4.3 Article

Bioactive constituents of Helianthus tuberosus (Jerusalem artichoke)

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

  1. Consortium for Plant Biotechnology Research, Inc./Ohio Plant Biotechnology Symposium

向作者/读者索取更多资源

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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