| Literature DB >> 26301500 |
Dong Liang1, Haixia Wu1, Ming Wah Wong2, Dejian Huang1,3.
Abstract
Diallyl trisulfide (DATS) reacts rapidly with glutathione (GSH) to release H2S through thiol-disulfide exchange followed by allyl perthiol reduction by GSH. Yet diallyl disulfide (DADS) only releases a minute amount of H2S via a sluggish reaction with GSH through an α-carbon nucleophilic substitution pathway. The results clarify the misunderstanding of DADS as a rapid H2S donor, which is attributed to its DATS impurity.Entities:
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Year: 2015 PMID: 26301500 DOI: 10.1021/acs.orglett.5b01962
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005