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Updated: Jul 4, 2026

Bioinformatics Resources for the Study of Glycan-Mediated Protein Interactions
Published on: January 20, 2022
Protein subtype-targeting through ligand epimerization: talose-selectivity of galectin-4 and galectin-8
Christopher T Oberg1, Helen Blanchard, Hakon Leffler
1Organic Chemistry, Lund University, PO Box 124, SE-221 00 Lund, Sweden.
Abstract:
A series of O2 and O3-derivatized methyl beta-d-talopyranosides were synthesized and evaluated in vitro as inhibitors of the galactose-binding galectin-1, -2, -3, -4 (N- and C-terminal domains), 8 (N-terminal domain), and 9 (N-terminal domain). Galectin-4C and 8N were found to prefer the d-talopyranose configuration to the natural ligand d-galactopyranose configuration. Derivatization at talose O2 and/or O3 provided selective submillimolar inhibitors for these two galectins.
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