JP2023548657A - がんの処置に使用するための、egfrおよび/またはher2のヘテロ環阻害剤 - Google Patents

がんの処置に使用するための、egfrおよび/またはher2のヘテロ環阻害剤 Download PDF

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JP2023548657A
JP2023548657A JP2023521702A JP2023521702A JP2023548657A JP 2023548657 A JP2023548657 A JP 2023548657A JP 2023521702 A JP2023521702 A JP 2023521702A JP 2023521702 A JP2023521702 A JP 2023521702A JP 2023548657 A JP2023548657 A JP 2023548657A
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JPWO2022076831A5 (https=
JP2023548657A5 (https=
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エンジェル グズマン-ペレス
ベンジャミン シー. ミルグラム
ライアン ディー. ホワイト
ジーン ジュニア デイビッド セイント
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Scorpion Therapeutics Inc
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    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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    • A61K31/4375Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
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    • C07D491/12Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
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JP2023521702A 2020-10-09 2021-10-08 がんの処置に使用するための、egfrおよび/またはher2のヘテロ環阻害剤 Pending JP2023548657A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US202063089965P 2020-10-09 2020-10-09
US63/089,965 2020-10-09
US202163151468P 2021-02-19 2021-02-19
US63/151,468 2021-02-19
PCT/US2021/054191 WO2022076831A2 (en) 2020-10-09 2021-10-08 Methods for treating cancer

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JP2023548657A true JP2023548657A (ja) 2023-11-20
JPWO2022076831A5 JPWO2022076831A5 (https=) 2024-10-15
JP2023548657A5 JP2023548657A5 (https=) 2024-10-15

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US (1) US20240101576A1 (https=)
EP (1) EP4225445A2 (https=)
JP (1) JP2023548657A (https=)
KR (1) KR20230107419A (https=)
AU (1) AU2021358596A1 (https=)
BR (1) BR112023006531A2 (https=)
CA (1) CA3198202A1 (https=)
CL (2) CL2023001012A1 (https=)
IL (1) IL301929A (https=)
MX (1) MX2023004085A (https=)
PH (1) PH12023500010A1 (https=)
TW (1) TW202227063A (https=)
WO (1) WO2022076831A2 (https=)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201905721D0 (en) 2019-04-24 2019-06-05 Univ Dundee Compounds
EP4323356A1 (en) 2021-04-13 2024-02-21 Nuvalent, Inc. Amino-substituted heterocycles for treating cancers with egfr mutations
IL321504A (en) * 2022-12-23 2025-08-01 Tay Therapeutics Ltd Selective beta inhibitors and their uses
CN115819418B (zh) * 2023-02-14 2023-04-28 山东绿叶制药有限公司 Plk1激酶抑制剂及其制备方法和应用
CN121909190A (zh) * 2023-06-08 2026-04-21 安塔列斯疗法股份有限公司 1,5-二氢-4H-吡咯并[3,2-c]吡啶-4-酮用于癌症治疗
CN121712773A (zh) 2023-06-08 2026-03-20 安塔列斯疗法股份有限公司 1,5-二氢-4h-吡咯并[3,2-c]吡啶-4-酮用于癌症治疗
CN119528906A (zh) * 2023-08-30 2025-02-28 中国科学院上海药物研究所 氮杂螺环类化合物及其制备方法、药物组合物和应用
EP4534085A1 (en) * 2023-10-03 2025-04-09 Scorpion Therapeutics, Inc. Compounds for use in methods of treating cancer
WO2025251058A1 (en) * 2024-05-31 2025-12-04 Celyn Therapeutics, Inc. Egfr inhibitors in cancer treatment

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012530099A (ja) * 2009-06-15 2012-11-29 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ 置換ピリミジニルピロロピリジノン誘導体、これらの製造のための方法およびキナーゼ阻害剤としてのこれらの使用
JP2018503648A (ja) * 2015-01-28 2018-02-08 バイエル ファーマ アクチエンゲゼルシャフト 4H−ピロロ[3,2−c]ピリジン−4−オン誘導体
WO2019081486A1 (en) * 2017-10-24 2019-05-02 Bayer Aktiengesellschaft 4h-pyrrolo[3,2-c]pyridin-4-one derivatives
WO2020161257A1 (en) * 2019-02-07 2020-08-13 Bayer Aktiengesellschaft 3-amino-2-[2-(acylamino)pyridin-4-yl]-1,5,6,7-tetrahydro-4h-pyrrolo[3,2-c]pyridin-4-one as csnk1 inhibitors

