Antimalarial β-carbolines from the New Zealand ascidian Pseudodistoma opacum

J Nat Prod. 2011 Sep 23;74(9):1972-9. doi: 10.1021/np200509g. Epub 2011 Aug 16.

Abstract

One tetrahydro-β-carboline, (-)-7-bromohomotrypargine (1), and three alkylguanidine-substituted β-carbolines, opacalines A, B, and C (2-4), have been isolated from the New Zealand ascidian Pseudodistoma opacum. The structures of the metabolites were determined by analysis of mass spectrometric and 2D NMR spectroscopic data. Natural products 2 and 3, synthetic debromo analogues 8 and 9, and intermediate 16 exhibited moderate antimalarial activity toward a chloroquine-resistant strain of Plasmodium falciparum, with an IC50 range of 2.5-14 μM. The biosynthesis of 1-4 is proposed to proceed via a Pictet-Spengler condensation of 6-bromotryptamine and the α-keto acid transamination product of either arginine or homoarginine. Cell separation and 1H NMR analysis of P. opacum identified tetrahydro-β-carboline 1 to be principally located in the zooids, while fully aromatized analogues 2-4 were localized to the test.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimalarials / chemistry
  • Antimalarials / isolation & purification*
  • Antimalarials / pharmacology*
  • Carbolines / chemistry
  • Carbolines / isolation & purification*
  • Carbolines / pharmacology*
  • Chloroquine / pharmacology
  • Drug Resistance / drug effects
  • Molecular Structure
  • New Zealand
  • Nuclear Magnetic Resonance, Biomolecular
  • Plasmodium falciparum / drug effects*
  • Stereoisomerism
  • Urochordata / chemistry*

Substances

  • Antimalarials
  • Carbolines
  • Chloroquine