Hybrid analogues of SFTI-1 modified in P1 position by ß- and γ-amino acids and N-substituted ß-alanines.

A series of compounds containing either non-proteinogenic ß-/γ-amino acids or N-substituted ß-alanine residues (ß-peptoid units) in P1 specificity position were synthesized based on the structure of sunflower trypsin inhibitor 1 (SFTI-1). The compounds were synthesized on a solid support; the N-substituted ß-alanines (ßNhlys and ßNhphe) were introduced into a peptidomimetic chain via a two-step approach using acryloyl chloride and an appropriate primary amine. The inhibitory activities were characterized in vitro against bovine α-chymotrypsin or bovine ß-trypsin. Three analogues displayed activity comparable to fully proteinogenic counterparts-monocyclic SFTI-1 and [Phe(5)]SFTI-1. Moreover, all active peptidomimetics were resistant toward proteolytic degradation, even after 24-h incubation at room temperature.