JP2018515514A5 - - Google Patents

Download PDF

Info

Publication number
JP2018515514A5
JP2018515514A5 JP2017558660A JP2017558660A JP2018515514A5 JP 2018515514 A5 JP2018515514 A5 JP 2018515514A5 JP 2017558660 A JP2017558660 A JP 2017558660A JP 2017558660 A JP2017558660 A JP 2017558660A JP 2018515514 A5 JP2018515514 A5 JP 2018515514A5
Authority
JP
Japan
Prior art keywords
amino
alkyl
substituted
compound according
cancer
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.)
Granted
Application number
JP2017558660A
Other languages
English (en)
Japanese (ja)
Other versions
JP6863901B2 (ja
JP2018515514A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2016/031996 external-priority patent/WO2016183278A1/en
Publication of JP2018515514A publication Critical patent/JP2018515514A/ja
Publication of JP2018515514A5 publication Critical patent/JP2018515514A5/ja
Application granted granted Critical
Publication of JP6863901B2 publication Critical patent/JP6863901B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017558660A 2015-05-13 2016-05-12 キナーゼ阻害のためのヘテロアリール化合物 Expired - Fee Related JP6863901B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562160989P 2015-05-13 2015-05-13
US62/160,989 2015-05-13
PCT/US2016/031996 WO2016183278A1 (en) 2015-05-13 2016-05-12 Heteroaryl compounds for kinase inhibition

Publications (3)

Publication Number Publication Date
JP2018515514A JP2018515514A (ja) 2018-06-14
JP2018515514A5 true JP2018515514A5 (enExample) 2019-06-13
JP6863901B2 JP6863901B2 (ja) 2021-04-28

Family

ID=57249337

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017558660A Expired - Fee Related JP6863901B2 (ja) 2015-05-13 2016-05-12 キナーゼ阻害のためのヘテロアリール化合物

Country Status (5)

Country Link
US (1) US20210323976A1 (enExample)
EP (1) EP3294712A4 (enExample)
JP (1) JP6863901B2 (enExample)
HK (1) HK1251567A1 (enExample)
WO (1) WO2016183278A1 (enExample)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101884010B1 (ko) 2011-05-04 2018-07-31 어리어드 파마슈티칼스, 인코포레이티드 Egfr-유도된 암의 세포 증식을 억제하는 화합물
JP6469567B2 (ja) 2012-05-05 2019-02-13 アリアド・ファーマシューティカルズ・インコーポレイテッド Egfr発動性がんの細胞増殖阻害用化合物
WO2017120429A1 (en) 2016-01-07 2017-07-13 CS Pharmasciences, Inc. Selective inhibitors of clinically important mutants of the egfr tyrosine kinase
CN108299419B (zh) * 2017-01-11 2022-04-26 南京圣和药业股份有限公司 一种新型egfr激酶抑制剂的几种新晶型及其制备方法
CN109705117A (zh) * 2017-10-25 2019-05-03 南京圣和药业股份有限公司 三环类化合物、其制备方法及用途
CN109705118B (zh) * 2017-10-25 2021-12-28 南京圣和药业股份有限公司 三环类egfr激酶抑制剂的制备方法
CN108191861B (zh) * 2018-03-01 2020-10-02 天津大学 N-[5-(嘧啶-2-氨基)-2,4-二取代苯基]-反式-2,4-戊二烯酰胺
AU2020296620B2 (en) * 2019-06-20 2023-07-13 Oncobix Co.Ltd. Pyrimidine derivative inhibiting growth of cancer cell and medicinal use thereof
EP4100409B1 (en) 2020-02-03 2024-08-28 Boehringer Ingelheim International GmbH [1,3]diazino[5,4-d]pyrimidines as her2 inhibitors
CN115052881B (zh) * 2020-02-03 2024-07-09 勃林格殷格翰国际有限公司 作为HER2抑制剂的[1,3]二嗪并[5,4-d]嘧啶
US11608343B2 (en) 2020-04-24 2023-03-21 Boehringer Ingelheim International Gmbh Substituted pyrimido[5,4-d]pyrimidines as HER2 inhibitors
CN112409192A (zh) * 2020-11-26 2021-02-26 启东东岳药业有限公司 一种4-氟-2-甲氧基苯胺的纯化方法
PE20240327A1 (es) 2021-04-13 2024-02-22 Nuvalent Inc Heterociclos con sustitucion amino para tratar canceres con mutaciones de egfr

