A series of prodrugs is described which have improved antimicrobial activity and physico-chemical properties. The structures of the biologically active ingredients are characterized by having a selected oligopeptide backbone attached, via the α-carbon of an L-alanyl unit thereof, by means of a disulfide link to the residue of an antimicrobial mercaptan.
本文介绍了一系列具有更好的抗菌活性和理化性质的原药。这些
生物活性成分的结构特征是,通过二
硫键将选定的低聚肽骨架经由其 L-丙
氨酰单元的 α-碳连接到抗菌
硫醇的残基上。