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Updated: Apr 30, 2026

Author Spotlight: Development and Characterization of Eco-Friendly Lignin-Based Microparticles for Enhanced Delivery of Bioflavonoids
Published on: March 1, 2024
Recent syntheses and biological activity of lentiginosine and its analogues
Franca M Cordero, Donatella Giomi, Alberto Brandi1
1Dipartimento di Chimica 'Ugo Schiff', Università di Firenze, Via della Lastruccia 3-13 I-50019 Sesto Fiorentino (FI), Italy. alberto.brandi@unifi.it.
Abstract:
(+)-Lentiginosine, a natural trans-1,2-dihydroxyindolizidine belonging to the class of iminosugars, is a potent inhibitor of amyloglucosidase, and a good inhibitor of Hsp90. The non-natural enantiomer, (-)-lentiginosine, induces apoptosis on tumor cells of different origin and is poorly cytotoxic towards non-transformed cells. The significant biological activity of these compounds has resulted in the development of many synthetic approaches for their preparation. This review is an update of a previous survey and summarizes the most recent achievements on biological studies as well as total syntheses of lentiginosine and trans-1,2-dihydroxyindolizidine analogues.
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