Polyhydroxylated Quinolizidine Iminosugars as Nanomolar Selective Inhibitors of α-Glucosidases.

Polyhydroxylated quinolizidines, e.g. I, bearing a hydroxymethyl group at the ring junction were synthesized from a readily available L-sorbose-derived keto-nitrone. Evaluated as glycoside hydrolase inhibitors, these quinolizidines revealed to be potent and selective alpha-glucosidase inhibitors. Quinolizidine I is the first quinolizidine-scaffolded iminosugar exhibiting nanomolar inhibition of a glycoenzyme.

Références

Titre
Polyhydroxylated Quinolizidine Iminosugars as Nanomolar Selective Inhibitors of α-Glucosidases.
Type de publication
Article de revue
Année de publication
2017
Revue
J. Org. Chem.
Volume
82
Pagination
9866–9872
ISSN
0022-3263
Soumis le 12 avril 2018