<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Bege M</submitter><funding>University of Debrecen</funding><pubmed_abstract>Hydrogen sulfide (H&lt;sub>2&lt;/sub>S) is an endogenous gasotransmitter with cardioprotective and antiviral effects. In this work, new cysteine-selective nucleoside-H&lt;sub>2&lt;/sub>S-donor hybrid molecules were prepared by conjugating nucleoside biomolecules with a thiol-activatable dithioacetyl group. 5'-Dithioacetate derivatives were synthesized from the canonical nucleosides (uridine, adenosine, cytidine, guanosine and thymidine), and the putative 5'-thio metabolites were also produced from uridine and adenosine. According to our measurements made with an H&lt;sub>2&lt;/sub>S-specific sensor, nucleoside dithioacetates are moderately fast H&lt;sub>2&lt;/sub>S donors, the guanosine derivative showed the fastest kinetics and the adenosine derivative the slowest. The antioxidant activity of 5'-thionucleosides </pubmed_abstract><journal>Scientific reports</journal><pagination>2876</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11754443</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis, H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;S releasing properties, antiviral and antioxidant activities and acute cardiac effects of nucleoside 5'-dithioacetates.</pubmed_title><pmcid>PMC11754443</pmcid><pubmed_authors>Lovas M</pubmed_authors><pubmed_authors>Priksz D</pubmed_authors><pubmed_authors>Kajtar R</pubmed_authors><pubmed_authors>Weber J</pubmed_authors><pubmed_authors>Eskeif S</pubmed_authors><pubmed_authors>Borbas A</pubmed_authors><pubmed_authors>Herczegh P</pubmed_authors><pubmed_authors>Bege M</pubmed_authors><pubmed_authors>Lekli I</pubmed_authors><pubmed_authors>Bernat B</pubmed_authors><pubmed_authors>Hodek J</pubmed_authors><pubmed_authors>Bereczki I</pubmed_authors><pubmed_authors>Novak L</pubmed_authors><pubmed_authors>Kattoub RG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis, H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;S releasing properties, antiviral and antioxidant activities and acute cardiac effects of nucleoside 5'-dithioacetates.</name><description>Hydrogen sulfide (H&lt;sub>2&lt;/sub>S) is an endogenous gasotransmitter with cardioprotective and antiviral effects. In this work, new cysteine-selective nucleoside-H&lt;sub>2&lt;/sub>S-donor hybrid molecules were prepared by conjugating nucleoside biomolecules with a thiol-activatable dithioacetyl group. 5'-Dithioacetate derivatives were synthesized from the canonical nucleosides (uridine, adenosine, cytidine, guanosine and thymidine), and the putative 5'-thio metabolites were also produced from uridine and adenosine. According to our measurements made with an H&lt;sub>2&lt;/sub>S-specific sensor, nucleoside dithioacetates are moderately fast H&lt;sub>2&lt;/sub>S donors, the guanosine derivative showed the fastest kinetics and the adenosine derivative the slowest. The antioxidant activity of 5'-thionucleosides </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2025-04-19T18:22:52.985Z</modification><creation>2025-04-19T18:22:52.985Z</creation></dates><accession>S-EPMC11754443</accession><cross_references><pubmed>39843902</pubmed><doi>10.1038/s41598-025-85351-1</doi></cross_references></HashMap>