Semisynthesis of justicidone and a 1,2-quinone lignan. Cytotoxic activity of some natural and synthetic lignans

Nat Prod Commun. 2009 Feb;4(2):235-8.

Abstract

The dioxo-lignans of the arylnaphthalene-type named justicidone (2) and elenodione (3) were obtained from elenoside (1) through a short and efficient semisynthetic process. Justicidone (2), one of its synthetic precursors, 4-(benzo[d][1,3]dioxol-5-yl)-5,6,8-trimethoxy-3a,4-dihydronaphtho[2,3-c]furan-1(3H)-one (9), and the aglycone of elenoside (5) showed cytotoxic activity towards the HL-60 cell line (IC50 = 7.25 miroM, 5.41 microM and 2.06 miroM, respectively).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acanthaceae / chemistry
  • Antineoplastic Agents, Phytogenic / chemistry*
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Cell Line, Tumor
  • Humans
  • Lignans / chemical synthesis*
  • Lignans / chemistry
  • Molecular Structure
  • Quinones / chemical synthesis*

Substances

  • Antineoplastic Agents, Phytogenic
  • Lignans
  • Quinones
  • elenoside
  • justicidone