Abstract
The synthesis and characterization of a small series of cyclic triimidazole derivatives functionalized with methylated pyridine or guanidine moieties is reported. These compounds were tested for their ability to bind to G‐quadruplexes from both telomeric and oncogene promoter sequences. Some of them exhibited high affinity and effective G‐quadruplex‐stabilizing properties. Overall, these compounds may represent useful leads for developing more potent and selective analogues.

This publication has 42 references indexed in Scilit: