Ostreol A: a new cytotoxic compound isolated from the epiphytic dinoflagellate Ostreopsis cf. ovata from the coastal waters of Jeju Island, Korea

Bioorg Med Chem Lett. 2013 May 15;23(10):3023-7. doi: 10.1016/j.bmcl.2013.03.020. Epub 2013 Mar 16.

Abstract

Ostreol A was isolated from cultures of the epiphytic dinoflagellate Ostreopsis cf. ovata from the coastal waters of Jeju Island, Korea. The compound, a non-palytoxin derivative, has a polyhydroxy chain ending with the primary amino group and contains an amide bond, along with two tetrahydropyran rings in the chain. Its chemical structure was elucidated by nuclear magnetic resonance (NMR) spectroscopy methods and confirmed by mass analysis. The compound exhibited significant cytotoxicity in the brine shrimp lethality test at a concentration of 0.9μg/mL.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Artemia / cytology
  • Artemia / drug effects*
  • Cell Survival / drug effects
  • Dinoflagellida / chemistry*
  • Dose-Response Relationship, Drug
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Polyhydroxyalkanoates / chemistry
  • Polyhydroxyalkanoates / isolation & purification
  • Polyhydroxyalkanoates / pharmacology*
  • Pyrans / chemistry
  • Pyrans / isolation & purification
  • Pyrans / pharmacology*
  • Republic of Korea
  • Seawater / chemistry*
  • Structure-Activity Relationship

Substances

  • Polyhydroxyalkanoates
  • Pyrans
  • ostreol A