JP2021518366A5 - - Google Patents

Info

Publication number
JP2021518366A5
JP2021518366A5 JP2020549740A JP2020549740A JP2021518366A5 JP 2021518366 A5 JP2021518366 A5 JP 2021518366A5 JP 2020549740 A JP2020549740 A JP 2020549740A JP 2020549740 A JP2020549740 A JP 2020549740A JP 2021518366 A5 JP2021518366 A5 JP 2021518366A5
Authority
JP
Japan
Prior art keywords
lymphoma
cell
disorders
compound according
alkyl
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.)
Granted
Application number
JP2020549740A
Other languages
English (en)
Japanese (ja)
Other versions
JP2021518366A (ja
JP7254094B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2019/052252 external-priority patent/WO2019180631A1/en
Publication of JP2021518366A publication Critical patent/JP2021518366A/ja
Publication of JP2021518366A5 publication Critical patent/JP2021518366A5/ja
Priority to JP2023052481A priority Critical patent/JP2023082088A/ja
Application granted granted Critical
Publication of JP7254094B2 publication Critical patent/JP7254094B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2020549740A 2018-03-22 2019-03-20 Prmt5阻害剤としての置換イミダゾリジン-2-オン誘導体 Active JP7254094B2 (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2023052481A JP2023082088A (ja) 2018-03-22 2023-03-28 Prmt5阻害剤としての置換イミダゾリジン-2-オン誘導体

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IN201841010656 2018-03-22
IN201841010656 2018-03-22
PCT/IB2019/052252 WO2019180631A1 (en) 2018-03-22 2019-03-20 Substituted imidazolidin-2-one derivatives as prmt5 inhibitors

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2023052481A Division JP2023082088A (ja) 2018-03-22 2023-03-28 Prmt5阻害剤としての置換イミダゾリジン-2-オン誘導体

Publications (3)

Publication Number Publication Date
JP2021518366A JP2021518366A (ja) 2021-08-02
JP2021518366A5 true JP2021518366A5 (enExample) 2022-03-29
JP7254094B2 JP7254094B2 (ja) 2023-04-07

Family

ID=67986029

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2020549740A Active JP7254094B2 (ja) 2018-03-22 2019-03-20 Prmt5阻害剤としての置換イミダゾリジン-2-オン誘導体
JP2023052481A Pending JP2023082088A (ja) 2018-03-22 2023-03-28 Prmt5阻害剤としての置換イミダゾリジン-2-オン誘導体

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2023052481A Pending JP2023082088A (ja) 2018-03-22 2023-03-28 Prmt5阻害剤としての置換イミダゾリジン-2-オン誘導体

Country Status (18)

Country Link
US (1) US11542275B2 (enExample)
EP (1) EP3768671B1 (enExample)
JP (2) JP7254094B2 (enExample)
KR (1) KR102767362B1 (enExample)
CN (1) CN112105609A (enExample)
AU (1) AU2019237329B2 (enExample)
BR (1) BR112020019111A2 (enExample)
CA (1) CA3092770A1 (enExample)
CU (1) CU24627B1 (enExample)
EA (1) EA202092253A1 (enExample)
ES (1) ES2982859T3 (enExample)
IL (1) IL277518B2 (enExample)
MX (1) MX2020009738A (enExample)
MY (1) MY203159A (enExample)
PH (1) PH12020551494A1 (enExample)
SG (1) SG11202008526VA (enExample)
WO (1) WO2019180631A1 (enExample)
ZA (1) ZA202006137B (enExample)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019180628A1 (en) * 2018-03-22 2019-09-26 Aurigene Discovery Technologies Limited Imidazolidin-2-one compounds as prmt5 modulators
BR112020019111A2 (pt) * 2018-03-22 2021-01-12 Aurigene Discovery Technologies Limited Derivados de imidazolidin-2-ona substituída como inibidores de prmt5
US11077101B1 (en) 2018-07-18 2021-08-03 Tango Therapeutics, Inc. Compounds and methods of use
US12403137B2 (en) 2019-10-28 2025-09-02 Tango Therapeutics, Inc. Compounds and methods of use
WO2022026892A1 (en) 2020-07-31 2022-02-03 Tango Therapeutics, Inc. Piperidin-1- yl-n-pyrydi ne-3-yl-2-oxoacet am ide derivatives useful for the treatment of mtap-deficient and/or mt a-accumulating cancers
CN116940571A (zh) * 2021-03-15 2023-10-24 诺华股份有限公司 苯并异噁唑衍生物及其用途
CN115232147B (zh) * 2022-08-09 2023-10-13 南方科技大学 一种作为HIF-2α激动剂的杂环衍生物
TW202508595A (zh) 2023-05-04 2025-03-01 美商銳新醫藥公司 用於ras相關疾病或病症之組合療法
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
AU2024360465A1 (en) 2023-10-12 2026-04-09 Revolution Medicines, Inc. Macrocyclic ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
TW202547461A (zh) 2024-05-17 2025-12-16 美商銳新醫藥公司 Ras抑制劑
WO2025255438A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (en) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Therapeutic compositions and methods for managing treatment-related effects
WO2026006747A1 (en) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Ras inhibitors
WO2026015801A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015790A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015796A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015825A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Use of ras inhibitor for treating pancreatic cancer
WO2026050446A1 (en) 2024-08-29 2026-03-05 Revolution Medicines, Inc. Ras inhibitors
WO2026072904A2 (en) 2024-09-26 2026-04-02 Revolution Medicines, Inc. Compositions and methods for treating lung cancer

