Abstract
An investigation of Thapsia garganica afforded a series of tetracyclic C-19 dilactones, whose production was dependent on the time and location of the collection. These unusual tetrahomosesquiterpenoids are presumably biosynthesized via a carbon dioxide-triggered electrophilic polyolefin cyclization. Despite the structural differences with thapsigargin, these compounds showed SERCA-inhibiting properties.
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | 1213-1217 |
| Numero di pagine | 5 |
| Rivista | Journal of Natural Products |
| Volume | 68 |
| Numero di pubblicazione | 8 |
| DOI | |
| Stato di pubblicazione | Pubblicato - ago 2005 |
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