Fluorene/fluorenone carboxamide derivatives as selective light-up fluorophores for c-myc G-quadruplex

被引:6
|
作者
Duyar, Halil [1 ,2 ]
Portakal, Huseyin S. [3 ]
Yalcin, Ergin [1 ,4 ]
Kanat, Beyza [3 ]
Doluca, Osman [3 ]
Seferoglu, Zeynel [1 ]
机构
[1] Gazi Univ, Dept Chem, TR-06560 Ankara, Turkey
[2] Gebze Tech Univ, Dept Chem, TR-41400 Kocaeli, Turkey
[3] Izmir Univ Econ, Dept Biomed Engn, TR-35330 Izmir, Turkey
[4] Iskenderun Tech Univ, Dept Engn Basic Sci, TR-31200 Antakya, Turkey
关键词
Fluorene; Fluorenone; G-Quadruplex; c-myc; Light-up probe;
D O I
10.1016/j.bmcl.2021.127824
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The development of fluorescent dyes capable of selective recognition of G-quadruplexes is essential for studying its localization and biological functions. However, considering the G-quadruplex topologies may vary significantly, the synthesis of compounds showing both selectivity and strong fluorescence properties still remains a great challenge. Recently we have developed fluorene/fluorenone derivatives with structure-specific binding towards dsRNA, indicating its potential for structure-selective ligands. Herein, we report the synthesis of novel fluorene/fluorenone derivatives and their selectivity towards various DNA structures, particularly G-quadruplexes, two of which showed strong affinity to the proto-oncogene c-myc promoter G-quadruplex.
引用
收藏
页数:6
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