American Chemical Society
ol0c03070_si_001.pdf (1.94 MB)

Synthesis and Biological Evaluation of N‑Aminoimidazolidin-2-one-Containing Angiotensin-(1–7) Peptidomimetics

Download (1.94 MB)
journal contribution
posted on 2020-10-26, 18:13 authored by Chuan Dai, Fang Wang, Dandan Zhang, Lei Xu, Xuefeng Xia, Jinqiang Zhang
N-Aminoimidazolidin-2-one (Aid)-containing peptides with a constrained backbone present a novel class of peptidomimetics for drug discovery. The introduction of Aid residues into peptide sequences has been achieved by intramolecular Mitsunobu cyclization of a serine side chain onto the α-NH of an aza-glycine residue. The effectiveness of this new strategy was demonstrated by synthesizing six Aid-containing analogues of angiotensin-(1–7) on solid support. The Aid analogues of angiotensin-(1–7) exhibited increased peptidase stability against human ACE and DPP3 and improved anti-inflammation and antiproliferation activity.