JP2013532652A5 - - Google Patents

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JP2013532652A5
JP2013532652A5 JP2013520164A JP2013520164A JP2013532652A5 JP 2013532652 A5 JP2013532652 A5 JP 2013532652A5 JP 2013520164 A JP2013520164 A JP 2013520164A JP 2013520164 A JP2013520164 A JP 2013520164A JP 2013532652 A5 JP2013532652 A5 JP 2013532652A5
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JP
Japan
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alkyl
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compound according
cycloalkyl
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JP2013520164A
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English (en)
Japanese (ja)
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JP2013532652A (ja
JP5991974B2 (ja
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Priority claimed from PCT/EP2011/062683 external-priority patent/WO2012010704A1/en
Publication of JP2013532652A publication Critical patent/JP2013532652A/ja
Publication of JP2013532652A5 publication Critical patent/JP2013532652A5/ja
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JP2013520164A 2010-07-23 2011-07-22 新規アミノピラゾロキナゾリン Active JP5991974B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP10170683 2010-07-23
EP10170683.6 2010-07-23
PCT/EP2011/062683 WO2012010704A1 (en) 2010-07-23 2011-07-22 New aminopyrazoloquinazolines

Publications (3)

Publication Number Publication Date
JP2013532652A JP2013532652A (ja) 2013-08-19
JP2013532652A5 true JP2013532652A5 (US07794700-20100914-C00152.png) 2015-09-03
JP5991974B2 JP5991974B2 (ja) 2016-09-14

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ID=43037625

Family Applications (1)

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JP2013520164A Active JP5991974B2 (ja) 2010-07-23 2011-07-22 新規アミノピラゾロキナゾリン

Country Status (22)

