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作 者:Hui Chen Hui Wang Xiao-Jun Qin Chen Chen Lu Feng Lai-Zhong Chen Lu-Pei Du Min-Yong Li
机构地区:[1]Department of Medicinal Chemistry,Key Laboratory of Chemical Biology(MOE),School of Pharmacy,Shandong University [2]China Pharmaceutical University Pharmaceutical Co.Ltd.
出 处:《Chinese Chemical Letters》2015年第5期513-516,共4页中国化学快报(英文版)
基 金:supported by the Program for New Century Excellent Talents in University(No.NCET-11-0306);the Shandong Natural Science Foundation(No.JQ201019);the Independent Innovation Foundation of Shandong University, IIFSDU(No.2014JC008);the Graduate Independent Innovation Foundation of Shandong University,GIIFSDU(No.yzcl2096)
摘 要:Aminopeptidase N (APN) is an important drug target and biomarker for various tumors. The current work characterizes a novel APN-targeted fluorescent probe (Bes-Green, 2) that manifests comparable inhibitory activity with Bestatin. This probe has capacity of tightly binding to the APN for imaging endogenous APN in living human ovarian clear cell carcinoma cells (ES-2) and has potential application in biological study of cellular APN.Aminopeptidase N (APN) is an important drug target and biomarker for various tumors. The current work characterizes a novel APN-targeted fluorescent probe (Bes-Green, 2) that manifests comparable inhibitory activity with Bestatin. This probe has capacity of tightly binding to the APN for imaging endogenous APN in living human ovarian clear cell carcinoma cells (ES-2) and has potential application in biological study of cellular APN.
关 键 词:Aminopeptidase N Bestatin Cell imaging Fluorescent probe
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