Arabidopsis Compound Description
| Knapsack ID | C00001486 |
| PubChem ID | 5281139 |
| Compound name | (2R)-2-Hydroxy 3-butenyl glucosinolate |
| Common Name | Progoitrin |
| Formula | C11H19NO10S2 |
| SCC Type | Methionine-derived glucosinolates; Hydroxy alkenyl glucosinolates |
| SCC Function | The antiproliferative activity found for isothiocyanates, derived from progoitrin potentially responsible for the reduction of colorectal cancer associated with diets rich in cruciferous vegetables (Leoni et al 1997). |
| Chemical Structure |  |
| Pubmed ID | Authors | Year | Title | Journal | Description |
|---|---|---|---|---|---|
|
Kliebenstein, D. J., Kroymann, J., Brown, P., Figuth, A., Pedersen, D., Gershenzon, J. & Mitchell-Olds, T. |
2001 |
Genetic Control of Natural Variation in Arabidopsis Glucosinolate Accumulation |
Plant Physiology |
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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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Leoni, O., Iori, R., Palmieri, S., Esposito, E., Menegatti, E., Cortesi, R., & Nastruzzi, C. |
1997 |
Myrosinase-generated isothiocyanate from glucosinolates: isolation, characterization and in vitro antiproliferative studies. |
Bioorganic & medicinal chemistry |