JP2020502116A5 - - Google Patents

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Publication number
JP2020502116A5
JP2020502116A5 JP2019531713A JP2019531713A JP2020502116A5 JP 2020502116 A5 JP2020502116 A5 JP 2020502116A5 JP 2019531713 A JP2019531713 A JP 2019531713A JP 2019531713 A JP2019531713 A JP 2019531713A JP 2020502116 A5 JP2020502116 A5 JP 2020502116A5
Authority
JP
Japan
Prior art keywords
compound according
group
structural formula
compound
pyridinyl
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.)
Pending
Application number
JP2019531713A
Other languages
English (en)
Japanese (ja)
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JP2020502116A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2017/067050 external-priority patent/WO2018118793A1/en
Publication of JP2020502116A publication Critical patent/JP2020502116A/ja
Publication of JP2020502116A5 publication Critical patent/JP2020502116A5/ja
Pending legal-status Critical Current

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JP2019531713A 2016-12-19 2017-12-18 突然変異イソクエン酸デヒドロゲナーゼの阻害およびその組成物と方法 Pending JP2020502116A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201662436328P 2016-12-19 2016-12-19
US62/436,328 2016-12-19
US201762536367P 2017-07-24 2017-07-24
US62/536,367 2017-07-24
PCT/US2017/067050 WO2018118793A1 (en) 2016-12-19 2017-12-18 Inhibitors of mutant isocitrate dehydrogenases and compositions and methods thereof

Publications (2)

Publication Number Publication Date
JP2020502116A JP2020502116A (ja) 2020-01-23
JP2020502116A5 true JP2020502116A5 (enExample) 2021-02-04

Family

ID=62627122

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2019531713A Pending JP2020502116A (ja) 2016-12-19 2017-12-18 突然変異イソクエン酸デヒドロゲナーゼの阻害およびその組成物と方法

Country Status (8)

Country Link
US (2) US11149032B2 (enExample)
EP (1) EP3555079A4 (enExample)
JP (1) JP2020502116A (enExample)
KR (1) KR20190092476A (enExample)
CN (1) CN110291085B (enExample)
AU (1) AU2017379796B2 (enExample)
CA (1) CA3047136A1 (enExample)
WO (1) WO2018118793A1 (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109311863B (zh) * 2016-06-06 2021-10-29 伊莱利利公司 突变型idh1抑制剂
WO2019213403A1 (en) 2018-05-02 2019-11-07 Kinnate Biopharma Inc. Inhibitors of cyclin-dependent kinases
AU2019291935A1 (en) * 2018-06-29 2021-02-04 Kinnate Biopharma Inc. Inhibitors of cyclin-dependent kinases
CN111825666B (zh) * 2019-04-23 2024-03-08 上海仕谱生物科技有限公司 二聚或多聚体形式的突变型idh抑制剂
WO2022056453A1 (en) * 2020-09-14 2022-03-17 Totus Medicines Inc. Therapeutic conjugates
CN120554346A (zh) * 2024-02-28 2025-08-29 中国科学院上海药物研究所 一类噁唑酮取代的嘧啶胺化合物及其制备方法、药物组合物和用途

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030004174A9 (en) * 2000-02-17 2003-01-02 Armistead David M. Kinase inhibitors
WO2008080937A1 (en) * 2006-12-28 2008-07-10 Basf Se 2-substituted pyrimidines i in therapy
MX342326B (es) * 2011-09-27 2016-09-26 Novartis Ag 3-pirimidin-4-il-oxazolidin-2-onas como inhibidoras de idh mutante.
CA2961793C (en) * 2014-09-19 2021-03-16 Forma Therapeutics, Inc. Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors
WO2017140758A1 (en) * 2016-02-19 2017-08-24 Debiopharm International S.A. Derivatives of 2-amino-4-(2-oxazolidinon-3-yl)-pyrimidine fused with a five-membered heteroaromatic ring in 5,6-position which are useful for the treatment of various cancers
CN109311863B (zh) * 2016-06-06 2021-10-29 伊莱利利公司 突变型idh1抑制剂

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