Macrocyclic bis-quinolizidine alkaloids from Xestospongia muta

Nat Prod Res. 2019 Feb;33(3):400-406. doi: 10.1080/14786419.2018.1455043. Epub 2018 Mar 29.

Abstract

A new stereoisomer Meso-araguspongine C together with nine reported macrocyclic bis-quinolizidine alkaloids araguspongines A, C, E, L, N-P, petrosin, and petrosin A were isolated from marine sponge Xestospongia muta. Stereochemistry of meso-araguspongine C (2) and araguspongines N-P (3-5) were established by their NMR data and conformational analyses. Both araguspongine C (1) and meso-araguspongine C (2) exhibited great cytotoxic activity towards HepG-2, HL-60, LU-1, MCF-7, and SK-Mel-2 human cancer cells (IC50 in the range of 0.43-1.02 μM). At a concentration of 20 μM, isolated compounds (1-10) also showed modest inhibitory effects (from 7.6 to 40.8%) on the NO production in LPS activated RAW264.7 macrophages.

Keywords: araguspongine C; quinolizidine alkaloid; cytotoxicity.

MeSH terms

  • Alkaloids / chemistry
  • Alkaloids / isolation & purification*
  • Animals
  • Cell Line, Tumor
  • Humans
  • Lipopolysaccharides
  • Macrocyclic Compounds / isolation & purification
  • Mice
  • Molecular Conformation
  • Nitric Oxide / antagonists & inhibitors
  • Nitric Oxide / biosynthesis
  • Quinolizidines / isolation & purification*
  • Quinolizines / isolation & purification*
  • RAW 264.7 Cells
  • Xestospongia / chemistry*

Substances

  • Alkaloids
  • Lipopolysaccharides
  • Macrocyclic Compounds
  • Quinolizidines
  • Quinolizines
  • araguspongine C
  • petrosin
  • Nitric Oxide