Novel Naphthalimide Derivatives as Selective G-Quadruplex DNA Binders

被引:4
|
作者
Yildiz, Ufuk [1 ]
Coban, Burak [1 ]
机构
[1] Bulent Ecevit Univ, Fac Arts & Sci, Dept Chem, TR-67100 Zonguldak, Turkey
关键词
4-Bromo-1,8-naphthalic anhydride; Quaternized; Naphthalimide; DNA binding; G-Quadruplex DNA selectivity; HETEROCYCLIC FUSED NAPHTHALIMIDES; AMINOALKYL SIDE-CHAINS; BINDING-PROPERTIES; IN-VITRO; TELOMERASE INHIBITION; BIOLOGICAL EVALUATION; DISPLACEMENT ASSAY; ANTITUMOR-ACTIVITY; ANTICANCER AGENTS; MOLECULAR DESIGN;
D O I
10.1007/s12010-018-2749-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A new derivate of 4-bromo-1,8-naphthalic anhydride and its quaternized analogue have been prepared and characterized. The interactions of both derivatives with human telomere quadruplex-DNA and ds-DNA have been comparatively studied by UV-visible (UV-Vis), fluorescent intercalator displacement assays, competition dialysis, circular dichroism (CD), agarose gel electrophoresis, and polyacrylamide gel electrophoresis. The results show that both derivatives can stabilize G-quadruplexes DNA, and they show different binding affinities for G-quadruplexes-DNA and ds-DNA. All spectroscopic studies have shown that the derivatives have a modest selectivity for G-quadruplex versus ds-DNA.
引用
收藏
页码:547 / 562
页数:16
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