Synthesis and biological evaluation of novel pentacyclic triterpene α-cyclodextrin conjugates as HCV entry inhibitors.

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第一作者： Sulong,Xiao

第一单位： State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China. Electronic address: slxiao@bjmu.edu.cn.

作者： Sulong,Xiao ^[1] ; Qi,Wang ^[2] ; Longlong,Si ^[3] ; Xiaoshu,Zhou ^[3] ; Yongmin,Zhang ^[4] ; Lihe,Zhang ^[3] ; Demin,Zhou ^[5]

作者单位： State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China. Electronic address: slxiao@bjmu.edu.cn. ^[1] State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China; Department of Molecular and Cellular Pharmacology, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China. ^[2] State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China. ^[3] Institut Parisien de Chimie Moléculaire, CNRS UMR 8232, Université Pierre & Marie Curie-Paris 6, 4 Place Jussieu, 75005, Paris, France. ^[4] State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China. Electronic address: deminzhou@bjmu.edu.cn. ^[5]

关键词 Click chemistry HCV entry inhibitor Pentacyclic triterpene α-Cyclodextrin