A new anticancer dihydroflavanoid from the root of Spiranthes australis (R. Brown) Lindl

Nat Prod Res. 2007 Jun;21(7):641-5. doi: 10.1080/14786410701371165.

Abstract

A new dihydroflavanoid was obtained from the root of Spiranthes australis (R. Brown) Lindl, a traditional Chinese medicinal herb. The structure was elucidated as (2S)-5,2',6'-trihydroxy-6-lavandulyl-4''-(gamma,gamma-dimethylallyl)-2'',2''-dimethylpyrano-[5'',6'' : 7,8]-flavanone by spectroscopic methods including UV, IR, HR-EI-MS, ESI-MS, 1D NMR and 2D NMR techniques, and subsequently, the anticancer activities of the compound to inhibit human cancer cells' growth including A549, BEL-7402, SGC-7901, MCF-7, HT-29, K562, and A498 cell lines by MTT method was evaluated in vitro.

MeSH terms

  • Antineoplastic Agents, Phytogenic / chemistry
  • Antineoplastic Agents, Phytogenic / isolation & purification*
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Cell Survival / drug effects
  • Drug Screening Assays, Antitumor
  • Flavonoids / chemistry
  • Flavonoids / isolation & purification*
  • Flavonoids / pharmacology*
  • Formazans / chemistry
  • HT29 Cells
  • Humans
  • Inhibitory Concentration 50
  • K562 Cells
  • Mass Spectrometry
  • Nuclear Magnetic Resonance, Biomolecular
  • Orchidaceae / chemistry*
  • Plant Roots / chemistry
  • Plants, Medicinal / chemistry
  • Spectrophotometry, Infrared
  • Spectrophotometry, Ultraviolet
  • Tetrazolium Salts / chemistry

Substances

  • Antineoplastic Agents, Phytogenic
  • Flavonoids
  • Formazans
  • Tetrazolium Salts
  • MTT formazan