Structural Elucidation and Free Radical Scavenging Activity of a new o-Orsellinic Acid Derivative Isolated from the Lichen Cladonia rappii

Nat Prod Commun. 2016 Sep;11(9):1311-1312.

Abstract

Rappiidic acid, a new o-orsellinic acid derivative, was isolated from the lichen Cladonia rappii. Its capability to scavenge reactive oxygen species (ROS) and reactive nitrogen species (RNS) was investigated and compared with resveratrol and (+)-usnic acid. Usnic acid at 100 μM was the most efficient ROS scavenger, exhibiting activity 3-fold higher than that of resveratrol. At the same concentration, rappidic acid scavenged 23.1% of ROS formed, demonstrating that this compound is twice as active as resveratrol. Both compounds were shown to be poor RNS scavengers.

MeSH terms

  • Benzofurans / chemistry
  • Brazil
  • Free Radical Scavengers / chemistry*
  • Lichens / chemistry*
  • Molecular Structure
  • Resorcinols / chemistry*
  • Resorcinols / isolation & purification
  • Resveratrol / chemistry

Substances

  • Benzofurans
  • Free Radical Scavengers
  • Resorcinols
  • usnic acid
  • orsellinic acid
  • Resveratrol