This study utilized phloridzin (P1) and its aglucone phloretin (P2), t
wo known inhibitors of glucose transmembrane transport, to inhibit tum
or cell growth in vivo. The efficacy of hydrazine sulfate as an antica
chexic agent was also evaluated. Utilizing the rat mammary adenocarcin
oma and Fischer bladder cell carcinoma cell lines, it has been shown t
hat the i.p. administration of P1 and P2 can produce significant diffe
rences in mean tumor diameters as compared to the untreated controls.