Synthesis and Cytotoxicity of 1,4-Naphthoquinone Oxime Derivatives


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详细

A series of hydroxylated 1,4-naphthoquinone oximes were designed and synthesized. The in vitro cytotoxicity of these compounds was evaluated against five human cancer cell lines and human skin fibroblast cell line. Among them, compounds (1E,4E)-6-{1-[(5-Hydroxypentyl)oxy]-2,2-dimethylbut-3-en-1-yl}-5,8- dimethoxynaphthalene-1,4-dione dioxime and (1E,4E)-6-{1-[(6-Hydroxyhexyl)oxy]-2,2-dimethylbut-3-en-1-yl}-5,8-dimethoxynaphthalene-1,4-dione dioxime displayed higher cytotoxicity in three cancer cell lines than the positive drug 5-fluorouracil

作者简介

Q. Zhang

School of Pharmacy

编辑信件的主要联系方式.
Email: lianyi1126@sjtu.edu.cn
中国, 800 Dongchuan Road, Shanghai, 200240

J. Dong

School of Pharmacy

Email: lianyi1126@sjtu.edu.cn
中国, 800 Dongchuan Road, Shanghai, 200240

Q. Meng

School of Pharmacy

Email: lianyi1126@sjtu.edu.cn
中国, 800 Dongchuan Road, Shanghai, 200240

G. Huang

School of Pharmacy

Email: lianyi1126@sjtu.edu.cn
中国, 800 Dongchuan Road, Shanghai, 200240

S. Li

School of Pharmacy

Email: lianyi1126@sjtu.edu.cn
中国, 800 Dongchuan Road, Shanghai, 200240


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