JP2023504143A5 - - Google Patents

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Publication number
JP2023504143A5
JP2023504143A5 JP2022532095A JP2022532095A JP2023504143A5 JP 2023504143 A5 JP2023504143 A5 JP 2023504143A5 JP 2022532095 A JP2022532095 A JP 2022532095A JP 2022532095 A JP2022532095 A JP 2022532095A JP 2023504143 A5 JP2023504143 A5 JP 2023504143A5
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JP
Japan
Prior art keywords
hydrogen
nhr
alkyl
aryl
compound according
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JP2022532095A
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English (en)
Japanese (ja)
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JP7760167B2 (ja
JP2023504143A (ja
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Priority claimed from PCT/EP2020/083597 external-priority patent/WO2021105335A1/en
Publication of JP2023504143A publication Critical patent/JP2023504143A/ja
Publication of JP2023504143A5 publication Critical patent/JP2023504143A5/ja
Application granted granted Critical
Publication of JP7760167B2 publication Critical patent/JP7760167B2/ja
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JP2022532095A 2019-11-27 2020-11-27 セレブロンに結合するピペリジン-2,6-ジオン誘導体、及びその使用方法 Active JP7760167B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
PLPCT/PL2019/000108 2019-11-27
PL2019000108 2019-11-27
PCT/EP2020/083597 WO2021105335A1 (en) 2019-11-27 2020-11-27 Piperidine-2, 6-dione derivatives which bind to cereblon, and methods of use thereof

Publications (3)

Publication Number Publication Date
JP2023504143A JP2023504143A (ja) 2023-02-01
JP2023504143A5 true JP2023504143A5 (https=) 2023-12-05
JP7760167B2 JP7760167B2 (ja) 2025-10-27

Family

ID=69024571

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2022532095A Active JP7760167B2 (ja) 2019-11-27 2020-11-27 セレブロンに結合するピペリジン-2,6-ジオン誘導体、及びその使用方法

Country Status (4)

Country Link
US (1) US20230065745A1 (https=)
EP (1) EP4065576A1 (https=)
JP (1) JP7760167B2 (https=)
WO (1) WO2021105335A1 (https=)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022255888A1 (en) * 2021-06-01 2022-12-08 Captor Therapeutics S.A. Targeted protein degradation using bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein
CN113501807A (zh) * 2021-06-10 2021-10-15 重庆科技学院 四氢苯并噻吩类化合物及药物组合物的制备方法和用途
IL311606A (en) * 2021-09-27 2024-05-01 Univ Pennsylvania Molluscum contagiosum infection inhibitors and methods of using them
WO2023101556A1 (en) * 2021-12-02 2023-06-08 Rijksuniversiteit Groningen Novel inhibitors of aspartate transcarbamoylase (atcase) and compositions, methods and uses related thereto.
EP4626875A1 (en) * 2022-12-02 2025-10-08 Avammune Therapeutics Inc. Adar1 inhibitors and methods of using the same
WO2024123195A1 (en) * 2022-12-06 2024-06-13 Captor Therapeutics S.A. Targeted protein degradation using prodrugs of bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein
KR20250130610A (ko) * 2022-12-06 2025-09-02 캡터 테라퓨틱스 에스.에이. 유비퀴틴 리가제 및 표적 mcl-1 단백질에 결합하는 이작용성 화합물을 사용하는 표적화된 단백질 분해

Family Cites Families (15)

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US5635517B1 (en) 1996-07-24 1999-06-29 Celgene Corp Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines
JP2002105073A (ja) * 2000-09-27 2002-04-10 Shionogi & Co Ltd 新規マトリックスメタロプロテアーゼ阻害剤
US7323479B2 (en) 2002-05-17 2008-01-29 Celgene Corporation Methods for treatment and management of brain cancer using 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4-methylisoindoline
CN1939922B (zh) * 2005-09-27 2010-10-13 天津和美生物技术有限公司 可抑制细胞释放肿瘤坏死因子的5H-噻吩[3,4-c]吡咯-4,6-二酮衍生物
CL2007002513A1 (es) 2006-08-30 2008-04-04 Celgene Corp Soc Organizada Ba Compuestos derivados de isoindolina sustituidos, compuestos intermediarios; composicion farmaceutica; y uso en el tratamiento y prevencion de enfermedades tales como cancer, dolor, degeneracion macular, entre otras.
ES2565683T3 (es) * 2006-09-15 2016-04-06 Xcovery, Inc. Compuestos inhibidores de quinasa
ME02420B (me) 2006-09-26 2016-09-20 Celgene Corp 5-supstituirani derivati kinazolinona kao sredstva protiv raka
PL3202460T3 (pl) 2010-02-11 2019-12-31 Celgene Corporation Pochodne arylometoksyizoindoliny i zawierające je kompozycje oraz sposoby ich zastosowania
BR112018068906A2 (pt) * 2016-03-16 2019-01-22 H. Lee Moffitt Cancer Center And Research Institute, Inc. composição, método, método de redução de risco, prevenção ou tratamento de um indivíduo que tem uma doença ou distúrbio autoimune, método de indução de degradação de uma proteína-alvo numa célula, método para reduzir o risco, prevenir ou tratar um estado da doença ou afecção num paciente em que a atividade proteica desregulada é responsável pelo referido estado da doença ou afecção, método para reduzir o risco, prevenir ou tratar câncer num indivíduo e método de tratamento de uma doença ou distúrbio genético num indivíduo
EP3454856B1 (en) 2016-05-10 2024-09-11 C4 Therapeutics, Inc. Heterocyclic degronimers for target protein degradation
CN109790143A (zh) * 2016-05-10 2019-05-21 C4医药公司 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体
CN110769822A (zh) 2017-06-20 2020-02-07 C4医药公司 用于蛋白降解的n/o-连接的降解决定子和降解决定子体
EP4467143B1 (en) 2017-07-10 2026-03-11 Celgene Corporation Method for preparing 4-(4-(4-(((2-(2,6-dioxopiperidin-3-yl)-l-oxoisoindolin-4-yl)oxy)methyl)benzyl)piperazin-l-yl)-3-fluorobenzonitrile
CN118108706A (zh) * 2017-09-04 2024-05-31 C4医药公司 戊二酰亚胺
CA3094988A1 (en) * 2018-03-30 2019-10-03 Biotheryx, Inc. Thienopyrimidinone compounds

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