Synthesis and biological evaluation of (+)-labdadienedial, derivatives and precursors from (+)-sclareolide

Eur J Med Chem. 2010 Sep;45(9):4403-8. doi: 10.1016/j.ejmech.2010.06.029. Epub 2010 Jun 25.

Abstract

Labdadienedial and a series of C15,C16-functionalized derivatives were synthesized from commercial (+)-sclareolide and evaluated for their cytotoxic, antimycotic, and antiviral activities. Their precursors were similarly evaluated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antifungal Agents / chemical synthesis
  • Antifungal Agents / chemistry
  • Antifungal Agents / pharmacology
  • Antifungal Agents / toxicity
  • Antineoplastic Agents / chemical synthesis
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / toxicity
  • Antiviral Agents / chemical synthesis
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology
  • Antiviral Agents / toxicity
  • Chlorocebus aethiops
  • Diterpenes / chemical synthesis*
  • Diterpenes / chemistry
  • Diterpenes / pharmacology*
  • Diterpenes / toxicity
  • Fungi / drug effects
  • HeLa Cells
  • Herpesvirus 1, Human / drug effects
  • Humans
  • Inhibitory Concentration 50
  • Vero Cells

Substances

  • Antifungal Agents
  • Antineoplastic Agents
  • Antiviral Agents
  • Diterpenes
  • labdadienedial
  • sclareolide