A new application of click chemistry in situ: development of fluorescent probe for specific G-quadruplex topology.

ABSTRACT: Target-guided synthesis is an approach to drug discovery that allows the target to self-assemble its own binding agents. So far, target-guided synthesis and especially in situ click chemistry have attracted extensive attention and have led to the identification of highly potent inhibitors for proteins. In this study, we expand the application of in situ click chemistry and present a procedure using this approach to identify selective fluorescent probes for a specific topology of G-quadruplex nucleic acids, the parallel G-quadruplexes. On this basis, compound 15 assembled by triarylimidazole scaffold and carboxyl side chain was a positive hit, demonstrating highly potential in the sensitive and selective detection of parallel G-quadruplexes. Such selective fluorescence response can be ratio

SUBMITTER: Hu MH 

PROVIDER: S-EPMC4658637 | biostudies-literature | 2015 Nov

REPOSITORIES: biostudies-literature