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公开(公告)号:US20070293516A1
公开(公告)日:2007-12-20
申请号:US11732856
申请日:2007-04-04
申请人: Zachary Knight , Beth Apsel , Kevan Shokat
发明人: Zachary Knight , Beth Apsel , Kevan Shokat
IPC分类号: A61K31/519 , A61P35/00 , A61P35/02 , C07D487/02 , C12N9/99
CPC分类号: C07D487/04
摘要: The present invention provides novel compounds that are antagonists of PI3 kinase, PI3 kinase and tryosine kinase, PI3Kinase and mTOR, or PI3Kinase, mTOR and tryosine kinase.
摘要翻译: 本发明提供了作为PI3激酶,PI3激酶和软糖激酶,PI3Kinase和mTOR或PI3Kinase,mTOR和软糖激酶的拮抗剂的新型化合物。
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公开(公告)号:US07585868B2
公开(公告)日:2009-09-08
申请号:US11732856
申请日:2007-04-04
申请人: Zachary A. Knight , Beth Apsel , Kevan M. Shokat
发明人: Zachary A. Knight , Beth Apsel , Kevan M. Shokat
IPC分类号: C07D487/04 , A61K31/519 , A61P35/04 , A61P35/02
CPC分类号: C07D487/04
摘要: The present invention provides novel compounds that can be used as antagonists of a lipid kinase such as a PI3 kinase, protein tyrosine kinase, and/or protein serine-threonine kinases such as mTOR. The present invention also provides methods of using the compounds for treating various disease conditions. The compounds include those having the formula: wherein the R1, R2 and R36 are as defined herein.
摘要翻译: 本发明提供可用作脂质激酶如PI3激酶,蛋白酪氨酸激酶和/或蛋白丝氨酸 - 苏氨酸激酶(如mTOR)的拮抗剂的新型化合物。 本发明还提供了使用该化合物治疗各种疾病状况的方法。 化合物包括具有下式的化合物:其中R 1,R 2和R 36如本文所定义。
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公开(公告)号:US20110301144A1
公开(公告)日:2011-12-08
申请号:US13016961
申请日:2011-01-29
申请人: Zachary A. Knight , Beth Apsel , Kevan M. Shokat
发明人: Zachary A. Knight , Beth Apsel , Kevan M. Shokat
IPC分类号: A61K31/519 , A61P35/02 , A61P19/08 , A61P35/04 , A61P37/00 , A61P7/02 , A61P11/06 , A61P35/00 , C07D487/04 , A61P29/00
CPC分类号: C07D487/04
摘要: The present invention provides novel compounds that are antagonists of PI3 kinase, PI3 kinase and tyrosine kinase, PI3 kinase and mTOR, or PI33 kinase, mTOR and tyrosine kinase.
摘要翻译: 本发明提供了作为PI3激酶,PI3激酶和酪氨酸激酶,PI3激酶和mTOR或PI33激酶,mTOR和酪氨酸激酶的拮抗剂的新型化合物。
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公开(公告)号:US08642604B2
公开(公告)日:2014-02-04
申请号:US12509281
申请日:2009-07-24
申请人: Zachary A. Knight , Beth Apsel , Kevan M. Shokat
发明人: Zachary A. Knight , Beth Apsel , Kevan M. Shokat
IPC分类号: A61K31/519 , A61P35/00 , C07D487/04
CPC分类号: C07D487/04
摘要: The present invention provides novel compounds that are antagonists of PI3 kinase, PI3 kinase and tyrosine kinase, PI3 kinase and mTOR, or PI33 kinase, mTOR and tyrosine kinase.
摘要翻译: 本发明提供了作为PI3激酶,PI3激酶和酪氨酸激酶,PI3激酶和mTOR或PI33激酶,mTOR和酪氨酸激酶的拮抗剂的新型化合物。
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公开(公告)号:US20110224223A1
公开(公告)日:2011-09-15
申请号:US13003562
申请日:2009-07-08
申请人: Kevan M. Shokat , David Fruman , Pingda Ren , Troy Edward Wilson , Liansheng Li , Andrew Hsieh , Morris Feldman , Beth Apsel , Yi Liu , Christian Rommel , Katrina Chan , Davide Ruggero , David Pearce , Matthew Janes
发明人: Kevan M. Shokat , David Fruman , Pingda Ren , Troy Edward Wilson , Liansheng Li , Andrew Hsieh , Morris Feldman , Beth Apsel , Yi Liu , Christian Rommel , Katrina Chan , Davide Ruggero , David Pearce , Matthew Janes
IPC分类号: A61K31/506 , C12N5/09 , C12N9/99 , A61K31/519 , A61K31/436 , A61P35/00 , A61P13/12 , A61P9/12 , A61P9/04 , A61P1/16
CPC分类号: A61K31/519 , C12Q1/485 , G01N2500/04 , G01N2510/00
摘要: The present invention provides methods and compositions for selective modulation of certain protein kinases, and especially mTor complexes. The methods and compositions are particularly useful in inhibiting mTor selectively for therapeutic applications.
摘要翻译: 本发明提供了选择性调节某些蛋白激酶,特别是mTor复合物的方法和组合物。 所述方法和组合物特别可用于抑制mTor用于治疗应用。
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