Trisaccharide inhibitors often exhibit higher avidity due to multivalent interactions with SLT-1. Understanding the optimal spacing and orientation of the carbohydrate moieties is crucial.
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methyl 2,3,6-tri-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside
(4-fluoro-benzyl)-{4-[(4-fluoro-benzylamino)-methyl]-benzyl}-amine
Propanoic acid, 3-[3-hydroxy-2-(hydroxymethyl)-2-methyl-1-oxopropoxy]-2-[[3-hydroxy-2- (hydroxymethyl)-2-methyl-1-oxopropoxy]methyl]-2-methyl-, phenylmethyl ester
