JP2021519308A5 - - Google Patents

Info

Publication number
JP2021519308A5
JP2021519308A5 JP2020551963A JP2020551963A JP2021519308A5 JP 2021519308 A5 JP2021519308 A5 JP 2021519308A5 JP 2020551963 A JP2020551963 A JP 2020551963A JP 2020551963 A JP2020551963 A JP 2020551963A JP 2021519308 A5 JP2021519308 A5 JP 2021519308A5
Authority
JP
Japan
Prior art keywords
alkyl
groups
cancer
alkoxy
haloalkyl
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
JP2020551963A
Other languages
English (en)
Japanese (ja)
Other versions
JP2021519308A (ja
JP7387627B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2019/024976 external-priority patent/WO2019191667A1/en
Publication of JP2021519308A publication Critical patent/JP2021519308A/ja
Publication of JP2021519308A5 publication Critical patent/JP2021519308A5/ja
Application granted granted Critical
Publication of JP7387627B2 publication Critical patent/JP7387627B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2020551963A 2018-03-29 2019-03-29 転写活性化タンパク質のイミダゾピペラジン阻害剤 Active JP7387627B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201862650151P 2018-03-29 2018-03-29
US62/650,151 2018-03-29
PCT/US2019/024976 WO2019191667A1 (en) 2018-03-29 2019-03-29 Imidazopiperazine inhibitors of transcription activating proteins

Publications (3)

Publication Number Publication Date
JP2021519308A JP2021519308A (ja) 2021-08-10
JP2021519308A5 true JP2021519308A5 (enExample) 2022-03-30
JP7387627B2 JP7387627B2 (ja) 2023-11-28

Family

ID=68057632

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2020551963A Active JP7387627B2 (ja) 2018-03-29 2019-03-29 転写活性化タンパク質のイミダゾピペラジン阻害剤

Country Status (12)

Country Link
US (3) US11058688B2 (enExample)
EP (1) EP3773587A4 (enExample)
JP (1) JP7387627B2 (enExample)
KR (1) KR102815607B1 (enExample)
CN (1) CN112165944B (enExample)
AU (2) AU2019245403B2 (enExample)
BR (1) BR112020019824A2 (enExample)
CA (1) CA3095367A1 (enExample)
IL (1) IL277628A (enExample)
RU (1) RU2020131507A (enExample)
WO (1) WO2019191667A1 (enExample)
ZA (1) ZA202006092B (enExample)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2020131507A (ru) 2018-03-29 2022-05-04 Боард Оф Реджентс, Де Юниверсити Оф Техас Систем Имидазопиперазиновые ингибиторы белков-активаторов транскрипции
WO2019195846A1 (en) 2018-04-06 2019-10-10 Board Of Regents, The University Of Texas System Imidazopiperazinone inhibitors of transcription activating proteins
KR102939417B1 (ko) 2020-04-25 2026-03-17 파마블럭 사이언시스 (난징), 인코포레이티드 Cbp/ep 300 억제제 및 이의 용도
EP4221708A4 (en) 2020-10-02 2024-11-06 Board of Regents, The University of Texas System IMIDAZOPIPERAZINE INHIBITORS OF TRANSCRIPTION-ACTIVATING PROTEINS
CA3193745A1 (en) * 2020-10-02 2022-04-07 Kang Le Imidazopiperazine inhibitors of transcription activating proteins
US20240122941A1 (en) * 2020-12-25 2024-04-18 National Cancer Center Therapy based on synthetic lethality in swi/snf complex-dysfunction cancer
CN121851016A (zh) * 2021-04-21 2026-04-14 长春金赛药业有限责任公司 含咪唑稠环类衍生物、其制备方法及其在医药上的应用
CN113429427A (zh) * 2021-07-05 2021-09-24 湖南南新制药股份有限公司 杂环化合物及其制备方法和药物用途
CN115724857B (zh) * 2021-08-25 2024-06-21 杭州禹泓医药科技有限公司 一种芳杂环类化合物、含其的药物组合物及其应用
CN116410211A (zh) * 2021-12-29 2023-07-11 山东新时代药业有限公司 一种苯并呋喃类化合物
CN116478130B (zh) * 2022-01-21 2025-05-30 深圳默元生物科技有限公司 N-羟基喹啉甲酰胺化合物及其用途
WO2023235809A1 (en) * 2022-06-02 2023-12-07 Eli Lilly And Company Cgas inhibitors
WO2025111184A1 (en) 2023-11-21 2025-05-30 Fmc Corporation Substituted tetrahydroquinoline and tetrahydroquinoxaline herbicides

