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Molecules 2018, 23(2), 493;

Natural Alkaloids and Heterocycles as G-Quadruplex Ligands and Potential Anticancer Agents

School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China
Author to whom correspondence should be addressed.
Received: 30 December 2017 / Revised: 4 February 2018 / Accepted: 20 February 2018 / Published: 23 February 2018
(This article belongs to the Special Issue G-Quadruplex Ligands and Cancer)
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G-quadruplexes are four-stranded nucleic acid secondary structures that are formed in guanine-rich sequences. G-quadruplexes are widely distributed in functional regions of the human genome and transcriptome, such as human telomeres, oncogene promoter regions, replication initiation sites, and untranslated regions. Many G-quadruplex-forming sequences are found to be associated with cancer, and thus, these non-canonical nucleic acid structures are considered to be attractive molecular targets for cancer therapeutics with novel mechanisms of action. In this mini review, we summarize recent advances made by our lab in the study of G-quadruplex-targeted natural alkaloids and their derivatives toward the development of potential anticancer agents. View Full-Text
Keywords: natural alkaloids; anticancer agents; drug design; G-quadruplex natural alkaloids; anticancer agents; drug design; G-quadruplex

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Che, T.; Wang, Y.-Q.; Huang, Z.-L.; Tan, J.-H.; Huang, Z.-S.; Chen, S.-B. Natural Alkaloids and Heterocycles as G-Quadruplex Ligands and Potential Anticancer Agents. Molecules 2018, 23, 493.

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