno que tiene un efecto de activacion del factor 2 relacionado con el factor nuclear eritroide 2 (nrf2).
JP2021528421A5 (enExample)
JP2025160251A5 (enExample)