1,2,3-Triazoles as peptide bond isosteres: synthesis and biological evaluation of cyclotetrapeptide mimics

V.D. Bock, D. Speijer, H. Hiemstra, J.H. van Maarseveen

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Abstract

Since the discovery of Cu(I)-catalysed click chemistry, the field of peptidomimetics has expanded to include 1,4-connected 1,2,3-triazoles as useful peptide bond isosteres. Here, we report the synthesis of triazole-containing analogues of the naturally occurring tyrosinase inhibitor cyclo-[Pro-Val-Pro-Tyr] and show that the analogues retain enzyme inhibitory activity, demonstrating the effectiveness of a 1,4-connected 1,2,3-triazole as a trans peptide bond isostere
Original languageUndefined/Unknown
Pages (from-to)971-975
JournalOrganic & biomolecular chemistry
Volume5
Issue number6
DOIs
Publication statusPublished - 2007

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