Chen Huai, Zhang Yuan, Li Qian-Qian, Zhao Yu-Fen, Chen Yong-Xiang, Li Yan-Mei
Key Lab of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry , Tsinghua University , Beijing 100084 , P.R. China.
Beijing Institute for Brain Disorders , Beijing 100069 , P.R. China.
J Org Chem. 2018 Jul 20;83(14):7528-7533. doi: 10.1021/acs.joc.8b00259. Epub 2018 Jul 2.
Lanthipeptides are a family of ribosomally synthesized peptides that have crucial biological functions. However, due to their complicated structures, the total synthesis of lanthipeptides is challenging. Here, a novel strategy to construct lanthipeptides is described, which involves cascade reactions of cysteine, including Cys disalkylation elimination, Michael reaction, and native chemical ligation. We utilized this strategy to synthesize lanthipeptide SapB as an example. This methodology has the potential to obtain lanthipeptides and their analogues for biological research and drug discovery.
羊毛硫肽是一类具有关键生物学功能的核糖体合成肽。然而,由于其结构复杂,羊毛硫肽的全合成具有挑战性。在此,描述了一种构建羊毛硫肽的新策略,该策略涉及半胱氨酸的级联反应,包括半胱氨酸二烷基化消除、迈克尔反应和天然化学连接。我们以利用该策略合成羊毛硫肽SapB为例。这种方法有潜力获得用于生物学研究和药物发现的羊毛硫肽及其类似物。