Kinetic Insights into Hydrogen Sulfide Delivery from Caged-Carbonyl Sulfide Isomeric Donor Platforms

Article abstract of DOI:10.1021/jacs.7b09527

Hydrogen sulfide (H₂S) is a biologically important small gaseous molecule that exhibits promising protective effects against a variety of physiological and pathological processes. To investigate the expanding roles of H₂S in biology, researchers often use H₂S donors to mimic enzymatic H₂S synthesis or to provide increased H₂S levels under specific circumstances. Aligned with the need for new broad and easily modifiable platforms for H₂S donation, we report here the preparation and H₂S release kinetics from a series of isomeric caged-carbonyl sulfide (COS) compounds, including thiocarbamates, thiocarbonates, and dithiocarbonates, all of which release COS that is quickly converted to H₂S by the ubiquitous enzyme carbonic anhydrase. Each donor is designed to release COS/H₂S after the activation of a trigger by activation by hydrogen peroxide (H₂O₂). In addition to providing a broad palette of new, H₂O₂-responsive donor motifs, we also demonstrate the H₂O₂ dose-dependent COS/H₂S release from each donor core, establish that release profiles can be modified by structural modifications, and compare COS/H₂S release rates and efficiencies from isomeric core structures. Supporting our experimental investigations, we also provide computational insights into the potential energy surfaces for COS/H₂S release from each platform. In addition, we also report initial investigations into dithiocarbamate cores, which release H₂S directly upon H₂O₂-mediated activation. As a whole, the insights on COS/H₂S release gained from these investigations provide a foundation for the expansion of the emerging area of responsive COS/H₂S donor systems.

Full text of DOI:10.1021/jacs.7b09527

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Article
2
Kinetic Insights into Hydrogen Sulfide (HS) Delivery from
Caged-Carbonyl Sulfide (COS) Isomeric Donor Platforms
Yu Zhao, Hillary A. Henthorn, and Michael D Pluth
J. Am. Chem. Soc., Just Accepted Manuscript • Publication Date (Web): 22 Oct 2017
Downloaded from http://pubs.acs.org on October 23, 2017
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