Anti-inflammatory cyathane diterpenoids from Sarcodon scabrosus

Biosci Biotechnol Biochem. 2004 Jun;68(6):1362-5. doi: 10.1271/bbb.68.1362.

Abstract

Four novel diterpenoids were isolated from the fruiting bodies of Sarcodon scabrosus (Fr.) Karst. (Boraginaceae) together with neosarcodonin A. One of the novel compounds was elucidated to be a cyathane diterpenoid, namely neosarcodonin O, by its spectral data. The others were characterized as 19-O-linoleoyl, 19-O-oleoyl and 19-O-stearoyl derivatives of sarcodonin A, after comparison with the authentic samples synthetically prepared from sarcodonin A. These compounds, together with the five 19-O-acyl derivatives synthesized from sarcodonin A, each exhibited inhibitory activity against 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced inflammation on mouse ears by topical application.

MeSH terms

  • Administration, Topical
  • Animals
  • Anti-Inflammatory Agents / isolation & purification*
  • Anti-Inflammatory Agents / pharmacology
  • Anti-Inflammatory Agents / therapeutic use
  • Boraginaceae / chemistry*
  • Diterpenes / isolation & purification*
  • Diterpenes / pharmacology
  • Diterpenes / therapeutic use
  • Inflammation / drug therapy
  • Mice
  • Terpenes

Substances

  • Anti-Inflammatory Agents
  • Diterpenes
  • Terpenes
  • sarcodonin M