Ligand Interactions with E-Selectin. Identification of a New Binding Site for Recognition of N-Acyl Aromatic Glucosamine Substituents of Sialyl Lewis X

Several N-acylglucosamine derivatives of sialyl Lewis X (1−3) were prepared using a combined chemical enzymatic approach and evaluated as an inhibitor of E-selectin-mediated cellular adhesion. Compounds with aromatic functionality, 1 and 2, were found to be 3−10 times more potent than the N-acetyl d...

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Veröffentlicht in:Journal of medicinal chemistry 1996-03, Vol.39 (7), p.1357-1360
Hauptverfasser: Ramphal, John Y, Hiroshige, Mariann, Lou, Boliang, Gaudino, John J, Hayashi, Masaji, Chen, Shiow Meei, Chiang, Lin C, Gaeta, Federico C. A, DeFrees, Shawn A
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Sprache:eng
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