Antitubercular resorcinol analogs and benzenoid C-glucoside from the roots of Ardisia cornudentata

Planta Med. 2011 Jan;77(1):60-5. doi: 10.1055/s-0030-1250094. Epub 2010 Jul 6.

Abstract

Bioassay-guided fractionation of the roots of Ardisia cornudentata Mez (Myrsinaceae) led to the isolation of three new compounds, 3-methoxy-2-methyl-5-pentylphenol (1), 3-methoxy-2-methyl-5-(1'-ketopentyl)phenol (2), and cornudoside (3), together with twenty-six known compounds. Their structures were elucidated by analysis of spectroscopic data. Thirteen of these isolates, 1, 2, 4- 6, 9- 15, and 21 showed antitubercular activities against Mycobacterium tuberculosis H37R (V) IN VITRO, with MIC values of 2.5-60 µg/mL. Two alkyl benzoquinones, ardisianone (7) and cornudentanone ( 8), were reported for their selective cytotoxic activity against the NCI-H460 cancer cell line (IC (50) values of 2.3, 2.5 µg/mL).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antitubercular Agents / chemistry
  • Antitubercular Agents / isolation & purification
  • Antitubercular Agents / pharmacology*
  • Ardisia / chemistry*
  • Benzoquinones / chemistry
  • Benzoquinones / isolation & purification
  • Benzoquinones / pharmacology
  • Cell Line, Tumor
  • Chemical Fractionation
  • Humans
  • Inhibitory Concentration 50
  • Microbial Sensitivity Tests
  • Mycobacterium tuberculosis / drug effects
  • Plant Roots / chemistry
  • Resorcinols / chemistry
  • Resorcinols / isolation & purification
  • Resorcinols / pharmacology*

Substances

  • Antitubercular Agents
  • Benzoquinones
  • Resorcinols
  • resorcinol