国家自然科学基金(30772650)

作品数:4被引量:0H指数:0
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相关作者:邹晓民徐萍周博王超牛彦更多>>
相关机构:北京大学中国医学科学院北京协和医学院更多>>
相关期刊:《Journal of Chinese Pharmaceutical Sciences》更多>>
相关主题:INHIBITORSSYNTHESISPROTEASOMEMIDIINTERMEDIATES更多>>
相关领域:医药卫生更多>>
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Synthesis of acyclic analogs of Syringolin A as potential 20S proteasome inhibitors
《Journal of Chinese Pharmaceutical Sciences》2010年第6期423-435,共13页袁悦 邹晓民 牛彦 许凤荣 牟科 周博 王超 李勇剑 杨冠宇 徐萍 
National Natural Science Foundation of China (Grant No.20772008 and 30772650)
A series of acyclic analogs of natural product Syringolin A (SylA) were designed and synthesized during our synthetic efforts for SylA. These acyclic analogs were prepared through a seven-step linear strategy, with ...
关键词:Syringolin A 20S proteasome Peptidyl vinyl amide 
Structure-based design of hexahydropyrimidin-5-ols as novel non-peptidic β-secretase inhibitors
《Journal of Chinese Pharmaceutical Sciences》2010年第5期341-345,共5页周博 牛彦 邹晓民 许凤荣 袁悦 王超 高海飞 刘鹏 徐萍 
National Natural Science Foundation of China (Grant No.20772008 and 30772650)
Based upon the crystal structure of a previously reported fragment hit that binds to Corresponding author. β-secretase, a novel series of non-peptidic small-molecule β-secretase inhibitors, namely hexahydropyrimidin...
关键词:β-Secretase inhibitors Hexahydropyrimidin-5-ols Structure-based drug design Computer-aided drug design 
Efficient synthesis of terminal α,β-unsaturated ketones as the intermediates of the proteasome epoxyketone inhibitors via Weinreb amide
《Journal of Chinese Pharmaceutical Sciences》2009年第1期33-36,共4页吕杨 邹晓民 牟科 傅翌秋 马超 周博 徐萍 
National Natural Science Foundation of China (Grant No. 30772650 and 20772008)
Peptidyl epoxyketones were potential antitumor agents due to their 20S proteasome inhibitory activities. Based on their structures and special inhibitory mechanism, a series of compounds were designed by linking the e...
关键词:Epoxyketone SYNTHESIS α β-Unsaturated ketone Weinreb amide 
Synthesis and activity of hydroxyethylene peptidomimetic inhibitors of humanβ-secretase
《Journal of Chinese Pharmaceutical Sciences》2008年第3期215-220,共6页马超 王月华 杨晓鸣 邹晓民 吕杨 杜冠华 徐萍 
National Natural Science Foundation of China(Grant No.30772650 and 20772008).
A series of β-secretase peptidomimetic inhibitors with Leu*Ala hydroxyethylene dipeptide isostere were synthesized and their β-secretase inhibitory activities were measured. The most potent compound N9 showed an in...
关键词:β-Secretase inhibitors Hydroxyethylene isostere SYNTHESIS Bioactivity 
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