JP2024525740A5 - - Google Patents

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Publication number
JP2024525740A5
JP2024525740A5 JP2024501799A JP2024501799A JP2024525740A5 JP 2024525740 A5 JP2024525740 A5 JP 2024525740A5 JP 2024501799 A JP2024501799 A JP 2024501799A JP 2024501799 A JP2024501799 A JP 2024501799A JP 2024525740 A5 JP2024525740 A5 JP 2024525740A5
Authority
JP
Japan
Prior art keywords
cancer
pharmaceutically acceptable
compound according
stereoisomer
pharmaceutical composition
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
JP2024501799A
Other languages
English (en)
Japanese (ja)
Other versions
JP2024525740A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2022/073782 external-priority patent/WO2023288305A1/en
Publication of JP2024525740A publication Critical patent/JP2024525740A/ja
Publication of JP2024525740A5 publication Critical patent/JP2024525740A5/ja
Pending legal-status Critical Current

Links

JP2024501799A 2021-07-16 2022-07-15 小分子サイクリン依存性キナーゼ4/6(cdk4/6)およびikzf2(helios)分解剤並びにその使用方法 Pending JP2024525740A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US202163222646P 2021-07-16 2021-07-16
US63/222,646 2021-07-16
PCT/US2022/073782 WO2023288305A1 (en) 2021-07-16 2022-07-15 Small molecule cyclin dependent kinase 4/6 (cdk4/6) and ikzf2 (helios) degraders and methods of use thereof

Publications (2)

Publication Number Publication Date
JP2024525740A JP2024525740A (ja) 2024-07-12
JP2024525740A5 true JP2024525740A5 (https=) 2025-07-23

Family

ID=84919760

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2024501799A Pending JP2024525740A (ja) 2021-07-16 2022-07-15 小分子サイクリン依存性キナーゼ4/6(cdk4/6)およびikzf2(helios)分解剤並びにその使用方法

Country Status (7)

Country Link
US (1) US20240376096A1 (https=)
EP (1) EP4370126A4 (https=)
JP (1) JP2024525740A (https=)
CN (1) CN117396208A (https=)
AU (1) AU2022311961A1 (https=)
CA (1) CA3217661A1 (https=)
WO (1) WO2023288305A1 (https=)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20240020735A (ko) 2021-05-07 2024-02-15 카이메라 쎄라퓨틱스 인코포레이티드 Cdk2 분해제 및 그 용도
US12122764B2 (en) 2021-12-22 2024-10-22 Gilead Sciences, Inc. IKAROS zinc finger family degraders and uses thereof
WO2023178181A1 (en) 2022-03-17 2023-09-21 Gilead Sciences, Inc. Ikaros zinc finger family degraders and uses thereof
CN118420612A (zh) * 2023-02-01 2024-08-02 沈阳药科大学 一种基于cdk4/6抑制剂的靶向蛋白降解化合物及制备方法和用途
WO2025245178A1 (en) * 2024-05-21 2025-11-27 Innovo Therapeutics, Inc. Pak4, cstf2, or cstf2t protein degraders, pharmaceutical compositions, and therapeutic applications

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MXPA04005939A (es) 2002-01-22 2005-01-25 Warner Lambert Co 2-(piridin-2-ilamino)-pirido[2,3-d]pirimidin-7-onas.
US7968569B2 (en) 2002-05-17 2011-06-28 Celgene Corporation Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione
TWI398252B (zh) 2006-05-26 2013-06-11 諾華公司 吡咯并嘧啶化合物及其用途
US20090030005A1 (en) * 2007-07-19 2009-01-29 Amgen Inc. Combinations for the treatment of cancer
ES2522346T3 (es) 2008-08-22 2014-11-14 Novartis Ag Compuestos de pirrolopirimidina como inhibidores de CDK
TW201014830A (en) 2008-09-30 2010-04-16 Theravance Inc Crystalline form of an alkoxyimidazol-1-ylmethyl biphenyl carboxylic acid
US20120115878A1 (en) 2010-11-10 2012-05-10 John Vincent Calienni Salt(s) of 7-cyclopentyl-2-(5-piperazin-1-yl-pyridin-2-ylamino)-7h-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide and processes of making thereof
WO2013039854A1 (en) 2011-09-15 2013-03-21 Merck Sharp & Dohme Corp. Compositions and methods for treating cancer
MX386473B (es) 2013-02-21 2025-03-18 Pfizer Formas solidas de un inhibidor de cdk4/6 selectivo
CN107530292B (zh) 2015-04-16 2022-11-01 诺华股份有限公司 瑞博西尼片剂
CA3018429A1 (en) * 2016-04-22 2017-10-26 Dana-Farber Cancer Institute, Inc. Degradation of cyclin-dependent kinase 9 (cdk9) by conjugation of cdk9 inhibitors with e3 ligase ligand and methods of use
AU2018351050B2 (en) * 2017-10-18 2025-09-18 Novartis Ag Compositions and methods for selective protein degradation
WO2019196812A1 (zh) * 2018-04-09 2019-10-17 上海科技大学 蛋白降解靶向化合物、其抗肿瘤应用、其中间体及中间体应用
CA3123519A1 (en) * 2019-02-15 2020-08-20 Novartis Ag Substituted 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof

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