Anti-HBV agents. Part 3: Preliminary structure–activity relationships of tetra-acylalisol A derivatives as potent hepatitis B virus inhibitors

Abstract

Thirty-two tetra-acylated derivatives of alisol A were synthesized and evaluated for their anti-hepatitis B virus (HBV) activities and cytotoxicities in vitro. Among the series of alisol A derivatives examined, five analogues were active against HBV surface antigen (HBsAg) and HBV e antigen (HBeAg) secretion in HepG 2.2.15 cells. These results also provide interesting structure–activity relationships of tetra-acylalisol A derivatives. Compounds tetra-acetyl alisol A ( A1), tetra-methoxyacetyl alisol A ( A23), and tetra-ethoxyacetyl alisol A ( A24) exhibited high activities against secretion of HBsAg with IC 50 values of 0.0048, 0.0044, and 0.014 mM, respectively, HBeAg with IC 50 values of 0.011, 0.012, and 0.018 mM, respectively, and remarkable selective index values SI HBsAg >333, SI HBeAg >145; SI HBsAg = 209, SI HBeAg = 77; and SI HBsAg >200, SI HBeAg >156, respectively. Additional studies in rats showed that compound A1 has favorable pharmacokinetic prosperities for further development purpose, with elimination half-time ( t 1/2) of 1.63 h and oral bioavailability ( F) of 40.9%.