<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>36(2)</volume><submitter>Simonyan H</submitter><pubmed_abstract>This study delves into the impact of two synthetic non-natural amino acids, &lt;b>7&lt;/b> and &lt;b>8&lt;/b>, on the structural dynamics of serum albumin and their potential significance in anticancer drug delivery systems. Crucially, the dihydrofuran-containing compound &lt;b>7&lt;/b> has been identified to bind to the G-quadruplex (G4) DNA sequence 22-mer Pu22, a mimic of the proto-oncogene c-Myc, as ascertained by circular dichroism (CD) and UV spectroscopy. Our docking studies suggest that &lt;b>7&lt;/b> binds to the G4 structure from the side of the G-quartet in a quasi-parallel manner, engaging in ten intermolecular interactions, including hydrogen bonds, π-lone pair and π-alkyl interactions. Notably, one interaction involves the heterocyclic ring of the compound. Compound &lt;b>7&lt;/b> emerges as a notable str</pubmed_abstract><journal>Molecular therapy. Nucleic acids</journal><pagination>102478</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11995079</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Binding of G-quadruplex DNA and serum albumins by synthetic non-proteinogenic amino acids: Implications for c-Myc-related anticancer activity and drug delivery.</pubmed_title><pmcid>PMC11995079</pmcid><pubmed_authors>Petrosyan S</pubmed_authors><pubmed_authors>Melikyan G</pubmed_authors><pubmed_authors>Simonyan H</pubmed_authors><pubmed_authors>Palumbo R</pubmed_authors><pubmed_authors>Roviello GN</pubmed_authors><pubmed_authors>Vicidomini C</pubmed_authors><pubmed_authors>Scognamiglio PL</pubmed_authors><pubmed_authors>Saghyan A</pubmed_authors><pubmed_authors>Sahakyan L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Binding of G-quadruplex DNA and serum albumins by synthetic non-proteinogenic amino acids: Implications for c-Myc-related anticancer activity and drug delivery.</name><description>This study delves into the impact of two synthetic non-natural amino acids, &lt;b>7&lt;/b> and &lt;b>8&lt;/b>, on the structural dynamics of serum albumin and their potential significance in anticancer drug delivery systems. Crucially, the dihydrofuran-containing compound &lt;b>7&lt;/b> has been identified to bind to the G-quadruplex (G4) DNA sequence 22-mer Pu22, a mimic of the proto-oncogene c-Myc, as ascertained by circular dichroism (CD) and UV spectroscopy. Our docking studies suggest that &lt;b>7&lt;/b> binds to the G4 structure from the side of the G-quartet in a quasi-parallel manner, engaging in ten intermolecular interactions, including hydrogen bonds, π-lone pair and π-alkyl interactions. Notably, one interaction involves the heterocyclic ring of the compound. Compound &lt;b>7&lt;/b> emerges as a notable str</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jun</publication><modification>2026-06-01T10:45:38.429Z</modification><creation>2026-04-08T11:27:16.072Z</creation></dates><accession>S-EPMC11995079</accession><cross_references><pubmed>40230622</pubmed><doi>10.1016/j.omtn.2025.102478</doi></cross_references></HashMap>