[Coumarins of Anemone raddeana Regel and their biological activity]

Yao Xue Xue Bao. 2012 Feb;47(2):206-9.
[Article in Chinese]

Abstract

To study the coumarins of Anemone raddeana Regel, the compounds were separated by silica gel column chromatography and HPLC. Their structures were identified by their physicochemical property and spectral analysis. Two new compounds were isolated and identified as 4, 7-dimethoxyl-5-methyl-6-hydroxy coumarin (1) and 4, 7-dimethoxyl-5-formyl-6-hydroxycoumarin (2). The bioassays indicated that compounds 1 and 2 could significantly inhibit the proliferation of cancer cell, and showed the agonist effect on the transactivity of retinoic acid receptor-alpha (RARalpha). In addition, the two compounds had inhibitory effect against human leukocyte elastase (HLE).

MeSH terms

  • Anemone / chemistry*
  • Antineoplastic Agents, Phytogenic / chemistry
  • Antineoplastic Agents, Phytogenic / isolation & purification*
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Coumarins / chemistry
  • Coumarins / isolation & purification*
  • Coumarins / pharmacology
  • Humans
  • Inhibitory Concentration 50
  • Leukocyte Elastase / metabolism
  • Molecular Structure
  • Plants, Medicinal / chemistry
  • Receptors, Retinoic Acid / genetics
  • Receptors, Retinoic Acid / metabolism
  • Retinoic Acid Receptor alpha
  • Rhizome / chemistry
  • Transcriptional Activation

Substances

  • 4,7-dimethoxyl-5-formyl-6-hydroxycoumarin
  • 4,7-dimethoxyl-5-methyl-6-hydroxycoumarin
  • Antineoplastic Agents, Phytogenic
  • Coumarins
  • RARA protein, human
  • Receptors, Retinoic Acid
  • Retinoic Acid Receptor alpha
  • Leukocyte Elastase