<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gilbert AK</submitter><funding>National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><funding>National Science Foundation</funding><pagination>17651-17660</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9896967</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>144(38)</volume><pubmed_abstract>Hydrogen sulfide (H&lt;sub>2&lt;/sub>S) is an endogenously produced gaseous signaling molecule with important roles in regulating organelle function and stress. Because of its high reactivity, targeted delivery of H&lt;sub>2&lt;/sub>S using small molecule H&lt;sub>2&lt;/sub>S donors has garnered significant interest to minimize off-target effects. Although mitochondrially targeted H&lt;sub>2&lt;/sub>S donors, such as AP39, have been reported previously and exhibit significantly higher potency than nontargeted donors, the expansion of targeted H&lt;sub>2&lt;/sub>S delivery to other subcellular organelles remains largely absent. To fill this key unmet need, we report a library of organelle-targeted H&lt;sub>2&lt;/sub>S donors that localize H&lt;sub>2&lt;/sub>S delivery to specific subcellular organelles, including the Golgi apparatu</pubmed_abstract><journal>Journal of the American Chemical Society</journal><pubmed_title>Subcellular Delivery of Hydrogen Sulfide Using Small Molecule Donors Impacts Organelle Stress.</pubmed_title><pmcid>PMC9896967</pmcid><funding_grant_id>R01GM113030</funding_grant_id><funding_grant_id>DGE-1842486</funding_grant_id><funding_grant_id>R01 GM113030</funding_grant_id><pubmed_authors>Pluth MD</pubmed_authors><pubmed_authors>Gilbert AK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Subcellular Delivery of Hydrogen Sulfide Using Small Molecule Donors Impacts Organelle Stress.</name><description>Hydrogen sulfide (H&lt;sub>2&lt;/sub>S) is an endogenously produced gaseous signaling molecule with important roles in regulating organelle function and stress. Because of its high reactivity, targeted delivery of H&lt;sub>2&lt;/sub>S using small molecule H&lt;sub>2&lt;/sub>S donors has garnered significant interest to minimize off-target effects. Although mitochondrially targeted H&lt;sub>2&lt;/sub>S donors, such as AP39, have been reported previously and exhibit significantly higher potency than nontargeted donors, the expansion of targeted H&lt;sub>2&lt;/sub>S delivery to other subcellular organelles remains largely absent. To fill this key unmet need, we report a library of organelle-targeted H&lt;sub>2&lt;/sub>S donors that localize H&lt;sub>2&lt;/sub>S delivery to specific subcellular organelles, including the Golgi apparatu</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-03T23:17:23.407Z</modification><creation>2025-04-03T23:17:23.407Z</creation></dates><accession>S-EPMC9896967</accession><cross_references><pubmed>36121306</pubmed><doi>10.1021/jacs.2c07225</doi></cross_references></HashMap>