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US (1) US8735386B2 (US07794700-20100914-C00152.png)
EP (1) EP2595987B1 (US07794700-20100914-C00152.png)
JP (1) JP5991974B2 (US07794700-20100914-C00152.png)
KR (1) KR20130132394A (US07794700-20100914-C00152.png)
CN (1) CN103097388A (US07794700-20100914-C00152.png)
AP (1) AP2012006640A0 (US07794700-20100914-C00152.png)
AR (1) AR082850A1 (US07794700-20100914-C00152.png)
AU (1) AU2011281504A1 (US07794700-20100914-C00152.png)
BR (1) BR112013000107A2 (US07794700-20100914-C00152.png)
CA (1) CA2803467A1 (US07794700-20100914-C00152.png)
CL (1) CL2012003745A1 (US07794700-20100914-C00152.png)
CO (1) CO6670575A2 (US07794700-20100914-C00152.png)
EA (1) EA201201661A1 (US07794700-20100914-C00152.png)
EC (1) ECSP13012448A (US07794700-20100914-C00152.png)
GE (1) GEP20156289B (US07794700-20100914-C00152.png)
MA (1) MA34389B1 (US07794700-20100914-C00152.png)
MX (1) MX2013000821A (US07794700-20100914-C00152.png)
PE (1) PE20131143A1 (US07794700-20100914-C00152.png)
SG (1) SG187548A1 (US07794700-20100914-C00152.png)
TW (1) TW201217380A (US07794700-20100914-C00152.png)
UY (1) UY33526A (US07794700-20100914-C00152.png)
WO (1) WO2012010704A1 (US07794700-20100914-C00152.png)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9150578B2 (en) * 2012-01-23 2015-10-06 Boehringer Ingelheim International Gmbh 5,8-dihydro-6H-pyrazolo[3,4-h]quinazolines as IGF-1R/IR inhibitors
US9376437B2 (en) 2013-03-13 2016-06-28 Oncoceutics, Inc 7-benzyl-4-(2-methylbenzyl)-2,4,6,7,8,9-hexahydroimidazo[1,2-a]pyrido[3,4-e]pyrimidin-5(1H)-one, salts thereof and methods of using the same in combination therapy
CN110669047A (zh) * 2013-11-15 2020-01-10 昂克希尔迪克斯有限公司 用于治疗癌症的化合物、其组合物及应用方法
MX2021001096A (es) 2015-01-30 2023-01-17 Oncoceutics Inc 7-bencil-4-(2-metilbencilo)-2,4,6,7,8,9-hexahidroimidazo [1,2-a]pirido[3,4-e]pirimidin-5(1h)-ona, analogos y sales del mismo y su uso en terapia.
US10414769B2 (en) 2015-05-13 2019-09-17 Boehringer Ingelheim International Gmbh 5,8-dimethyl-9-phenyl-5,8-dihydro-6H-pyrazolo[3,4-h]quinazolin-2-yl)-(1H-pyrazol-3-yl)-amines as IGF-1R/IR inhibitors
CN113264935B (zh) * 2016-11-11 2022-09-20 上海海雁医药科技有限公司 吡啶胺取代的杂三环化合物及其中间体和医药上的用途
US11597725B2 (en) * 2017-05-26 2023-03-07 Jiangsu Atom Bioscience And Pharmaceutical Co., Ltd. URAT1 inhibitor for promoting uric acid excretion
CN107383019B (zh) * 2017-07-28 2019-10-15 江苏艾凡生物医药有限公司 吡唑并[4,3-h]喹唑啉类化合物及其用途
EP3786161A4 (en) * 2018-04-24 2021-05-05 Shanghai Haiyan Pharmaceutical Technology Co., Ltd CDK4 / 6 INHIBITOR, PHARMACEUTICALLY ACCEPTABLE SALT, POLYMORPHIC OF THEM AND ASSOCIATED USE
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
CA3128200A1 (en) * 2019-01-30 2020-08-06 Yale University Compounds, compositions, and methods for treating fibrosis
US11384083B2 (en) 2019-02-15 2022-07-12 Incyte Corporation Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors
WO2020180959A1 (en) 2019-03-05 2020-09-10 Incyte Corporation Pyrazolyl pyrimidinylamine compounds as cdk2 inhibitors
CN113518775A (zh) * 2019-03-07 2021-10-19 生物技术公司 用于制备经取代的咪唑并喹啉的方法
WO2020205560A1 (en) 2019-03-29 2020-10-08 Incyte Corporation Sulfonylamide compounds as cdk2 inhibitors
US20220175819A1 (en) * 2019-04-19 2022-06-09 Fount Bio, Inc. Delivery and retention of active agents within the skin
US11447494B2 (en) 2019-05-01 2022-09-20 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
WO2020223469A1 (en) 2019-05-01 2020-11-05 Incyte Corporation N-(1-(methylsulfonyl)piperidin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine derivatives and related compounds as cyclin-dependent kinase 2 (cdk2) inhibitors for treating cancer
AR119765A1 (es) 2019-08-14 2022-01-12 Incyte Corp Compuestos de imidazolil pirimidinilamina como inhibidores de cdk2
MX2022004390A (es) 2019-10-11 2022-08-08 Incyte Corp Aminas biciclicas como inhibidores de la cinasa dependiente de ciclina 2 (cdk2).
JP2023529867A (ja) 2020-06-05 2023-07-12 キネート バイオファーマ インク. 線維芽細胞増殖因子受容体キナーゼの阻害剤
CN111960974A (zh) * 2020-08-28 2020-11-20 山东潍坊润丰化工股份有限公司 一种烯草酮中间体的合成方法
WO2022166725A1 (zh) * 2021-02-08 2022-08-11 南京明德新药研发有限公司 5,6-二氢噻吩并[3,4-h]喹唑啉类化合物
US11981671B2 (en) 2021-06-21 2024-05-14 Incyte Corporation Bicyclic pyrazolyl amines as CDK2 inhibitors
US11976073B2 (en) 2021-12-10 2024-05-07 Incyte Corporation Bicyclic amines as CDK2 inhibitors

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2233003A1 (en) * 1995-10-02 1997-04-10 F. Hoffmann-La Roche Ag Pyrimidine derivatives as 5ht2c-receptor antagonists
RS20050944A (en) 2003-05-22 2008-06-05 Nerviano Medical Sciences S.R.L., Pyrazolo-quinazoline derivatives, process for their preparation and their use as kinase inhibitors
CN1897950A (zh) 2003-10-14 2007-01-17 惠氏公司 稠合芳基和杂芳基衍生物及其使用方法

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