Pyranoanthocyanin
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The pyranoanthocyanins are a type of pyranoflavonoids. They are chemical compounds formed in
red wine Red wine is a type of wine made from dark-colored grape varieties - (red grapes.) The color of the wine can range from intense violet, typical of young wines, through to brick red for mature wines and brown for older red wines. The juice fro ...
s by
yeast Yeasts are eukaryotic, single-celled microorganisms classified as members of the fungus kingdom (biology), kingdom. The first yeast originated hundreds of millions of years ago, and at least 1,500 species are currently recognized. They are est ...
during
fermentation Fermentation is a type of anaerobic metabolism which harnesses the redox potential of the reactants to make adenosine triphosphate (ATP) and organic end products. Organic molecules, such as glucose or other sugars, are catabolized and reduce ...
processes or during controlled oxygenation processes during the
aging of wine The aging of wine is potentially able to improve the quality of wine. This distinguishes wine from most other consumable goods. While wine is perishable and capable of deteriorating, complex chemical reactions involving a wine's sugars, acids ...
. The different classes of pyranoanthocyanins are carboxypyranoanthocyanins, methylpyranoanthocyanins, pyranoanthocyanin-flavanols, pyranoanthocyanin-phenols, portisins, oxovitisins and pyranoanthocyanin dimers; their general structure includes an additional ring (formed between the OH group at C-5 and the C-4 of the anthocyanin pyranic ring) that may have different substituents linked directly at C-10.


Examples

* Carboxypyranoanthocyanidins, can be considered markers of microoxygenation techniques * Hydroxyphenyl-pyranoanthocyanins * Vitisin A and B * Pinotins *
Portosins Portosins are Vinyl group, vinylpyranoanthocyanins, a type of blueish phenolic pigments, found in aged port wine. See also * Wine color References

Pyranoanthocyanins {{aromatic-stub ...
(vinylpyranoanthocyanins)


Vitisin A type

* Cyanidin-3-O-glucoside-pyruvic acid (m/z of +H ion:517, λmax 506 nm) * Cyanidin-3-O-acetylglucoside-pyruvic acid (559 - 507) * Cyanidin-coumaroylglucoside-pyruvic acid (661 - 507 nm) * Delphinidin-3-O-glucoside-pyruvic acid (533 - 507 nm) * Delphinidin-3-O-acetylglucoside-pyruvic acid (575 - 509 nm) * Delphinidin-3-O-coumaroylglucoside-pyruvic acid (679 - 511 nm) * Peonidin-3-O-glucoside-pyruvic acid (531 - 509 nm) * Peonidin-3-O-acetylglucoside-pyruvic acid (573 - 510 nm) * Peonidin-3-O-coumaroylglucoside-pyruvic acid (677 - 511 nm) * Petunidin-3-O-glucoside-pyruvic acid (547 - 508 nm) * Petunidin-3-O-acetylglucoside-pyruvic acid (589 - 509 nm) * Petunidin-3-O-coumaroylglucoside-pyruvic acid (693 - 510 nm) * Malvidin-3-O-glucoside-pyruvic acid (561 - 513 nm) * Malvidin-3-O-acetylglucoside-pyruvic acid (603 - 516 nm) * Malvidin-3-O-coumaroylglucoside-pyruvic acid (707 - 513 nm)


Vitisin B type

* Malvidin-3-O-glucoside-acetaldehyde (517 - 490 nm) * Malvidin-3-O-acetylglucoside-acetaldehyde (559 - 494 nm) * Malvidin-3-O-coumaroylglucoside-acetaldehyde (663 - 497 nm)


Oxovitisins

Oxovitisins are pyranone-anthocyanin derivatives * Pyranone-malvidin-3-glucoside ( Oxovitisin A) * Pyranone-malvidin-3-coumaroylglucoside


