
Bioorganic and Medicinal Chemistry Letters p. 2755 - 2760 (1996)
Update date:2022-08-03
Topics:
Lin, Chun-Cheng
Kimura, Teiji
Wu, Shih-Hsiung
Weitz-Schmidt, Gabriele
Wong, Chi-Huey
Several fucodipeptides and their liposome-like derivatives were prepared and tested as inhibitors of sialyl Lewis X binding to E-selectin. It has been found that trans-hydroxyproline (D or L) can be used to mimic the galactose residue of sialyl Lewis X, and the mimetic containing 3,4-dihydroxy-D-proline is the most active with IC50 value (50 μM) 10-fold greater than sialyl Lewis X. Derivatization of a hydroxythreonine-containing fucodipeptides into a covalent liposome-like derivative, however, provides a mimetic with only IC50 ~ 30 μM.
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