2',3'-Di-O-acetyluridine 5'-p-styrenesulfonate was synthesized by the
reaction of 2',3'-di-O-acetyluridine with p-styrenesulfonyl chloride a
nd polymerized. After removal of acetyl groups, the polymeric product
was shown by NMR spectroscopy and gel permeation chromatography to be
poly(uridine 5'-p-styrenesulfonate). This uridine-containing polymer w
as tested against the galactosyl transferase that synthesizes lactose
in the presence of alpha-lactalbumin. The polymeric compound did inhib
it the enzyme with 75% inhibition requiring 120 mu M which is only one
percent of the concentration of glycosyl donor substrate (UDP-galacto
se, 12 mM).