Design, synthesis, and biological evaluation of prenylated chalcones as 5-LOX inhibitors

In this study, a series of 10 novel mono- and di- O-prenylated chalcone derivatives were designed, synthesized, and screened for their in vitro 5-LOX inhibition activity and anti-proliferative activity. Ten novel mono- and di- O-prenylated chalcone derivatives were designed on the basis of a homology derived molecular model of 5-lipoxygenase (5-LOX). The compounds were docked into 5-LOX active site and the binding characteristics were quantified using LUDI. To verify our theoretical assumption, the molecules were synthesized and tested for their 5-LOX inhibitory activities. The synthesis was carried out by Claisen–Schmidt condensation reaction of mono- and di- O-prenylated acetophenones with appropriate aldehydes. 5-LOX in vitro inhibition assay showed higher potency of di- O-prenylated chalcones than their mono- O-prenylated chalcone analogs. Compound 5e exhibited good inhibition with an IC 50 at 4 μM. The overall trend for the binding energies calculated and LUDI score was in good qualitative agreement with the experimental data. Further, the compound 5e showed potent anti-proliferative effects (GI 50 at 9 μM) on breast cancer cell line, MCF-7.