Synthesis of thiodisaccharides related to 4-thiolactose. Specific structural modifications in the glucose residue increase the inhibitory activity against the E. coli β-galactosidase.

OSCAR VARELA

BIOORGANIC & MEDICINAL CHEMISTRY.

PERGAMON-ELSEVIER SCIENCE LTD

Lugar: Amsterdam; Año: 2023

0968-0896

earching for new glycosidase inhibitors, a set of benzyl β-D-Gal-S-(1→4)-3-deoxy-4-thio-α-D-hexopyranosides was synthesized. Diverse configurations have been installed at C-2 and C-4 of the glucose residue. The benzyl glycosidic group was kept intact or substituted by an electron donating or withdrawing group that could also participate in hydrogen bonding. All thiodisaccharides were found to be inhibitors of the E. coli β-galactosidase. In general, benzyl thiodisaccharides were better inhibitors than those substituted (NO2 or NH2) on the benzyl ring. Thiodisaccharides containing a hexopyranoside, instead of pentopyranoside, showed a weaker inhibitory activity, except for those having the α-D-xylo configuration, which displayed inhibition constants of the same order of magnitude. These and previous results were indicative that the inhibition process by thiodisaccharides is strongly dependent on the configuration of the 3-deoxy-4-thiopyranoside, as well as its