Synthesis and anti-hepatitis B virus evaluation of novel ethyl 6-hydroxyquinoline-3-carboxylates in vitro

Bioorg Med Chem. 2008 Jul 1;16(13):6522-7. doi: 10.1016/j.bmc.2008.05.029. Epub 2008 May 17.

Abstract

A series of non-nucleoside ethyl 6-hydroxyquinoline-3-carboxylate derivatives were prepared and evaluated in HepG2.2.15 cells. Most compounds inhibited the expression of viral antigens HBsAg or HBeAg at low concentration. Six compounds, 9f(3), 12b(6), 12f(6), 13b(2), 13b(6), and 13f(6), displayed excellent intracellular inhibitory activity and selectivity towards the replication of HBV DNA. Of these six initial hits, compound 13b(6) was the most active.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / chemical synthesis*
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • Cell Line, Tumor
  • Hepatitis B virus / drug effects*
  • Humans
  • Hydroxyquinolines / chemical synthesis*
  • Hydroxyquinolines / chemistry
  • Hydroxyquinolines / pharmacology*
  • Molecular Structure
  • Structure-Activity Relationship

Substances

  • Antiviral Agents
  • Hydroxyquinolines