Natural products and their derivatives as G-quadruplex binding ligands

被引:20
|
作者
Shan Chan [1 ]
Tan Jia-Heng [1 ]
Ou Tian-Miao [1 ]
Huang Zhi-Shu [1 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
G-quadruplex binding ligands; natural products; derivatives; TELOMERIC G-QUADRUPLEX; HIGHLY SELECTIVE LIGANDS; C-MYC PROMOTER; SMALL-MOLECULE; QUINDOLINE DERIVATIVES; CELL-GROWTH; QUINAZOLINE DERIVATIVES; BERBERINE DERIVATIVES; STABILIZING LIGANDS; CATIONIC PORPHYRINS;
D O I
10.1007/s11426-013-4920-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
G-quadruplexes comprise a class of secondary structures that are formed in guanine-rich sequences in eukaryotic genomes and play a crucial role in the regulation of many biological events. G-quadruplexes have become targets for anticancer drugs with high selectivity vs. duplex DNA and low cytotoxicity against normal cells. Natural products and their derivatives display polymorphism, structural complexity, and potent activity. It is, therefore, reasonable to seek ligands targeting G-quadruplexes from natural products. Recently, many successful examples have been reported, showing ligands with excellent anticancer activities. In this review, we summarized the development of research on natural products and derivatives that target G-quadruplex structures in an effort to guide future studies.
引用
收藏
页码:1351 / 1363
页数:13
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