Unknown

Dataset Information

0

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.

SUBMITTER: Matassini C 

PROVIDER: S-EPMC4685925 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

altmetric image

Publications

Exploring architectures displaying multimeric presentations of a trihydroxypiperidine iminosugar.

Matassini Camilla C   Mirabella Stefania S   Goti Andrea A   Robina Inmaculada I   Moreno-Vargas Antonio J AJ   Cardona Francesca F  

Beilstein journal of organic chemistry 20151216


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 huma  ...[more]

Similar Datasets

| S-EPMC8448365 | biostudies-literature
| S-EPMC4267727 | biostudies-literature
2024-09-25 | PXD041931 | Pride
| S-EPMC3351140 | biostudies-literature
| S-EPMC5390498 | biostudies-literature
| S-EPMC6745470 | biostudies-literature
| S-EPMC7330713 | biostudies-literature
| S-EPMC11478570 | biostudies-literature
| S-EPMC6354729 | biostudies-literature
| S-EPMC9149629 | biostudies-literature