蒽
哌嗪
化学
选择性
药理学
组合化学
药物化学
有机化学
医学
催化作用
作者
Margrate Anyanwu,Matteo Giannangeli,Xing‐Xing Fan,Paolo Coghi,Giovanni Ribaudo,Alessandra Gianoncelli
标识
DOI:10.1021/acsmedchemlett.4c00340
摘要
G-Quadruplexes (G4s) are appealing targets for anticancer therapy because of their location in the genome and their role in regulating physiological and pathological processes. In this article, we report the characterization of the molecular interaction and selectivity of OAF89, a 9,10-disubstituted G4-binding anthracene derivative, with different DNA sequences. Advanced analytical methods, including mass spectrometry and nuclear magnetic resonance, were used to conduct the investigation, together with the use of
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