WO2015039612A8 - 抑制btk和/或jak3激酶活性的化合物 - Google Patents

抑制btk和/或jak3激酶活性的化合物 Download PDF

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Publication number
WO2015039612A8
WO2015039612A8 PCT/CN2014/086820 CN2014086820W WO2015039612A8 WO 2015039612 A8 WO2015039612 A8 WO 2015039612A8 CN 2014086820 W CN2014086820 W CN 2014086820W WO 2015039612 A8 WO2015039612 A8 WO 2015039612A8
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Prior art keywords
btk
compound
jak3
compound inhibiting
inhibiting activities
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PCT/CN2014/086820
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English (en)
French (fr)
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WO2015039612A1 (zh
Inventor
刘金明
车美英
李功
李占梅
邱红娟
金孟燮
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北京韩美药品有限公司
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Publication date
Priority to US15/022,248 priority Critical patent/US9840517B2/en
Priority to MX2016003582A priority patent/MX368781B/es
Application filed by 北京韩美药品有限公司 filed Critical 北京韩美药品有限公司
Priority to EP14846251.8A priority patent/EP3048105A4/en
Priority to NZ718728A priority patent/NZ718728A/en
Priority to AU2014323777A priority patent/AU2014323777C1/en
Priority to SG11201601980XA priority patent/SG11201601980XA/en
Priority to RU2016110755A priority patent/RU2650512C2/ru
Priority to KR1020167009680A priority patent/KR101879422B1/ko
Priority to CA2924362A priority patent/CA2924362C/en
Priority to BR112016005881A priority patent/BR112016005881A2/pt
Priority to JP2016543306A priority patent/JP6458039B2/ja
Publication of WO2015039612A1 publication Critical patent/WO2015039612A1/zh
Publication of WO2015039612A8 publication Critical patent/WO2015039612A8/zh
Priority to IL24461116A priority patent/IL244611B/en
Priority to PH12016500531A priority patent/PH12016500531B1/en
Priority to US15/799,315 priority patent/US10273242B2/en

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Abstract

本发明涉及抑制BTK(布鲁顿酪氨酸激酶)和/或JAK3(Janus酪氨酸激酶3)激酶活性的化合物、其药物组合物、其在制药中的用途、使用其抑制BTK和/或JAK3活性的方法以及使用其治疗和/或预防哺乳动物(尤其是人)中BTK和/或JAK3介导的疾病或病症的方法。所述化合物具有结构式(I)。
PCT/CN2014/086820 2013-09-18 2014-09-18 抑制btk和/或jak3激酶活性的化合物 WO2015039612A1 (zh)

Priority Applications (14)

Application Number Priority Date Filing Date Title
CA2924362A CA2924362C (en) 2013-09-18 2014-09-18 Compound inhibiting activities of btk and/or jak3 kinases
KR1020167009680A KR101879422B1 (ko) 2013-09-18 2014-09-18 Btk 및/또는 jak3 키나제의 활성을 억제하는 화합물
EP14846251.8A EP3048105A4 (en) 2013-09-18 2014-09-18 Compound inhibiting activities of btk and/or jak3 kinases
MX2016003582A MX368781B (es) 2013-09-18 2014-09-18 Compuesto inhibidor de las actividades de las cinasas btk y/o jak3.
AU2014323777A AU2014323777C1 (en) 2013-09-18 2014-09-18 Compound inhibiting activities of BTK and/or JAK3 kinases
SG11201601980XA SG11201601980XA (en) 2013-09-18 2014-09-18 Compound inhibiting activities of btk and/or jak3 kinases
BR112016005881A BR112016005881A2 (pt) 2013-09-18 2014-09-18 composto, composição farmacêutica e uso do composto
US15/022,248 US9840517B2 (en) 2013-09-18 2014-09-18 Compound inhibiting activities of BTK and/or JAK3 kinases
NZ718728A NZ718728A (en) 2013-09-18 2014-09-18 Compound inhibiting activities of btk and/or jak3 kinases
RU2016110755A RU2650512C2 (ru) 2013-09-18 2014-09-18 Соединение, ингибирующее активности киназ ВТК и/или JAK3
JP2016543306A JP6458039B2 (ja) 2013-09-18 2014-09-18 Btk及び/又はjak3キナーゼの活性を抑制する化合物
IL24461116A IL244611B (en) 2013-09-18 2016-03-15 Compounds containing compressed pyrimidine/4,2,1-triazine two-ring systems as inhibitors of jak3 and/or btk kinase activity
PH12016500531A PH12016500531B1 (en) 2013-09-18 2016-03-18 Compound inhibiting activities of btk and/or jak3 kinases
US15/799,315 US10273242B2 (en) 2013-09-18 2017-10-31 Compound inhibiting activities of BTK and/or JAK3 kinases

