Inhibition of L- and P-selectin by a rationally synthesized novel core 2-like branched structure containing GalNAc-Lewisx and Neu5Ac 2-3Gal 1-3GalNAc sequences-Reference-Cited by-同舟云学术

Inhibition of L- and P-selectin by a rationally synthesized novel core 2-like branched structure containing GalNAc-Lewisx and Neu5Ac 2-3Gal 1-3GalNAc sequences

Published:1998-07-01 Issue:7 Volume:8 Page:707-717
ISSN:0959-6658
Container-title:Glycobiology
language:en
Short-container-title:Glycobiology

Author:

Jain R. K.,Piskorz C. F.,Huang B.-G.,Locke R. D.,Han H.-L.,Koenig A.,Varki A.,Khushi L. M.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry

Link

http://academic.oup.com/glycob/article-pdf/8/7/707/2086651/8-7-707.pdf

Reference59 articles.

1. Preparation of disaccharides having a β-d-mannopyranosyl group from N-phthaloyllactosamine derivatives by double or triple SN2 substitution

2. A novel mimic of the sialyl Lewis x determinant

3. Synthesis and biological activity of conformationally constrained sialyl Lewis X analogues with reduced carbohydrate character

4. Binding of L-Selectin to the Vascular Sialomucin CD34

5. A carbohydrate domain common to both sialyl Le(a) and sialyl Le(X) is recognized by the endothelial cell leukocyte adhesion molecule ELAM-1

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