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.
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Authors | Jinyong Peng, Qiwei Xu, Youwei Xu, Yan Qi, Xu Han, Lina Xu |
Journal | Natural product research
(Nat Prod Res)
Vol. 21
Issue 7
Pg. 641-5
(Jun 2007)
ISSN: 1478-6419 [Print] England |
PMID | 17613822
(Publication Type: Journal Article)
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Chemical References |
- Antineoplastic Agents, Phytogenic
- Flavonoids
- Formazans
- Tetrazolium Salts
- MTT formazan
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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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