Isolation, structure elucidation, and synthesis of antiplasmodial quinolones from Crinum firmifolium

Bioorg Med Chem. 2017 Aug 1;25(15):4203-4211. doi: 10.1016/j.bmc.2017.06.017. Epub 2017 Jun 13.

Abstract

Antiplasmodial bioassay guided fractionation of a Madagascar collection of Crinum firmifolium led to the isolation of seven compounds. Five of the seven compounds were determined to be 2-alkylquinolin-4(1H)-ones with varying side chains. Compounds 1 and 4 were determined to be known compounds with reported antiplasmodial activities, while 5 was believed to be a new branched 2-alkylquinolin-4(1H)-one, however, it was isolated in limited quantities and in admixture and therefore was synthesized to confirm its structure as a new antiplasmodial compound. Along with 5, two other new and branched compounds 6 and 7 were synthesized as well. Accompanying the five quinolones were two known compounds 2 and 3 which are inactive against Plasmodium falciparum. The isolation, structure elucidation, total synthesis, and biological evaluation of these compounds are discussed in this article.

Keywords: Amaryllidaceae; Antiplasmodial; Crinum; Quinolone.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, N.I.H., Extramural

MeSH terms

  • Antimalarials / chemical synthesis
  • Antimalarials / chemistry*
  • Antimalarials / isolation & purification*
  • Crinum / chemistry*
  • Mass Spectrometry
  • Plasmodium falciparum / drug effects*
  • Proton Magnetic Resonance Spectroscopy
  • Quinolones / chemical synthesis
  • Quinolones / chemistry*
  • Quinolones / isolation & purification*
  • Spectrophotometry, Ultraviolet

Substances

  • Antimalarials
  • Quinolones