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pubmed-article:9873626pubmed:abstractTextMonocyclic and bicyclic lactam units representing beta-turn surrogates were incorporated into a sialyl Le(X) structure by replacement of the natural sugar components. Low micromolar activity was found in a new P-selectin binding assay.lld:pubmed
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pubmed-article:9873626pubmed:articleTitleExploration of beta-turn scaffolding motifs as components of sialyl Le(X) mimetics and their relevance to P-selectin.lld:pubmed
pubmed-article:9873626pubmed:affiliationDepartment of Chemistry, Université de Montréal, Centre-ville, Montréal, Québec, Canada.lld:pubmed
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