Cyclic peptide-based potent and selective SIRT1/2 dual inhibitors harboring Nε-thioacetyl-lysine
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摘要
<正>In the current study,we discovered that several N-terminus-to-side chain cyclic tripeptides harboring the catalytic mechanismbased SIRT1/2/3 inhibitory warhead Nε-thioacetyl-lysine at their central positions exhibited a comparably strong inhibition(nM level)against the SIRT1/2-catalyzed Nε-acetyl-lysine deacetylation reactions.Their dual SIRT1/2 inhibitory action was also
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