Fishing in the Toolbox of Cyclic Turn Mimics: a Literature Overview of the Last Decade

The main goal in developing peptidomimetics is the stabilization of the bioactive conformation of peptides. Among all the secondary structures, turns are of paramount importance. This review highlights the recent advances in the design and synthesis of cyclic turn mimics. Both amino acids, carbo- and hetero-cyclic scaffolds have been considered, focusing on their use in the preparation of peptidomimetics and on their ability to induce gamma-, beta-, and alpha-turns.

Automated summary

This review emphasizes the recent advances in the design and synthesis of cyclic turn mimics, focusing on their ability to induce gamma-, beta-, and alpha-turns in peptidomimetics.