Isolation and characterization of a new compound from Prunus mume fruit that inhibits cancer cells

J Agric Food Chem. 2006 Mar 22;54(6):2123-8. doi: 10.1021/jf0523770.

Abstract

An active compound that inhibits cancer cells was isolated from the fruit of Prunus mume, and its structure and in vitro activities were characterized. The n-hexane fraction obtained from methanol extracts exhibited the strongest inhibitory effect on the growth of cancer cells. From the n-hexane fraction, a new compound named B-1 was purified through preparative thin-layer chromatography, ODS column chromatography, and reverse phase high-performance liquid chromatography and its structure was analyzed by fast atom bombardment mass spectrometry and 1H and 13C NMR. The molecular formula of B-1 was C19H22O6 {2-hydroxy-1-[(7-hydroxy-2-oxo-2H-chromen-6-yl)methyl]-2-methylpropyl-(2Z)-3-methyl-but-e-enoate:prunate}, and the IC50 value was in the range of 39-58 microg/mL in descending order of the cancer cell lines Hep-2, SW-156, HEC-1-B, and SK-OV-3. B-1 exhibited 81-96% inhibition at a concentration level of 100 microg/mL against all cells, based on an 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide assay. However, B-1 showed little effect against normal cells with only 23% or less growth inhibition at 100 microg/mL. Thus, B-1 has a highly specific inhibitory effect against cancer cells but little effect against normal cells. When the cancer cell lines Hep-2 and SK-OV-3 were incubated with B-1 for 72 h, most of the tested cells suffered strong growth inhibition. The compound has the potential to be developed as a nutraceutical.

MeSH terms

  • Animals
  • Antineoplastic Agents / isolation & purification
  • Antineoplastic Agents / pharmacology
  • Benzopyrans / isolation & purification*
  • Benzopyrans / pharmacology
  • Butyrates / isolation & purification*
  • Butyrates / pharmacology
  • Cell Division / drug effects*
  • Cell Line, Tumor
  • Chromatography, High Pressure Liquid
  • Chromatography, Thin Layer
  • Fruit / chemistry*
  • Humans
  • Kidney Neoplasms
  • Laryngeal Neoplasms
  • Magnetic Resonance Spectroscopy
  • Mice
  • NIH 3T3 Cells
  • Neoplasms / pathology*
  • Prunus / chemistry*
  • Spectrometry, Mass, Fast Atom Bombardment

Substances

  • 2-hydroxy-1-((7-hydroxy-2-oxo-2H-chromen-6-yl)methyl)-2-methylpropyl-(2Z)-3-methyl-but-e-enoate
  • Antineoplastic Agents
  • Benzopyrans
  • Butyrates