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

Organic & Biomolecular Chemistry · 2007 · Vol. 5(6) · pp. 971–971
Victoria D. BockDave SpeijerHenk HiemstraJan H. van Maarseveen

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.

Click Chemistry and ApplicationsChemical Synthesis and AnalysisMonoclonal and Polyclonal Antibodies ResearchIsostereChemistryPeptidomimeticPeptideClick chemistryPeptide bondStereochemistryTriazoleTyrosinaseCombinatorial chemistry

MeSH terms

Peptides, CyclicTriazolesMonophenol MonooxygenaseBiomimetic Materials
Citations
282
FWCI
12.52
field-weighted impact
References
42
Percentile
99%
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