Abstract
Four phenylpropanoids and a thapsigargin analogue have been isolated from the fruits of Thapsia garganica. A spectroscopic method for elucidating the relative stereochemistry at the two pairs of stereogenic centers in the phenylpropanoids has been developed. The phenylpropanoids were found to be potent cytotoxins.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 2651-2658 |
| Number of pages | 8 |
| Journal | Phytochemistry |
| Volume | 67 |
| Issue number | 24 |
| DOIs | |
| State | Published - Dec 2006 |
Keywords
- 2,3-Dihydroxy-2-methylbutanoic acid
- Apiaceae
- Cytotoxicity
- Phenylpropanoids
- Relative configuration
- Thapsia garganica
- Thapsigargin
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Plant Science
- Horticulture
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