Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
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Cytotoxicity of Labdane-Type Diterpenoids from Hedychium forrestii
Qing ZhaoChen QingXiao Jiang HaoJun HanGuo Ying ZuoCheng ZouGui Li Xu
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JOURNAL FREE ACCESS

2008 Volume 56 Issue 2 Pages 210-212

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Abstract

Two new labdane-type diterpenoids, hedyforrestin D (1) and 15-ethoxy-hedyforrestin D (2), and three known compounds, yunnancoronarin A (4), B (3) and C (5) were isolated from the rhizomes of Hedychium forrestii. The structure of the new diterpenoids was established as 6β,15ξ-dihydroxylabda-8(17),11,13-trien-15,16-olide (1), and 6β-hydroxy-15ξ-ethoxylabda-8(17),11,13-trien-15,16-olide (2) on the basis of spectroscopic analyses. In addition, the isolated compounds were evaluated for their cytotoxicity against the lung adenocarcinoma cells A549 and leukemia cells K562 through 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assays. Of these, compounds 3 and 4 exhibited the most activity with IC50 values of 0.92 and 2.20 μM, respectively, whereas 5 was inactive against A549 cells and 1 was inactive against both cell lines up to a concentration of 300.81 μM. This shows that both the hydroxy substitution and orientation of unsaturated lactone group in the five-membered ring of C-13 to C-16 seem to play an important role in the anti-tumor activities of human lung adenocarcinoma and leukemia.

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© 2008 The Pharmaceutical Society of Japan
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