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公开(公告)号:US20110028507A1
公开(公告)日:2011-02-03
申请号:US12672785
申请日:2008-08-08
申请人: Sun Nam Kim , Yong Rae Hong , Dongkyu Shin , Seonggu Ro , Joong Myung Cho , Mi Jung Lee , Ho Jin Chang
发明人: Sun Nam Kim , Yong Rae Hong , Dongkyu Shin , Seonggu Ro , Joong Myung Cho , Mi Jung Lee , Ho Jin Chang
IPC分类号: A61K31/4365 , C07D513/04 , C12N5/00 , C12N9/99 , C07D491/04 , A61K31/4355 , A61P9/10 , A61P7/06 , A61P19/02 , A61P29/00 , A61P1/00 , A61P25/00 , A61P25/08 , A61P31/18 , A61P13/12 , A61P3/00 , A61P37/06
CPC分类号: C07D495/04 , C07D471/04 , C07D491/048
摘要: Disclosed herein are pyridine derivatives, or a pharmaceutically acceptable salt, ester, amide, or prodrug thereof, pharmaceutical compositions comprising the same, and methods of modulating the level or activity of HIF in a subject, inhibiting hydroxylation of HIF α in a subject, modulating expression of HIF-regulated genes in a subject, treating an HIF-related disorder in a subject, increasing levels of endogenous EPO in a subject, or treating a disorder in a subject, using the disclosed compounds.
摘要翻译: 本文公开的是吡啶衍生物或其药学上可接受的盐,酯,酰胺或前药,包含其的药物组合物和调节受试者中HIF水平或活性的方法,抑制受试者中HIFα的羟化作用,调节 使用所公开的化合物在受试者中表达HIF调节的基因,治疗受试者中的HIF相关病症,增加受试者中内源性EPO的水平或治疗受试者中的病症。
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2.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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3.Glycogen synthase kinase 3β inhibitor, composition and process for the preparation thereof 失效
标题翻译: 糖原合酶激酶3β抑制剂,其制备及其制备方法公开(公告)号:US07179832B2
公开(公告)日:2007-02-20
申请号:US10543177
申请日:2004-01-20
申请人: Joong Myung Cho , Seonggu Ro , Tae Gyu Lee , Kyung Joo Lee , Dongkyu Shin , Young-Lan Hyun , Seung Chul Lee , Jin Hwan Kim , Young Ho Jeon
发明人: Joong Myung Cho , Seonggu Ro , Tae Gyu Lee , Kyung Joo Lee , Dongkyu Shin , Young-Lan Hyun , Seung Chul Lee , Jin Hwan Kim , Young Ho Jeon
IPC分类号: A61K31/4184 , C07D235/18
CPC分类号: C07D235/18 , C07D401/12 , C07D403/12 , C07D409/12
摘要: Novel compounds having hydroxybenzoimidazole carboxylic amide are useful for inhibiting glycogen synthase kinase 3β(GSK-3β).
摘要翻译: 具有羟基苯并咪唑羧酰胺的新型化合物可用于抑制糖原合成酶激酶3β(GSK-3β)。
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4.Glycogen synthase kinase 3beta inhibitor, composition and process for the preparation thereof 失效
标题翻译: 糖原合酶激酶3β抑制剂,其制备及其制备方法公开(公告)号:US20060079521A1
公开(公告)日:2006-04-13
申请号:US10543177
申请日:2004-01-20
申请人: Joong Cho , Seonggu Ro , Tae Lee , Kyung Lee , Dongkyu Shin , Young-Lan Hyun , Seung Lee , Jin Kim , Young Jeon
发明人: Joong Cho , Seonggu Ro , Tae Lee , Kyung Lee , Dongkyu Shin , Young-Lan Hyun , Seung Lee , Jin Kim , Young Jeon
IPC分类号: A61K31/5377 , A61K31/4184 , C07D413/02
CPC分类号: C07D235/18 , C07D401/12 , C07D403/12 , C07D409/12
摘要: Novel compounds having hydroxybenzoimidazole carboxylic amide are useful for inhibiting glycogen synthase kinase 3β (GSK-3β).
摘要翻译: 具有羟基苯并咪唑羧酰胺的新型化合物可用于抑制糖原合成酶激酶3β(GSK-3β)。
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5.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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