New Cerebroside and Nucleoside Derivatives from a Red Sea Strain of the Marine Cyanobacterium Moorea producens

Molecules. 2016 Mar 9;21(3):324. doi: 10.3390/molecules21030324.

Abstract

In the course of our ongoing efforts to identify marine-derived bioactive compounds, the marine cyanobacterium Moorea producens was investigated. The organic extract of the Red Sea cyanobacterium afforded one new cerebroside, mooreaside A (1), two new nucleoside derivatives, 3-acetyl-2'-deoxyuridine (2) and 3-phenylethyl-2'-deoxyuridine (3), along with the previously reported compounds thymidine (4) and 2,3-dihydroxypropyl heptacosanoate (5). The structures of the compounds were determined by different spectroscopic studies (UV, IR, 1D, 2D NMR, and HRESIMS), as well as comparison with the literature data. Compounds 1-5 showed variable cytotoxic activity against three cancer cell lines.

Keywords: Moorea producens; cerebroside; cytotoxic activity; marine cyanobacterium; nucleosides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cerebrosides / chemistry
  • Cerebrosides / isolation & purification
  • Cerebrosides / pharmacology*
  • Cyanobacteria / chemistry*
  • Humans
  • Indian Ocean
  • Molecular Structure
  • Neoplasms / drug therapy*
  • Nucleosides / chemistry
  • Nucleosides / isolation & purification
  • Nucleosides / pharmacology*

Substances

  • Cerebrosides
  • Nucleosides