JP2022551950A5 - - Google Patents

Info

Publication number
JP2022551950A5
JP2022551950A5 JP2022522065A JP2022522065A JP2022551950A5 JP 2022551950 A5 JP2022551950 A5 JP 2022551950A5 JP 2022522065 A JP2022522065 A JP 2022522065A JP 2022522065 A JP2022522065 A JP 2022522065A JP 2022551950 A5 JP2022551950 A5 JP 2022551950A5
Authority
JP
Japan
Prior art keywords
difluoro
methyl
amino
cyclopropyl
oxazepino
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
JP2022522065A
Other languages
English (en)
Japanese (ja)
Other versions
JP2022551950A (ja
JP7668273B2 (ja
Filing date
Publication date
Priority claimed from GB201914860A external-priority patent/GB201914860D0/en
Application filed filed Critical
Publication of JP2022551950A publication Critical patent/JP2022551950A/ja
Publication of JP2022551950A5 publication Critical patent/JP2022551950A5/ja
Application granted granted Critical
Publication of JP7668273B2 publication Critical patent/JP7668273B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2022522065A 2019-10-14 2020-10-14 Bcl6阻害剤としての[1,4]オキサゼピノ[2,3-c]キノリノン誘導体 Active JP7668273B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB201914860A GB201914860D0 (en) 2019-10-14 2019-10-14 Inhibitor compounds
GB1914860.0 2019-10-14
PCT/GB2020/052588 WO2021074620A1 (en) 2019-10-14 2020-10-14 [1,4]oxazepino[2,3-c]qui noli none derivatives as blc6 inhibitors

Publications (3)

Publication Number Publication Date
JP2022551950A JP2022551950A (ja) 2022-12-14
JP2022551950A5 true JP2022551950A5 (enExample) 2023-10-19
JP7668273B2 JP7668273B2 (ja) 2025-04-24

Family

ID=68619494

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2022522065A Active JP7668273B2 (ja) 2019-10-14 2020-10-14 Bcl6阻害剤としての[1,4]オキサゼピノ[2,3-c]キノリノン誘導体

Country Status (13)

Country Link
US (1) US12528826B2 (enExample)
EP (1) EP4045510B1 (enExample)
JP (1) JP7668273B2 (enExample)
KR (1) KR20220083761A (enExample)
CN (1) CN114650995A (enExample)
AU (1) AU2020365518B2 (enExample)
CA (1) CA3157716A1 (enExample)
ES (1) ES3047908T3 (enExample)
GB (1) GB201914860D0 (enExample)
IL (1) IL292182B1 (enExample)
MX (1) MX2022004419A (enExample)
WO (1) WO2021074620A1 (enExample)
ZA (1) ZA202203520B (enExample)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA3095371A1 (en) 2018-04-13 2019-10-17 Cancer Research Technology Limited Bcl6 inhibitors
GB201914860D0 (en) 2019-10-14 2019-11-27 Cancer Research Tech Ltd Inhibitor compounds
CA3154386A1 (en) 2019-10-17 2021-04-22 Michael Berlin Bifunctional molecules containing an e3 ubiquitine ligase binding moiety linked to a bcl6 targeting moiety
KR20230171979A (ko) 2021-04-16 2023-12-21 아비나스 오퍼레이션스, 인코포레이티드 Bcl6 단백질 분해의 조절제 및 관련 사용 방법
PE20250756A1 (es) 2022-06-06 2025-03-13 Treeline Biosciences Inc Degradadores bifuncionales de bcl6 de quinolona triciclica
EP4536649A1 (en) 2022-06-13 2025-04-16 Treeline Biosciences, Inc. Quinolone bcl6 bifunctional degraders
KR20250023481A (ko) 2022-06-13 2025-02-18 트리라인 바이오사이언시스, 인크. 1,8-나프티리딘-2-온 이종이작용성 bcl6 분해제
KR20240161027A (ko) * 2023-05-03 2024-11-12 인제대학교 산학협력단 BTK 분해제 및 Bcl-6 분해제를 포함하는 암의 예방 또는 치료용 약학적 조성물
AU2024331309A1 (en) * 2023-09-01 2026-03-19 Treeline Biosciences, Inc. Tricyclic quinolone bcl6 bifunctional degraders

