JP2010526814A5 - - Google Patents

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Publication number
JP2010526814A5
JP2010526814A5 JP2010507532A JP2010507532A JP2010526814A5 JP 2010526814 A5 JP2010526814 A5 JP 2010526814A5 JP 2010507532 A JP2010507532 A JP 2010507532A JP 2010507532 A JP2010507532 A JP 2010507532A JP 2010526814 A5 JP2010526814 A5 JP 2010526814A5
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JP
Japan
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pharmaceutically acceptable
acceptable salt
compound according
halo
trifluoromethyl
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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.)
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JP2010507532A
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English (en)
Japanese (ja)
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JP5503532B2 (ja
JP2010526814A (ja
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Priority claimed from PCT/US2008/062143 external-priority patent/WO2008140947A1/en
Publication of JP2010526814A publication Critical patent/JP2010526814A/ja
Publication of JP2010526814A5 publication Critical patent/JP2010526814A5/ja
Application granted granted Critical
Publication of JP5503532B2 publication Critical patent/JP5503532B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2010507532A 2007-05-11 2008-05-01 P70s6キナーゼ阻害剤 Expired - Fee Related JP5503532B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US91733107P 2007-05-11 2007-05-11
US60/917,331 2007-05-11
PCT/US2008/062143 WO2008140947A1 (en) 2007-05-11 2008-05-01 P70 s6 kinase inhibitors

Publications (3)

Publication Number Publication Date
JP2010526814A JP2010526814A (ja) 2010-08-05
JP2010526814A5 true JP2010526814A5 (cg-RX-API-DMAC7.html) 2011-06-16
JP5503532B2 JP5503532B2 (ja) 2014-05-28

Family

ID=39765082

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010507532A Expired - Fee Related JP5503532B2 (ja) 2007-05-11 2008-05-01 P70s6キナーゼ阻害剤

Country Status (33)

Country Link
US (2) US8093383B2 (cg-RX-API-DMAC7.html)
EP (1) EP2148880B1 (cg-RX-API-DMAC7.html)
JP (1) JP5503532B2 (cg-RX-API-DMAC7.html)
KR (1) KR101088219B1 (cg-RX-API-DMAC7.html)
CN (1) CN101679439B (cg-RX-API-DMAC7.html)
AR (1) AR066344A1 (cg-RX-API-DMAC7.html)
AU (1) AU2008251692B2 (cg-RX-API-DMAC7.html)
BR (1) BRPI0811212A2 (cg-RX-API-DMAC7.html)
CA (1) CA2687265C (cg-RX-API-DMAC7.html)
CL (1) CL2008001230A1 (cg-RX-API-DMAC7.html)
CO (1) CO6241109A2 (cg-RX-API-DMAC7.html)
CR (1) CR11106A (cg-RX-API-DMAC7.html)
DK (1) DK2148880T3 (cg-RX-API-DMAC7.html)
DO (1) DOP2009000257A (cg-RX-API-DMAC7.html)
EA (1) EA016445B1 (cg-RX-API-DMAC7.html)
EC (1) ECSP099721A (cg-RX-API-DMAC7.html)
ES (1) ES2483726T3 (cg-RX-API-DMAC7.html)
GT (1) GT200900292A (cg-RX-API-DMAC7.html)
HR (1) HRP20140611T1 (cg-RX-API-DMAC7.html)
IL (1) IL201564A (cg-RX-API-DMAC7.html)
MA (1) MA31433B1 (cg-RX-API-DMAC7.html)
MX (1) MX2009012075A (cg-RX-API-DMAC7.html)
MY (1) MY154898A (cg-RX-API-DMAC7.html)
NZ (1) NZ580423A (cg-RX-API-DMAC7.html)
PE (1) PE20090887A1 (cg-RX-API-DMAC7.html)
PL (1) PL2148880T3 (cg-RX-API-DMAC7.html)
PT (1) PT2148880E (cg-RX-API-DMAC7.html)
RS (1) RS53451B (cg-RX-API-DMAC7.html)
SI (1) SI2148880T1 (cg-RX-API-DMAC7.html)
TN (1) TN2009000446A1 (cg-RX-API-DMAC7.html)
TW (1) TWI423805B (cg-RX-API-DMAC7.html)
UA (1) UA99284C2 (cg-RX-API-DMAC7.html)
WO (1) WO2008140947A1 (cg-RX-API-DMAC7.html)

