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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.
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页数:6
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