JP2019524883A5 - - Google Patents

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JP2019524883A5
JP2019524883A5 JP2019529309A JP2019529309A JP2019524883A5 JP 2019524883 A5 JP2019524883 A5 JP 2019524883A5 JP 2019529309 A JP2019529309 A JP 2019529309A JP 2019529309 A JP2019529309 A JP 2019529309A JP 2019524883 A5 JP2019524883 A5 JP 2019524883A5
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JP
Japan
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JP2019529309A
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Japanese (ja)
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JP6959663B2 (ja
JP2019524883A (ja
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Priority claimed from CN201610647295.0A external-priority patent/CN107698593A/zh
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JP2019529309A 2016-08-09 2017-07-27 Fgfr阻害剤としての複素環化合物 Active JP6959663B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN201610647295.0A CN107698593A (zh) 2016-08-09 2016-08-09 作为fgfr抑制剂的杂环化合物
CN201610647295.0 2016-08-09
PCT/CN2017/094620 WO2018028438A1 (zh) 2016-08-09 2017-07-27 作为fgfr抑制剂的杂环化合物

Publications (3)

Publication Number Publication Date
JP2019524883A JP2019524883A (ja) 2019-09-05
JP2019524883A5 true JP2019524883A5 (US07794700-20100914-C00125.png) 2020-07-16
JP6959663B2 JP6959663B2 (ja) 2021-11-02

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ID=61162708

Family Applications (1)

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JP2019529309A Active JP6959663B2 (ja) 2016-08-09 2017-07-27 Fgfr阻害剤としての複素環化合物

Country Status (7)

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US (1) US10752631B2 (US07794700-20100914-C00125.png)
EP (1) EP3498706A4 (US07794700-20100914-C00125.png)
JP (1) JP6959663B2 (US07794700-20100914-C00125.png)
KR (1) KR20190035870A (US07794700-20100914-C00125.png)
CN (2) CN107698593A (US07794700-20100914-C00125.png)
CA (1) CA3032921A1 (US07794700-20100914-C00125.png)
WO (1) WO2018028438A1 (US07794700-20100914-C00125.png)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2018266705B2 (en) 2017-05-08 2023-05-04 Gritstone Bio, Inc. Alphavirus neoantigen vectors
CA3129665A1 (en) 2019-03-21 2020-09-24 Onxeo A dbait molecule in combination with kinase inhibitor for the treatment of cancer
WO2020236524A1 (en) * 2019-05-17 2020-11-26 Kinnate Biopharma Inc. Inhibitors of fibroblast growth factor receptor kinases
CA3140019A1 (en) 2019-05-30 2020-12-03 Gritstone Bio, Inc. Modified adenoviruses
KR20220098759A (ko) 2019-11-08 2022-07-12 인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) 키나제 억제제에 대해 내성을 획득한 암의 치료 방법
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
AU2021285974A1 (en) * 2020-06-05 2023-01-19 Kinnate Biopharma Inc. Inhibitors of fibroblast growth factor receptor kinases
WO2022032196A2 (en) 2020-08-06 2022-02-10 Gritstone Bio, Inc. Multiepitope vaccine cassettes
CN112480109B (zh) * 2020-11-16 2022-04-01 浙江大学 吡啶并[2,3-b]吡嗪-3(4H)-酮类衍生物及其用途
JP2024503661A (ja) * 2021-01-12 2024-01-26 ベイジン・イノケア・ファーマ・テク・カンパニー・リミテッド (s)-1-(1-アクリロイルピロリジン-3-イル)-3-((3,5-ジメトキシフェニル)エチニル)-5-(メチルアミノ)-1h-ピラゾール-4-カルボキサミドの製造方法
CN114853739B (zh) * 2021-02-03 2023-09-22 药雅科技(上海)有限公司 一种炔代吡嗪类fgfr抑制剂及其制备方法和用途
CN115043832B (zh) * 2021-03-08 2023-08-22 药雅科技(上海)有限公司 一种fgfr抑制剂炔代杂环类化合物及其制备方法和用途
WO2024083111A1 (zh) * 2022-10-18 2024-04-25 首药控股(北京)股份有限公司 一种新型杂环化合物

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7659274B2 (en) * 2006-01-25 2010-02-09 Osi Pharmaceuticals, Inc. Unsaturated mTOR inhibitors
PL2657233T3 (pl) 2012-01-19 2015-01-30 Taiho Pharmaceutical Co Ltd 3,5-dipodstawiony związek alkinylobenzenowy i jego sól
EP2970206A1 (en) * 2013-03-13 2016-01-20 Boston Biomedical, Inc. 3-(aryl or heteroaryl) methyleneindolin-2-one derivatives as inhibitors of cancer stem cell pathway kinases for the treatment of cancer
DK3023100T3 (da) * 2013-07-18 2019-05-27 Taiho Pharmaceutical Co Ltd Antitumorlægemiddel til intermitterende administration af fgfr-hæmmer
WO2015008844A1 (ja) * 2013-07-18 2015-01-22 大鵬薬品工業株式会社 Fgfr阻害剤耐性癌の治療薬
CN104341425B (zh) * 2013-08-08 2018-11-02 上海医药集团股份有限公司 氘代乙炔衍生物、其药物组合物及应用
SG11201602070TA (en) * 2013-09-30 2016-04-28 Beijing Synercare Pharma Tech Co Ltd Substituted nicotinimide inhibitors of btk and their preparation and use in the treatment of cancer, inflammation and autoimmune disease
MX2017002206A (es) * 2014-08-19 2018-01-23 Shanghai Haihe Pharmaceutical Co Ltd Compuestos de indazol como inhibidores de cinasa fgfr, preparacion y uso de los mismos.

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