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Design and synthesis of sialyl Lewis x mimics as E-selectin inhibitors

N Kaila1, B E Thomas, P Thakker

  • 1Department of Chemical Sciences, Wyeth Research, Cambridge, MA 02140, USA. nkaila@genetics.com

Bioorganic & Medicinal Chemistry Letters
|February 24, 2001
PubMed

Abstract:

The design and synthesis of novel beta-C-mannosides that inhibit the binding of sialyl Lewis x to E-selectin are described. Compounds that contained a phenyl substituent at the C-6 position were found to have increased potency.

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