期刊
PHYTOCHEMISTRY LETTERS
卷 2, 期 1, 页码 15-18出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.phytol.2008.10.003
关键词
Helianthus tuberosus L (Asteraceae); ent-kaurane diterpenes; ent-norlabdane diterpene; Germacrane-type sesquiterpene lactones; Norisoprenoid; Cytotoxicity; Soybean defense assay
资金
- Consortium for Plant Biotechnology Research, Inc./Ohio Plant Biotechnology Symposium
In a cytotoxicity-guided study using the MCF-7 human breast cancer cell line, nine known compounds, ent-17-oxokaur-15(16)-en-19-oic acid (1). ent-17-hydroxykaur-15(16)-en-19-oic acid (2), ent-15-hydroxykaur-16(17)-en-19-oic acid methyl ester (3), ent-15-nor-14-oxolabda-8(17), 12E-dien-18-oic acid (4), 4,15-isoatriplicolide angelate (5). 4,15-isoatriplicolide methylacrylate (6). (+)-pinoresinol (7), (-)-loliolide (8), and vanillin (9) were isolated from the chloroform-soluble subfraction of a methanol extract of the whole plant of Helianthus tuberosus collected in Ohio, USA. This is the first time that diterpenes have been isolated and identified from this economically important plant. The bioactivities of all isolates were evaluated using the MCF-7 human breast cancer cell line as well as a soybean isoflavonoid defense activation bioassay. The results showed that two germacrane-type sesquiterpene lactones, 5 and 6, are cytotoxic agents. While compounds 2, 3, 5 and 6 blocked isoflavone accumulation in the soybean, the norisoprenoid (-)-loliolide (8) was somewhat stimulatory of these defense metabolites. (c) 2008 Phytochemical Society of Europe Published by Elsevier B.V. All rights reserved.
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