JP2012524103A5 - - Google Patents

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Publication number
JP2012524103A5
JP2012524103A5 JP2012506209A JP2012506209A JP2012524103A5 JP 2012524103 A5 JP2012524103 A5 JP 2012524103A5 JP 2012506209 A JP2012506209 A JP 2012506209A JP 2012506209 A JP2012506209 A JP 2012506209A JP 2012524103 A5 JP2012524103 A5 JP 2012524103A5
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JP
Japan
Prior art keywords
phenyl
azabicyclo
oxa
alkyl
oct
Prior art date
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Application number
JP2012506209A
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English (en)
Japanese (ja)
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JP2012524103A (ja
JP5649643B2 (ja
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Priority claimed from PCT/US2010/031191 external-priority patent/WO2010120998A1/en
Publication of JP2012524103A publication Critical patent/JP2012524103A/ja
Publication of JP2012524103A5 publication Critical patent/JP2012524103A5/ja
Application granted granted Critical
Publication of JP5649643B2 publication Critical patent/JP5649643B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2012506209A 2009-04-17 2010-04-15 ピリミジン化合物、ｍＴＯＲキナーゼおよびＰＩ３キナーゼ阻害剤としてのそれらの使用、ならびにそれらの合成 Expired - Fee Related JP5649643B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US17013809P 2009-04-17 2009-04-17
US61/170,138 2009-04-17
PCT/US2010/031191 WO2010120998A1 (en) 2009-04-17 2010-04-15 Pyrimidine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses

Publications (3)

Publication Number Publication Date
JP2012524103A JP2012524103A (ja) 2012-10-11
JP2012524103A5 true JP2012524103A5 (OSRAM) 2013-04-04
JP5649643B2 JP5649643B2 (ja) 2015-01-07

Family

ID=42269326

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012506209A Expired - Fee Related JP5649643B2 (ja) 2009-04-17 2010-04-15 ピリミジン化合物、ｍＴＯＲキナーゼおよびＰＩ３キナーゼ阻害剤としてのそれらの使用、ならびにそれらの合成

Country Status (6)

Country Link
US (1) US8835429B2 (OSRAM)
EP (1) EP2419432B9 (OSRAM)
JP (1) JP5649643B2 (OSRAM)
CA (1) CA2755554C (OSRAM)
ES (1) ES2439793T3 (OSRAM)
WO (1) WO2010120998A1 (OSRAM)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2535116T3 (es) 2010-03-04 2015-05-05 Cellzome Limited Derivados de urea sustituida con morfolino como inhibidores de mtor
US20120258967A1 (en) * 2011-03-09 2012-10-11 Avila Therapeutics, Inc. Pi3 kinase inhibitors and uses thereof
EP2694511A1 (en) * 2011-04-04 2014-02-12 Cellzome Limited Dihydropyrrolo pyrimidine derivatives as mtor inhibitors
JP5995975B2 (ja) 2011-09-21 2016-09-21 セルゾーム リミテッド Ｍｔｏｒ阻害剤としてのモルホリノ置換尿素またはカルバメート誘導体
WO2013050508A1 (en) 2011-10-07 2013-04-11 Cellzome Limited Morpholino substituted bicyclic pyrimidine urea or carbamate derivatives as mtor inhibitors
WO2013067141A1 (en) * 2011-11-01 2013-05-10 Exelixis, Inc. N- (3- { [ (3- { [2-chloro-5- (methoxy) phenyl] amino} quinoxalin- 2 -yl) amino] sulfonyl} phe nyl) - 2 -methylalaninamide as phosphatidylinositol 3 - kinase inhibitor for the treatment of lymphoproliferative malignancies
CN104230952B (zh) * 2014-08-16 2017-02-01 沈阳药科大学 含有嘧啶骨架的化合物及其制备方法和用途
AU2015366357B2 (en) * 2014-12-17 2018-07-19 Shanghai Haiyan Pharmaceutical Technology Co. Ltd. 2-morpholin-4,6-disubstituted pyrimidine derivative, and preparation method and pharmaceutical use thereof

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9009A (en) * 1852-06-08 Bat-trap
WO2004108130A1 (en) * 2003-06-03 2004-12-16 Beth Israel Deaconess Medical Center Methods and compounds for the treatment of vascular stenosis
GB0520657D0 (en) * 2005-10-11 2005-11-16 Ludwig Inst Cancer Res Pharmaceutical compounds
GB0525083D0 (en) * 2005-12-09 2006-01-18 Astrazeneca Ab Pyrimidine derivatives
MX2009002046A (es) * 2006-08-24 2009-03-06 Astrazeneca Ab Derivados de morfolino pirimidina utiles en el tratamiento de trastornos proliferativos.
JP2010527924A (ja) * 2007-05-18 2010-08-19 メルク・シャープ・エンド・ドーム・コーポレイション オキソ架橋ジアゼパンオレキシン受容体アンタゴニスト
AU2008312631A1 (en) * 2007-10-16 2009-04-23 Wyeth Llc Thienopyrimidine and pyrazolopyrimidine compounds and their use as mTOR kinase and PI3 kinase inhibitors

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