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作 者:Li Chen Wen Qiu Jia Tang Zhi Feng Wang Shu Ying He
机构地区:[1]Department of Phytochemistry, China Pharmaceutical University, Nanjing 210009, China [2]Tianjin Hankang Medicinal & Biological Technology Co., Ltd., Tianjin 300203, China [3]School of Life Science and Technology, China Pharmaceutical University, Nanjing 210009, China
出 处:《Chinese Chemical Letters》2011年第4期413-416,共4页中国化学快报(英文版)
基 金:supported by a grant from the National Natural Science Foundation of China(No.2097210);research grants from the Natural Science Foundation of Jiangsu Province(No.BK2009302);Tianjin Application Bases and Advanced Technology Research Program Key Projects(No.JCZDJC21400)
摘 要:A series of furoxan-based novel nitric oxide-donating ursolic acid(UA) derivatives(7a-f) were synthesized,and their cytotoxic activities against HepG2 cells in vitro were evaluated by MTT method.It was found that 7a-d and 7f showed more potent cytotoxic activities than control 5-fluorouracil and UA.A series of furoxan-based novel nitric oxide-donating ursolic acid(UA) derivatives(7a-f) were synthesized,and their cytotoxic activities against HepG2 cells in vitro were evaluated by MTT method.It was found that 7a-d and 7f showed more potent cytotoxic activities than control 5-fluorouracil and UA.
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