The synthesis and biological evaluation of some new glycose esters bearing the 1,2-O-isopropylidene-D-hexofuranose functionality and belonging to the 3-O-acyl-D-allose and 6-O-acyl-D-glucose series are reported. When the results concerning cell growth inhibition are compared, it appears that the 6-O-acyl-D-glucose derivatives are more active than the 3-O-acyl-D-allose compounds. Within both 6-O-acyl-D-glucose and 3-O-acyl-D-allose derivatives, butyric esters displayed the highest inhibitory effects. Inhibition of cell growth is not associated with high induction levels of erythroid differentiation, despite the fact that pivaloates induce erythroid differentiation to an extent similar to that exhibited by previously reported molecules [Bioorg. Med. Chem. Lett. 1999, 9, 3153–3158].

Preparation and biological evaluation of some 1,2-O-isopropylidene-D-hexopyranose esters

CATELANI, GIORGIO;D'ANDREA, FELICIA;
2006

Abstract

The synthesis and biological evaluation of some new glycose esters bearing the 1,2-O-isopropylidene-D-hexofuranose functionality and belonging to the 3-O-acyl-D-allose and 6-O-acyl-D-glucose series are reported. When the results concerning cell growth inhibition are compared, it appears that the 6-O-acyl-D-glucose derivatives are more active than the 3-O-acyl-D-allose compounds. Within both 6-O-acyl-D-glucose and 3-O-acyl-D-allose derivatives, butyric esters displayed the highest inhibitory effects. Inhibition of cell growth is not associated with high induction levels of erythroid differentiation, despite the fact that pivaloates induce erythroid differentiation to an extent similar to that exhibited by previously reported molecules [Bioorg. Med. Chem. Lett. 1999, 9, 3153–3158].
Catelani, Giorgio; D'Andrea, Felicia; Landi, M; Zuccato, C; Bianchi, N; Gambari, R.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11568/201957
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