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Polyphenolics flavonol glycosides

The effects of catechin, epicatechin, procyanidin B2, caffeic acid, / -coumaric acid, myricetrin, and quercetrin on the color intensity and stability of malvidin 3-glucoside at a molar ratio of 1 1 under conditions similar to red wine were evaluated. " Flavan 3-ols appeared to have the lowest protective effects and flavonols the highest strong color changes were visually perceptible. " In the complexation of malvin chloride and natural polyphenols, flavonol glycosides by far exerted the best protector effect. ... [Pg.265]

TLC-FID of lipid classes, 491 -503 Flavonoids. see also Polyphenolics Flavonols. see also Flavonol glycosides Flavor analysis, see also Aroma compounds... [Pg.760]

Tetrahydroxy-flavonol-3-rutinoside (flavonol glycoside) Theaflavin (polyphenol)... [Pg.627]

Glycosides of polyphenolic compounds, e. g. those of flavonoids, constitute a large group and novel findings increase their number extremely quickly. The list of flavone and flavonol glycosides known up to 1986 contains about 900 entries [1]. In the survey of Harbome and Williams [2] covering discoveries in anthocyanins and other flavonoids from January 1995 to December 1997 over 160 new glycosides of flavonoids are reported. [Pg.2592]

Recently, Romani et al. [200] published a sophisticated solid phase extraction procedure for the qualitative analysis of grape skins. In a first extraction on Extrelut 20 (kieselguhr, Merck) polyphenols are separated from anthocyanins. The polyphenols are subsequently fractionated on a C-18 cartridge (Bond Elut , Varian) into phenolic acids and esters, procyanidins, flavonol glycosides and acylated anthocyanins. [Pg.530]

Grape pomace polyphenol composition is affected by many different factors. It is variety dependant [10-11] and, within the same variety, different parts have significantly different compositions. For example, the grape skins, have been found to be rich in anthocyanins, hydroxycinnamic acids, flavanols and flavonol glycosides, whereas the seed portion is a good source of gallic acid and flavanols [3, 11]. Polyphenol composition is also influenced by the growing location, climate, maturity and fermentation time [12]. [Pg.71]

It is generally considered that polyphenol oxidase, which has at least three isoforms, is the key enzyme in the fermentation processes that produce black teas, but there is evidence also for an important contribution from peroxidases with the essential hydrogen peroxide being generated by polyphenol oxidase (Subramanian et al. 1999). The primary substrates for polyphenol oxidase are the flavan-3-ols which are converted to quinones. These quinones react further, and may be reduced back to phenols by oxidizing other phenols, such as gallic acid, flavonol glycosides and theaflavins, that are not direct substrates for polyphenol oxidase (Opie etal. 1993,1995). [Pg.267]

Unlike some classes of polyphenols such as flavonols and flavones, flavanols are almost always present in the nonglycosylated form. Removal of glycoside from flavonoids, usually necessary before the transport across the intestinal barrier, is not required in the case of flavanols [Scalbert and Williamson, 2000]. The absorption of procyanidins by the small intestine was investigated by studying 14C-( + )-catechin, dimer, trimer, and procyanidin polymers permeation through Caco-2 cell cultures [Deprez et al., 2001]. There was little difference in permeability between monomer, dimmer, and trimer, based on the measurement of radioactivity present on the basal side of the cultures, whereas the permeability of the polymers was 10 times lower. The authors reported the absence of catechin metabolism but did not determine whether the radioactivity measured on the basal side of the cultures was from the parent dimers to polymers or from their products of degradation or metabolites, which could have resulted from instability of the parent compounds in the culture... [Pg.57]

Flavonoids constitute a large class of polyphenols found in fruits and vegetables that share a common skeleton of phenylchromane. This basic structure allows a large number of substitution patterns leading to several subclasses of flavonoids, such as flavonols, flavones, flavanones, flavanols, anthocyanidins, isoflavones, dihydroflavonols, and chalcones. Among the diverse flavonoid subclasses, flavonols (especially quercetin) and flavanols (catechins) are the most abundant in our food. Flavonols are present in foods as diverse glycosides, whereas flavanols are usually found as aglycones. [Pg.198]

The tea bush and in particular its young leaves contain a high concentration of polyphenols and oxidative enzymes, thus the young leaves are better for tea manufacture. Tea polyphenols, previously called tea tannins, are also known as tea flavonoids. Among the polyphenols in fresh tea leaves, catechins are the predominant form of polyphenols, which account for 12-24% of the dry weight. Besides catechins, flavonol, and their glycosides, anthocyanidin and leucoanthocyanidin, phenolic acids and depsides are also present. Their typical concentrations are shown in table 8.1. These phenolic compounds are directly or indirectly associated with the characteristics of tea, including its color, taste, and aroma. [Pg.131]

Apple polyphenols are present in different parts of the fruit. A major source is the skin, which contains all the flavonols and anthocyanins in addition to an important amount of dihydrochalcones. ° Phenolic acids are present in the flesh whereas most of the dihydrochalcones are in the core and the seeds. This distribution in different parts of the fruit also affects polyphenol concentration of apple juice where only small amounts of quercetin glycosides and dihydrochalcones are present. However, polyphenol content is also affected by the technological procedure. The oxidative conditions and the clarification process during the production of clear apple juice reduces the phenolic content. In contrast, the anaerobic conditions and the lack of a clarification step during cloudy apple juice production prevents an important loss of polyphenols. ... [Pg.176]


See other pages where Polyphenolics flavonol glycosides is mentioned: [Pg.22]    [Pg.63]    [Pg.324]    [Pg.366]    [Pg.786]    [Pg.789]    [Pg.93]    [Pg.86]    [Pg.279]    [Pg.175]    [Pg.2163]    [Pg.649]    [Pg.196]    [Pg.143]    [Pg.11]    [Pg.321]    [Pg.295]    [Pg.607]    [Pg.1247]    [Pg.776]    [Pg.186]    [Pg.306]    [Pg.183]    [Pg.492]    [Pg.91]    [Pg.37]    [Pg.913]    [Pg.163]    [Pg.222]    [Pg.90]    [Pg.2717]    [Pg.347]    [Pg.268]   
See also in sourсe #XX -- [ Pg.511 , Pg.512 , Pg.513 , Pg.514 , Pg.515 , Pg.516 ]




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Flavonol

Flavonol glycosides

Flavonoles

Flavonols glycosides

Polyphenol glycoside

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