Isolation of new phenylacetylingol derivatives that reactivate HIV-1 latency and a novel spirotriterpenoid from Euphorbia officinarum latex

Bioorg Med Chem. 2007 Jul 1;15(13):4577-84. doi: 10.1016/j.bmc.2007.04.009. Epub 2007 Apr 10.

Abstract

Three new, highly functionalized ingol diterpenes, ingol 7,8,12-triacetate 3-phenylacetate (1), ingol 7,8,12-triacetate 3-(4-methoxyphenyl)acetate (2) and 8-methoxyingol 7,12-diacetate 3-phenylacetate (3), together with the novel spirotriterpene, 3S,4S,5R,7S,9R,14R-3,7-dihydroxy-4,14-dimethyl-7[8-->9]-Abeo-cholestan-8-one (4), have been isolated from Euphorbia officinarum latex. Structures were established on the basis of their spectroscopic data, including two-dimensional NMR analysis and NOE experiments. The biological effects of 1-3 on cell cycle and HIV-1 gene transcription were analysed in the Jurkat T cell line. Compound 3 induced cell-cycle arrest and HIV-1-LTR promoter activation and could represent a novel lead compound for the development of therapies against HIV-1 latency.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle / drug effects
  • Crystallography, X-Ray
  • Diterpenes / isolation & purification*
  • Diterpenes / pharmacology*
  • Euphorbia / chemistry*
  • Flow Cytometry
  • Gene Expression Regulation, Viral / drug effects
  • HIV-1 / drug effects*
  • HIV-1 / genetics
  • Humans
  • Indicators and Reagents
  • Jurkat Cells
  • Latex / chemistry
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Phenylacetates / isolation & purification*
  • Phenylacetates / pharmacology*
  • Spectroscopy, Fourier Transform Infrared
  • Spiro Compounds / isolation & purification*
  • Spiro Compounds / pharmacology*
  • Triterpenes / isolation & purification*
  • Triterpenes / pharmacology*
  • Virus Latency / drug effects*

Substances

  • Diterpenes
  • Indicators and Reagents
  • Latex
  • Phenylacetates
  • Spiro Compounds
  • Triterpenes