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Superiority of an Asymmetric Perylene Diimide in Terms of Hydrosolubility, G-Quadruplex Binding, Cellular Uptake, and Telomerase Inhibition in Prostate Cancer Cells

Ratasark Summart, Pak Thaichana, Jutharat Supan, Puttinan Meepowpan, T. Randall Lee, Wirote Tuntiwechapikul

2020ACS Omega11 citationsDOIOpen Access PDF

Abstract

-ethyl piperidine side chain of PDI is sufficient for G-quadruplex binding, while another side chain can be tuned to elicit desirable properties. These findings might lead to better PDIs for use as anticancer drugs.

Topics & Concepts

TelomeraseChemistryTelomereG-quadruplexPerylenePiperSide chainDNACancer cellCancerBiochemistryBiologyGeneGeneticsPaleontologyPolymerOrganic chemistryMoleculeDNA and Nucleic Acid ChemistryAdvanced biosensing and bioanalysis techniquesRNA Interference and Gene Delivery
Superiority of an Asymmetric Perylene Diimide in Terms of Hydrosolubility, G-Quadruplex Binding, Cellular Uptake, and Telomerase Inhibition in Prostate Cancer Cells | Litcius