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Merck

Rational design of novel glycomimetics: inhibitors of concanavalin A.

Bioorganic & medicinal chemistry letters (2008-11-08)
Karen T Welch, Trent A Turner, Callie E Preast
RÉSUMÉ

A virtual screening approach was used to identify new glycomimetics. The National Cancer Institute Diversity Set was docked into the carbohydrate binding site of the lectin concanavalin A (ConA). The resulting poses were analyzed and 19 molecules were tested for inhibition with an enzyme-linked lectin assay (ELLA). Eight of the 19 molecules inhibited ConA-carbohydrate binding. The two most potent inhibitors have IC(50) values that are an order of magnitude smaller than the monosaccharide methyl alpha-D-mannopyranoside.

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Sigma-Aldrich
Méthyl α-D-mannopyranoside, ≥99.0% (HPLC)
Millipore
Méthyl α-D-mannopyranoside, ≥99.0%, suitable for microbiology, enables differentiation between species of Listeria