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Synthesis and Investigation of the G-Quadruplex Binding Properties of Kynurenic Acid Derivatives with a Dihydroimidazoquinoline-3,5-dione Core

Title: Synthesis and Investigation of the G-Quadruplex Binding Properties of Kynurenic Acid Derivatives with a Dihydroimidazoquinoline-3,5-dione Core
Authors: Mazzini, Stefania; Princiotto, Salvatore; Musso, Loana; Passarella, Daniele; Beretta, Giovanni Luca; Perego, Paola; Dallavalle, Sabrina
Contributors: S. Mazzini; S. Princiotto; L. Musso; D. Passarella; G.L. Beretta; P. Perego; S. Dallavalle
Publisher Information: MDPI
Publication Year: 2022
Collection: The University of Milan: Archivio Istituzionale della Ricerca (AIR)
Subject Terms: kynurenic acid; KYNA; G-quadruplex; DNA; stabilization; cytotoxicity; Settore CHIM/06 - Chimica Organica; Settore CHEM-05/A - Chimica organica
Description: G-quadruplexes are secondary structures originating from nucleic acid regions rich in guanines, which are well known for their involvement in gene transcription and regulation and DNA damage repair. In recent studies from our group, kynurenic acid (KYNA) derivative 1 was synthesized and found to share the structural features typical of G-quadruplex binders. Herein, structural modifications were conducted on this scaffold in order to assist the binding with a G quadruplex, by introducing charged hydrophilic groups. The antiproliferative activity of the new analogues was evaluated on an IGROV-1 human ovarian cancer cell line, and the most active compound, compound 9, was analyzed with NMR spectrometry in order to investigate its binding mode with DNA. The results indicated that a weak, non-specific interaction was set with duplex nucleotides; on the other hand, titration in the presence of a G-quadruplex from human telomere d(TTAGGGT)4 showed a stable, although not strong, interaction at the 3-end of the nucleotidic 4 sequence, efficiently assisted by salt bridges between the quaternary nitrogen and the external phosphate groups. Overall, this work can be considered a platform for the development of a new class of potential G-quadruplex stabilizing molecules, confirming the crucial role of a planar system and the ability of charged nitrogen-containing groups to facilitate the binding to G-quadruplex grooves and loops.
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/35566141; info:eu-repo/semantics/altIdentifier/wos/WOS:000795382200001; volume:27; issue:9; firstpage:1; lastpage:17; numberofpages:17; journal:MOLECULES; https://hdl.handle.net/2434/927034
DOI: 10.3390/molecules27092791
Availability: https://hdl.handle.net/2434/927034; https://doi.org/10.3390/molecules27092791
Rights: info:eu-repo/semantics/openAccess ; license:Creative commons ; license uri:http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.F9EA08B7
Database: BASE