5-Substituted Flavones—Another Class of Potent Triplex DNA-Specific Ligands as Antigene Enhancers

Authors

• Landy Gu, University of the PacificFollow
• Nghia Tran, University of the PacificFollow
• Vanessa M. Rangel, University of the PacificFollow
• Mandeep Singh, University of the PacificFollow
• Krege M. Christison, University of the PacificFollow
• Geoff P. Lin-Cereghino, University of the PacificFollow
• Liang Xue, University of the PacificFollow

Document Type

Article

Publication Title

Molecules

Department

Biological Sciences

ISSN

14203049

Volume

29

Issue

24

DOI

10.3390/molecules29245862

First Page

1

Last Page

25

Publication Date

12-12-2024

Abstract

In the field of drug development, the quest for novel compounds that bind to DNA with high affinity and specificity never ends. In the present work, we report the newest development in this field, namely, triplex DNA-specific binding ligands based on the 5-substituted flavone scaffold in our lab. Biophysical studies showed that the newly synthesized flavone derivatives (depending on the side chains) bind to triplex DNA with binding affinities better than or similar to 5-substituted 3,3′,4′,7-tetramethoxyflavonoids. These compounds selectively stabilize triplex DNA while having little effect on duplex DNA, as verified by various biophysical methods. A detailed structural analysis suggested that the binding of these compounds to triplex DNA depends on the type of amino groups in the side chains and the length of the side chains. Viscosity studies suggested that these ligands bind to triplex DNA via intercalation. A representative ligand, compound 4b, showed a positive inhibitory effect on the activity of a restriction endonuclease (DraI) via ligand-mediated triplex formation. Several of these compounds exhibited excellent cytotoxicity toward various cancer cell lines (HT-29, HCT116, and HL-60), as indicated by the MTT assay. The work presented here is part of a continued effort from our laboratory to explore the novel structural motifs of natural product flavonoids for the development of triplex-specific ligands as antigene enhancers.

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

Recommended Citation

Gu, Landy; Tran, Nghia; Rangel, Vanessa M.; Singh, Mandeep; Christison, Krege M.; Lin-Cereghino, Geoff P.; and Xue, Liang, "5-Substituted Flavones—Another Class of Potent Triplex DNA-Specific Ligands as Antigene Enhancers" (2024). Pacific Faculty Work. 3.
https://scholarlycommons.pacific.edu/all-faculty/3