Source:http://linkedlifedata.com/resource/pubmed/id/18239312
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2008-2-1
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pubmed:abstractText |
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 6beta,15xi-dihydroxylabda-8(17),11,13-trien-15,16-olide (1), and 6beta-hydroxy-15xi-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 IC(50) values of 0.92 and 2.20 microM, respectively, whereas 5 was inactive against A549 cells and 1 was inactive against both cell lines up to a concentration of 300.81 microM. 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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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents, Phytogenic,
http://linkedlifedata.com/resource/pubmed/chemical/Diterpenes,
http://linkedlifedata.com/resource/pubmed/chemical/Tetrazolium Salts,
http://linkedlifedata.com/resource/pubmed/chemical/Thiazoles,
http://linkedlifedata.com/resource/pubmed/chemical/labdane,
http://linkedlifedata.com/resource/pubmed/chemical/thiazolyl blue
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0009-2363
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
56
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
210-2
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pubmed:meshHeading |
pubmed-meshheading:18239312-Antineoplastic Agents, Phytogenic,
pubmed-meshheading:18239312-Cell Line, Tumor,
pubmed-meshheading:18239312-Crystallography, X-Ray,
pubmed-meshheading:18239312-Diterpenes,
pubmed-meshheading:18239312-Drug Screening Assays, Antitumor,
pubmed-meshheading:18239312-Humans,
pubmed-meshheading:18239312-K562 Cells,
pubmed-meshheading:18239312-Magnetic Resonance Spectroscopy,
pubmed-meshheading:18239312-Molecular Conformation,
pubmed-meshheading:18239312-Spectrometry, Mass, Electrospray Ionization,
pubmed-meshheading:18239312-Spectrophotometry, Infrared,
pubmed-meshheading:18239312-Structure-Activity Relationship,
pubmed-meshheading:18239312-Tetrazolium Salts,
pubmed-meshheading:18239312-Thiazoles,
pubmed-meshheading:18239312-Zingiberaceae
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pubmed:year |
2008
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pubmed:articleTitle |
Cytotoxicity of labdane-type diterpenoids from Hedychium forrestii.
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pubmed:affiliation |
State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, The Chinese Academy of Sciences, Heilongtan, Kunming, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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