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
CN201310429844 2013-09-18
CN201310429844.3 2013-09-18
CN201310430071 2013-09-18
CN201310430071.0 2013-09-18
CN201310430761 2013-09-18
CN201310430761.6 2013-09-18

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US15/022,248 A-371-Of-International US9840517B2 (en) 2013-09-18 2014-09-18 Compound inhibiting activities of BTK and/or JAK3 kinases
US15/799,315 Division US10273242B2 (en) 2013-09-18 2017-10-31 Compound inhibiting activities of BTK and/or JAK3 kinases

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Publication Number Publication Date
WO2015039612A1 WO2015039612A1 (zh) 2015-03-26
WO2015039612A8 true WO2015039612A8 (zh) 2016-03-03

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US (2) US9840517B2 (zh)
EP (1) EP3048105A4 (zh)
JP (1) JP6458039B2 (zh)
KR (1) KR101879422B1 (zh)
CN (3) CN106083887B (zh)
AU (1) AU2014323777C1 (zh)
BR (1) BR112016005881A2 (zh)
CA (1) CA2924362C (zh)
IL (1) IL244611B (zh)
MX (1) MX368781B (zh)
NZ (1) NZ718728A (zh)
PH (1) PH12016500531B1 (zh)
RU (1) RU2650512C2 (zh)
SG (1) SG11201601980XA (zh)
WO (1) WO2015039612A1 (zh)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015039612A1 (zh) 2013-09-18 2015-03-26 北京韩美药品有限公司 抑制btk和/或jak3激酶活性的化合物
CN110526912B (zh) 2014-06-19 2023-02-14 武田药品工业株式会社 用于激酶抑制的杂芳基化合物
CN106188060A (zh) 2015-04-29 2016-12-07 厦门大学 嘧啶并吡咯类化合物、其制备方法、药用组合物及其应用
WO2017004134A1 (en) * 2015-06-29 2017-01-05 Nimbus Iris, Inc. Irak inhibitors and uses thereof
WO2017004133A1 (en) * 2015-06-29 2017-01-05 Nimbus Iris, Inc. Irak inhibitors and uses thereof
JP6851367B2 (ja) * 2015-08-13 2021-03-31 北京韓美薬品有限公司Beijing Hanmi Pharm. Co., Ltd. Irak4阻害剤、及びその応用
KR102048719B1 (ko) * 2015-08-13 2019-11-26 베이징 한미 파마슈티컬 컴퍼니 리미티드 Irak4억제제 및 이의 용도
WO2017205766A1 (en) * 2016-05-27 2017-11-30 Pharmacyclics Llc Inhibitors of interleukin-1 receptor-associated kinase
EP3950691A1 (en) * 2016-06-30 2022-02-09 Daewoong Pharmaceutical Co., Ltd. Pyrazolopyrimidine derivatives as kinase inhibitor
CN107698603B (zh) 2016-08-09 2022-04-08 南京红云生物科技有限公司 噻吩并嘧啶类化合物、其制备方法、药用组合物及其应用
KR102398659B1 (ko) * 2017-03-17 2022-05-16 주식회사 대웅제약 카이네이즈 저해제로서의 피롤로트리아진 유도체
CN110709402B (zh) * 2017-06-15 2022-05-10 浙江海正药业股份有限公司 杂芳基并嘧啶酮类衍生物、其制备方法及其在医药上用途
CN107312006B (zh) * 2017-06-28 2019-11-15 郑州大学第一附属医院 吡咯并嘧啶类衍生物及其应用
CN109206435B (zh) * 2017-06-29 2020-09-08 中国医药研究开发中心有限公司 噻吩并[3,2-d]嘧啶类化合物及其制备方法和医药用途
PL3733673T3 (pl) * 2017-12-28 2022-09-26 Daewoong Pharmaceutical Co., Ltd. Pochodna oksyfluoropiperydyny jako inhibitor kinazy
KR102577242B1 (ko) 2017-12-28 2023-09-11 주식회사 대웅제약 카이네이즈 저해제로서의 아미노-메틸피페리딘 유도체
KR102577241B1 (ko) 2017-12-28 2023-09-11 주식회사 대웅제약 카이네이즈 저해제로서의 아미노-플루오로피페리딘 유도체
CA3108065A1 (en) 2018-07-31 2020-02-06 Loxo Oncology, Inc. Spray-dried dispersions, formulations, and polymorphs of (s)-5-amino-3-(4-((5-fluoro-2-methoxybenzamido)methyl)phenyl)-1-(1,1,1-trifluoropropan-2-yl)-1h-pyrazole-4-carboxamide
EP3898615A1 (en) 2018-12-19 2021-10-27 Array Biopharma, Inc. 7-((3,5-dimethoxyphenyl)amino)quinoxaline derivatives as fgfr inhibitors for treating cancer
EP3898626A1 (en) 2018-12-19 2021-10-27 Array Biopharma, Inc. Substituted pyrazolo[1,5-a]pyridine compounds as inhibitors of fgfr tyrosine kinases
AU2020242287A1 (en) 2019-03-21 2021-09-02 INSERM (Institut National de la Santé et de la Recherche Médicale) A Dbait molecule in combination with kinase inhibitor for the treatment of cancer
ES2962852T3 (es) 2019-05-10 2024-03-21 Deciphera Pharmaceuticals Llc Inhibidores de la autofagia de heteroarilaminopirimidina amida y métodos de uso de los mismos
FI3966207T3 (fi) 2019-05-10 2023-11-30 Deciphera Pharmaceuticals Llc Autofagian fenyyliaminopyrimidiiniamidi-inhibiittoreita ja menetelmiä niiden käyttämiseksi
CN114258318A (zh) 2019-06-17 2022-03-29 德西费拉制药有限责任公司 氨基嘧啶酰胺自噬抑制剂及其使用方法
WO2021089791A1 (en) 2019-11-08 2021-05-14 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
CN115244055A (zh) * 2020-01-21 2022-10-25 江苏先声药业有限公司 嘧啶并五元环类衍生物及其应用
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
CA3181162A1 (en) 2020-06-05 2021-12-09 Stephen W. Kaldor Inhibitors of fibroblast growth factor receptor kinases
WO2023220439A1 (en) * 2022-05-12 2023-11-16 Skyhawk Therapeutics, Inc. Compositions useful for modulating splicing

