A novel aryl-hydrazide from the marine lichen Lichina pygmaea: isolation, synthesis of derivatives, and cytotoxicity assays

Bioorg Med Chem Lett. 2010 Aug 1;20(15):4582-6. doi: 10.1016/j.bmcl.2010.06.013. Epub 2010 Jun 8.

Abstract

A new aryl-hydrazide l-glutamic acid derivative, pygmeine (3), was isolated from a methanolic extract of Lichina pygmaea, a marine lichen. Synthetic derivatives obtained via a two-step coupling of l-glutamic acid with phenylhydrazine moieties were useful to elucidate the structure of 3 and to carry out biological assays. Thus, the cytotoxicity of the ortho-, meta-, and para-hydroxyl isomers along with their respective benzyl intermediates, and a natural methoxylated analog, were evaluated on murine and human melanoma cells (B16, A375). The para-hydroxyl isomer 6 was found to be the most active (IC(50)=1.6 microM) on B16 cells.

MeSH terms

  • Animals
  • Benzyl Compounds / chemistry
  • Cell Line, Tumor
  • Glutamic Acid / chemistry
  • Humans
  • Hydrazines / chemical synthesis
  • Hydrazines / chemistry*
  • Hydrazines / isolation & purification
  • Hydrazines / therapeutic use
  • Isomerism
  • Lichens / chemistry*
  • Magnetic Resonance Spectroscopy
  • Melanoma, Experimental / drug therapy
  • Mice
  • Molecular Conformation
  • Phenylhydrazines / chemistry

Substances

  • Benzyl Compounds
  • Hydrazines
  • Phenylhydrazines
  • pygmeine
  • phenylhydrazine
  • hydrazine
  • Glutamic Acid