Pinotin type

* Delphinidin-3-O-glucoside-4-vinylcatechol (597 - 510 nm) * Delphinidin-3-O-acetylglucoside-4-vinylcatechol (639 - 512 nm) * Delphinidin-3-O-coumaroylglucoside-4-vinylcatechol (743 - 514 nm) * Peonidin-3-O-glucoside-4-vinylcatechol (595 - 504 nm) * Peonidin-3-O-acetylglucoside-4-vinylcatechol (637 - 506 nm) * Peonidin-3-O-coumaroylglucoside-4-vinylcatechol (741 - 508 nm) * Petunidin-3-O-glucoside-4-vinylcatechol (611 - 510 nm) * Petunidin-3-O-acetylglucoside-4-vinylcatechol (653 - 512 nm) * Petunidin-3-O-coumaroylglucoside-4-vinylcatechol (757 - 516 nm) * Malvidin-3-O-glucoside-4-vinylcatechol (625 - 512 nm) * Malvidin-3-O-acetylglucoside-4-vinylcatechol (667 - 514 nm) * Malvidin-3-O-coumaroylglucoside-4-vinylcatechol (771 - 514 nm) * Delphinidin-3-O-glucoside-4-vinylphenol (581 - 504 nm) * Delphinidin-3-O-acetylglucoside-4-vinylphenol (623 - 506 nm) * Delphinidin-3-O-coumaroylglucoside-4-vinylphenol (727 - 506 nm) * Peonidin-3-O-glucoside-4-vinylphenol (579 - 499 nm) * Peonidin-3-O-acetylglucoside-4-vinylphenol (621 - 504 nm) * Peonidin-3-O-coumaroylglucoside-4-vinylphenol (725 - 505 nm) * Petunidin-3-O-glucoside-4-vinylphenol (595 - 504 nm) * Petunidin-3-O-acetylglucoside-4-vinylphenol (636 - 506 nm) * Petunidin-3-O-coumaroylglucoside-4-vinylphenol (741 - 507 nm) * Malvidin-3-O-glucoside-4-vinylphenol (609 - 504 nm) * Malvidin-3-O-acetylglucoside-4-vinylphenol (651 - 507 nm) * Malvidin-3-O-coumaroylglucoside-4-vinylphenol (755 - 509 nm) * Malvidin-3-O-caffeoylglucoside-4-vinylphenol (771 - 532 nm) * Delphinidin-3-O-glucoside-4-vinylguaiacol (611 - 502 nm) * Peonidin-3-O-glucoside-4-vinylguaiacol (609 - 499 nm) * Petunidin-3-O-glucoside-4-vinylguaiacol (625 - 502 nm) * Malvidin-3-O-glucoside-4-vinylguaiacol (639 - 504 nm) * Malvidin-3-O-acetylglucoside-4-vinylguaiacol (681 - 506 nm) * Malvidin-3-O-coumaroylglucoside-vinylguaiacol (755 477 508 nm)


Flavanyl-pyranoanthocyanin type

* Delphinidin-3-O-glucoside-4-vinyl(epi)catechin (777 - 501 nm) * Delphinidin-3-O-acetylglucoside-4-vinyl(epi)catechin (819 - 503 nm) * Peonidin-3-O-glucoside-4-vinyl(epi)catechin (775 - 199 nm) * Peonidin-3-O-acetylglucoside-4-vinyl(epi)catechin (817 - 501 nm) * Petunidin-3-O-glucoside-4-vinyl(epi)catechin (791 - 502 nm) * Petunidin-3-O-acetylglucoside-4-vinyl(epi)catechin (833 - 504 nm) * Malvidin-3-O-glucoside-4-vinyl(epi)catechin (805 - 503 nm) * Malvidin-3-O-acetylglucoside-4-vinyl(epi)catechin (847 - 508 nm) * Malvidin-3-O-coumaroylglucoside-4-vinyl(epi)catechin (951 - 503 nm)Anthocyanins and Their Variation in Red Wines II. Anthocyanin Derived Pigments and Their Color Evolution. Fei He, Na-Na Liang, Lin Mu, Qiu-Hong Pan, Jun Wang, Malcolm J. Reeves and Chang-Qing Duan, Molecules, 2012, 17, pages 1483-1519,


References


See also

*
Phenolic compounds in wine Phenolic compounds— natural phenol and polyphenols—occur naturally in wine. These include a large group of several hundred chemical compounds that affect the taste, color and mouthfeel of wine. These compounds include phenolic acids, sti ...
{{Pyranoanthocyanidin