Unique polyacetylenic ester-neolignan derivatives from Mitrephora tomentosa and their antimalarial activities

Phytochemistry. 2021 Mar:183:112615. doi: 10.1016/j.phytochem.2020.112615. Epub 2020 Dec 17.

Abstract

The phytochemical investigation of the methanol extracts of the leaves and twigs of Mitrephora tomentosa Hook. f. & Thomson resulted in the isolation and identification of undescribed polyacetylenic ester-neolignan derivatives, along with six known compounds. These six undescribed natural products were named as mitrephentosins A-F. The structures of these compounds were determined by spectroscopic techniques including UV, IR, NMR, and mass spectrometric analyses. The absolute configurations of mitrephentosins A-F were determined based on specific rotations values and ECD spectral data by comparisons made with the known parent neoligan compound mitredrusin. Mitrephentosins C, E, and F showed moderate antimalarial activities (IC50 values of 13.3-24.6 μM) against the Plasmodium falciparum strains TM4/8.2 and K1CB1 and were not toxic to Vero cells, while the other isolated compounds were not active against these P. falciparum strains.

Keywords: Annonaceae; Antimalarial activity; Mitrephora tomentosa; Neolignan; Polyacetylenic ester.

MeSH terms

  • Animals
  • Antimalarials* / pharmacology
  • Chlorocebus aethiops
  • Esters
  • Lignans*
  • Plant Extracts / pharmacology
  • Plasmodium falciparum
  • Polyacetylene Polymer
  • Vero Cells

Substances

  • Antimalarials
  • Esters
  • Lignans
  • Plant Extracts
  • Polyacetylene Polymer