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
- Auteurs
- Da Cruz, Anais Vieira, Kanazawa Alice, Poisson Jean-François, Behr Jean-Bernard, and Py Sandrine
- Revue
- J. Org. Chem.
- Volume
- 82
- Pagination
- 9866–9872
- ISSN
- 0022-3263
Soumis le 12 avril 2018