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CA2743295A1 (en) 2008-11-11 2010-05-20 Eli Lilly And Company P70 s6 kinase inhibitor and egfr inhibitor combination therapy
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JP5581390B2 (ja) * 2009-10-23 2014-08-27 イーライ リリー アンド カンパニー Akt阻害剤
SG183155A1 (en) 2010-02-03 2012-09-27 Signal Pharm Llc Identification of lkb1 mutation as a predictive biomarker for sensitivity to tor kinase inhibitors
CA2803387C (en) 2010-07-29 2017-12-05 Bayard R. Huck Cyclic amine azaheterocyclic carboxamides
UA110113C2 (xx) 2010-07-29 2015-11-25 Біциклічні азагетероциклічні карбоксаміди
US8946247B2 (en) 2010-11-24 2015-02-03 Merck Patent Gmbh Quinazoline carboxamide azetidines
HUE034979T2 (en) 2011-09-12 2018-05-02 Merck Patent Gmbh Aminopyrimidine derivatives for use as modulators of kinase activity
MX346095B (es) * 2011-09-12 2017-03-07 Merck Patent Gmbh Nuevas imidazol-aminas como moduladores de la actividad de cinasas.
MX2015002887A (es) * 2012-09-06 2015-07-06 Plexxikon Inc Compuestos y metodos para la modulacion de cinasas, e indicaciones para ello.
AU2013203714B2 (en) 2012-10-18 2015-12-03 Signal Pharmaceuticals, Llc Inhibition of phosphorylation of PRAS40, GSK3-beta or P70S6K1 as a marker for TOR kinase inhibitory activity
EP3299362B1 (en) * 2012-11-16 2020-04-22 Merck Patent GmbH Imidazol-piperidinyl derivatives as modulators of kinase activity
US9580443B2 (en) 2012-11-16 2017-02-28 Merck Patent Gmbh Heterocyclic derivatives as modulators of kinase activity
PE20151782A1 (es) 2012-11-29 2015-12-02 Merck Patent Gmbh Derivados de azaquinolin-carboxamida
ES2746756T3 (es) * 2013-03-11 2020-03-06 Merck Patent Gmbh Derivados de 6-[4-(1H-imidazol-2-il)piperidin-1-il]pirimidin-4-amina como moduladores de la actividad cinasa
KR102271344B1 (ko) 2013-04-17 2021-07-01 시그날 파마소티칼 엘엘씨 디하이드로피라지노-피라진을 사용한 암의 치료
ES2744198T3 (es) 2013-04-17 2020-02-24 Signal Pharm Llc Formulaciones farmacéuticas, procesos, formas sólidas y procedimientos de uso relacionados con 1-etil-7-(2-metil-6-(1H-1,2,4-triazol-3-il)piridin-3-il)-3, 4 dihidropirazino[2,3-b]pirazin-2(1H)-ona
JP6382947B2 (ja) 2013-04-17 2018-08-29 シグナル ファーマシューティカルズ,エルエルシー 前立腺癌を治療するためのジヒドロピラジノ−ピラジン化合物及びアンドロゲン受容体アンタゴニストを含む組合せ療法
CN105392499B (zh) 2013-04-17 2018-07-24 西格诺药品有限公司 用于治疗癌症的包含tor激酶抑制剂和胞苷类似物的组合疗法
KR102240356B1 (ko) 2013-04-17 2021-04-14 시그날 파마소티칼 엘엘씨 Tor 키나제 억제제와 5-치환된 퀴나졸리논 화합물을 포함하는 암 치료용 조합 요법
CN105377260B (zh) 2013-04-17 2020-06-12 西格诺药品有限公司 二氢吡嗪并-吡嗪类化合物在制备治疗癌症的药物中的应用
BR112015026021A2 (pt) 2013-04-17 2017-07-25 Signal Pharm Llc terapia de combinação compreendendo um inibidor de tor quinase e n-(3-(5-flúor-2-(4-(2-met-oxietoxi)fenilamino)pirimidin-4-ilamino)fenil)acrilamida para o tratamento de câncer
WO2014193912A1 (en) 2013-05-29 2014-12-04 Signal Pharmaceuticals, Llc Pharmaceutical compositions of 7-(6-(2-hydroxypropan-2-yl)pyridin-3-yl)-1-((trans)-4-methoxycyclohexyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1h)-one, a solid form thereof and methods of their use
US9771369B2 (en) 2014-03-04 2017-09-26 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
CN106456752B (zh) 2014-04-03 2020-11-20 默克专利股份公司 癌症治疗剂的组合
WO2015160880A1 (en) 2014-04-16 2015-10-22 Signal Pharmaceuticals, Llc SOLID FORMS COMPRISING 1-ETHYL-7-(2-METHYL-6-(1H-1,2,4-TRIAZOL-3-YL) PYRIDIN-3-YL)-3,4-DIHYDROPYRAZINO(2,3-b)PYRAZIN-2(1H)-ONE, AND A COFORMER, COMPOSITIONS AND METHODS OF USE THEREOF
NZ714742A (en) 2014-04-16 2017-04-28 Signal Pharm Llc Solid forms of 1-ethyl-7-(2-methyl-6-(1h-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1h)-one, compositions thereof and methods of their use
WO2016040078A1 (en) * 2014-09-10 2016-03-17 Eli Lilly And Company Substituted phenyl imidazolyl piperidyl compounds as p70s6k1 inhibitors
WO2016164641A1 (en) 2015-04-08 2016-10-13 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
CN106187899B (zh) * 2016-06-28 2019-07-16 绍兴文理学院 一种氟代氮杂芳烃的合成方法
EA202090103A1 (ru) 2017-06-22 2020-04-24 Селджин Корпорейшн Лечение гепатоцеллюлярной карциномы, которая характеризуется вирусной инфекцией гепатита b
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UA99284C2 (ru) * 2007-05-11 2012-08-10 Елі Ліллі Енд Компані ИНГИБИТОРЫ р70 S6-КИНАЗЫ

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