JP2012502010A5 - - Google Patents

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Publication number
JP2012502010A5
JP2012502010A5 JP2011525573A JP2011525573A JP2012502010A5 JP 2012502010 A5 JP2012502010 A5 JP 2012502010A5 JP 2011525573 A JP2011525573 A JP 2011525573A JP 2011525573 A JP2011525573 A JP 2011525573A JP 2012502010 A5 JP2012502010 A5 JP 2012502010A5
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JP
Japan
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alkyl
hydrogen
independently
membered
different
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JP2011525573A
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English (en)
Japanese (ja)
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JP5576379B2 (ja
JP2012502010A (ja
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Priority claimed from PCT/EP2009/061656 external-priority patent/WO2010026262A1/en
Publication of JP2012502010A publication Critical patent/JP2012502010A/ja
Publication of JP2012502010A5 publication Critical patent/JP2012502010A5/ja
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JP2011525573A 2008-09-08 2009-09-08 細胞増殖阻害剤としてのピリド[5,4−d]ピリミジン Active JP5576379B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP08163897 2008-09-08
EP08163897.5 2008-09-08
PCT/EP2009/061656 WO2010026262A1 (en) 2008-09-08 2009-09-08 Pyrido [5, 4-d] pyrimidines as cell proliferation inhibitors

Publications (3)

Publication Number Publication Date
JP2012502010A JP2012502010A (ja) 2012-01-26
JP2012502010A5 true JP2012502010A5 (https=) 2012-10-18
JP5576379B2 JP5576379B2 (ja) 2014-08-20

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ID=40297852

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011525573A Active JP5576379B2 (ja) 2008-09-08 2009-09-08 細胞増殖阻害剤としてのピリド[5,4−d]ピリミジン

Country Status (16)

Country Link
US (1) US8653087B2 (https=)
EP (1) EP2350083B1 (https=)
JP (1) JP5576379B2 (https=)
KR (1) KR20110063528A (https=)
CN (1) CN102203098A (https=)
AR (1) AR073501A1 (https=)
AU (1) AU2009289196A1 (https=)
CA (1) CA2736306A1 (https=)
CL (1) CL2011000489A1 (https=)
IL (1) IL211136A0 (https=)
MX (1) MX2011002431A (https=)
NZ (1) NZ591493A (https=)
RU (1) RU2011113402A (https=)
TW (1) TW201014860A (https=)
WO (1) WO2010026262A1 (https=)
ZA (1) ZA201101090B (https=)

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TW201014860A (en) 2008-09-08 2010-04-16 Boehringer Ingelheim Int New chemical compounds
US8778929B2 (en) 2008-09-29 2014-07-15 Boehringer Ingelheim International Gmbh Substituted heteroaryl inhibitors of B-RAF
EP2398797B1 (en) * 2009-02-17 2013-11-06 Boehringer Ingelheim International GmbH Pyrimido[5,4-d]pyrimidine derivatives for the inhibition of tyrosine kinases
NZ596538A (en) 2009-05-12 2014-04-30 Romark Lab Lc Haloalkyl heteroaryl benzamide compounds
CN108042535A (zh) 2009-06-26 2018-05-18 罗马克实验室有限公司 用于治疗流感的化合物和方法
WO2011117382A1 (en) 2010-03-26 2011-09-29 Boehringer Ingelheim International Gmbh Pyridyltriazoles
WO2011117381A1 (en) 2010-03-26 2011-09-29 Boehringer Ingelheim International Gmbh B-raf kinase inhibitors
US8710055B2 (en) 2010-12-21 2014-04-29 Boehringer Ingelheim International Gmbh Triazolylphenyl sulfonamides as serine/threonine kinase inhibitors
ES2882807T3 (es) 2011-09-16 2021-12-02 Novartis Ag Heterociclil carboxamidas N-sustituidas
EP2825533B1 (en) 2012-03-13 2016-10-19 Basf Se Fungicidal pyrimidine compounds
WO2015036059A1 (en) 2013-09-16 2015-03-19 Basf Se Fungicidal pyrimidine compounds
CA2923101A1 (en) 2013-09-16 2015-03-19 Basf Se Fungicidal pyrimidine compounds
WO2018165718A1 (en) 2017-03-17 2018-09-20 Cardio Therapeutics Pty Ltd Heterocyclic inhibitors of pcsk9
TW202309022A (zh) 2021-04-13 2023-03-01 美商努法倫特公司 用於治療具egfr突變之癌症之胺基取代雜環
US20240239801A1 (en) * 2021-04-19 2024-07-18 Université de Montréal Pyrimido[5,4,d]pyrimidine compounds, compositions comprising them and uses thereof
JP2024514227A (ja) 2021-04-19 2024-03-28 ユニヴェルシテ ド モントリオール ピリド[3,2-d]ピリミジン化合物、該化合物を含む組成物、及びそれらの使用方法
CN120035595A (zh) * 2022-10-13 2025-05-23 蒙特利尔大学 噻唑并[5,4-d]嘧啶化合物、包含其的组合物及其用途
AU2023410324A1 (en) 2022-12-22 2025-05-15 Boehringer Ingelheim International Gmbh Crystalline forms of a her2 inhibitor
CN121568696A (zh) 2023-07-28 2026-02-24 勃林格殷格翰国际有限公司 制备her2抑制剂的方法

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TW414798B (en) 1994-09-07 2000-12-11 Thomae Gmbh Dr K Pyrimido (5,4-d) pyrimidines, medicaments comprising these compounds, their use and processes for their preparation
JP3290666B2 (ja) 1995-06-07 2002-06-10 ファイザー・インコーポレーテッド 複素環式の縮合環ピリミジン誘導体
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AR007857A1 (es) 1996-07-13 1999-11-24 Glaxo Group Ltd Compuestos heterociclicos fusionados como inhibidores de proteina tirosina quinasa, sus metodos de preparacion, intermediarios uso en medicina ycomposiciones farmaceuticas que los contienen.
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CL2008001943A1 (es) 2007-07-02 2009-09-11 Boehringer Ingelheim Int Compuestos derivados de fenil-triazol, inhibidores de enzimas de señales especificas que participan del control de la proliferacion celular; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar cancer, infecciones, enfermedades inflamatorias y autoinmunes.
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US8778929B2 (en) 2008-09-29 2014-07-15 Boehringer Ingelheim International Gmbh Substituted heteroaryl inhibitors of B-RAF
US20110183975A1 (en) 2008-10-07 2011-07-28 Yasuhiro Goto Novel 6-azaindole aminopyrimidine derivatives having nik inhibitory activity
EP2398797B1 (en) 2009-02-17 2013-11-06 Boehringer Ingelheim International GmbH Pyrimido[5,4-d]pyrimidine derivatives for the inhibition of tyrosine kinases
WO2011117382A1 (en) 2010-03-26 2011-09-29 Boehringer Ingelheim International Gmbh Pyridyltriazoles
WO2011117381A1 (en) 2010-03-26 2011-09-29 Boehringer Ingelheim International Gmbh B-raf kinase inhibitors
US8710055B2 (en) 2010-12-21 2014-04-29 Boehringer Ingelheim International Gmbh Triazolylphenyl sulfonamides as serine/threonine kinase inhibitors
US20130023531A1 (en) 2011-01-27 2013-01-24 Boehringer Ingelheim International Gmbh Pyrimido[5,4-d]pyrimidylamino phenyl sulfonamides as serine/threonine kinase inhibitors
US8889684B2 (en) 2011-02-02 2014-11-18 Boehringer Ingelheim International Gmbh Azaindolylphenyl sulfonamides as serine/threonine kinase inhibitors

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