Family Cites Families (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0259572A (ja) 1988-08-23 1990-02-28 Mitsubishi Kasei Corp ベンズイミダゾロン誘導体又はその塩類
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
CA2349616A1 (en) 1998-12-04 2000-06-15 Neurosearch A/S New benzimidazolone-, benzoxazolone-, or benzothiazolone derivatives as ion channel modulating agents
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
PT1154774E (pt) 1999-02-10 2005-10-31 Astrazeneca Ab Derivados de quinazolina como inibidores de angiogenese
IL147309A0 (en) 1999-07-21 2002-08-14 Fujisawa Pharmaceutical Co Benzimidazolone derivatives and pharmaceutical compositions containg the same
AU2001258628A1 (en) 2000-05-31 2001-12-11 Astrazeneca Ab Indole derivatives with vascular damaging activity
UA73993C2 (uk) 2000-06-06 2005-10-17 Астразенека Аб Хіназолінові похідні для лікування пухлин та фармацевтична композиція
WO2001094311A1 (en) 2000-06-08 2001-12-13 Mitsubishi Pharma Corporation Cytoprotectors
MXPA02012905A (es) 2000-07-07 2004-07-30 Angiogene Pharm Ltd Derivados de colquinol como agentes de dano vascular..
MXPA02012903A (es) 2000-07-07 2004-07-30 Angiogene Pharm Ltd Derivados de colquinol como inhibidores de angiogenesis.
UY27304A1 (es) 2001-05-24 2002-12-31 Avanir Pharmaceuticals Inhibidores del factor inhibidor de la migración de los macrófagos y métodos para su identificación
WO2003095448A1 (en) 2002-05-06 2003-11-20 Bayer Pharmaceuticals Corporation Pyridinyl amino pyrimidine derivatives useful for treating hyper-proliferative disorders
US7825132B2 (en) 2002-08-23 2010-11-02 Novartis Vaccines And Diagnostics, Inc. Inhibition of FGFR3 and treatment of multiple myeloma
US20050256157A1 (en) 2002-08-23 2005-11-17 Chiron Corporation Combination therapy with CHK1 inhibitors
WO2008011032A1 (en) 2006-07-17 2008-01-24 Amgen Inc. Quinazoline and pyridopyrimidine derivatives as p38 kinase inhibitors
WO2008066887A2 (en) 2006-11-30 2008-06-05 Albert Einstein College Of Medicine Of Yeshiva University Small molecule inhibitors of bcl6
US8686008B2 (en) 2007-08-16 2014-04-01 The University Of Mississippi Highly selective sigma receptor ligands
WO2009063240A1 (en) 2007-11-16 2009-05-22 Arrow Therapeutics Limited 2,4-diaminopyrimidine derivatives useful as inhibitors of aurora kinase
SG187502A1 (en) 2008-02-01 2013-02-28 Takeda Pharmaceutical Oxim derivatives as hsp90 inhibitors
AU2009314760B2 (en) 2008-11-11 2011-11-10 Je Il Pharmaceutical Co.,Ltd Novel tricyclic derivative or pharmaceutically acceptable salts thereof, preparation method thereof, and pharmaceutical composition containing the same
BRPI1006942A2 (pt) 2009-01-23 2016-04-12 Rigel Pharmaceuticals Inc composto, composição farmacêutica, kit, métodos para inibir uma atividade de uma jak quinase, para tratar uma doença, para tratar a rejeição de transplante de aloenxerto em um receptor de transplante, para tratar uma reação de hipersensibilidade, e para inibir uma cascata de transdução de sinal, e, uso do composto
KR20120114355A (ko) 2010-01-13 2012-10-16 글락소스미스클라인 엘엘씨 화합물 및 방법
CA2840883C (en) 2011-07-07 2019-07-16 Merck Patent Gmbh Substituted azaheterocycles
CA2877146C (en) 2012-06-18 2020-10-20 Dart Neuroscience (Cayman) Ltd Substituted thiophene- and furan-fused azolopyrimidine-5-(6h)-one compounds
EP2964642B1 (en) 2013-03-05 2017-11-15 F. Hoffmann-La Roche AG Inhibitors of bruton's tyrosine kinase
US9943506B2 (en) 2013-06-17 2018-04-17 Cornell University BCL6 inhibitors as anticancer agents
CN105017159B (zh) 2014-04-28 2019-05-17 四川大学 5-氟-2,4-二取代氨基嘧啶衍生物及其制备方法和用途
US10266549B2 (en) 2014-08-25 2019-04-23 Salk Institute For Biological Studies ULK1 inhibitors and methods using same
US20160060260A1 (en) 2014-08-29 2016-03-03 Board Of Regents, The University Of Texas System Bromodomain inhibitors for treating disease
HK1244427A1 (zh) 2014-12-06 2018-08-10 Intra-Cellular Therapies, Inc. 有机化合物
WO2017007658A1 (en) 2015-07-07 2017-01-12 Rigel Pharmaceuticals, Inc. A combination for immune mediated cancer treatment
US11001570B2 (en) * 2016-12-13 2021-05-11 Boehringer Ingelheim International Gmbh 6-amino-quinolinone compounds and derivatives as BCL6 inhibitors
US11161839B2 (en) 2017-05-26 2021-11-02 The Institute Of Cancer Research: Royal Cancer Hospital 2-quinolone derived inhibitors of BCL6
JP7202315B2 (ja) 2017-05-26 2023-01-11 キャンサー・リサーチ・テクノロジー・リミテッド ベンズイミダゾロン由来のbcl6阻害剤
CA3095371A1 (en) 2018-04-13 2019-10-17 Cancer Research Technology Limited Bcl6 inhibitors
GB201819136D0 (en) 2018-11-23 2019-01-09 Cancer Research Tech Ltd Inhibitor compounds
GB201914860D0 (en) 2019-10-14 2019-11-27 Cancer Research Tech Ltd Inhibitor compounds

