H. Ohmoto et al., STUDIES ON SELECTIN BLOCKER .1. STRUCTURE-ACTIVITY-RELATIONSHIPS OF SIALYL-LEWIS-X ANALOGS, Journal of medicinal chemistry, 39(6), 1996, pp. 1339-1343
As a part of our studies of selectin blockers, we prepared 1-deoxy-3'-
O-sulfo Le(x) analogs (1-3), 1-deoxy-3'-O-phosphono Le(x) analogs (4),
and 1-deoxy sLe(x) analogs (5-7), and examined their inhibitory activ
ities against natural ligand (sLe(x)) binding to E-selectin, P-selecti
n, and L-selectin. The 1-deoxy sLe(x) 5 was up to 20 times more potent
an inhibitor than the sLe(x) tetrasaccharide toward P- and L-selectin
binding. This indicates that the modification of the 1 or 2 position
of sLe(x) is useful in the design of a more potent selectin blocker.