Evaluation of anti-HCV activity and SAR study of (+)-lycoricidine through targeting of host heat-stress cognate 70 (Hsc70)

Bioorg Med Chem Lett. 2013 May 1;23(9):2679-82. doi: 10.1016/j.bmcl.2013.02.089. Epub 2013 Mar 1.

Abstract

The anti hepatitis C virus (HCV) activity of (+)-lycoricidine (1) was evaluated for the first time in this letter, yielding an EC50 value of 0.55 nmol/mL and an selection index (SI) value of 12.72. Further studies indicated that 1 induced this effect by down-regulating host heat-stress cognate 70 (Hsc70) expression. In addition, 20 derivatives were designed and synthesised to investigate the basic structure-activity relationship (SAR) of the title compound. Several of these derivatives exhibit a good inhibition of HCV, such as compound 3 (EC50=0.68 nmol/mL, SI=33.86), compound 2d (EC50=15 nmol/mL, SI=12) and compound 5 (EC50=33 nmol/mL, SI >10.91). Meanwhile, the experimental data suggest that the modification of certain groups of (+)-lycoricidine can reduce the cytotoxicity of the compounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amaryllidaceae Alkaloids / chemical synthesis
  • Amaryllidaceae Alkaloids / chemistry*
  • Amaryllidaceae Alkaloids / pharmacology
  • Antiviral Agents / chemical synthesis
  • Antiviral Agents / chemistry*
  • Antiviral Agents / pharmacology
  • Cell Line
  • Gene Expression / drug effects
  • HSC70 Heat-Shock Proteins / antagonists & inhibitors
  • HSC70 Heat-Shock Proteins / metabolism*
  • Hepacivirus / drug effects*
  • Humans
  • Phenanthridines / chemical synthesis
  • Phenanthridines / chemistry*
  • Phenanthridines / pharmacology
  • Stereoisomerism
  • Structure-Activity Relationship

Substances

  • Amaryllidaceae Alkaloids
  • Antiviral Agents
  • HSC70 Heat-Shock Proteins
  • Phenanthridines
  • lycoricidine