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

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.
AuthorsJinyong Peng, Qiwei Xu, Youwei Xu, Yan Qi, Xu Han, Lina Xu
JournalNatural product research (Nat Prod Res) Vol. 21 Issue 7 Pg. 641-5 (Jun 2007) ISSN: 1478-6419 [Print] England
PMID17613822 (Publication Type: Journal Article)
Chemical References
  • Antineoplastic Agents, Phytogenic
  • Flavonoids
  • Formazans
  • Tetrazolium Salts
  • MTT formazan
Topics
  • Antineoplastic Agents, Phytogenic (chemistry, isolation & purification, pharmacology)
  • Cell Survival (drug effects)
  • Drug Screening Assays, Antitumor
  • Flavonoids (chemistry, isolation & purification, 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)

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