| Literature DB >> 21431154 |
Yu-Jing Lu1, Siu-Cheong Yan, Fung-Yi Chan, Lan Zou, Wai-Hong Chung, Wing-Leung Wong, Bin Qiu, Ning Sun, Pak-Ho Chan, Zhi-Shu Huang, Lian-Quan Gu, Kwok-Yin Wong.
Abstract
A new switch-on fluorescent probe containing the natural product cryptolepine analogue benzofuroquinolinium moiety (binding scaffold) and a benzothiazole moiety (signalling unit) shows a remarkable fluorescence enhancement selective for the G-quadruplex nucleic acid structure. Binding studies revealed that the highly selective response of the fluorescent probe arises from end-stack binding to G-quadruplex. © The Royal Society of Chemistry 2011Entities:
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Year: 2011 PMID: 21431154 DOI: 10.1039/c1cc00020a
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222