β‐Mannosyl Triazoles as Mimics of Galactosyl Galectin‐3 and Galectin‐9 N‐Terminal Domain Inhibitors
Mannosyl β-C-1 amidotriazoles have previously been reported to have higher selectivity for galectin-9N (N-terminal domain) than the corresponding galactoside C3 amidotriazoles have, which were more selective for galectin-3. This study further investigated this by synthesis of mono- and bis-aryltriazolyl mannoside analogues to known high-affinity galectin-3 galactosyl-derived inhibitors. Following synthesis, affinity measurements using competititve fluorescence polarization assays were performed which indicated low affinity of the bis-aryltriazolyl mannosyls, while the mono-aryltriazolyl mannosyls analogs possessed improved affinity, albeit with lower and selectivity. From conformational calculations it was implied that the weak-binding bis-aryltriazolyl mannosyl analogues do not find the same conformation and binding pose as the parent galactoside compounds.
Authors
- Ulf J. Nilsson (ORCID: https://orcid.org/0000-0001-5815-9522)
- Fredrik Sjövall
Institutions
- Lund University (SE)
Publication Details
- Journal
- ChemBioChem
- Published
- 2026-04-13
- DOI
- https://doi.org/10.1002/cbic.70319
- Primary Topic
- Galectins and Cancer Biology
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Galecto
- Vetenskapsrådet
- Kungliga Fysiografiska Sällskapet i Lund