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, Claudia; Dal Bello, Giovanna; Cea, Michele; Nahimana, Aimable; Aubry, Dominique; Garuti, Anna; Motta, Giulia; Moran, Eva; Fruscione, Floriana; Pronzato, Paolo; Grossi, Francesco; Patrone, Franco; Ballestrero, Alberto; Dupuis, Marc; Sordat, Bernard; Zimmermann, Kaspar; Loretan, Jacqueline; Wartmann, Markus; Duchosal, Michel A.; Nencioni, Alessio; Vogel, Pierre. - 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; Pronzato, Paolo; Grossi, Francesco; Patrone, Franco; Ballestrero, Alberto; Dupuis, Marc; Sordat, Bernard; Zimmermann, Kaspar; Loretan, Jacqueline; Wartmann, Markus; Duchosal, Michel A.; Nencioni, Alessio; Vogel, Pierre
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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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