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Aryl fucosides: synthesis and evaluation of their binding affinity towards the DC-SIGN receptor
Rohit Chavan1, Maurice Besch2,3,4, Jonathan Lefèbre2,3,4
1University of Chemistry and Technology, Prague, Technická 5, 16628 Prague 6, Czech Republic. petra.menova@vscht.cz.
Abstract:
DC-SIGN, a C-type lectin receptor expressed on antigen presenting cells, is crucial for pathogen recognition and immune modulation. While most glycomimetic DC-SIGN ligands are mannose-based, fucose-based ligands offer enhanced selectivity, potentially reducing off-target effects. This study reports the stereoselective synthesis of aryl α-L-fucosides and their binding affinity for DC-SIGN. Using 1H-15N HSQC NMR and a competition assay, we identified 3-trifluoromethylphenyl α-L-fucoside as the best ligand, exhibiting both KD and IC50 values in a three-digit micromolar range and binding not only to the canonical site, but also to a secondary allosteric site.
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