Design, synthesis and biological evaluation of fluorescent derivatives of ursolic acid in living cells

被引:1
|
作者
Mei, Wenyi [1 ]
Xie, Lijuan [1 ]
Zhang, Xiaodong [1 ]
Shi, Cunjian [1 ]
Wang, Fengzhi [1 ]
Fu, Qiqi [1 ]
Zhao, Zhenjiang [1 ]
Li, Honglin [1 ,2 ,3 ]
Xu, Yufang [1 ]
Chen, Zhuo [1 ]
机构
[1] East China Univ Sci & Technol, Sch Pharm, Shanghai Key Lab New Drug Design, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
[2] East China Normal Univ, Innovat Ctr AI & Drug Discovery, Shanghai 200062, Peoples R China
[3] Lingang Lab, Shanghai 200031, Peoples R China
基金
中国国家自然科学基金;
关键词
Pentacyclic triterpenoid; Ursolic acid; Fluorescent derivatives; Autophagy; Apoptosis; SUBCELLULAR-LOCALIZATION; DOWN-REGULATION; OLEANOLIC ACID; PROBES; VOLUNTEERS; METABOLISM; TURNOVER; PATHWAY;
D O I
10.1016/j.cclet.2023.108825
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ursolic acid (UA) is a naturally occurring ursane triterpenoid, which exhibits a wide range of unique biological activities. To clarify its mechanism of action (MOA), a series of fluorescent derivatives of UA ( 5a -c ) were designed and synthesized by conjugation with 7-nitrobenzo-2-oxa-1,3-diazole (NBD) fluorophore. Among them, 5c exhibited similar anti-proliferative activity with UA against HCT116 cells (half maximal inhibitory concentration (IC50 ) = 9.21 +/- 0.50 mu mol/L). Cell imaging experiment indicated that 5c was rapidly taken up in HCT116 cells in a dose and time-dependent manner. Then, 5c was found to localize in endoplasmic reticulum (ER), lysosomes, and mitochondria, but not in nucleus of HCT116 cells by confocal microscopy studies. Preliminary MOA proved that UA induced autophagy with a unique intracellular distribution mechanism involving ER and lysosome. In all, our work provides new clues for revealing the molecular mechanism of UA as an antitumor agent. (c) 2024 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
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页数:3
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