Insights into self-degradation of cysteine esters and amides under physiological conditions yield new cleavable chemistry

Xueying Kang, Haishun Ye, Shanshan Liu, Xiaoqiang Tu, Jiqin Zhu, Hongyan Sun, Long Yi*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

2 Citations (Scopus)

Abstract

An unprecedented H2S release from cysteine esters and amides (CysO/NHR) under physiological conditions was discovered and the plausible mechanism was proposed. Alkylation of the amino moiety of cysteine esters enables the H2S release to be tuned and further provides support to the mechanistic insights. This discovery not only provides new insights into several fundamental science issues including non-enzymatic H2S-produced pathways, but also inspires new tunable cleavable motifs for sustained release of arylthiols and even for prodrug design.
Original languageEnglish
Pages (from-to)4233-4236
JournalChemical Communications
Volume59
Issue number28
Online published14 Mar 2023
DOIs
Publication statusPublished - 11 Apr 2023

Research Keywords

  • HYDROGEN-SULFIDE
  • SMALL-MOLECULE
  • H2S DONORS
  • AMINO-ACIDS
  • IDENTIFICATION
  • DERIVATIVES
  • MODULATION
  • DELIVERY
  • CANCER
  • PROBES

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