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0960104B1 (en) * 1996-04-17 2004-06-16 Bristol-Myers Squibb Pharma Company N-(amidinophenyl)-n'-(subst.)-3h-2,4-benzodiazepin-3-one derivatives as factor xa inhibitors
WO2010149755A1 (en) * 2009-06-26 2010-12-29 Novartis Ag 1, 3-disubstituted imidazolidin-2-one derivatives as inhibitors of cyp 17
US9029399B2 (en) * 2011-04-28 2015-05-12 Novartis Ag 17α-hydroxylase/C17,20-lyase inhibitors
IN2012CH00067A (enExample) * 2012-01-06 2017-08-04
DK2935222T3 (en) * 2012-12-21 2019-01-07 Epizyme Inc PRMT5 INHIBITORS AND APPLICATIONS THEREOF
US9745291B2 (en) 2012-12-21 2017-08-29 Epizyme, Inc. PRMT5 inhibitors containing a dihydro- or tetrahydroisoquinoline and uses thereof
JP2016511744A (ja) 2012-12-21 2016-04-21 エピザイム,インコーポレイティド Prmt5を阻害する方法
JP2016505597A (ja) 2012-12-21 2016-02-25 エピザイム,インコーポレイティド Prmt5阻害剤およびその使用
CA2899363A1 (en) * 2012-12-21 2014-06-26 Epizyme, Inc. Prmt5 inhibitors and uses thereof
WO2014108820A1 (en) 2013-01-08 2014-07-17 Aurigene Discovery Technologies Limited Substituted 2-pyrazinone derivatives as kinase inhibitors
GB201302927D0 (en) 2013-02-20 2013-04-03 Cancer Therapeutics Crc Pty Ltd Compounds
CA2942833A1 (en) 2013-03-15 2014-09-18 Ohio State Innovation Foundation Inhibitors of prmt5 and methods of their use
TWI690521B (zh) * 2014-04-07 2020-04-11 美商同步製藥公司 作為隱花色素調節劑之含有咔唑之醯胺類、胺基甲酸酯類及脲類
US20170210751A1 (en) 2014-06-25 2017-07-27 Epizyme, Inc. Prmt5 inhibitors and uses thereof
US20170198006A1 (en) 2014-06-25 2017-07-13 Epizyme, Inc. Prmt5 inhibitors and uses thereof
WO2016022605A1 (en) 2014-08-04 2016-02-11 Epizyme, Inc. Prmt5 inhibitors and uses thereof
GB201415573D0 (en) 2014-09-03 2014-10-15 Cancer Therapeutics Crc Pty Ltd Compounds
GB201604020D0 (en) 2016-03-09 2016-04-20 Ctxt Pty Ltd Compounds
GB201604027D0 (en) * 2016-03-09 2016-04-20 Ctxt Pty Ltd Compounds
EP3266784A1 (en) 2016-06-08 2018-01-10 Pierre Fabre Medicament Protein arginine n-methyltransferases inhibitors and uses thereof
BR112020019111A2 (pt) * 2018-03-22 2021-01-12 Aurigene Discovery Technologies Limited Derivados de imidazolidin-2-ona substituída como inibidores de prmt5

Similar Documents

Publication Publication Date Title
JP2021518366A5 (enExample)
JP2025023997A (ja) Fak阻害剤およびその併用薬物
EP3632907B1 (en) N-(azaaryl)cyclolactam-1-carboxamide derivative, preparation method therefor, and use thereof
ES2665073T3 (es) Inhibidores de serina/treonina cinasa
TWI805255B (zh) 拮抗藥與免疫核查點阻礙藥而成之組合的用途
CA2545942A1 (en) Aryl imidazoles and their use as anti-cancer agents
JP2019535744A5 (enExample)
ES2908938T3 (es) Nuevos derivados de benzamida como moduladores de PPAR-gamma
ES2660215T3 (es) Potenciador de efecto antitumoral que comprende un compuesto de imidazooxazina
JP2013522292A5 (enExample)
RU2016107884A (ru) Фармацевтическая композиция для лечения и/или профилактики рака
CA2736177A1 (en) Compositions of kinase inhibitors and their use for treatment of cancer and other diseases related to kinases
EP3632906B1 (en) Azaaryl derivative, preparation method therefor, and application thereof for use in pharmacy
JP2010538091A5 (enExample)
MX2010013699A (es) Derivados de azacarbolinas, su preparacion y su uso terapeutico.
CN110563703A (zh) 基于crbn配体诱导parp-1降解的化合物及制备方法和应用
JP2017524013A5 (enExample)
JP2023533350A (ja) 脳透過性btk又はher2阻害剤としての化合物およびその製造方法と応用
KR101739083B1 (ko) 세포 증식성 질환 치료용 플래티넘 화합물, 그 제조방법 및 용도
JP2022519719A (ja) プロスタグランジンe2(pge2)受容体調節薬としての新規なn-ベンジル-2-フェノキシベンズアミド誘導体
WO2021218319A1 (zh) 一种具有含氟取代基的苯并咪唑衍生物的制备及其应用
CN103450133A (zh) 具有抗肿瘤活性的东莨菪素衍生物、其制备方法及用途
CN104292233B (zh) 一种吡唑并[1,5-a]嘧啶衍生物及其抗肿瘤用途
Yang et al. Synthesis, crystal structure, and in vitro antitumor activities of copper (II) complexes containing tetradentate pyridine-based ligands
Pandey et al. In vitro and in vivo studies on antitumor potential of Ni (II) and Pd (II) complexes based on a series of thiourea-based ligands