<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yuan Z</submitter><funding>NIDDK NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>Georgia Research Alliance</funding><funding>Georgia State University</funding><pagination>5317-5326</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8248650</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>93(12)</volume><pubmed_abstract>Ruthenium-based CO-releasing molecules (CO-RMs), CORM-2 and CORM-3, have been widely used as surrogates of CO for studying its biological effects &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i> with much success. However, several previous solution-phase and &lt;i>in vitro&lt;/i> studies have revealed the ability of such CO-RMs to chemically modify proteins and reduce aromatic nitro groups due to their intrinsic chemical reactivity under certain conditions. In our own work of studying the cytoprotective effects of CO donors, we were in need of assessing chemical factors that could impact the interpretation of results from CO donors including CORM-2,3 in various &lt;i>in vitro&lt;/i> assays. For this, we examined the effects of CORM-2,3 toward representative reagents commonly used in various bioassays including resa</pubmed_abstract><journal>Analytical chemistry</journal><pubmed_title>Chemical Reactivities of Two Widely Used Ruthenium-Based CO-Releasing Molecules with a Range of Biologically Important Reagents and Molecules.</pubmed_title><pmcid>PMC8248650</pmcid><funding_grant_id>R01DK119202</funding_grant_id><funding_grant_id>R01 DK119202</funding_grant_id><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Tripathi R</pubmed_authors><pubmed_authors>Ye Y</pubmed_authors><pubmed_authors>Yuan Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chemical Reactivities of Two Widely Used Ruthenium-Based CO-Releasing Molecules with a Range of Biologically Important Reagents and Molecules.</name><description>Ruthenium-based CO-releasing molecules (CO-RMs), CORM-2 and CORM-3, have been widely used as surrogates of CO for studying its biological effects &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i> with much success. However, several previous solution-phase and &lt;i>in vitro&lt;/i> studies have revealed the ability of such CO-RMs to chemically modify proteins and reduce aromatic nitro groups due to their intrinsic chemical reactivity under certain conditions. In our own work of studying the cytoprotective effects of CO donors, we were in need of assessing chemical factors that could impact the interpretation of results from CO donors including CORM-2,3 in various &lt;i>in vitro&lt;/i> assays. For this, we examined the effects of CORM-2,3 toward representative reagents commonly used in various bioassays including resa</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-04T20:16:15.749Z</modification><creation>2025-04-04T20:16:15.749Z</creation></dates><accession>S-EPMC8248650</accession><cross_references><pubmed>33745269</pubmed><doi>10.1021/acs.analchem.1c00533</doi></cross_references></HashMap>