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9903762D0 (en) * 1999-02-18 1999-04-14 Novartis Ag Organic compounds
JP2008013527A (ja) 2006-07-10 2008-01-24 Sankyo Co Ltd チエノ[3,2−d]ピリミジン−2,4−ジアミン誘導体
EP2081936B1 (en) * 2006-11-03 2014-04-02 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
AU2008312624B2 (en) 2007-10-18 2014-07-10 Boehringer Ingelheim International Gmbh Preparation of dihydrothieno [3, 2-D] pyrimidines and intermediates used therein
CA2723185A1 (en) 2008-04-22 2009-10-29 Portola Pharmaceuticals, Inc. Inhibitors of protein kinases
KR20110025224A (ko) * 2008-06-27 2011-03-09 아빌라 테라퓨틱스, 인크. 헤테로아릴 화합물 및 이의 용도
WO2010111406A2 (en) 2009-03-24 2010-09-30 Myriad Pharmaceuticals, Inc. Compounds and therapeutic uses thereof
WO2010129053A2 (en) 2009-05-05 2010-11-11 Dana Farber Cancer Institute Egfr inhibitors and methods of treating disorders
US20110207736A1 (en) * 2009-12-23 2011-08-25 Gatekeeper Pharmaceuticals, Inc. Compounds that modulate egfr activity and methods for treating or preventing conditions therewith
NZ627709A (en) * 2010-06-23 2014-12-24 Hanmi Science Co Ltd Novel fused pyrimidine derivatives for inhibition of tyrosine kinase activity
EP2624698A4 (en) 2010-10-08 2014-10-08 Abbvie Inc Furo [3,2-D] PYRIMIDINE COMPOUNDS
SG2014014450A (en) * 2011-09-22 2014-09-26 Pfizer Pyrrolopyrimidine and purine derivatives
AU2014229468A1 (en) * 2013-03-14 2015-09-03 Pfizer Inc. Combination of an EGFR T790m inhibitor and an EGFR inhibitor for the treatment of non-small cell lung cancer
WO2015039612A1 (zh) 2013-09-18 2015-03-26 北京韩美药品有限公司 抑制btk和/或jak3激酶活性的化合物
UA115388C2 (uk) * 2013-11-21 2017-10-25 Пфайзер Інк. 2,6-заміщені пуринові похідні та їх застосування в лікуванні проліферативних захворювань
DK3318565T3 (da) * 2013-12-05 2021-05-25 Pfizer Pyrrolo[2,3-D]pyrimidinyl-, pyrrolo[2,3-B]pyrazinyl- og pyrrolo[2,3-D]pyridinylacrylamider

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PH12016500531A1 (en) 2016-05-16
BR112016005881A2 (pt) 2017-09-12
AU2014323777A1 (en) 2016-04-28
IL244611B (en) 2019-10-31
SG11201601980XA (en) 2016-04-28
WO2015039612A1 (zh) 2015-03-26
JP2016530335A (ja) 2016-09-29
JP6458039B2 (ja) 2019-01-23
AU2014323777B2 (en) 2017-03-09
KR20160054014A (ko) 2016-05-13
CA2924362A1 (en) 2015-03-26
PH12016500531B1 (en) 2016-05-16
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IL244611A0 (en) 2016-04-21
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EP3048105A1 (en) 2016-07-27
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CN106065017A (zh) 2016-11-02
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CN106083887A (zh) 2016-11-09
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