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Mimics of the sialyl Lewis X tetrasaccharide. Replacement of the N-Acetylglucosamine sugar with simple C2-symmetric 1,2-diols

✍ Scribed by Jeremy C. Prodger; Mark J. Bamford; Michael I. Bird; Paul M. Gore; Duncan S. Holmes; Richard Priest; Victoria Saez


Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
960 KB
Volume
4
Category
Article
ISSN
0968-0896

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✦ Synopsis


~.bstract--Analogues of sialyl Lewis X have been synthesized that feature replacement of the N-acetylglucosamine residue with C2-symmetric diols. The diols used contain different levels of torsional constraint and various functional groups. The cyclohexyl derived compound 27 was equipotent to sLex in vitro (IC5o 0.5 mM).