A novel 3,6-diamino-1,8-naphthalimide derivative as a highly selective fluorescent "turn-on" probe for thiols

Authors:Dong Cheng; Zhou Chun Qiong*; Yang Jian Wei; Liao Ting Cong; Chen Jin Xiang; Yin Cai Xia; Chen Wen Hua
Source:RSC Advances, 2015, 5(42): 32990-32993.
DOI:10.1039/c5ra03849a

Summary

A novel 1,8-naphthalimide derivative bearing 3-amino and 6-(2,4-dinitrobenzenesulfonamido) groups was synthesized and found to exhibit a fluorescent "turn-on" response to biothiols, including Cys, Hcy and GSH. This compound exhibited high selectivity and low detection limit, in particular toward Cys. The sensing mechanism involved the cleavage of the 2,4-dinitrobenzenesulfonamido group and the formation of an electron-donating amino group. In addition, its properties for cellular imaging were also briefly discussed.

  • Institution
    南方医科大学; 山西大学

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