The important proapoptotic activity of (–)-lentiginosine, the enantiomer of a natural glycosidase inhibitor, associated with its low cytotoxicity, suggests the study of the unknown receptor responsible for the triggering of the proapoptotic cascade. To this purpose two derivatives of (–)- lentiginosine which contain the biotin moiety as an affinity label and fluorescein as fluorophore, have been synthesized. Significantly, the compounds maintain a good activity as the hydroxylentiginosine precursor.

Synthesis of biotin and fluorescein labeled (–)-lentiginosine / Franca Maria Cordero; Carolina Vurchio; Beatrice Macchi; Antonella Minutolo; Alberto Brandi. - In: ARKIVOC. - ISSN 1551-7012. - ELETTRONICO. - 3:(2014), pp. 215-227. [10.3998/ark.5550190.p008.495]

Synthesis of biotin and fluorescein labeled (–)-lentiginosine

CORDERO, FRANCA MARIA;VURCHIO, CAROLINA;BRANDI, ALBERTO
2014

Abstract

The important proapoptotic activity of (–)-lentiginosine, the enantiomer of a natural glycosidase inhibitor, associated with its low cytotoxicity, suggests the study of the unknown receptor responsible for the triggering of the proapoptotic cascade. To this purpose two derivatives of (–)- lentiginosine which contain the biotin moiety as an affinity label and fluorescein as fluorophore, have been synthesized. Significantly, the compounds maintain a good activity as the hydroxylentiginosine precursor.
2014
3
215
227
Franca Maria Cordero; Carolina Vurchio; Beatrice Macchi; Antonella Minutolo; Alberto Brandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/841503
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