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Exploring architectures displaying multimeric presentations of a trihydroxypiperidine iminosugar.

ABSTRACT: The synthesis of new multivalent architectures based on a trihydroxypiperidine α-fucosidase inhibitor is reported herein. Tetravalent and nonavalent dendrimers were obtained by means of the click chemistry approach involving the copper azide-alkyne-catalyzed cycloaddition (CuAAC) between suitable scaffolds bearing terminal alkyne moieties and an azido-functionalized piperidine as the bioactive moiety. A preliminary biological investigation is also reported towards commercially available and human glycosidases.

PROVIDER: S-EPMC4685925 | BioStudies |

REPOSITORIES: biostudies

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