NEOGLYCOPOLYMER INHIBITORS OF THE SELECTINS

Citation
Dd. Manning et al., NEOGLYCOPOLYMER INHIBITORS OF THE SELECTINS, Tetrahedron, 53(35), 1997, pp. 11937-11952
Citations number
57
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404020
Volume
53
Issue
35
Year of publication
1997
Pages
11937 - 11952
Database
ISI
SICI code
0040-4020(1997)53:35<11937:NIOTS>2.0.ZU;2-P
Abstract
The selectin class of proteins plays an important role in the inflamma tory response. These proteins, which bind saccharide ligands, facilita te the recruitment of leukocytes to the inflamed endothelium. The ring -opening metathesis polymerization (ROMP) has been used to generate sy nthetic multidentate Ligands, which display multiple copies of sulfate d saccharide residues. By altering the structure of the appended sacch aride residues, multivalent ligands that selectively target one member of the selectin family, P-selectin, were created. The biological acti vities of materials prepared from the same monomer unit varied, depend ing on the method of polymer preparation. This result suggests that po lymers containing more repeat elements exhibit higher selectin inhibit ory activities. (C) 1997 Elsevier Science Ltd.