JP2024500562A5 - - Google Patents

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Publication number
JP2024500562A5
JP2024500562A5 JP2023557491A JP2023557491A JP2024500562A5 JP 2024500562 A5 JP2024500562 A5 JP 2024500562A5 JP 2023557491 A JP2023557491 A JP 2023557491A JP 2023557491 A JP2023557491 A JP 2023557491A JP 2024500562 A5 JP2024500562 A5 JP 2024500562A5
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JP
Japan
Prior art keywords
alkyl
group
substituted
aryl
optionally substituted
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
JP2023557491A
Other languages
English (en)
Japanese (ja)
Other versions
JP2024500562A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2021/084089 external-priority patent/WO2022117782A1/en
Publication of JP2024500562A publication Critical patent/JP2024500562A/ja
Publication of JP2024500562A5 publication Critical patent/JP2024500562A5/ja
Pending legal-status Critical Current

Links

JP2023557491A 2020-12-03 2021-12-03 Alc1阻害剤およびparpiとの相乗効果 Pending JP2024500562A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP20211730.5 2020-12-03
EP20211730 2020-12-03
PCT/EP2021/084089 WO2022117782A1 (en) 2020-12-03 2021-12-03 Alc1 inhibitors and synergy with parpi

Publications (2)

Publication Number Publication Date
JP2024500562A JP2024500562A (ja) 2024-01-09
JP2024500562A5 true JP2024500562A5 (https=) 2024-12-11

Family

ID=73792931

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2023557491A Pending JP2024500562A (ja) 2020-12-03 2021-12-03 Alc1阻害剤およびparpiとの相乗効果

Country Status (13)

Country Link
US (1) US20240033363A1 (https=)
EP (1) EP4255910A1 (https=)
JP (1) JP2024500562A (https=)
KR (1) KR20230116832A (https=)
CN (1) CN117120448A (https=)
AR (1) AR124235A1 (https=)
AU (1) AU2021393770A1 (https=)
CA (1) CA3198803A1 (https=)
CL (1) CL2023001587A1 (https=)
IL (1) IL303333A (https=)
MX (1) MX2023006549A (https=)
TW (1) TW202237095A (https=)
WO (1) WO2022117782A1 (https=)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116283828A (zh) * 2023-02-03 2023-06-23 广州安岩仁医药科技有限公司 一种parp1抑制剂中间体及其制备方法与应用
WO2025088087A1 (en) 2023-10-25 2025-05-01 Eisbach Bio Gmbh A pyrido-thieno-pyrimidin derivative as alc1 inhibitor for use in the treatment of homologous recombination deficiency (hrd) cancers
AU2024366320A1 (en) 2023-10-25 2026-04-16 Eisbach Bio Gmbh Alc1 inhibitors for use in treating cancer by potentiating the effects of several classes of approved cancer drugs
WO2025093706A1 (en) 2023-10-31 2025-05-08 Eisbach Bio Gmbh Alc1 inhibitors alc1i-1 and alc1i-2 for use in treating pancreatic cancer by potentiating the effect of irinotecan
WO2025242703A1 (en) 2024-05-21 2025-11-27 Eisbach Bio Gmbh Crystalline forms of an alc1 inhibitor useful in the treatment of cancer

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT72878B (en) 1980-04-24 1983-03-29 Merck & Co Inc Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents
WO2000022110A2 (en) 1998-10-09 2000-04-20 President And Fellows Of Harvard College Targeted proteolysis by recruitment to ubiquitin protein ligases
US6306663B1 (en) 1999-02-12 2001-10-23 Proteinex, Inc. Controlling protein levels in eucaryotic organisms
KR100774855B1 (ko) * 2000-04-27 2007-11-08 아스텔라스세이야쿠 가부시키가이샤 축합 헤테로아릴 유도체
WO2002020740A2 (en) 2000-09-08 2002-03-14 California Institute Of Technology Proteolysis targeting chimeric pharmaceutical
WO2006010568A2 (de) * 2004-07-23 2006-02-02 Curacyte Discovery Gmbh Substituierte pyrido [3',2':4,5]thieno[3,2-d]pyrimidin-2,4(1 h,3h)-diones und -4(3h)-one sowie pyrido [3',2' :4,5] furo[3,2-d]pyrimidin -2,4(1 h,3h)-dione und -4(3h)-one zur verwendung als inhibitoren der tnf-allpha freisetzung
WO2010151664A2 (en) * 2009-06-26 2010-12-29 Massachusetts Institute Of Technology Compositions and methods for treating cancer and modulating stress granule formation
EP2806875B1 (en) * 2012-01-25 2017-07-19 Proteostasis Therapeutics, Inc. Proteasome activity modulating compounds
RU2738833C9 (ru) 2014-04-14 2022-02-28 Арвинас, Оперэйшнз, Инк. Имидные модуляторы протеолиза и способы их применения
CN107108613B (zh) 2014-11-10 2020-02-25 基因泰克公司 布罗莫结构域抑制剂及其用途
MA40940A (fr) 2014-11-10 2017-09-19 Constellation Pharmaceuticals Inc Pyrrolopyridines substituées utilisées en tant qu'inhibiteurs de bromodomaines
WO2016105518A1 (en) 2014-12-23 2016-06-30 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
US9694084B2 (en) 2014-12-23 2017-07-04 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
WO2017007612A1 (en) 2015-07-07 2017-01-12 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
WO2017024317A2 (en) 2015-08-06 2017-02-09 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
US10154992B2 (en) * 2016-07-12 2018-12-18 The Regents Of The University Of California Compounds and methods for treating HIV infection

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