Molecules (Oct 2021)

Design, Synthesis, and Biological Evaluation of Desmuramyl Dipeptides Modified by Adamantyl-1,2,3-triazole

  • Vesna Petrović Peroković,
  • Željka Car,
  • Josip Draženović,
  • Ranko Stojković,
  • Lidija Milković,
  • Mariastefania Antica,
  • Đani Škalamera,
  • Srđanka Tomić,
  • Rosana Ribić

DOI
https://doi.org/10.3390/molecules26216352
Journal volume & issue
Vol. 26, no. 21
p. 6352

Abstract

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Muramyl dipeptide (MDP) is the smallest peptidoglycan fragment able to trigger the immune response. Structural modification of MDP can lead to the preparation of analogs with improved immunostimulant properties, including desmuramyl peptides (DMPs). The aim of this work was to prepare the desmuramyl peptide (L-Ala-D-Glu)-containing adamantyl-triazole moiety and its mannosylated derivative in order to study their immunomodulatory activities in vivo. The adjuvant activity of the prepared compounds was evaluated in a murine model using ovalbumin as an antigen, and compared to the reference adjuvant ManAdDMP. The results showed that the introduction of the lipophilic adamantyl-triazole moiety at the C-terminus of L-Ala-D-Glu contributes to the immunostimulant activity of DMP, and that mannosylation of DMP modified with adamantyl-triazole causes the amplification of its immunostimulant activity.

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