| Literature DB >> 31901381 |
Shi Xu1, Yingying Wang1, Zoel Parent1, Ming Xian2.
Abstract
While hydrogen polysulfides (H2Sn, n ≥ 2) are believed to play regulatory roles in biology, their fundamental chemistry and reactivity are still poorly understood. Compounds that can produce H2Sn are useful tools. In this work we found that H2S2 could be effectively produced from diacyl disulfide precursors, triggered by certain nucleophiles, in both aqueous solutions and organic solvents. This method was used to explore redox reactions of H2S2, such as scavenging 1,1-diphenyl-2-picrylhydrazyl radical (DPPH) and reduction of tetrazines.Entities:
Keywords: Donor; Hydrogen persulfide; Hydrogen sulfide
Year: 2019 PMID: 31901381 PMCID: PMC7000109 DOI: 10.1016/j.bmcl.2019.126903
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823