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Names | |
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IUPAC name
(S)-2,3-Dihydro-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one
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Identifiers | |
520-33-2 ![]() |
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3D model (Jmol) | Interactive image |
ChEBI |
CHEBI:28230 ![]() |
ChEMBL |
ChEMBL399121 ![]() |
ChemSpider |
65234 ![]() |
DrugBank |
DB01094 ![]() |
ECHA InfoCard | 100.007.538 |
EC Number | 208-290-2 |
KEGG |
C01709 ![]() |
PubChem | 72281 |
UNII |
Q9Q3D557F1 ![]() |
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Properties | |
C16H14O6 | |
Molar mass | 302.28 g·mol−1 |
Melting point | 226–228 °C (439–442 °F; 499–501 K) |
Solubility in other solvents | Sol. EtOH, alkalis |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
Hesperetin (5,7,3',4'-OMe-flavan-on) is the 4'-methoxy derivative of eriodictyol, a flavanone. Hesperetin's 7-O-glycoside, hesperidin, is a naturally occurring flavanon-glycoside, the main flavonoid in lemons and sweet oranges. Hesperetin (and naringenin, the parent flavanone of naringin) are not found to a significant extent in Citrus spp.
A variety of glycosides of hesperetin are known, including:
Hesperidin 6-O-α-L-rhamnosyl-β-D-glucosidase is an enzyme that uses hesperidin and H2O to produce hesperetin and rutinose. It is found in the hyphomycetes species Stilbella fimetaria.