JP2023502458A5 - - Google Patents

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Publication number
JP2023502458A5
JP2023502458A5 JP2022529505A JP2022529505A JP2023502458A5 JP 2023502458 A5 JP2023502458 A5 JP 2023502458A5 JP 2022529505 A JP2022529505 A JP 2022529505A JP 2022529505 A JP2022529505 A JP 2022529505A JP 2023502458 A5 JP2023502458 A5 JP 2023502458A5
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JP
Japan
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group
heterocyclyl
heteroaryl
cycloalkyl
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JP2022529505A
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Japanese (ja)
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JP2023502458A (ja
JP7781059B2 (ja
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Priority claimed from PCT/CN2020/130326 external-priority patent/WO2021098811A1/zh
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JP2022529505A 2019-11-21 2020-11-20 ピラゾロヘテロアリール系誘導体、その調製方法及びその医薬的応用 Active JP7781059B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
CN201911147956 2019-11-21
CN201911147956.3 2019-11-21
CN202010837381.4 2020-08-19
CN202010837381 2020-08-19
PCT/CN2020/130326 WO2021098811A1 (zh) 2019-11-21 2020-11-20 吡唑并杂芳基类衍生物、其制备方法及其在医药上的应用

Publications (3)

Publication Number Publication Date
JP2023502458A JP2023502458A (ja) 2023-01-24
JP2023502458A5 true JP2023502458A5 (https=) 2023-11-30
JP7781059B2 JP7781059B2 (ja) 2025-12-05

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JP2022529505A Active JP7781059B2 (ja) 2019-11-21 2020-11-20 ピラゾロヘテロアリール系誘導体、その調製方法及びその医薬的応用

Country Status (11)

Country Link
US (1) US12559488B2 (https=)
EP (1) EP4063363A4 (https=)
JP (1) JP7781059B2 (https=)
KR (1) KR20220103987A (https=)
CN (5) CN120004887A (https=)
AU (1) AU2020386587A1 (https=)
BR (1) BR112022008000A2 (https=)
CA (1) CA3159376A1 (https=)
MX (1) MX2022005985A (https=)
TW (1) TW202128690A (https=)
WO (1) WO2021098811A1 (https=)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112142744A (zh) 2019-06-28 2020-12-29 上海瑛派药业有限公司 取代的稠合杂芳双环化合物作为激酶抑制剂及其应用
TW202220993A (zh) * 2020-08-07 2022-06-01 香港商德琪研發有限公司 Atr抑制劑及其用途
WO2022135560A1 (en) * 2020-12-25 2022-06-30 Impact Therapeutics (Shanghai) , Inc Substituted imidazo[1,5-b]pyridazine compounds as kinase inhibitors and use thereof
KR20240012471A (ko) 2021-05-21 2024-01-29 지앙수 헨그루이 파마슈티컬스 컴퍼니 리미티드 피라졸로헤테로아릴계 유도체의 약학적으로 허용 가능한 염 및 이의 결정형
WO2023109883A1 (zh) * 2021-12-15 2023-06-22 上海翊石医药科技有限公司 一类芳杂环取代的化合物及其制备方法和用途
WO2024109727A1 (zh) * 2022-11-21 2024-05-30 江苏恒瑞医药股份有限公司 一种吡唑并杂芳基类衍生物的可药用盐的结晶形式
CN119143753B (zh) * 2023-06-14 2026-01-02 石药集团中奇制药技术(石家庄)有限公司 一种杂环类抗肿瘤化合物的盐及其晶型

Family Cites Families (15)

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ES2921576T3 (es) 2008-12-19 2022-08-29 Vertex Pharma Compuestos útiles como inhibidores de la quinasa ATR
US20110053923A1 (en) * 2008-12-22 2011-03-03 Astrazeneca Chemical compounds 610
SA111320519B1 (ar) * 2010-06-11 2014-07-02 Astrazeneca Ab مركبات بيريميدينيل للاستخدام كمثبطات atr
CA2819373A1 (en) * 2010-12-09 2012-06-14 Amgen Inc. Bicyclic compounds as pim inhibitors
ME03336B (me) 2013-03-12 2019-10-20 Vertex Pharma Inhibitori dnk-pk
AR095443A1 (es) 2013-03-15 2015-10-14 Fundación Centro Nac De Investig Oncológicas Carlos Iii Heterociclos condensados con acción sobre atr
TWI656121B (zh) * 2014-08-04 2019-04-11 德商拜耳製藥公司 2-(嗎啉-4-基)-1,7-萘啶
US20190000850A1 (en) 2015-02-09 2019-01-03 The Regents Of The University Of California Combination cancer therapy
WO2017118734A1 (en) 2016-01-08 2017-07-13 The Institute Of Cancer Research: Royal Cancer Hospital Inhibitors of ataxia-telangiectasia mutated and rad3-related protein kinase (atr) for use in methods of treating cancer
CA3011189C (en) 2016-01-14 2024-02-20 Bayer Pharma Aktiengesellschaft 5-substituted 2-(morpholin-4-yl)-1,7-naphthyridines
US11730734B2 (en) 2016-09-12 2023-08-22 University Of Florida Research Foundation, Incorporated Use of ATR and Chk1 inhibitor compounds
WO2018153970A1 (en) 2017-02-24 2018-08-30 Bayer Pharma Aktiengesellschaft Solid forms of 2-[(3r)-3-methylmorpholin-4-yl]-4-(1-methyl-1h-pyrazol-5-yl)-8-(1h-pyrazol-5-yl)-1,7-naphthyridine
EP3679041B1 (en) 2017-09-08 2022-07-06 Newave Pharmaceutical Inc. Substituted pyrrolopyridines as atr inhibitors
CN112654396B (zh) * 2018-09-07 2025-07-01 默克专利股份公司 5-吗啉-4-基-吡唑并[4,3-b]吡啶衍生物
WO2020068729A1 (en) 2018-09-25 2020-04-02 Incyte Corporation Pyrazolo[4,3-d]pyrimidine compounds as alk2 abd/or fgfr modulators

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