摘要
<正>We discovered in the current study that six side chain-to-side chain cyclic pentapeptides harboring a central Nε-dodecyl(or tetradecyl)-thiocarbamoyl-lysine residue all behaved as highly potent(n M level)inhibitors against human SIRT6-catalyzed deacylation reaction.Moreover,one compound was also found to be selective for SIRT6 versus SIRT2/3/5(~20-,~11-,and
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