Similar Documents

Publication Publication Date Title
JP2022551950A5 (enExample)
US12479849B2 (en) EGFR inhibitors for the treatment of cancer
US8957074B2 (en) Pyrrolopyrimidine compounds as inhibitors of CDK4/6
US20250122222A1 (en) Heterocyclic compounds and methods of use
US20250059179A1 (en) Heterocyclic Compounds and Methods of Use
US20240417412A1 (en) Heterocyclic compounds and methods of use
US20250163064A1 (en) Quinazoline compounds and uses thereof as inhibitors of mutant kras proteins
JP2021521165A5 (enExample)
JP2024517693A5 (enExample)
US20250289801A1 (en) Egfr inhibitors
JP2025525356A (ja) アザキナゾリン汎Kras阻害剤
US20240317721A1 (en) Pyrazolyl derivatives as inhibitors of the kras mutant protein
US20240124474A1 (en) Her2 mutation inhibitors
JP2018500376A5 (enExample)
US8288396B2 (en) Pyrimidopyrimidoindazole derivative
US11236104B2 (en) Heteroaromatic NMDA receptor modulators and uses thereof
JP2017531672A5 (enExample)
EP4419525B1 (en) Heterocyclic compounds for use in the treatment of cancer
US11702414B2 (en) Thiadiazole IRAK4 inhibitors
US12590099B2 (en) Inhibitors of histone deacetylase useful for the treatment or prevention of HIV infection
JP2018535958A5 (enExample)
JP2024511841A5 (enExample)
JP2024539130A (ja) がんの治療における使用のためのヘテロ環式化合物
JP2022508523A5 (enExample)
US12180226B2 (en) Spirotricycle RIPK1 inhibitors and methods of uses thereof