New derivatives of 1,4-dideoxy-1,4-imino-D-ribitol have been prepared and evaluated for their cytotoxicity on solid and haematological malignancies. 1,4-Dideoxy-5-O-[(9Z)-octadec-9-en-1-yl]-1,4-imino-Dribitol (13, IC(50) similar to 2 mu M) and its C(18)-analogues (IC(50) < 10 mu M) are cytotoxic toward SKBR3 (breast cancer) cells. 13 also inhibits (IC(50) similar to 8 mu M) growth of JURKAT cells.

Anti-cancer activity of 5-O-alkyl 1,4-imino-1,4-dideoxyribitols / Bello, C., Dal Bello, G., Cea, M., Nahimana, A., Aubry, D., Garuti, A., Motta, G., Moran, E., Fruscione, F., Pronzato, P., Grossi, F., Patrone, F., Ballestrero, A., Dupuis, M., Sordat, B., Zimmermann, K., Loretan, J., Wartmann, M., Duchosal, M.A., Nencioni, A., et al.. - In: BIOORGANIC & MEDICINAL CHEMISTRY. - ISSN 0968-0896. - ELETTRONICO. - 19:(2011), pp. 7720-7727. [10.1016/j.bmc.2011.07.053]

Anti-cancer activity of 5-O-alkyl 1,4-imino-1,4-dideoxyribitols

Bello, Claudia;
2011

Abstract

New derivatives of 1,4-dideoxy-1,4-imino-D-ribitol have been prepared and evaluated for their cytotoxicity on solid and haematological malignancies. 1,4-Dideoxy-5-O-[(9Z)-octadec-9-en-1-yl]-1,4-imino-Dribitol (13, IC(50) similar to 2 mu M) and its C(18)-analogues (IC(50) < 10 mu M) are cytotoxic toward SKBR3 (breast cancer) cells. 13 also inhibits (IC(50) similar to 8 mu M) growth of JURKAT cells.
2011
19
7720
7727
Bello, Claudia; Dal Bello, Giovanna; Cea, Michele; Nahimana, Aimable; Aubry, Dominique; Garuti, Anna; Motta, Giulia; Moran, Eva; Fruscione, Floriana; ...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1109769
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