Design, synthesis and biological evaluation of immunostimulating mannosylated desmuramyl peptides

  1. Rosana Ribić ORCID Logo,
  2. Ranko Stojković,
  3. Lidija MilkovićORCID Logo,
  4. Mariastefania AnticaORCID Logo,
  5. Marko Cigler and
  6. Srđanka Tomić

Submitting author affiliation: University North, Varaždin, Croatia

Beilstein Arch. 2019, 20198. doi:10.3762/bxiv.2019.8.v1

Published 16 Apr 2019

  • Preprint

Abstract

Muramyl dipeptide is the minimal structure of peptidoglycan with adjuvant properties. Replacement of the N-acetylmuramyl moiety and increase of lipophilicity are important approaches in the preparation of muramyl dipeptide analogues with improved pharmacological properties. Mannose receptors present on immunocompetent cells are pattern-recognition receptors and by mannose ligands binding they affect the immune system. Here we present design, synthesis and biological evaluation of novel mannosylated desmuramyl peptide derivatives. Mannose was coupled to dipeptide containing lipophilic adamantane on N- or C-terminus through glycolyl or hydroxyisobutyryl linker. Adjuvant activities of synthesized compounds were investigated in the mouse model using ovalbumin as an antigen. Their activities were compared to the previously described mannosylated adamantane-containing desmuramyl peptide and peptidoglycan monomer. Tested compounds exhibited adjuvant activity and the strongest enhancement of IgG production was stimulated by the compound 21 (Man-OCH2-D-(1-Ad)Gly-L-Ala-D-isoGln).

Keywords: adamantane; adjuvant activity; desmuramyl peptide; mannose

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When a peer-reviewed version of this preprint is available in the Beilstein Journals, this information will be updated in the information box above. If no peer-reviewed version is available, please cite this preprint using the following information:

Ribić, R.; Stojković, R.; Milković, L.; Antica, M.; Cigler, M.; Tomić, S. Beilstein Arch. 2019, 20198. doi:10.3762/bxiv.2019.8.v1

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© 2019 Ribić et al.; licensee Beilstein-Institut.
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