JP2020502157A5 - - Google Patents

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Publication number
JP2020502157A5
JP2020502157A5 JP2019532088A JP2019532088A JP2020502157A5 JP 2020502157 A5 JP2020502157 A5 JP 2020502157A5 JP 2019532088 A JP2019532088 A JP 2019532088A JP 2019532088 A JP2019532088 A JP 2019532088A JP 2020502157 A5 JP2020502157 A5 JP 2020502157A5
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JP
Japan
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ethyl
pharmaceutically acceptable
cancer
glioblastoma
enoylpiperazin
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JP2019532088A
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English (en)
Japanese (ja)
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JP2020502157A (ja
JP6793836B2 (ja
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Priority claimed from PCT/US2017/065246 external-priority patent/WO2018111707A1/en
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Publication of JP2020502157A5 publication Critical patent/JP2020502157A5/ja
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JP2019532088A 2016-12-16 2017-12-08 変異体idh1およびidh2阻害剤としての7−フェニルエチルアミノ−4h−ピリミド[4,5−d][1,3]オキサジン−2−オン化合物 Active JP6793836B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662435283P 2016-12-16 2016-12-16
US62/435,283 2016-12-16
PCT/US2017/065246 WO2018111707A1 (en) 2016-12-16 2017-12-08 7-phenylethylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant idh1 and idh2 inhibitors

Publications (3)

Publication Number Publication Date
JP2020502157A JP2020502157A (ja) 2020-01-23
JP2020502157A5 true JP2020502157A5 (https=) 2020-03-05
JP6793836B2 JP6793836B2 (ja) 2020-12-02

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ID=60888651

Family Applications (1)

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JP2019532088A Active JP6793836B2 (ja) 2016-12-16 2017-12-08 変異体idh1およびidh2阻害剤としての7−フェニルエチルアミノ−4h−ピリミド[4,5−d][1,3]オキサジン−2−オン化合物

Country Status (37)