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003000251A1 (en) * 2001-06-21 2003-01-03 Ariad Pharmaceuticals, Inc. Novel idolinones and uses thereof
AU2008314632B2 (en) * 2007-10-19 2015-05-28 Celgene Avilomics Research, Inc. Heteroaryl compounds and uses thereof
ES2645689T5 (en) * 2008-05-21 2025-06-24 Takeda Pharmaceuticals Co Phosphorous derivatives as kinase inhibitors
US9273077B2 (en) * 2008-05-21 2016-03-01 Ariad Pharmaceuticals, Inc. Phosphorus derivatives as kinase inhibitors
TWI546290B (zh) * 2008-06-27 2016-08-21 賽基艾維洛米斯研究股份有限公司 雜芳基化合物及其用途
JP5427321B2 (ja) * 2011-07-27 2014-02-26 アストラゼネカ アクチボラグ 2−(2,4,5−置換−アニリノ)ピリミジン化合物
AU2014337067B2 (en) * 2013-10-18 2019-01-24 Syros Pharmaceuticals, Inc. Heteroaromatic compounds useful for the treatment of proliferative diseases
US20170166598A1 (en) * 2014-05-13 2017-06-15 Ariad Pharmaceuticals, Inc. Heteroaryl compounds for kinase inhibition
JP6230205B2 (ja) * 2014-06-19 2017-11-15 アリアド ファーマシューティカルズ, インコーポレイテッド キナーゼ阻害のためのヘテロアリール化合物
CN107614503B (zh) * 2015-04-29 2020-03-10 广东众生药业股份有限公司 稠环或三环芳基嘧啶化合物用作激酶抑制剂

Similar Documents

Publication Publication Date Title
JP2018515514A5 (enExample)
JP2018012712A5 (enExample)
JP2015514808A5 (enExample)
PE20230161A1 (es) Inhibidores de proteinas kras mutantes
IL275762B2 (en) History of PHENYL-SO2-NH-C(=O)-PHENYL-PIPERAZINE-CH2-1,2-CYCLOHEXANE-BICYCLO[1.1.1]PENTANE and spirit preparations containing them
PH12021500049A1 (en) 2,3-dihydroquinazolin compounds as nav1.8 inhibitors
MX2020005363A (es) Compuestos heterociclicos como inhibidores de prmt5.
MX2023004309A (es) Inhibidores de quinasa alk2 que contienen imidazol.
CY1120248T1 (el) Ενωσεις ιμιδαζο[4,5-c]κινολιν-2-ονης και η χρηση τους στη θεραπευτικη αντιμετωπιση του καρκινου
JP2014500265A5 (enExample)
JP2020503271A5 (enExample)
MY191938A (en) Novel pyrazolo[3,4-d]pyrimidine compound or salt thereof
CY1114908T1 (el) Παραγωγα κινολινης ως αντιβακτηριακοι παραγοντες
RU2018102365A (ru) Новые гидроксисложноэфирные производные, способ их получения и фармацевтические композиции, содержащие их
JP2017533968A5 (enExample)
CN114430740A (zh) Egfr抑制剂、组合物及其制备方法
PH12019500804A1 (en) Liposomal formulation for use in the treatment of cancer
HRP20191268T1 (hr) Derivati tieno[2,3-c]pirol-4-ona kao inhibitori erk
MX2019015371A (es) Derivados de dihidro-pirrolo-piridina.
JP2009541223A5 (enExample)
MY189118A (en) Pyrazolo[1,5-a]pyrazin-4-yl derivatives
MX2010001677A (es) Derivados de 4-(9-(3,3-difluorociclopentil)-5,7,7-trimetil-6-oxo-6 ,7,8,9-tetrahidro-5h-pirimido[4,5-b][1,4]diazepin-2-ilamino)-3-me toxibenzamida como inhibidores de las proteinas cinasas humanas plk1 a plk4 para el tratamiento de enfermedades proli
JP2016527217A5 (enExample)
JP2016512520A5 (enExample)
JP2005527587A5 (enExample)