JP2019518770A5 - - Google Patents

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Publication number
JP2019518770A5
JP2019518770A5 JP2018567108A JP2018567108A JP2019518770A5 JP 2019518770 A5 JP2019518770 A5 JP 2019518770A5 JP 2018567108 A JP2018567108 A JP 2018567108A JP 2018567108 A JP2018567108 A JP 2018567108A JP 2019518770 A5 JP2019518770 A5 JP 2019518770A5
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JP
Japan
Prior art keywords
compound
salt
atropisomer
formula
pharmaceutical composition
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JP2018567108A
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English (en)
Japanese (ja)
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JP2019518770A (ja
JP6987798B2 (ja
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Priority claimed from PCT/US2017/038549 external-priority patent/WO2017223202A1/en
Publication of JP2019518770A publication Critical patent/JP2019518770A/ja
Publication of JP2019518770A5 publication Critical patent/JP2019518770A5/ja
Application granted granted Critical
Publication of JP6987798B2 publication Critical patent/JP6987798B2/ja
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JP2018567108A 2016-06-22 2017-06-21 癌の治療に変異体idh1阻害剤として有用なチアゾール誘導体 Active JP6987798B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662353298P 2016-06-22 2016-06-22
US62/353,298 2016-06-22
PCT/US2017/038549 WO2017223202A1 (en) 2016-06-22 2017-06-21 Thiazole derivatives useful as mutant idh1 inhibitors for treating cancer

Publications (3)

Publication Number Publication Date
JP2019518770A JP2019518770A (ja) 2019-07-04
JP2019518770A5 true JP2019518770A5 (https=) 2020-07-30
JP6987798B2 JP6987798B2 (ja) 2022-01-05

Family

ID=59276859

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2018567108A Active JP6987798B2 (ja) 2016-06-22 2017-06-21 癌の治療に変異体idh1阻害剤として有用なチアゾール誘導体

Country Status (8)

Country Link
US (1) US10836759B2 (https=)
EP (1) EP3475276B1 (https=)
JP (1) JP6987798B2 (https=)
CN (1) CN109641887B (https=)
AU (1) AU2017281088B2 (https=)
CA (1) CA3028999A1 (https=)
ES (1) ES2880347T3 (https=)
WO (1) WO2017223202A1 (https=)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016044789A1 (en) 2014-09-19 2016-03-24 Forma Therapeutics, Inc. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
ES2768694T3 (es) 2014-09-19 2020-06-23 Forma Therapeutics Inc Composiciones de quinolinona pirimidinas como inhibidores de isocitrato dehidrogenasa mutante
CA2961811C (en) 2014-09-19 2021-11-02 Forma Therapeutics, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
CA2961807A1 (en) 2014-09-19 2016-03-24 Forma Therapeutics, Inc. Phenyl 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
US10294206B2 (en) 2015-04-21 2019-05-21 Forma Tm2, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US10532047B2 (en) 2018-05-16 2020-01-14 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
WO2019222553A1 (en) 2018-05-16 2019-11-21 Forma Therapeutics, Inc. Inhibiting mutant idh-1
US11013734B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation
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)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2010223919B2 (en) * 2009-03-13 2016-03-31 Les Laboratoires Servier Methods and compositions for cell-proliferation-related disorders
CA2756347A1 (en) 2009-03-24 2010-09-30 Gilead Calistoga Llc Atropisomers of 2-purinyl-3-tolyl-quinazolinone derivatives and methods of use
CN105209460A (zh) * 2013-03-14 2015-12-30 诺华股份有限公司 作为突变idh抑制剂的3-嘧啶-4-基-噁唑烷-2-酮化合物
ES2905564T3 (es) * 2014-12-22 2022-04-11 Us Health Inhibidores mutantes de IDH1 útiles para tratar el cáncer

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