Woodylides A-C, new cytotoxic linear polyketides from the South China Sea sponge Plakortis simplex

Mar Drugs. 2012 May;10(5):1027-1036. doi: 10.3390/md10051027. Epub 2012 May 7.

Abstract

Three new polyketides, woodylides A-C (1-3), were isolated from the ethanol extract of the South China Sea sponge Plakortis simplex. The structures were elucidated by spectroscopic data (IR, 1D and 2D NMR, and HRESIMS). The absolute configurations at C-3 of 1 and 3 were determined by the modified Mosher's method. Antifungal, cytotoxic, and PTP1B inhibitory activities of these polyketides were evaluated. Compounds 1 and 3 showed antifungal activity against fungi Cryptococcus neoformans with IC₅₀ values of 3.67 and 10.85 µg/mL, respectively. In the cytotoxicity test, compound 1 exhibited a moderate effect against the HeLa cell line with an IC₅₀ value of 11.2 µg/mL, and compound 3 showed cytotoxic activity against the HCT-116 human colon tumor cell line and PTP1B inhibitory activity with IC₅₀ values of 9.4 and 4.7 µg/mL, respectively.

Keywords: PTP1B inhibitory activity; Plakortis simplex; cytotoxicity; woodylides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antifungal Agents / chemistry
  • Antifungal Agents / isolation & purification
  • Antifungal Agents / pharmacology
  • Aquatic Organisms / chemistry
  • Biological Products / chemistry*
  • Biological Products / isolation & purification*
  • Biological Products / pharmacology
  • Cell Line, Tumor
  • China
  • Cryptococcus neoformans / drug effects
  • Drug Screening Assays, Antitumor / methods
  • HCT116 Cells
  • HeLa Cells
  • Humans
  • Inhibitory Concentration 50
  • Magnetic Resonance Spectroscopy / methods
  • Plakortis / chemistry*
  • Polyketides / chemistry*
  • Polyketides / isolation & purification*
  • Polyketides / pharmacology
  • Seawater

Substances

  • Antifungal Agents
  • Biological Products
  • Polyketides