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- W2912017014 endingPage "426" @default.
- W2912017014 startingPage "426" @default.
- W2912017014 abstract "G-quadruplexes are four-stranded nucleic acids structures that can form in guanine-rich sequences. Following the observation that G-quadruplexes are particularly abundant in genomic regions related to cancer, such as telomeres and oncogenes promoters, several G-quadruplex-binding molecules have been developed for therapeutic purposes. Among them, naphthalene diimide derivatives have reported versatility, consistent selectivity and high affinity toward the G-quadruplex structures. In this review, we present the chemical features, synthesis and peculiar optoelectronic properties (absorption, emission, redox) that make naphtalene diimides so versatile for biomedical applications. We present the latest developments on naphthalene diimides as G-quadruplex ligands, focusing on their ability to bind G-quadruplexes at telomeres and oncogene promoters with consequent anticancer activity. Their different binding modes (reversible versus irreversible/covalent) towards G-quadruplexes and their additional use as antimicrobial agents are also presented and discussed." @default.
- W2912017014 created "2019-02-21" @default.
- W2912017014 creator A5044086948 @default.
- W2912017014 creator A5064443367 @default.
- W2912017014 creator A5068029711 @default.
- W2912017014 creator A5069115725 @default.
- W2912017014 date "2019-01-24" @default.
- W2912017014 modified "2023-10-18" @default.
- W2912017014 title "Naphthalene Diimides as Multimodal G-Quadruplex-Selective Ligands" @default.
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