9,10-Bis[(4-(2-hydroxyethyl)piperazine-1-yl)prop2-yne-1-yl]anthracene: G-Quadruplex Selectivity and Anticancer Activity.
Margrate AnyanwuMatteo GiannangeliXing-Xing FanPaolo CoghiGiovanni RibaudoAlessandra GianoncelliPublished in: ACS medicinal chemistry letters (2024)
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 in silico docking and molecular dynamics. Eventually, the compound was tested in vitro to assess its bioactivity against lung cancer cell lines.
Keyphrases
- molecular dynamics
- magnetic resonance
- mass spectrometry
- liquid chromatography
- density functional theory
- single molecule
- circulating tumor
- molecular docking
- cell free
- ionic liquid
- structural basis
- high resolution
- capillary electrophoresis
- gas chromatography
- high performance liquid chromatography
- contrast enhanced
- tandem mass spectrometry
- genome wide
- magnetic resonance imaging
- dna binding
- computed tomography
- nucleic acid
- circulating tumor cells
- mesenchymal stem cells
- genetic diversity