JP2024501537A5 - - Google Patents

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Publication number
JP2024501537A5
JP2024501537A5 JP2023539966A JP2023539966A JP2024501537A5 JP 2024501537 A5 JP2024501537 A5 JP 2024501537A5 JP 2023539966 A JP2023539966 A JP 2023539966A JP 2023539966 A JP2023539966 A JP 2023539966A JP 2024501537 A5 JP2024501537 A5 JP 2024501537A5
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JP
Japan
Prior art keywords
nhr
compound according
optionally
alkyl
hydrogen
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Application number
JP2023539966A
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English (en)
Japanese (ja)
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JP7853713B2 (ja
JP2024501537A (ja
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Publication date
Priority claimed from PCT/PL2020/000099 external-priority patent/WO2022146151A1/en
Application filed filed Critical
Publication of JP2024501537A publication Critical patent/JP2024501537A/ja
Publication of JP2024501537A5 publication Critical patent/JP2024501537A5/ja
Application granted granted Critical
Publication of JP7853713B2 publication Critical patent/JP7853713B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2023539966A 2020-12-30 2021-12-30 セレブロンに結合する新規な化合物、及びその使用方法 Active JP7853713B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
PCT/PL2020/000099 WO2022146151A1 (en) 2020-12-30 2020-12-30 Novel compounds which bind to cereblon, and methods of use thereof
PLPCT/PL2020/000099 2020-12-30
PCT/EP2021/087847 WO2022144416A1 (en) 2020-12-30 2021-12-30 Novel compounds which bind to cereblon, and methods of use thereof

Publications (3)

Publication Number Publication Date
JP2024501537A JP2024501537A (ja) 2024-01-12
JP2024501537A5 true JP2024501537A5 (https=) 2025-01-09
JP7853713B2 JP7853713B2 (ja) 2026-04-30

Family

ID=74347684

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2023539966A Active JP7853713B2 (ja) 2020-12-30 2021-12-30 セレブロンに結合する新規な化合物、及びその使用方法

Country Status (6)

Country Link
US (1) US20240307547A1 (https=)
EP (1) EP4271670A1 (https=)
JP (1) JP7853713B2 (https=)
KR (1) KR20230128083A (https=)
CN (1) CN116917275A (https=)
WO (2) WO2022146151A1 (https=)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4584259A1 (en) 2022-09-09 2025-07-16 Innovo Therapeutics, Inc. Ck1alpha and dual ck1alpha / gspt1 degrading compounds
WO2024167423A1 (en) * 2023-02-07 2024-08-15 Captor Therapeutics S.A. Gspt1 degrader compounds
WO2025063888A1 (en) 2023-09-19 2025-03-27 Kancure Pte. Ltd. Survivin-targeted compounds
WO2025097090A1 (en) * 2023-11-02 2025-05-08 Neomorph, Inc. Substituted (piperidin-4-yl)-1,5-naphthyridine and (piperidin-4-yl)quinoline derivatives and uses thereof
WO2025179161A1 (en) 2024-02-21 2025-08-28 Innovo Therapeutics, Inc. Protein degrading compounds

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
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
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.
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
KR102668696B1 (ko) * 2012-01-12 2024-05-29 예일 유니버시티 E3 유비퀴틴 리가아제에 의한 표적 단백질 및 다른 폴리펩티드의 증진된 분해를 위한 화합물 및 방법
RU2738833C9 (ru) * 2014-04-14 2022-02-28 Арвинас, Оперэйшнз, Инк. Имидные модуляторы протеолиза и способы их применения
EP3827836A1 (en) * 2014-06-27 2021-06-02 Celgene Corporation Compositions and methods for inducing conformational changes in cereblon and other e3 ubiquitin ligases
WO2016105518A1 (en) 2014-12-23 2016-06-30 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
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
CN109641874A (zh) * 2016-05-10 2019-04-16 C4医药公司 用于靶蛋白降解的c3-碳连接的戊二酰亚胺降解决定子体
EP3454856B1 (en) 2016-05-10 2024-09-11 C4 Therapeutics, Inc. Heterocyclic degronimers for target protein degradation
WO2018064589A1 (en) * 2016-09-29 2018-04-05 Dana-Farber Cancer Institute, Inc. Targeted protein degradation using a mutant e3 ubiquitin ligase
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
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

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