JP2016533366A5 - - Google Patents

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Publication number
JP2016533366A5
JP2016533366A5 JP2016523925A JP2016523925A JP2016533366A5 JP 2016533366 A5 JP2016533366 A5 JP 2016533366A5 JP 2016523925 A JP2016523925 A JP 2016523925A JP 2016523925 A JP2016523925 A JP 2016523925A JP 2016533366 A5 JP2016533366 A5 JP 2016533366A5
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JP
Japan
Prior art keywords
cancer
compound
pharmaceutically acceptable
pharmaceutical composition
acceptable salt
Prior art date
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Application number
JP2016523925A
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English (en)
Japanese (ja)
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JP6374959B2 (ja
JP2016533366A (ja
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Publication date
Priority claimed from US14/056,560 external-priority patent/US9376448B2/en
Application filed filed Critical
Priority claimed from PCT/US2014/061033 external-priority patent/WO2015058031A1/en
Publication of JP2016533366A publication Critical patent/JP2016533366A/ja
Publication of JP2016533366A5 publication Critical patent/JP2016533366A5/ja
Application granted granted Critical
Publication of JP6374959B2 publication Critical patent/JP6374959B2/ja
Active legal-status Critical Current
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JP2016523925A 2013-10-17 2014-10-17 Dna−pk阻害剤 Active JP6374959B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US14/056,560 US9376448B2 (en) 2012-04-24 2013-10-17 DNA-PK inhibitors
US14/056,560 2013-10-17
PCT/US2014/061033 WO2015058031A1 (en) 2013-10-17 2014-10-17 Dna-pk inhibitors

Publications (3)

Publication Number Publication Date
JP2016533366A JP2016533366A (ja) 2016-10-27
JP2016533366A5 true JP2016533366A5 (enExample) 2017-11-24
JP6374959B2 JP6374959B2 (ja) 2018-08-15

Family

ID=51932571

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016523925A Active JP6374959B2 (ja) 2013-10-17 2014-10-17 Dna−pk阻害剤

Country Status (17)

Country Link
EP (1) EP3057959B1 (enExample)
JP (1) JP6374959B2 (enExample)
CN (1) CN105636958B (enExample)
AU (1) AU2014337208B2 (enExample)
BR (1) BR112016008423B1 (enExample)
CA (1) CA2927392C (enExample)
DK (1) DK3057959T3 (enExample)
ES (1) ES2671354T3 (enExample)
HR (1) HRP20180804T1 (enExample)
HU (1) HUE037516T2 (enExample)
LT (1) LT3057959T (enExample)
PL (1) PL3057959T3 (enExample)
PT (1) PT3057959T (enExample)
RS (1) RS57306B1 (enExample)
SI (1) SI3057959T1 (enExample)
TR (1) TR201807411T4 (enExample)
WO (1) WO2015058031A1 (enExample)

