JP2010522770A5 - - Google Patents

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Publication number
JP2010522770A5
JP2010522770A5 JP2010501246A JP2010501246A JP2010522770A5 JP 2010522770 A5 JP2010522770 A5 JP 2010522770A5 JP 2010501246 A JP2010501246 A JP 2010501246A JP 2010501246 A JP2010501246 A JP 2010501246A JP 2010522770 A5 JP2010522770 A5 JP 2010522770A5
Authority
JP
Japan
Prior art keywords
cancer
methyl
amino
ethyl
pyrazol
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.)
Withdrawn
Application number
JP2010501246A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010522770A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2008/058603 external-priority patent/WO2008121786A1/en
Publication of JP2010522770A publication Critical patent/JP2010522770A/ja
Publication of JP2010522770A5 publication Critical patent/JP2010522770A5/ja
Withdrawn legal-status Critical Current

Links

JP2010501246A 2007-03-29 2008-03-28 Akt活性の阻害物質 Withdrawn JP2010522770A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US90874107P 2007-03-29 2007-03-29
PCT/US2008/058603 WO2008121786A1 (en) 2007-03-29 2008-03-28 Inhibitors of akt activity

Publications (2)

Publication Number Publication Date
JP2010522770A JP2010522770A (ja) 2010-07-08
JP2010522770A5 true JP2010522770A5 (en:Method) 2011-05-12

Family

ID=39808679

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010501246A Withdrawn JP2010522770A (ja) 2007-03-29 2008-03-28 Akt活性の阻害物質

Country Status (4)

Country Link
US (1) US8338434B2 (en:Method)
EP (1) EP2134175A4 (en:Method)
JP (1) JP2010522770A (en:Method)
WO (1) WO2008121786A1 (en:Method)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UY30892A1 (es) 2007-02-07 2008-09-02 Smithkline Beckman Corp Inhibidores de la actividad akt
EP2358371B1 (en) * 2008-10-31 2015-02-11 Merck Sharp & Dohme Corp. P2x3, receptor antagonists for treatment of pain
WO2010088331A1 (en) 2009-01-30 2010-08-05 Glaxosmithkline Llc Crystalline n-{(1-s)-2-amino-1-[(3-fluorophenyl)methyl]ethyl}-5-chloro-4-(4-chloro-1-methyl-1h-pyrazol-5-yl)-2-thiophenecarboxamide hydrochloride
WO2010094009A2 (en) * 2009-02-13 2010-08-19 Children's Hospital Medical Center Methods and compositions for the treatment of ras associated disorders
EP2635279A4 (en) * 2010-11-05 2014-10-29 Glaxosmithkline Ip No 2 Ltd CHEMICAL COMPOUNDS
US8895571B2 (en) 2011-10-14 2014-11-25 Incyte Corporation Isoindolinone and pyrrolopyridinone derivatives as Akt inhibitors
WO2013096153A1 (en) * 2011-12-22 2013-06-27 Glaxosmithkline Llc Chemical compounds
WO2013096151A1 (en) * 2011-12-22 2013-06-27 Glaxosmithkline Llc Chemical compounds
WO2013096637A1 (en) * 2011-12-23 2013-06-27 Millennium Pharmaceuticals, Inc. Heteroaryls and uses thereof
AU2014293011A1 (en) 2013-07-26 2016-03-17 Race Oncology Ltd. Compositions to improve the therapeutic benefit of bisantrene
CN112888440A (zh) 2018-10-16 2021-06-01 豪夫迈·罗氏有限公司 Akt抑制剂在眼科中的用途

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MXPA04001088A (es) * 2001-08-03 2004-05-20 Vertex Pharma Derivados de pirazol como inhibidores de cinasa y uso de los mismos.
TW200306819A (en) * 2002-01-25 2003-12-01 Vertex Pharma Indazole compounds useful as protein kinase inhibitors
GB0215844D0 (en) * 2002-07-09 2002-08-14 Novartis Ag Organic compounds
AU2003287366A1 (en) * 2002-10-31 2004-06-07 University Of Rochester Hyfroxyflutamide induced pathways related to androgen receptor negative prostate cancer cells
RU2342365C2 (ru) * 2003-05-01 2008-12-27 Бристол-Маерс Сквибб Компани Арилзамещенные пиразоламиды в качестве ингибиторов киназ
CA2620818A1 (en) * 2005-09-02 2007-03-08 Astellas Pharma Inc. Amide derivatives as rock inhibitors

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