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Cyclic Acyl Disulfides and Acyl Selenylsulfides as the Precursors for Persulfides (RSSH) Selenylsulfides (RSeSH) and Hydrogen Sulfide (H2S)

机译:环状酰基二硫化物和酰基烯丙基硫化物作为过硫化物(RSSH)烯丙基硫化物(RSeSH)和硫化氢(H2S)的前体

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摘要

The reactions of three model compounds (>1−>3) for cyclic acyl disulfides and cyclic acyl selenylsulfides are studied. These compounds were found to be effective precursors for persulfides (RSSH) and selenylsulfides (RSeSH) upon reacting with nucleophilic species. They could also act as H2S donors when interacting with cellular thiols. The most interesting discovery was the generation of RSeSH from compound >3 under mild conditions. Selenylsulfides (RSeSH) are expected to be important regulating molecules involved in Sec-related redox signaling. The method of producing RSeSH should allow researchers to better understand the chemical biology of RSeSH.
机译:研究了三种模型化合物(> 1 -> 3 )对环状酰基二硫化物和环状酰基硒基硫化物的反应。当与亲核物质反应时,发现这些化合物是过硫化物(RSSH)和硒烯基硫化物(RSeSH)的有效前体。当与细胞硫醇相互作用时,它们还可以充当H2S供体。最有趣的发现是在温和条件下由化合物> 3 生成RSeSH。硒烯硫化物(RSeSH)有望成为涉及Sec相关氧化还原信号的重要调控分子。 RSeSH的生产方法应使研究人员更好地了解RSeSH的化学生物学。

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