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK1537114T3 (da) 2002-08-07 2006-11-13 Novartis Ag Organiske forbindelser som midler til behandling af aldosteronmedierede tilstande
US20070004736A1 (en) 2002-11-22 2007-01-04 Keiji Kubo Imidazole derivative, process for producing the same, and use
MX2008015008A (es) 2006-05-26 2008-12-05 Novartis Ag INHIBIDORES DE SINTASA DE ALDOSTERONA Y/O DE 11ß-HIDROXILASA.
US7943617B2 (en) * 2006-11-27 2011-05-17 Bristol-Myers Squibb Company Heterobicyclic compounds useful as kinase inhibitors
WO2008078291A1 (en) 2006-12-22 2008-07-03 Actelion Pharmaceuticals Ltd 5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine derivatives
CN101686989B (zh) 2007-06-21 2016-10-19 卡拉治疗学股份有限公司 取代的咪唑并杂环
US8859538B2 (en) 2007-06-21 2014-10-14 Cara Therapeutics, Inc. Uses of substituted imidazoheterocycles
CN101417999A (zh) 2007-10-25 2009-04-29 上海恒瑞医药有限公司 哌嗪类衍生物,其制备方法及其在医药上的应用
CN101468988A (zh) 2007-12-26 2009-07-01 上海恒瑞医药有限公司 哌嗪类衍生物,其制备方法及其在医药上的应用
CN102076694A (zh) 2008-06-25 2011-05-25 埃科特莱茵药品有限公司 5,6,7,8-四氢-咪唑并[1,5-a]吡嗪化合物
PE20120121A1 (es) * 2008-12-08 2012-02-20 Gilead Connecticut Inc Derivados de imidazopirazina como inhibidores de syk
WO2011092120A1 (en) 2010-01-29 2011-08-04 Nerviano Medical Sciences S.R.L. 6,7- dihydroimidazo [1,5-a] pyrazin-8 (5h) - one derivatives as protein kinase modulators
CN102372716A (zh) 2010-08-09 2012-03-14 江苏恒瑞医药股份有限公司 酞嗪酮类衍生物、其制备方法及其在医药上的应用
US9145418B2 (en) 2011-10-07 2015-09-29 Nerviano Medical Sciences S.R.L. Substituted 3,4-dihydropyrrolo[1,2-a]pyrazin-1(2H)-ones as protein kinase inhibitors
CN103087067A (zh) * 2012-08-02 2013-05-08 盛世泰科生物医药技术(苏州)有限公司 作为二肽基酶抑制剂的化合物及其组合物,以及它们的用途
US9695176B2 (en) 2012-10-18 2017-07-04 Bristol-Myers Squibb Company Substituted imidazo[1,5-a]pyrazines as CGRP receptor antagonists
US20160113893A1 (en) * 2013-06-12 2016-04-28 Proximagen Limited New therapeutic uses of enzyme inhibitors
WO2014206150A1 (en) * 2013-06-28 2014-12-31 Abbvie Inc. Bromodomain inhibitors
JP6820254B2 (ja) 2014-10-10 2021-01-27 ジェネンテック, インコーポレイテッド 治療用化合物およびその使用
EP3632915A1 (en) 2014-11-27 2020-04-08 Genentech, Inc. 4,5,6,7-tetrahydro-1 h-pyrazolo[4,3-c]pyridin-3-amine compounds as cbp and/or ep300 inhibitors
MA41338B1 (fr) 2015-01-16 2019-07-31 Hoffmann La Roche Composés de pyrazine pour le traitement de maladies infectieuses
GB201506660D0 (en) 2015-04-20 2015-06-03 Cellcentric Ltd Pharmaceutical compounds
GB201506658D0 (en) 2015-04-20 2015-06-03 Cellcentric Ltd Pharmaceutical compounds
EP3445750A4 (en) 2016-04-18 2019-11-27 Celgene Quanticel Research, Inc. THERAPEUTIC COMPOUNDS
JP7014736B2 (ja) 2016-05-24 2022-02-01 ジェネンテック, インコーポレイテッド がんの処置のためのピラゾロピリジン誘導体
EP3464270B1 (en) 2016-05-24 2022-02-23 Genentech, Inc. Heterocyclic inhibitors of cbp/ep300 and their use in the treatment of cancer
RU2020131507A (ru) 2018-03-29 2022-05-04 Боард Оф Реджентс, Де Юниверсити Оф Техас Систем Имидазопиперазиновые ингибиторы белков-активаторов транскрипции
WO2019195846A1 (en) 2018-04-06 2019-10-10 Board Of Regents, The University Of Texas System Imidazopiperazinone inhibitors of transcription activating proteins

Similar Documents

Publication Publication Date Title
JP2021519308A5 (enExample)
JP2015534580A5 (enExample)
FI3328827T3 (fi) Glutamiinianalogien aihiolääkkeitä
JP2015534578A5 (enExample)
RU2020111366A (ru) Триспецифичные связывающие молекулы, которые специфически связывают антигены множества злокачественных опухолей, и способы их применения
MX2021005214A (es) Farmacos anti-estrogenicos tetrahidro-1h-pirido [3,4-b] indol.
JP2017510641A5 (enExample)
JP2017186337A5 (enExample)
JP2018536624A5 (enExample)
JP2015534579A5 (enExample)
RU2014101626A (ru) Полиморфы 2-амид 1-({4-метил-5-[2-(2, 2, 2-трифтор-1, 1-диметил-этил)-пиридин-4-ил]тиазол-2-ил}амида) (s)-пирролидин-1, 2-дикарбоновой кислоты
MX338831B (es) Moduladores selectivos de receptores de androgenos.
WO2009105214A3 (en) Selective androgen receptor modulators
WO2010118287A8 (en) Selective androgen receptor modulators
JP2018516966A5 (enExample)
JP2015527318A5 (enExample)
JP2020502271A5 (enExample)
JP2014055156A5 (enExample)
JP2019524714A5 (enExample)
AU2012288626A8 (en) 2 - (2, 4, 5 - substituted -anilino) pyrimidine derivatives as EGFR modulators useful for treating cancer
JP2013523784A5 (enExample)
JP2017509586A5 (enExample)
MY183927A (en) Pyridinyl and fused pyridinyl triazolone derivatives
JP2024519188A5 (enExample)
JP2019527239A5 (enExample)