Arabidopsis Compound Description
| Knapsack ID | C00007864 |
| PubChem ID | 5486194 |
| Compound name | (2S)-2-Hydroxy 3-butenyl glucosinolate |
| Common Name | Epiprogoitrin |
| Formula | C11H19NO10S2 |
| SCC Type | Methionine-derived glucosinolates; Hydroxy alkenyl glucosinolates |
| SCC Function | Antiproliferative activity found for Isothiocyanate and nitriles derived from epi-progoitrin demonstrated that in general nitriles are considerably less potent than the corresponding isothiocyanates in inhibiting cancer cell growth (Nastruzzi et al 2000). |
| Chemical Structure |  |
| Pubmed ID | Authors | Year | Title | Journal | Description |
|---|---|---|---|---|---|
|
Reichelt, M., Brown, P.D., Schneider, B., Oldham, N.J., Stauber, E., Tokuhisa, J., Kliebenstein, D.J., Mitchell-Olds, T. & Gershenzon, J. |
2002 |
Benzoic acid glucosinolate esters and other glucosinolates from Arabidopsis thaliana |
Phytochemistry |
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Nastruzzi, C., Cortesi, R., Esposito, E., Menegatti, E., Leoni, O., Iori, R., & Palmieri, S. |
2000 |
In vitro antiproliferative activity of isothiocyanates and nitriles generated by myrosinase-mediated hydrolysis of glucosinolates from seeds of cruciferous vegetables. |
Journal of agricultural and food chemistry |