JPWO2023092107A5 - - Google Patents

Info

Publication number
JPWO2023092107A5
JPWO2023092107A5 JP2024529341A JP2024529341A JPWO2023092107A5 JP WO2023092107 A5 JPWO2023092107 A5 JP WO2023092107A5 JP 2024529341 A JP2024529341 A JP 2024529341A JP 2024529341 A JP2024529341 A JP 2024529341A JP WO2023092107 A5 JPWO2023092107 A5 JP WO2023092107A5
Authority
JP
Japan
Prior art keywords
optionally substituted
halo
cancer
alkyl
independently selected
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
JP2024529341A
Other languages
English (en)
Japanese (ja)
Other versions
JP2024540483A5 (https=
JP2024540483A (ja
Publication date
Priority claimed from PCT/US2022/080165 external-priority patent/WO2023092088A1/en
Application filed filed Critical
Publication of JP2024540483A publication Critical patent/JP2024540483A/ja
Publication of JP2024540483A5 publication Critical patent/JP2024540483A5/ja
Publication of JPWO2023092107A5 publication Critical patent/JPWO2023092107A5/ja
Pending legal-status Critical Current

Links

JP2024529341A 2021-11-19 2022-11-19 Cdk2阻害剤及びその製造方法及び使用方法 Pending JP2024540483A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US202163281508P 2021-11-19 2021-11-19
US63/281,508 2021-11-19
USPCT/US2022/080165 2022-11-18
PCT/US2022/080165 WO2023092088A1 (en) 2021-11-19 2022-11-18 Cdk2 inhibitors and methods of making and using same
PCT/US2022/080199 WO2023092107A1 (en) 2021-11-19 2022-11-19 Cdk2 inhibitors and methods of making and using same

Publications (3)

Publication Number Publication Date
JP2024540483A JP2024540483A (ja) 2024-10-31
JP2024540483A5 JP2024540483A5 (https=) 2025-11-27
JPWO2023092107A5 true JPWO2023092107A5 (https=) 2025-11-27

Family

ID=84901264

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2024529341A Pending JP2024540483A (ja) 2021-11-19 2022-11-19 Cdk2阻害剤及びその製造方法及び使用方法

Country Status (5)

Country Link
US (1) US20250074895A1 (https=)
EP (1) EP4433470A1 (https=)
JP (1) JP2024540483A (https=)
CN (1) CN118265706A (https=)
WO (2) WO2023092088A1 (https=)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2022271290A1 (en) 2021-05-07 2023-11-23 Kymera Therapeutics, Inc. Cdk2 degraders and uses thereof
US11932648B2 (en) 2021-06-28 2024-03-19 Blueprint Medicines Corporation CDK2 inhibitors
CN119072471A (zh) * 2022-04-28 2024-12-03 正大天晴药业集团股份有限公司 一种吡唑取代环戊酯衍生物及其用途
CN120239698A (zh) * 2022-11-17 2025-07-01 山东绿叶制药有限公司 Cdk2抑制剂及其制备方法和应用
US20240317777A1 (en) * 2023-02-23 2024-09-26 Accutar Biotechnology Inc. Novel macrocyclic aminopyrazole compounds as cdk2 inhibitors
WO2025062334A1 (en) * 2023-09-20 2025-03-27 Beigene Switzerland Gmbh 4-((5-(3-(4-(pyridin-2-yl)cyclopentyl)-1 h-pyrazol-3-yl)amino)-benzenesulfonamide derivatives and similar compounds as cdk inhibitors for the treatment of cancer
WO2026024674A1 (en) 2024-07-22 2026-01-29 Genesis Therapeutics, Inc. Methods of treating skp2-associated cancers

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL154016A0 (en) * 2000-08-31 2003-07-31 Pfizer Prod Inc Pyrazole derivatives and their use as protein kinase inhibitors
WO2020050653A1 (ko) 2018-09-05 2020-03-12 삼성전자 주식회사 이동 통신 시스템에서 papr 감소를 위한 기준 신호 시퀀스 생성 방법 및 장치
CN113330000B (zh) * 2019-01-31 2024-12-24 辉瑞公司 具有对cdk2的抑制活性的3-羰基氨基-5-环戊基-1fi-吡咯化合物

Similar Documents

Publication Publication Date Title
Laali et al. Novel fluorinated curcuminoids and their pyrazole and isoxazole derivatives: Synthesis, structural studies, Computational/Docking and in-vitro bioassay
KR101668931B1 (ko) 항종양제의 효과 증강제
JP2022062168A5 (https=)
JP2021519783A5 (https=)
KR20240044469A (ko) 경구 생체이용률이 높은 jak 억제제
JP2005521713A (ja) 血管新生阻害剤
JPWO2019191470A5 (https=)
KR20110025741A (ko) 퀴나졸린 유도체
CA2716518A1 (en) Use of pyrimidine derivatives for the treatment of egfr dependent diseases or diseases that have acquired resistance to agents that target egfr family members
JPWO2023092107A5 (https=)
CN113082210B (zh) 一种肿瘤化疗药物组合物
Zhang et al. Discovery of a potent dual EGFR/HER-2 inhibitor L-2 (selatinib) for the treatment of cancer
WO2022083657A1 (zh) 取代苯并或吡啶并嘧啶胺类抑制剂及其制备方法和应用
JPWO2023278326A5 (https=)
Zhu et al. Chemotherapeutic and biologic agents as radiosensitizers in rectal cancer
JPWO2021195128A5 (https=)
WO2023143147A1 (zh) 一种哒嗪并吡啶酮类化合物、其药物组合物及应用
Chen et al. Discovery of pyrrolo [2, 3-d] pyrimidine-based molecules as a Wee1 inhibitor template
TWI638825B (zh) 抑制癌症及病毒之化合物
US20230399325A1 (en) Succinate and crystal form thereof as therapeutics
CN101291675B (zh) 抗癌组合药物
WO2020172906A1 (zh) 一种新型pan-RAF激酶抑制剂及其用途
CN111718350B (zh) 吡唑取代的吡唑并嘧啶化合物和药物组合物及其应用
CA3113408A1 (en) Cancer combination therapy using quinoline carboxamide derivative
EP4112608A1 (en) Aryl-fused isoselenazole compound containing tetrazine substituent, synthesis method therefor, and use thereof