Country Link
US (3) US11001596B2 (https=)
EP (2) EP3555105B1 (https=)
JP (1) JP6793836B2 (https=)
KR (1) KR102276022B1 (https=)
CN (2) CN115109075B (https=)
AU (2) AU2017378060B2 (https=)
CA (1) CA3045303C (https=)
CL (1) CL2019001551A1 (https=)
CO (1) CO2019005287A2 (https=)
CR (1) CR20190252A (https=)
CY (1) CY1123577T1 (https=)
DK (1) DK3555105T3 (https=)
DO (1) DOP2019000163A (https=)
EA (1) EA036112B1 (https=)
EC (1) ECSP19042682A (https=)
ES (2) ES2941631T3 (https=)
HR (1) HRP20201882T1 (https=)
HU (1) HUE052067T2 (https=)
IL (1) IL267236B (https=)
JO (1) JOP20190142B1 (https=)
LT (1) LT3555105T (https=)
MA (2) MA47399B1 (https=)
MD (1) MD3555105T2 (https=)
MX (1) MX385562B (https=)
MY (1) MY197313A (https=)
NZ (1) NZ754115A (https=)
PE (1) PE20190977A1 (https=)
PH (1) PH12019501328B1 (https=)
PL (1) PL3555105T3 (https=)
PT (1) PT3555105T (https=)
RS (1) RS61108B1 (https=)
SA (1) SA519401897B1 (https=)
SI (1) SI3555105T1 (https=)
TN (1) TN2019000158A1 (https=)
UA (1) UA123640C2 (https=)
WO (1) WO2018111707A1 (https=)
ZA (1) ZA201903125B (https=)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3194383B1 (en) 2014-09-19 2019-11-06 Forma Therapeutics, Inc. Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors
MA53352A (fr) 2014-09-19 2021-09-15 Forma Therapeutics Inc Dérivés de pyridin-2-(1h)-one-quinolinone en tant qu'inhibiteurs d'isocitrate déshydrogénase
MX372964B (es) 2014-09-19 2020-03-27 Forma Therapeutics Inc Derivados de fenil quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh)
AU2015317327B9 (en) 2014-09-19 2020-04-09 Forma Therapeutics, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US9624175B2 (en) 2015-04-21 2017-04-18 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US10407419B2 (en) 2015-04-21 2019-09-10 Forma Therapeutics, Inc. Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors
EP3640251B1 (en) 2016-10-24 2021-12-08 Astrazeneca AB 6,7,8,9-tetrahydro-3h-pyrazolo[4,3-f]isoquinoline derivatives useful in the treatment of cancer
JP7291077B2 (ja) 2016-12-16 2023-06-14 ヤンセン ファーマシューティカ エヌ.ベー. Jakファミリーのキナーゼの低分子阻害物質
ES2941631T3 (es) * 2016-12-16 2023-05-24 Lilly Co Eli Compuestos de Pirido[4,3-d][1,3]oxazin-2-ona como inhibidores de IDH1 e IDH2 mutantes
JOP20190144A1 (ar) 2016-12-16 2019-06-16 Janssen Pharmaceutica Nv إيميدازو بيرولو بيريدين كمثبطات لعائلة jak الخاصة بإنزيمات الكيناز
PL3494116T3 (pl) 2017-01-30 2020-04-30 Astrazeneca Ab Modulatory receptora estrogenowego
US11013734B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation
US20210196701A1 (en) 2018-05-16 2021-07-01 Forma Therapeutics, Inc. Inhibiting mutant idh-1
WO2019222551A1 (en) 2018-05-16 2019-11-21 Forma Therapeutics, Inc. Solid forms of ((s)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile
US11013733B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1)
US11311527B2 (en) 2018-05-16 2022-04-26 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
TW202016110A (zh) 2018-06-15 2020-05-01 比利時商健生藥品公司 Jak激酶家族之小分子抑制劑
CN115038700B (zh) * 2019-11-08 2025-07-25 内尔维亚诺医疗科学公司 偕二取代的杂环化合物及其作为idh抑制剂的用途
MX2022011846A (es) * 2020-03-23 2023-01-04 Lilly Co Eli Metodo para el tratamiento de sujetos resistentes al inhibidor idh1.
CN115443137B (zh) * 2020-03-23 2024-05-31 伊莱利利公司 使用突变idh抑制剂和bcl-2抑制剂的组合疗法
AU2021242260B2 (en) * 2020-03-23 2023-12-14 Eli Lilly And Company Combination therapy with a mutant IDH inhibitor
MX2022013258A (es) 2020-04-24 2022-11-14 Astrazeneca Ab Formulaciones farmaceuticas.
MX2022013391A (es) 2020-04-24 2022-11-30 Astrazeneca Ab Pauta posologica para el tratamiento del cancer.
US12559505B2 (en) 2020-06-28 2026-02-24 Wigen Biomedicine Technology (shanghai) Co., Ltd. IDH mutant inhibitor and use thereof
WO2022020281A1 (en) 2020-07-20 2022-01-27 Eli Lilly And Company Combination therapy with a mutant idh1 inhibitor, a deoxyadenosine analog, and a platinum agent
MX2023010642A (es) 2021-03-11 2023-11-28 Janssen Pharmaceutica Nv Lorpucitinib para uso en el tratamiento de trastornos mediados por jak.
CN113588768B (zh) * 2021-05-18 2022-07-05 国家卫生健康委科学技术研究所 一种以分子图像方式定量组织内内源性代谢物的质谱方法
US20240261294A1 (en) * 2021-06-09 2024-08-08 Eli Lilly And Company Method for treating idh inhibitor-resistant subjects
CA3217608A1 (en) 2021-06-15 2022-12-22 Yuli Xie Idh mutant inhibitor and use thereof
US11746115B2 (en) 2021-08-13 2023-09-05 Eli Lilly And Company Solid forms of 7-[[(1S)-1-[4-[(1S)-2-cyclopropyl-1-(4-prop-2-enoylpiperazin-1-yl)ethyl]phenyl]ethyl]amino]-1-ethyl-4H-pyrimido[4,5-d][1,3]oxazin-2-one
WO2023141087A1 (en) 2022-01-19 2023-07-27 Eli Lilly And Company Combination therapy with a mutant idh inhibitor

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112014007310A2 (pt) * 2011-09-27 2017-04-04 Novartis Ag 3-pirimidin-4-il-oxazolidin-2-onas como inibidores de idh mutante
AU2014229283B2 (en) * 2013-03-14 2016-07-28 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant IDH
WO2014147586A1 (en) * 2013-03-22 2014-09-25 Novartis Ag 1-(2-(ethylamino)pyrimidin-4-yl)pyrrolidin-2-ones as inhibitors of mutant idh
US9624175B2 (en) * 2015-04-21 2017-04-18 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
CN107405687A (zh) * 2015-04-24 2017-11-28 哈利伯顿能源服务公司 制作陶瓷或金属间化合物零件的方法
ES2764523T3 (es) * 2015-07-27 2020-06-03 Lilly Co Eli Compuestos de 7-feniletilamino-4H-pirimido[4,5-D][1,3]oxazin-2-ona y su uso como inhibidores de IDH1 mutantes
CN109311863B (zh) * 2016-06-06 2021-10-29 伊莱利利公司 突变型idh1抑制剂
ES2941631T3 (es) * 2016-12-16 2023-05-24 Lilly Co Eli Compuestos de Pirido[4,3-d][1,3]oxazin-2-ona como inhibidores de IDH1 e IDH2 mutantes

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