Caftaric acid

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Caftaric acid
Caftaric acid.svg
Identifiers
PubChem 6440397
ChemSpider 4944664 YesY
MeSH caftaric+acid
ChEMBL CHEMBL558557 N
Jmol-3D images Image 1
Image 2
Properties
Molecular formula C13H12O9
Molar mass 312.23 g mol−1
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 N (verify) (what is: YesY/N?)
Infobox references

Caftaric acid is a non-flavanoid phenolic compound.

It is found in grape[1] (Vitis vinifera) and impacts the color of white wine. Many believe[who?] this molecule is responsible for the yellowish-gold color seen in some whites wines[citation needed]. Aside from wine, it is abundantly present in raisins. It also occurs in Cichorium intybus (common chicory) and is one of the bioactive components of Echinacea purpurea (Eastern purple coneflower).[2]

Caftaric acid and caffeic acid are in a class of chemicals known as cinnamates (hydroxycinnamic acids). Caftaric acid is formed when caffeic acid and tartaric acid undergo esterification. But, during fermentation, caftaric acid is oxidized into its principal components.

Caftaric acid has a good bioavailability when fed in rats. Intact trans-caftaric acid was detected in rat plasma along with its O-methylated derivative trans-fertaric acid.[2]

In wine[edit]

Winemakers measure caftaric acid levels as their primary method to estimate the oxidation levels that a wine has undergone. For example, press wines, which undergo a high degree of oxidation[citation needed], will have little to no caftaric acid.

Grape reaction product (2-S glutathionyl caftaric acid) is an oxidation compound produced from caftaric acid and found in wine. Malvidin 3-glucoside alone is not oxidized in the presence of grape polyphenol oxidase (PPO), whereas it is degraded in the presence of a crude grape PPO extract and of caftaric acid, forming anthocyanidin-caftaric acid adducts.[3]

See also[edit]

References[edit]

  1. ^ C. Y. Lee and A. Jaworski (1987). abstract "Phenolic Compounds in White Grapes Grown in New York". Am. J. Enol. Vitic 38 (4): 277–281. 
  2. ^ a b Vanzo, A; Cecotti, R; Vrhovsek, U; Torres, AM; Mattivi, F; Passamonti, S (2007). "The fate of trans-caftaric acid administered into the rat stomach". Journal of agricultural and food chemistry 55 (4): 1604–11. doi:10.1021/jf0626819. PMID 17300159. 
  3. ^ Sarni-Manchado, Pascale; Cheynier, Véronique; Moutounet, Michel (1997). "Reactions of polyphenoloxidase generated caftaric acid o-quinone with malvidin 3-O-glucoside". Phytochemistry 45 (7): 1365. doi:10.1016/S0031-9422(97)00190-8.