JP2008531537A5 - - Google Patents

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Publication number
JP2008531537A5
JP2008531537A5 JP2007556664A JP2007556664A JP2008531537A5 JP 2008531537 A5 JP2008531537 A5 JP 2008531537A5 JP 2007556664 A JP2007556664 A JP 2007556664A JP 2007556664 A JP2007556664 A JP 2007556664A JP 2008531537 A5 JP2008531537 A5 JP 2008531537A5
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JP
Japan
Prior art keywords
group
compound according
composition according
halo
carbon atom
Prior art date
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.)
Pending
Application number
JP2007556664A
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English (en)
Japanese (ja)
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JP2008531537A (ja
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Publication date
Priority claimed from GBGB0503962.3A external-priority patent/GB0503962D0/en
Application filed filed Critical
Priority claimed from PCT/GB2006/000668 external-priority patent/WO2006090167A2/en
Publication of JP2008531537A publication Critical patent/JP2008531537A/ja
Publication of JP2008531537A5 publication Critical patent/JP2008531537A5/ja
Pending legal-status Critical Current

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JP2007556664A 2005-02-25 2006-02-24 化合物 Pending JP2008531537A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US65619305P 2005-02-25 2005-02-25
GBGB0503962.3A GB0503962D0 (en) 2005-02-25 2005-02-25 Compounds
PCT/GB2006/000668 WO2006090167A2 (en) 2005-02-25 2006-02-24 Hydrazinomethyl, hydr zonomethyl and 5-membered heterocylic compounds which act as mtor inhibitors and their use as anti cancer agents

Publications (2)

Publication Number Publication Date
JP2008531537A JP2008531537A (ja) 2008-08-14
JP2008531537A5 true JP2008531537A5 (https=) 2009-04-09

Family

ID=36729293

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007556664A Pending JP2008531537A (ja) 2005-02-25 2006-02-24 化合物

Country Status (10)

Country Link
US (1) US20100130473A1 (https=)
EP (1) EP1877388A2 (https=)
JP (1) JP2008531537A (https=)
KR (1) KR20070108916A (https=)
AU (1) AU2006217742A1 (https=)
CA (1) CA2599320A1 (https=)
IL (1) IL184900A0 (https=)
MX (1) MX2007010404A (https=)
NO (1) NO20074071L (https=)
WO (1) WO2006090167A2 (https=)

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US9029411B2 (en) 2008-01-25 2015-05-12 Millennium Pharmaceuticals, Inc. Thiophenes and uses thereof
LT2294072T (lt) 2008-05-23 2017-06-12 Wyeth Llc Triazino junginiai, kaip p13 kinazės ir mtor inhibitoriai
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US9090601B2 (en) 2009-01-30 2015-07-28 Millennium Pharmaceuticals, Inc. Thiazole derivatives
WO2010090716A1 (en) 2009-01-30 2010-08-12 Millennium Pharmaceuticals, Inc. Heteroaryls and their use as pi3k inhibitors
UY32470A (es) 2009-03-05 2010-10-29 Boehringer Ingelheim Int Derivados de 2-{2-cloro-5-[(sustituido) metil]fenilamino} -1-metil]fenilamino}-1-metilbencimidazol-5-carboxamidas-n-(sustituidas) y sus sales fisiológicamente aceptables, composiciones conteniéndolos y aplicaciones
US8242260B2 (en) 2009-08-28 2012-08-14 Novartis Ag Compounds and compositions as protein kinase inhibitors
WO2011067348A2 (en) 2009-12-03 2011-06-09 Novartis Ag Mek inhibitor salts and solvates thereof
WO2011067356A2 (en) 2009-12-03 2011-06-09 Novartis Ag Polymorphs of a mek inhibitor
CA2788678C (en) 2010-02-03 2019-02-26 Signal Pharmaceuticals, Llc Identification of lkb1 mutation as a predictive biomarker for sensitivity to tor kinase inhibitors
GB201004200D0 (en) * 2010-03-15 2010-04-28 Univ Basel Spirocyclic compounds and their use as therapeutic agents and diagnostic probes
KR101461767B1 (ko) 2010-03-30 2014-11-13 노파르티스 아게 만성 활성 b-세포-수용체 신호전달이 있는 b-세포 림프종의 치료를 위한 pkc 억제제
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US8486968B2 (en) 2010-12-10 2013-07-16 Boehringer Ingelheim International Gmbh Compounds
UY33779A (es) 2010-12-10 2012-07-31 Boehringer Ingelheim Int ?2-(fenilamino)-1H-bencimidazol-5-carboxamidas novedosas?
US8466186B2 (en) 2010-12-10 2013-06-18 Boehringer Ingelheim International Gmbh Compounds
HK1199068A1 (en) 2011-08-03 2015-06-19 西格诺药品有限公司 Identification of gene expression profile as a predictive biomarker for lkb1 status
BR112014007310A2 (pt) 2011-09-27 2017-04-04 Novartis Ag 3-pirimidin-4-il-oxazolidin-2-onas como inibidores de idh mutante
KR102040997B1 (ko) * 2011-12-02 2019-11-27 시그날 파마소티칼 엘엘씨 7-(6-(2-히드록시프로판-2-일)피리딘-3-일)-1-((트랜스)-4-메톡시시클로헥실)-3,4-디히드로피라지노[2,3-b]피라진-2(1H)-온, 그의 고체 형태의 제약 조성물 및 그의 사용 방법
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US9296733B2 (en) 2012-11-12 2016-03-29 Novartis Ag Oxazolidin-2-one-pyrimidine derivative and use thereof for the treatment of conditions, diseases and disorders dependent upon PI3 kinases
JP6120311B2 (ja) * 2013-02-12 2017-04-26 学校法人銀杏学園 ポリフェノール化合物
JP6387360B2 (ja) 2013-03-14 2018-09-05 ノバルティス アーゲー 変異idhの阻害薬としての3−ピリミジン−4−イル−オキサゾリジン−2−オン
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BR112016018691A2 (pt) * 2014-02-14 2017-08-08 Univ British Columbia Compostos do domínio de ligação ao dna (dbd) de receptor de andrógeno humano como terapêuticos e métodos para seu uso
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TWI787284B (zh) 2017-06-22 2022-12-21 美商西建公司 以b型肝炎病毒感染表徵之肝細胞癌之治療
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AU2024288001A1 (en) 2023-07-11 2026-01-15 Tay Therapeutics Limited Compounds comprising a naphthyridine or pyridopyrimidine core as ptc read-through agents

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