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Eriodictyol

From Wikipedia, the free encyclopedia
Eriodictyol
Names
IUPAC name
(2S)-3′,4′,5,7-Tetrahydroxyflavan-4-one
Systematic IUPAC name
(2S)-2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydro-4H-1-benzopyran-4-one
Other names
Eriodictiol
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.008.198Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2/t13-/m0/s1 ☒N
    Key: SBHXYTNGIZCORC-ZDUSSCGKSA-N ☒N
  • InChI=1/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2/t13-/m0/s1
    Key: SBHXYTNGIZCORC-ZDUSSCGKBZ
  • O=C2c3c(O[C@H](c1ccc(O)c(O)c1)C2)cc(O)cc3O
Properties
C15H12O6
Molar mass288.255 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Eriodictyol is abitter-maskingflavanone, aflavonoid extracted from yerba santa (Eriodictyon californicum), a plant native toNorth America.[1] Eriodictyol is one of the fourflavanones identified in this plant as having taste-modifying properties, the other three beinghomoeriodictyol, its sodium salt, andsterubin.[2]

Eriodictyol has garnered scientific attention for its strongantioxidant,anti-inflammatory, and neuroprotective properties. Structurally similar to other flavonoids, such as hesperidin and naringenin, eriodictyol scavenges free radicals and regulates inflammatory responses.

Eriodictyol was also found in the twigs ofMillettia duchesnei,[3] inEupatorium arnottianum,[4] and its glycosides (eriocitrin) in lemons androse hips (Rosa canina).[5]

Eriodictyol belongs to theflavanone subclass of flavonoids and has a chemical structure defined by the molecular formula C15H12O6, with a molecular weight of 288.25 g/mol.[6]

References

[edit]
  1. ^Kaminski, Patricia; Katz, Richard."Yerba SantaEriodictyon californicum".Flower Essence Society. Retrieved2022-01-20.
  2. ^Ley JP, Krammer G, Reinders G, Gatfield IL, Bertram HJ (July 2005). "Evaluation of bitter masking flavanones from Herba Santa (Eriodictyon californicum (H. and A.) Torr., Hydrophyllaceae)".J. Agric. Food Chem.53 (15):6061–6.doi:10.1021/jf0505170.PMID 16028996.
  3. ^Ngandeu F, Bezabih M, Ngamga D, et al. (January 2008). "Rotenoid derivatives and other constituents of the twigs of Millettia duchesnei".Phytochemistry.69 (1):258–63.doi:10.1016/j.phytochem.2007.05.038.PMID 17640692.
  4. ^Clavin M, Gorzalczany S, Macho A, et al. (July 2007). "Anti-inflammatory activity of flavonoids from Eupatorium arnottianum".J Ethnopharmacol.112 (3):585–9.doi:10.1016/j.jep.2007.04.007.PMID 17570627.
  5. ^Hvattum E (2002). "Determination of phenolic compounds in rose hip (Rosa canina) using liquid chromatography coupled to electrospray ionisation tandem mass spectrometry and diode-array detection".Rapid Commun. Mass Spectrom.16 (7):655–62.Bibcode:2002RCMS...16..655H.doi:10.1002/rcm.622.PMID 11921243.
  6. ^"Eriodictyol".FoodStruct. Retrieved1 October 2024.

External links

[edit]
Flavanones and theirglycosides
Flavanones
O-methylated flavanones
C-methylated flavanones
Glycosides
Acetylated
Acetylated glycosides
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