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公开(公告)号:US07722718B2
公开(公告)日:2010-05-25
申请号:US11873831
申请日:2007-10-17
申请人: Jessie English , Thierry Oliver Fischmann , Thomas Hesson , Alan William Hruza , Weihong Jin , Paul Reichert , Catherine Smith , Shahriar Shane Taremi
发明人: Jessie English , Thierry Oliver Fischmann , Thomas Hesson , Alan William Hruza , Weihong Jin , Paul Reichert , Catherine Smith , Shahriar Shane Taremi
CPC分类号: C12N9/1205 , C07K2299/00
摘要: The present invention relates to crystals of the ERK2 polypeptide and complexes thereof which are useful, inter alia, for structure assisted drug design.
摘要翻译: 本发明涉及ERK2多肽的结晶及其复合物,其特别用于结构辅助药物设计。
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公开(公告)号:US07312061B2
公开(公告)日:2007-12-25
申请号:US11233581
申请日:2005-09-23
申请人: Jessie English , Thierry Oliver Fischmann , Thomas Hesson , Alan William Hruza , Weihong Jin , Paul Reichert , Catherine Smith , Shahriar Shane Taremi
发明人: Jessie English , Thierry Oliver Fischmann , Thomas Hesson , Alan William Hruza , Weihong Jin , Paul Reichert , Catherine Smith , Shahriar Shane Taremi
IPC分类号: C12N9/12
CPC分类号: C12N9/1205 , C07K2299/00
摘要: The present invention relates to crystals of the ERK2 polypeptide and complexes thereof which are useful, inter alia, for structure assisted drug design.
摘要翻译: 本发明涉及ERK2多肽的结晶及其复合物,其特别用于结构辅助药物设计。
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公开(公告)号:US20100190231A1
公开(公告)日:2010-07-29
申请号:US12754029
申请日:2010-04-05
申请人: JESSIE M. ENGLISH , Thierry Oliver Fischmann , Thomas Hesson , Alan William Hruza , Weihong Jin , Paul Reichert , Catherine Smith , Shahriar Shane Taremi
发明人: JESSIE M. ENGLISH , Thierry Oliver Fischmann , Thomas Hesson , Alan William Hruza , Weihong Jin , Paul Reichert , Catherine Smith , Shahriar Shane Taremi
CPC分类号: C12N9/1205 , C07K2299/00
摘要: The present invention relates to crystals of the ERK2 polypeptide and complexes thereof which are useful, inter alia, for structure assisted drug design.
摘要翻译: 本发明涉及ERK2多肽的结晶及其复合物,其特别用于结构辅助药物设计。
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4.
公开(公告)号:US20130165450A1
公开(公告)日:2013-06-27
申请号:US13820913
申请日:2011-09-09
IPC分类号: C07D417/14 , C07D491/113 , C07D471/10
CPC分类号: C07D417/14 , A61K31/425 , C07D417/04 , C07D471/10 , C07D491/10
摘要: This invention relates to certain thiazole carboxamide derivatives of Formula (I) as inhibitors of 3-phosphoinositide-dependent protein kinase (PDK-1). The compounds can be useful in inhibiting the proliferation of cancer cells, and other aberrant conditions where the PDK-1 signaling pathway is overstimulated.
摘要翻译: 本发明涉及作为3-磷酸肌醇依赖性蛋白激酶(PDK-1)抑制剂的式(I)的某些噻唑羧酰胺衍生物。 该化合物可用于抑制癌细胞的增殖,以及PDK-1信号通路被过度刺激的其它异常状况。
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