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Quercitrin

Quercitrin
Quercitrin.png
Names
IUPAC name
2-(3,4-Dihydroxyphenyl)-5,7- dihydroxy-3-[ [(2S,3R,4R,5R,6S)- 3,4,5-trihydroxy-6-methyl-2- tetrahydropyranyl]oxy]-4-chromenone
Other names
Quercetin 3-O-a-L-rhamnoside
Thujin
Quercetin 3-rhamnoside
Quercetin-3-rhamnoside
Quercetin-3-L-rhamnoside
Identifiers
522-12-3 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:17558 N
ChEMBL ChEMBL82242 N
ChemSpider 4444112 N
ECHA InfoCard 100.007.567
PubChem 5280459
UNII 2Y8906LC5P N
Properties
C21H20O11
Molar mass 448.38 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YesYN ?)
Infobox references

Quercitrin is a glycoside formed from the flavonoid quercetin and the deoxy sugar rhamnose.

Austrian chemist Heinrich Hlasiwetz (1825-1875) is remembered for his chemical analysis of quercitrin.

Quercitrin is a constituent of the dye quercitron. It can be found in Tartary buckwheat (Fagopyrum tataricum) and in oaks species like the North American white oak (Quercus alba) and English oak (Quercus robur). It is also found in Nymphaea odorata or Taxillus kaempferi.

The enzyme quercitrinase catalyzes the chemical reaction between quercitrin and H2O to yield L-rhamnose and quercetin.


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