Grape reaction product
Chemical structure of grape reaction product | |
Names | |
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Other names
GRP
GRP1 2-S-Glutathionyl caftaric acid |
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Identifiers | |
Jmol 3D model | Interactive image |
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Properties | |
C23H27N3O15S | |
Molar mass | 617.54 g·mol−1 |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
The grape reaction product (GRP, GRP1 or 2-S-glutathionyl caftaric acid[1]) is a phenolic compound explaining the disappearance of caftaric acid from grape must during processing.[2] It is also found in aged red wines.[3] Its enzymatic production by polyphenol oxidase is important in limiting the browning of musts,[4] especially in white wine production. The product can be recreated in model solutions.[5][6]
It is possible to determine its concentration in wine by mass spectrometry.[7]
S-Glutathionyl caftaric acid is itself oxidizable.[8] It is not a substrate for grape polyphenol oxidase, but laccase from Botrytis cinerea can use it to form GRP2.[9]
Related molecules
Other related molecules are trans-caffeoyltartrate derivatives like GRP o-quinone[10] and 2,5-di-S-glutathionyl cafteoyl tartrate (GRP2)[11] or adducts with anthocyanidins.[12]
See also
References
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- ↑ Caftaric acid in grapes and conversion to a reaction product during processing. V.L. Singleton, J. Zaya, E. Trousdale and M. Salgues, Vitis, 1984, pages 113-120 (article)
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- ↑ Straightforward Method To Quantify GSH, GSSG, GRP, and Hydroxycinnamic Acids in Wines by UPLC-MRM-MS. Anna Vallverdú-Queralt, Arnaud Verbaere, Emmanuelle Meudec, Veronique Cheynier and Nicolas Sommerer, J. Agric. Food Chem. 2015, 63, 142−149, doi:10.1021/jf504383g
- ↑ Caftaric Acid Disappearance and Conversion to Products of Enzymic Oxidation in Grape Must and Wine. V. L. Singleton, M. Salgues, J. Zaya and E. Trousdale, Am. J. Enol. Vitic, 1985, volume 36, number 1, pages 50-56 'abstract)
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- Hydroxycinnamic acid esters