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Photochemistry of phytoalexins containing phenalenone-like chromophores: Photophysics and singlet oxygen photosensitizing properties of the plant oxoaporphine alkaloid oxoglaucine

  • Cristina Flors
  • , Chantal Prat
  • , Rafael Suau
  • , Francisco Nájera
  • , Santi Nonell*
  • *Corresponding author for this work

Research output: Indexed journal article Articlepeer-review

17 Citations (Scopus)

Abstract

Oxoglaucine (OG) is an oxoaporphine alkaloid, which has been linked to plant defense mechanisms. It contains a phenalenone (PN)-like chromophore, which suggests a role as singlet oxygen (1O2) photosensitizer. Indeed, OG is able to photosensitize 1O2 with 100% efficiency in nonpolar environments, similar to PN. However, this efficiency decreases in polar and protic media, although 1O2 is formed in all environments ranging from benzene to water. OG is a rather inefficient 1O2 quencher (kq = 8 × 105 M-1 s-1) unlike the related alkaloids boldine and glaucine, for which an antioxidant role has been suggested. The results of this study contribute to the view that plant defense mediated by PN-like secondary metabolites may have a photochemical component.

Original languageEnglish
Pages (from-to)120-124
Number of pages5
JournalPhotochemistry and Photobiology
Volume81
Issue number1
DOIs
Publication statusPublished - Jan 2005

Keywords

  • Isoquinoline alkaloids
  • Phosphorescence
  • Deactivation
  • Sensitizer
  • Lignans
  • Yields

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