Gallic acid derivatives with a lipophilic group (hydrogenated farnesyl gall
ate, lauryl gallate, gallic acid laurylamide and cholesteryl gallate) were
examined for their ability to induce apoptosis in human monoblastic leukemi
a U937 cells. Farnesyl ester derivative is the most potent apoptosis induce
r among the compounds examined, The results suggest that lipid derivatives
can augment the apoptosis-inducing activity of gallic acid depending on the
structure. These findings will provide useful information in developing an
ti-cancer agents.