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1.Naphthalenyloxypropenyl derivatives having inhibitory activity against histone deacetylase and pharmaceutical composition comprising the same 有权
标题翻译: 对组蛋白脱乙酰酶具有抑制活性的萘氧基丙烯基衍生物及其组合物公开(公告)号:US08053435B2
公开(公告)日:2011-11-08
申请号:US12513021
申请日:2007-11-01
申请人: Cheol Hae Lee , Hee Jung Jung , Jae Hak Kim , Won Jang Jeong , Joong Myung Cho , Seong Gu Ro , Young Lan Hyun , Cheol Soon Lee , Dongkyu Shin
发明人: Cheol Hae Lee , Hee Jung Jung , Jae Hak Kim , Won Jang Jeong , Joong Myung Cho , Seong Gu Ro , Young Lan Hyun , Cheol Soon Lee , Dongkyu Shin
IPC分类号: A61K31/165 , A61K31/341 , A61K31/381 , A61K31/4164 , A61K31/4166 , A61K31/40 , A61K31/4468 , A61K31/5375 , C07D207/50 , C07D233/88 , C07D295/027 , C07D211/98 , C07D307/66 , C07D333/36
CPC分类号: C07C259/10 , C07C259/06 , C07C2601/14 , C07C2601/16 , C07D207/27 , C07D207/335 , C07D211/10 , C07D211/58 , C07D233/64 , C07D295/13 , C07D307/14 , C07D307/52 , C07D333/20
摘要: The present invention discloses novel naphthalenyloxypropenyl derivatives useful for inhibiting the enzyme activity of histone deacetylase, leading effective suppression of cancer cell proliferation.
摘要翻译: 本发明公开了用于抑制组蛋白脱乙酰酶的酶活性的新型萘氧基丙烯基衍生物,有效抑制癌细胞增殖。
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2.NAPHTHALENYLOXYPROPENYL DERIVATIVES HAVING INHIBITORY ACTIVITY AGAINST HISTONE DEACETYLASE AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME 有权
标题翻译: 具有抗组胺脱乙酰酶的抑制活性的萘并戊烯衍生物和包含其的药物组合物公开(公告)号:US20100069630A1
公开(公告)日:2010-03-18
申请号:US12513021
申请日:2007-11-01
申请人: Cheol Hae Lee , Hee Jung Jung , Jae Hak Kim , Won Jang Jeong , Joong Myung Cho , Seong Gu Ro , Young Lan Hyun , Cheol Soon Lee
发明人: Cheol Hae Lee , Hee Jung Jung , Jae Hak Kim , Won Jang Jeong , Joong Myung Cho , Seong Gu Ro , Young Lan Hyun , Cheol Soon Lee
IPC分类号: C07D295/00 , C07D211/98 , C07D233/44 , C07C233/00 , C07D307/02 , C07D207/46 , C07D333/20
CPC分类号: C07C259/10 , C07C259/06 , C07C2601/14 , C07C2601/16 , C07D207/27 , C07D207/335 , C07D211/10 , C07D211/58 , C07D233/64 , C07D295/13 , C07D307/14 , C07D307/52 , C07D333/20
摘要: The present invention discloses novel naphthalenyloxypropenyl derivatives useful for inhibiting the enzyme activity of histone deacetylase, leading effective suppression of cancer cell proliferation.
摘要翻译: 本发明公开了用于抑制组蛋白脱乙酰酶的酶活性的新型萘氧基丙烯基衍生物,有效抑制癌细胞增殖。
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3.Imidazopyridine Derivatives Inhibiting Protein Kinase Activity, Method for the Preparation Thereof and Pharmaceutical Composition Containing Same 审中-公开
标题翻译: 抑制蛋白激酶活性的咪唑并吡啶衍生物及其制备方法和含有其的药物组合物公开(公告)号:US20090170847A1
公开(公告)日:2009-07-02
申请号:US12161916
申请日:2007-01-23
申请人: Seung Chul Lee , Jin Seok Choi , Jung Hoon Oh , Boonsaeng Park , Yong Eun Kim , Jun Hee Lee , Dongkyu Shin , Cheol Min Kim , Young-Lan Hyun , Cheol Soon Lee , Joong-Myung Cho , Seonggu Ro
发明人: Seung Chul Lee , Jin Seok Choi , Jung Hoon Oh , Boonsaeng Park , Yong Eun Kim , Jun Hee Lee , Dongkyu Shin , Cheol Min Kim , Young-Lan Hyun , Cheol Soon Lee , Joong-Myung Cho , Seonggu Ro
IPC分类号: A61K31/5377 , A61K31/53 , A61K31/506 , A61K31/496 , A61K31/4745 , C07D471/02
CPC分类号: C07D471/04
摘要: The inventive imidazopyridine derivative can be used in a pharmaceutical composition for preventing or treating diseases such as diabetes, obesity, dementia, cancer, and inflammation, since it can efficiently inhibit the activities of several protein kinases including glycogen synthase kinase-3 (GSK-3), aurora kinase, extracellular signal-regulated kinase (ERK), protein kinase B (AKT), and the likes, to control signal transductions thereof.
摘要翻译: 本发明的咪唑并吡啶衍生物可用于预防或治疗诸如糖尿病,肥胖症,痴呆,癌症和炎症等疾病的药物组合物中,因为它可有效抑制几种蛋白激酶(包括糖原合成酶激酶-3(GSK-3 ),极光激酶,细胞外信号调节激酶(ERK),蛋白激酶B(AKT)等,以控制其信号转导。
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