JPWO2021129653A5 - - Google Patents

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Publication number
JPWO2021129653A5
JPWO2021129653A5 JP2022539058A JP2022539058A JPWO2021129653A5 JP WO2021129653 A5 JPWO2021129653 A5 JP WO2021129653A5 JP 2022539058 A JP2022539058 A JP 2022539058A JP 2022539058 A JP2022539058 A JP 2022539058A JP WO2021129653 A5 JPWO2021129653 A5 JP WO2021129653A5
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JP
Japan
Prior art keywords
alkyl
pharmaceutically acceptable
acceptable salt
compound according
optical isomer
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.)
Pending
Application number
JP2022539058A
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English (en)
Japanese (ja)
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JP2023508097A (ja
Publication date
Application filed filed Critical
Priority claimed from PCT/CN2020/138572 external-priority patent/WO2021129653A1/zh
Publication of JP2023508097A publication Critical patent/JP2023508097A/ja
Publication of JPWO2021129653A5 publication Critical patent/JPWO2021129653A5/ja
Pending legal-status Critical Current

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JP2022539058A 2019-12-23 2020-12-23 タンパク質分解剤化合物の製造方法及び使用 Pending JP2023508097A (ja)

Applications Claiming Priority (9)

Application Number Priority Date Filing Date Title
CN201911342649.0 2019-12-23
CN201911342649 2019-12-23
CN202010200682.6 2020-03-20
CN202010200682 2020-03-20
CN202010496353 2020-06-03
CN202010496353.0 2020-06-03
CN202011486334.6 2020-12-16
CN202011486334 2020-12-16
PCT/CN2020/138572 WO2021129653A1 (zh) 2019-12-23 2020-12-23 一种蛋白降解剂化合物的制备方法和应用

Publications (2)

Publication Number Publication Date
JP2023508097A JP2023508097A (ja) 2023-02-28
JPWO2021129653A5 true JPWO2021129653A5 (ko) 2024-01-09

Family

ID=76573691

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2022539058A Pending JP2023508097A (ja) 2019-12-23 2020-12-23 タンパク質分解剤化合物の製造方法及び使用

Country Status (18)

Country Link
US (1) US20230111119A1 (ko)
EP (1) EP4083020A4 (ko)
JP (1) JP2023508097A (ko)
KR (1) KR20220120629A (ko)
CN (2) CN114829342A (ko)
AU (1) AU2020414151A1 (ko)
BR (1) BR112022012385A2 (ko)
CA (1) CA3162523A1 (ko)
CL (1) CL2022001724A1 (ko)
CO (1) CO2022010305A2 (ko)
EC (1) ECSP22056811A (ko)
IL (1) IL294225A (ko)
JO (1) JOP20220159A1 (ko)
MX (1) MX2022007885A (ko)
PE (1) PE20230114A1 (ko)
TW (1) TWI755992B (ko)
WO (1) WO2021129653A1 (ko)
ZA (1) ZA202208051B (ko)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN118638043A (zh) 2019-12-19 2024-09-13 阿尔维纳斯运营股份有限公司 用于雄激素受体的靶向降解的化合物和方法
EP4146642A1 (en) 2020-05-09 2023-03-15 Arvinas Operations, Inc. Methods of manufacturing a bifunctional compound, ultrapure forms of the bifunctional compound, and dosage forms comprising the same
CN113801098B (zh) 2020-06-12 2023-05-30 上海济煜医药科技有限公司 酞嗪酮类化合物及其制备方法和医药用途
US12097261B2 (en) 2021-05-07 2024-09-24 Kymera Therapeutics, Inc. CDK2 degraders and uses thereof
EP4367112A1 (en) 2021-07-09 2024-05-15 Plexium, Inc. Aryl compounds and pharmaceutical compositions that modulate ikzf2
WO2024002289A1 (en) * 2022-06-30 2024-01-04 Anhorn Medicines Co., Ltd. Protein degradation compounds and methods of use
WO2024012570A1 (zh) * 2022-07-15 2024-01-18 西藏海思科制药有限公司 一种含氮杂环衍生物及其组合物和药学上的应用
US11957759B1 (en) 2022-09-07 2024-04-16 Arvinas Operations, Inc. Rapidly accelerated fibrosarcoma (RAF) degrading compounds and associated methods of use

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180228907A1 (en) * 2014-04-14 2018-08-16 Arvinas, Inc. Cereblon ligands and bifunctional compounds comprising the same
CN107428734A (zh) * 2015-01-20 2017-12-01 阿尔维纳斯股份有限公司 用于雄激素受体的靶向降解的化合物和方法
KR102173463B1 (ko) * 2016-10-11 2020-11-04 아비나스 오퍼레이션스, 인코포레이티드 안드로겐 수용체의 표적 분해용 화합물 및 방법
CA3042301A1 (en) * 2016-11-22 2018-05-31 Dana-Farber Cancer Institute, Inc. Degradation of protein kinases by conjugation of protein kinase inhibitors with e3 ligase ligand and methods of use
WO2018098275A1 (en) * 2016-11-22 2018-05-31 Dana-Farber Cancer Institute, Inc. Degradation of bruton's tyrosine kinase (btk) by conjugation of btk inhibitors with e3 ligase ligand and methods of use

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