A new norcembranoid dimer from the red sea soft coral Sinularia gardineri

J Nat Prod. 1996 Jul;59(7):687-9. doi: 10.1021/np960207z.

Abstract

A study of Sinularia gardineri (Pratt) (Alcyoniidae), collected in the Red Sea, revealed a new heptacyclic norcembranoid dimer singardin (1). The structure of singardin was deduced by spectroscopic analysis. A known sesquiterpene, guaianediol (2), and the known cembranolides (1R,5S,8R,10S,11R)-11-hydroxy-1-isoprenyl-8-methyl-3,6-dioxo -5,8-epoxycyclotetradec-12-ene 10,12-carbolactone (5-epi-sinuleptolide) and sinuleptolide were also isolated. Compounds 1 and 2 show cytotoxicity to murine leukemia (P-388), human lung carcinoma (A-549), human colon carcinoma (HT-29), and human melanoma cells (MEL-28).

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antifungal Agents / pharmacology
  • Antineoplastic Agents / isolation & purification*
  • Antineoplastic Agents / pharmacology
  • Candida albicans / drug effects
  • Cnidaria / chemistry*
  • Cryptococcus neoformans / drug effects
  • Drug Screening Assays, Antitumor
  • Furans / isolation & purification*
  • Furans / pharmacology
  • Humans
  • Lactones / isolation & purification*
  • Lactones / pharmacology
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry
  • Mice
  • Spectrophotometry, Infrared
  • Tumor Cells, Cultured

Substances

  • Antifungal Agents
  • Antineoplastic Agents
  • Furans
  • Lactones
  • singardin