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Eriodictyol

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Eriodictyol
Names
IUPAC name
(2S)-3′,4′,5,7-Tetrahydroxyflavan-4-one
Preferred 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 InfoCard 100.008.198 Edit this at Wikidata
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 mass 288.255 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Eriodictyol is a bitter-masking flavanone, a flavonoid extracted from yerba santa (Eriodictyon californicum), a plant native to North America.[1] Eriodictyol is one of the four flavanones identified in this plant as having taste-modifying properties, the other three being homoeriodictyol, its sodium salt, and sterubin.[2]

Eriodictyol was also found in the twigs of Millettia duchesnei,[3] in Eupatorium arnottianum,[4] and its glycosides (eriocitrin) in lemons and rose hips (Rosa canina).[5]


References

  1. ^ Kaminski, Patricia; Katz, Richard. "Yerba Santa Eriodictyon californicum". Flower Essence Society. Retrieved 2022-01-20.
  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.
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