Design and synthesis of simplified sordaricin derivatives as inhibitors of fungal protein synthesis
作者:Juan C. Cuevas、JoséL. Lavandera、JoséL. Martos
DOI:10.1016/s0960-894x(98)00693-3
日期:1999.1
A reduction of the tetracyclic skeleton of sordarins and sordaricins to a cyclopentane ring bearing the pharmacophore functional groups led to new derivatives retaining part of their in vitro and whole-cell activity.