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Xanthones with quinone reductase-inducing activity from the fruits of Garcinia mangostana (Mangosteen)

  • Young Won Chin
  • , Hyun Ah Jung
  • , Heebyung Chai
  • , William J. Keller
  • , A. Douglas Kinghorn*
  • *Corresponding author for this work
  • Ohio State University
  • Nature's Sunshine Products

Research output: Contribution to journalJournal articlepeer-review

Abstract

Bioactivity-guided fractionation of a dichloromethane-soluble extract of Garcinia mangostana fruits has led to the isolation and identification of five compounds, including two xanthones, 1,2-dihydro-1,8,10-trihydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)furo[3,2-a]xanthen-11-one (1) and 6-deoxy-7-demethylmangostanin (2), along with three known compounds, 1,3,7-trihydroxy-2,8-di-(3-methylbut-2-enyl)xanthone (3), mangostanin (4), and α-mangostin (5). The structures of compounds 1 and 2 were determined from analysis of their spectroscopic data. All isolated compounds in the present study together with eleven other compounds previously isolated from the pericarp of mangosteen, were tested in an in vitro quinone reductase-induction assay using murine hepatoma cells (Hepa 1c1c7) and an in vitro hydroxyl radical antioxidant assay. Of these, compounds 1-4 induced quinone reductase (concentration to double enzyme induction, 0.68-2.2 μg/mL) in Hepa 1c1c7 cells and γ-mangostin (6) exhibited hydroxyl radical-scavenging activity (IC50, 0.20 μg/mL).

Original languageEnglish
Pages (from-to)754-758
Number of pages5
JournalPhytochemistry
Volume69
Issue number3
DOIs
StatePublished - 2008.02

Keywords

  • (6-deoxy-7-demethylmangostanin)
  • 1,2-Dihydro-1,8,10-trihydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)furo[3,2-a]xanthen-11-one
  • 2,3-Dihydro-4,7-dihydroxy-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enyl)furo[3,2-b]xanthen-5-one
  • Clusiaceae
  • Garcinia mangostana
  • Hydroxyl radical-scavenging activity
  • Quinone reductase induction

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