Abstractmagnified imageWe report herein the synthesis of 4‐(methoxycarbonyl)phenyl β‐lactoside and eight derivatives modified at C(6) or C(6′). These compounds were evaluated in hemagglutination inhibition assay using the lectin from Erythrina cristagalli. None of the compounds showed enhanced activity as compared to lactose.
Abstractmagnified imageWe report herein the synthesis of 4‐(methoxycarbonyl)phenyl β‐lactoside and eight derivatives modified at C(6) or C(6′). These compounds were evaluated in hemagglutination inhibition assay using the lectin from Erythrina cristagalli. None of the compounds showed enhanced activity as compared to lactose.
Synthesis of 4-(Methoxycarbonyl)phenyl<i>β</i>-Lactoside Derivatives Modified at C(6) or C(6′), and Evaluation of Their Inhibitory Activity on<i>Erythrina cristagalli</i>Lectin-Mediated Hemagglutination
作者:Anna Paola Butera、José Dias de Souza Filho、Maria Auxiliadôra Fontes Prado、Marilda Pereira Lisboa、Ricardo José Alves
DOI:10.1002/hlca.200800239
日期:2009.1
Abstractmagnified imageWe report herein the synthesis of 4‐(methoxycarbonyl)phenyl β‐lactoside and eight derivatives modified at C(6) or C(6′). These compounds were evaluated in hemagglutination inhibition assay using the lectin from Erythrina cristagalli. None of the compounds showed enhanced activity as compared to lactose.