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RS59512B1 (sr) 2012-09-25 2019-12-31 Hoffmann La Roche Derivati heksahidropirolo[3,4−c]pirola i srodna jedinjenja kao inhibitori autotaksina (atx) i kao inhibitori proizvodnje lizofosfatidne kiseline (lpa) za lečenje npr. bubrežnih bolesti
AR095079A1 (es) 2013-03-12 2015-09-16 Hoffmann La Roche Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo
WO2015078803A1 (en) 2013-11-26 2015-06-04 F. Hoffmann-La Roche Ag NEW OCTAHYDRO-CYCLOBUTA [1,2-c;3,4-c']DIPYRROL-2-YL
CN106103446B (zh) 2014-03-26 2019-07-30 豪夫迈·罗氏有限公司 作为自分泌运动因子(atx)和溶血磷脂酸(lpa)生产抑制剂的二环化合物
KR20160128428A (ko) 2014-03-26 2016-11-07 에프. 호프만-라 로슈 아게 오토탁신(atx) 및 리소포스파티드산(lpa) 생성 억제제로서의 축합형 [1,4]다이아제핀 화합물
MA41898A (fr) 2015-04-10 2018-02-13 Hoffmann La Roche Dérivés de quinazolinone bicyclique
CN108026077B (zh) 2015-09-04 2021-11-05 豪夫迈·罗氏有限公司 苯氧基甲基衍生物
CR20180143A (es) 2015-09-24 2018-05-03 Hoffmann La Roche Nuevos compuestos biciclicos como inhibidores duales de atx/ca
EP3353178B1 (en) 2015-09-24 2021-07-14 F. Hoffmann-La Roche AG Bicyclic compounds as dual atx/ca inhibitors
PE20180461A1 (es) 2015-09-24 2018-03-06 Hoffmann La Roche Nuevos compuestos biciclicos como inhibidores de la atx
KR20180054635A (ko) 2015-09-24 2018-05-24 에프. 호프만-라 로슈 아게 오토탁신(atx) 억제제로서 이환형 화합물
CR20180323A (es) 2015-11-20 2018-08-06 Idorsia Pharmaceuticals Ltd Derivados de indol n-sustituídos como moduladores de los receptores de pge2
US11110108B2 (en) 2016-09-27 2021-09-07 Vertex Pharmaceuticals Incorporated Method for treating cancer using a combination of DNA-damaging agents and DNA-PK inhibitors
RU2019132254A (ru) 2017-03-16 2021-04-16 Ф. Хоффманн-Ля Рош Аг Гетероциклические соединения, пригодные в качестве дуальных ингибиторов atx/ca
CN110382484B (zh) 2017-03-16 2022-12-06 豪夫迈·罗氏有限公司 新的作为atx抑制剂的二环化合物
AR111808A1 (es) * 2017-05-18 2019-08-21 Idorsia Pharmaceuticals Ltd Derivados de pirimidina como moduladores del receptor de pge2
TWI768043B (zh) 2017-05-18 2022-06-21 瑞士商愛杜西亞製藥有限公司 N-取代吲哚衍生物
US11325899B2 (en) 2017-05-18 2022-05-10 Idorsia Pharmaceuticals Ltd Benzofurane and benzothiophene derivatives as PGE2 receptor modulators
ES2896476T3 (es) * 2017-05-18 2022-02-24 Idorsia Pharmaceuticals Ltd Derivados de pirimidina
HRP20211533T1 (hr) 2017-05-18 2022-01-07 Idorsia Pharmaceuticals Ltd Derivati fenila kao modulatori receptora pge2
EP3717475B1 (en) 2017-11-20 2023-06-07 Icahn School of Medicine at Mount Sinai Kinase inhibitor compounds and compositions and methods of use
WO2019136320A1 (en) 2018-01-05 2019-07-11 Icahn School Of Medicine At Mount Sinai Method of increasing proliferation of pancreatic beta cells, treatment method, and composition
US12121524B2 (en) 2018-01-17 2024-10-22 Vertex Pharmaceuticals Incorporated DNA-PK inhibitors
EP3740483B1 (en) 2018-01-17 2023-01-11 Vertex Pharmaceuticals Incorporated Quinoxalinone compounds, compositions, methods, and kits for increasing genome editing efficiency
AU2019240065A1 (en) 2018-03-20 2020-09-24 Icahn School Of Medicine At Mount Sinai Kinase inhibitor compounds and compositions and methods of use
JP2022515650A (ja) * 2018-12-31 2022-02-21 アイカーン スクール オブ メディシン アット マウント サイナイ キナーゼ阻害剤化合物及び組成物ならびに使用方法
CN112300126A (zh) * 2019-07-31 2021-02-02 山东轩竹医药科技有限公司 杂环类dna-pk抑制剂
CN112574179B (zh) * 2019-09-29 2022-05-10 山东轩竹医药科技有限公司 Dna-pk抑制剂
CN112574211B (zh) * 2019-09-29 2022-06-14 山东轩竹医药科技有限公司 杂环类激酶抑制剂
WO2021136463A1 (zh) * 2019-12-31 2021-07-08 成都百裕制药股份有限公司 嘌呤衍生物及其在医药上的用途
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
WO2025034702A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Rmc-6291 for use in the treatment of ras protein-related disease or disorder
WO2025080946A2 (en) 2023-10-12 2025-04-17 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
WO2025217307A1 (en) 2024-04-09 2025-10-16 Revolution Medicines, Inc. Methods for predicting response to a ras(on) inhibitor and combination therapies
WO2025229177A1 (en) 2024-05-02 2025-11-06 Idorsia Pharmaceuticals Ltd Crystalline forms of an n-substituted indole derivative
WO2025240847A1 (en) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Ras inhibitors

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EP1351946A2 (en) * 2000-09-01 2003-10-15 Icos Corporation Materials and methods to potentiate cancer treatment
EP1678147B1 (en) * 2003-09-15 2012-08-08 Lead Discovery Center GmbH Pharmaceutically active 4,6-disubstituted aminopyrimidine derivatives as modulators of protein kinases
EP1901747A2 (en) * 2005-05-25 2008-03-26 Ingenium Pharmaceuticals AG Pyrimidine-based cdk inhibitors for treating pain
US8202876B2 (en) * 2006-10-02 2012-06-19 Irm Llc Compounds and compositions as protein kinase inhibitors
CN102834380B (zh) * 2010-03-10 2015-04-01 阿斯利康公司 蛋白激酶的抑制剂
SMT201800608T1 (it) * 2012-04-24 2019-01-11 Vertex Pharma Inibitori di dna-pk

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