Synthesis and the biological evaluation of arylnaphthalene lignans as anti-hepatitis B virus agents

Bioorg Med Chem. 2010 Feb;18(3):1213-26. doi: 10.1016/j.bmc.2009.12.038. Epub 2009 Dec 21.

Abstract

We have previously shown that helioxanthin can suppress human hepatitis B virus gene expression. A series of helioxanthin analogues were synthesized and evaluated for their anti-hepatitis B virus activity. Modifications at the lactone rings and methylenedioxy unit of helioxanthin can modulate the antiviral activity. Among them, compound 32 is the most effective anti-HBV agent. Compound 32 can suppress the secretion of viral surface antigen and e antigen in HepA2 cells with EC(50) values of 0.06 and 0.14 microM, respectively. Compound 32 not only inhibited HBV DNA with wild-type and lamivudine-resistant strain but also suppressed HBV mRNA, core protein and viral promoters. In this study, a full account of the preparation, structure-activity relationships of helioxanthin analogues, and the possible mechanism of anti-HBV activity of this class of compounds are presented. This type of compounds possesses unique mode of action differing from existing therapeutic drugs. They are potentially new anti-HBV agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Hepatitis B / drug therapy*
  • Hepatitis B Surface Antigens / genetics
  • Hepatitis B Surface Antigens / metabolism
  • Hepatitis B e Antigens / metabolism
  • Hepatitis B virus / drug effects*
  • Humans
  • Lignans / chemistry*
  • Lignans / pharmacology*
  • Promoter Regions, Genetic / drug effects
  • Structure-Activity Relationship
  • Viral Core Proteins / metabolism
  • Virus Replication / drug effects

Substances

  • Hepatitis B Surface Antigens
  • Hepatitis B e Antigens
  • Lignans
  • Viral Core Proteins
  • helioxanthin