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The structure-activity relationship of flavonoids as scavengers of peroxynitrite

  • Jae Sue Choi*
  • , Hae Young Chung
  • , Sam Sik Kang
  • , Mee Jung Jung
  • , Jung Won Kim
  • , Jae Kyung No
  • , Hyun Ah Jung
  • *Corresponding author for this work
  • Pukyong National University
  • Pusan National University
  • Seoul National University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Peroxynitrite is a cytotoxic intermediate produced by the reaction between a superoxide anion radical and nitric oxide. The scavenging activities of flavonoids on peroxynitrite were investigated to illustrate the structure-activity relationship. Peroxynitrite was scavenged by the presence of various flavonoids, whose structures seem to be closely related to the degree of scavenging. Of 31 compounds tested, the most active was quercetin, with an IC50 value of 0.93 μM. Others had IC50 values ranging from 0.96 to more than 10 μM. The scavenging activity was postulated to be governed by the position of the hydroxyl group. Ortho-hydroxyl structures increased the scavenging activity on peroxynitrite.

Original languageEnglish
Pages (from-to)232-235
Number of pages4
JournalPhytotherapy Research
Volume16
Issue number3
DOIs
StatePublished - 2002

Keywords

  • Flavonoid
  • Peroxynitrite
  • Structure-activity relationship

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