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6906194B2 (en) 2003-10-08 2005-06-14 Massachusetts Instititue Of Technology Fluorescence assay for kinase activity
US7964729B2 (en) 2006-08-28 2011-06-21 Massachusetts Institute Of Technology Sox-based kinase sensor
JP5825932B2 (ja) 2011-08-26 2015-12-02 キヤノン株式会社 撮像装置及びその制御方法、プログラム、及び記録媒体
WO2013092512A1 (en) 2011-12-21 2013-06-27 Bayer Intellectual Property Gmbh Substituted benzylpyrazoles
WO2013167698A1 (en) 2012-05-11 2013-11-14 Bayer Pharma Aktiengesellschaft Substituted cycloalkenopyrazoles as bub1 inhibitors for the treatment of cancer
EP2976335A1 (en) 2013-03-21 2016-01-27 Bayer Pharma Aktiengesellschaft Heteroaryl substituted indazoles
EP2976336A1 (en) 2013-03-21 2016-01-27 Bayer Pharma Aktiengesellschaft 3-heteroaryl substituted indazoles
CN105452237A (zh) 2013-06-21 2016-03-30 拜耳制药股份公司 杂芳基取代的吡唑
JP2016525076A (ja) 2013-06-21 2016-08-22 バイエル ファーマ アクチエンゲゼルシャフト 置換されたベンジルピラゾール類
WO2014202588A1 (en) 2013-06-21 2014-12-24 Bayer Pharma Aktiengesellschaft Heteroaryl substituted pyrazoles
JP2016526540A (ja) 2013-06-21 2016-09-05 バイエル ファーマ アクチエンゲゼルシャフト 置換ベンジルピラゾール
CA2928998A1 (en) 2013-10-30 2015-05-07 Bayer Pharma Aktiengesellschaft Heteroaryl substituted pyrazoles
EP3143015B1 (en) 2014-05-13 2019-02-20 ARIAD Pharmaceuticals, Inc. Heteroaryl compounds for kinase inhibition
AR100886A1 (es) 2014-06-17 2016-11-09 Bayer Pharma AG 3-amino-1,5,6,7-tetrahidro-4h-indol-4-onas
CA2989469A1 (en) 2015-06-17 2016-12-22 Bayer Pharma Aktiengesellschaft 3-amino-1,5,6,7-tetrahydro-4h-indol-4-ones
US10308629B2 (en) 2015-08-05 2019-06-04 Bayer Pharma Aktiengesellschaft 1H-pyrrol-3-amines
BR112018004175B8 (pt) 2015-09-01 2023-10-31 Taiho Pharmaceutical Co Ltd Composto pirazolo[3,4-d]pirimidina, composição farmacêutica e usos terapêuticos do dito composto
CA3091834A1 (en) 2018-02-23 2019-08-29 The Regents Of The University Of Michigan Egfr dimer disruptors and use of the same
WO2019241715A1 (en) 2018-06-14 2019-12-19 Dana-Farber Cancer Institute, Inc. Cyano quinoline amide compounds as her2 inhibitors and methods of use
WO2019246541A1 (en) 2018-06-21 2019-12-26 Dana-Farber Cancer Institute, Inc. Inhibitors of egfr and methods of use thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012530099A (ja) * 2009-06-15 2012-11-29 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ 置換ピリミジニルピロロピリジノン誘導体、これらの製造のための方法およびキナーゼ阻害剤としてのこれらの使用
JP2018503648A (ja) * 2015-01-28 2018-02-08 バイエル ファーマ アクチエンゲゼルシャフト 4H−ピロロ[3,2−c]ピリジン−4−オン誘導体
WO2019081486A1 (en) * 2017-10-24 2019-05-02 Bayer Aktiengesellschaft 4h-pyrrolo[3,2-c]pyridin-4-one derivatives
WO2020161257A1 (en) * 2019-02-07 2020-08-13 Bayer Aktiengesellschaft 3-amino-2-[2-(acylamino)pyridin-4-yl]-1,5,6,7-tetrahydro-4h-pyrrolo[3,2-c]pyridin-4-one as csnk1 inhibitors

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CA3198202A1 (en) 2022-04-14
MX2023004085A (es) 2023-06-29
TW202227063A (zh) 2022-07-16
KR20230107419A (ko) 2023-07-14
CL2023001012A1 (es) 2023-12-22
WO2022076831A2 (en) 2022-04-14
PH12023500010A1 (en) 2024-03-11
US20240101576A1 (en) 2024-03-28
AU2021358596A9 (en) 2024-10-24
WO2022076831A3 (en) 2022-07-07
CL2025004052A1 (es) 2026-03-20
AU2021358596A1 (en) 2023-05-25
EP4225445A2 (en) 2023-08-16
BR112023006531A2 (pt) 2023-10-03
IL301929A (en) 2023-06-01

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