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Updated: Dec 20, 2025

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Oxidation of 8-thioguanosine gives redox-responsive hydrogels and reveals intermediates in a desulfurization pathway
Songjun Xiao1, Wes Lee, Fu Chen
1Department of Chemistry & Biochemistry, University of Maryland, College Park, MD 20742, USA. jdavis@umd.edu sxiao@terpmail.umd.edu ogs@umd.edu.
Abstract:
A disulfide made by oxidation of 8-thioguanosine is a supergelator. The hydrogels are redox-responsive, as they disassemble upon either reduction or oxidation of the S-S bond. We also identified this disulfide, and 2 other compounds, as intermediates in oxidative desulfurization of 8-thioG to guanosine.
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