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公开(公告)号:US08957102B2
公开(公告)日:2015-02-17
申请号:US12920243
申请日:2009-08-28
申请人: Tae-Seong Kim , Eunkyung Lee , Doyoung Kim , Bu-mahn Park , Jiyeon Park , JungJe Joo
发明人: Tae-Seong Kim , Eunkyung Lee , Doyoung Kim , Bu-mahn Park , Jiyeon Park , JungJe Joo
IPC分类号: C07D231/00 , C07D231/06 , A01N43/42 , A01N43/56 , A61K31/44 , A61K31/415 , C07D471/04 , C07D487/04
CPC分类号: C07D471/04 , C07D487/04
摘要: Provided are novel heterocyclic compounds useful as anti-cancer drugs by suppressing protein kinase activities of growth factor receptors such as c-Met, pharmaceutical compositions containing the same, and methods for using the compound.
摘要翻译: 提供了通过抑制生长因子受体如c-Met的蛋白激酶活性,含有其的药物组合物和使用该化合物的方法,可用作抗癌药物的新型杂环化合物。
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公开(公告)号:US20110183983A1
公开(公告)日:2011-07-28
申请号:US12920243
申请日:2009-08-28
申请人: Tae-Seong Kim , Eunkyung Lee , Doyoung Kim , Bu-mahn Park , Jiyeon Park , JungJe Joo
发明人: Tae-Seong Kim , Eunkyung Lee , Doyoung Kim , Bu-mahn Park , Jiyeon Park , JungJe Joo
IPC分类号: A61K31/53 , C07D487/04 , C07D471/04 , C07D253/10 , A61K31/5025 , A61K31/437 , A61P35/00 , A61P17/06
CPC分类号: C07D471/04 , C07D487/04
摘要: Provided are novel heterocyclic compounds useful as anti-cancer drugs by suppressing protein kinase activities of growth factor receptors such as c-Met, pharmaceutical compositions containing the same, and methods for using the compound.
摘要翻译: 提供了通过抑制生长因子受体如c-Met的蛋白激酶活性,含有它们的药物组合物和使用该化合物的方法,可用作抗癌药物的新型杂环化合物。
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公开(公告)号:US20120289509A1
公开(公告)日:2012-11-15
申请号:US13542895
申请日:2012-07-06
申请人: Tae-Seong KIM , Eunkyung LEE , Doyoung KIM , Bu-mahn PARK , Jiyeon PARK , JungJe JOO
发明人: Tae-Seong KIM , Eunkyung LEE , Doyoung KIM , Bu-mahn PARK , Jiyeon PARK , JungJe JOO
IPC分类号: C07D487/04 , A61P35/00 , A61K31/437 , A61K31/53 , A61K31/5025 , C07D471/04
CPC分类号: C07D471/04 , C07D487/04
摘要: Provided are novel heterocyclic compounds useful as anti-cancer drugs by suppressing protein kinase activities of growth factor receptors such as c-Met, pharmaceutical compositions containing the same, and methods for using the compound.
摘要翻译: 提供了通过抑制生长因子受体如c-Met的蛋白激酶活性,含有其的药物组合物和使用该化合物的方法,可用作抗癌药物的新型杂环化合物。
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