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葡萄反应产物

维基百科，自由的百科全书
（重定向自GRP）
葡萄反应产物
Chemical structure of grape reaction product
IUPAC名
2-[(E)-3-[3-[2-[(4-amino-4-carboxybutanoyl)amino]-3-(carboxymethylamino)-3-oxopropyl]sulfanyl-4,5-dihydroxyphenyl]prop-2-enoyl]oxy-3-hydroxybutanedioic acid
别名 GRP
GRP1
2-S-Glutathionyl caftaric acid
2-S-谷胱酰基咖啡酰酒石酸
识别
CAS号
PubChem 71308212
SMILES
 
  • Oc1cc(cc(c1O)SCC(NC(=O)CCC(N)C(=O)O)C(=O)NCC(O)=O)\C=C\C(=O)OC(C(O)=O)C(O)C(O)=O
ChEBI 147433
性质
化学式 C23H27N3O15S
摩尔质量 617.54 g·mol−1
若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

葡萄反应产物（GRP、GRP1 或 2-S-谷硫酰基咖啡酰酒石酸）[1]是一种酚类化合物，可以解释为什么在加工过程中咖啡酰酒石酸会从葡萄汁中消失。[2]陈年红葡萄酒中也含有这种成分。[3]它由多酚氧化酶酶解产生，对限制葡萄汁的褐变非常重要，[4]特别是在白葡萄酒生产中。 该产品可在模型解决方案中再现。[5][6]

通过质谱法可以确定其在葡萄酒中的浓度。[7]S-谷胱酰基咖啡酰酒石酸本身能被氧化。[8] 它不是葡萄多酚氧化酶的底物，但灰葡萄孢菌的漆酶可以利用它形成 GRP2。[9]

相关分子

其他相关分子是“反式”-咖啡酰酒石酸衍生物，如 GRP1,2-苯醌[10]和 2,5-di-S-谷氨酰基咖啡酰酒石酸盐（GRP2）[11]或与花青素的加合物。[12]

咖啡酒石酸紫外可见光谱.png
咖啡酒石酸紫外可见光谱

参考文献

  1. ^ Veronique F. Cheynier; Eugene K. Trousdale; Vernon L. Singleton; Michel J. Salgues; Renee Wylde. Characterization of 2-S-glutathionyl caftaric acid and its hydrolysis in relation to grape wines. J. Agric. Food Chem. 1986, 34 (2): 217–221. doi:10.1021/jf00068a016. 
  2. ^ 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)
  3. ^ Anis Arnous; Dimitris P. Makris; Panagiotis Kefalas. Effect of Principal Polyphenolic Components in Relation to Antioxidant Characteristics of Aged Red Wines. J. Agric. Food Chem. 2001, 49 (12): 5736–5742. PMID 11743756. doi:10.1021/jf010827s. 
  4. ^ V.L. Singleton; M. Salgues; J. Zaya; E. Trousdale. Caftaric Acid Disappearance and Conversion to Products of Enzymic Oxidation in Grape Must and Wine (PDF). Am. J. Enol. Vitic. 1985, 36 (1): 50. 
  5. ^ V. Cheynier; C. Owe; J. Rigaud. Oxidation of Grape Juice Phenolic Compounds in Model Solutions. Journal of Food Science. 1988, 53 (6): 1729–1732. doi:10.1111/j.1365-2621.1988.tb07828.x. 
  6. ^ Veronique Cheynier; Jorge M. Ricardo da Silva. Oxidation of grape procyanidins in model solutions containing trans-caffeoyltartaric acid and polyphenol oxidase. J. Agric. Food Chem. 1991, 39 (6): 1047–1049. doi:10.1021/jf00006a008. 
  7. ^ 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
  8. ^ 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)
  9. ^ Salgues, M.; Cheynier, V.; Gunata, Z.; Wylde, R. Oxidation of Grape Juice 2-S-Glutathionyl Caffeoyl Tartaric Acid by Botrytis cinerea Laccase and Characterization of a New Substance: 2,5-di-S-Glutathionyl Caffeoyl Tartaric Acid. Journal of Food Science. 1986, 51 (5): 1191. doi:10.1111/j.1365-2621.1986.tb13081.x. 
  10. ^ Cheynier V.; Rigaud J.; Souquet J.-M.; Duprat F.; Moutounet M. Must browning in relation to the behavior of phenolic compounds during oxidation. American Journal of Enology and Viticulture. 1990, 41 (4): 346–349. INIST（法语：Institut de l'information scientifique et technique）:5402970
  11. ^ Véronique Cheynier; Jacques Rigaud; Michel Moutounet. Oxidation kinetics of trans-caffeoyltartrate and its glutathione derivatives in grape musts. Phytochemistry. 1990, 29 (6): 1751–1753. doi:10.1016/0031-9422(90)85008-4. 
  12. ^ Petros Kneknopoulos; George K. Skouroumounis; Yoji Hayasaka; Dennis K. Taylor. New Phenolic Grape Skin Products from Vitis vinifera cv. Pinot Noir. J. Agric. Food Chem. 2011, 59 (3): 1005–1011. PMID 21214245. doi:10.1021/jf103682x. 
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