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74565

Sigma-Aldrich

Eriodictyol

≥95.0% (HPLC)

Synonym(s):

(S)-3′,4′,5,7-Tetrahydroxyflavanone, Eriodictiol, Huazhongilexone

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About This Item

Empirical Formula (Hill Notation):
C15H12O6
CAS Number:
552-58-9
Molecular Weight:
288.25
Beilstein:
5104930
EC Number:
209-016-4
MDL number:
MFCD00135890
UNSPSC Code:
12352200
PubChem Substance ID:
329764998
NACRES:
NA.25

Quality Level

100

Assay

≥95.0% (HPLC)

form

powder

storage temp.

2-8°C

SMILES string

Oc1cc(O)c2C(=O)C[C@H](Oc2c1)c3ccc(O)c(O)c3

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

InChI key

SBHXYTNGIZCORC-ZDUSSCGKSA-N

Gene Information

mouse ... Hexa(15211)

Biochem/physiol Actions

The flavanone eriodictyol is a metabolite in the flavonoid biosynthesis pathway. Eriodictyol has anti-inflammatory and antioxidant activities[1] and taste-modifying properties; it is extracted from plants such as Eriodictyon californicum[2], the twigs of Millettia duchesnei,[3] in Eupatorium arnottianum,[4] lemons and as glycoside in rose hips (Rosa canina).[5]

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Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBX0041
BCBW5582
BCBW4677
BCBW1769

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Erlend Hvattum
Rapid communications in mass spectrometry : RCM, 16(7), 655-662 (2002-03-29)
Liquid chromatography coupled with negative and positive electrospray ionisation (ESI) tandem mass spectrometry (MS/MS) and diode-array detection (DAD) was used for determination of phenols in rose hip (Rosa canina) extract. ESI mass spectra of the chromatographically separated phenols gave the
Manar M Salem et al.
Journal of natural products, 68(1), 108-111 (2005-02-01)
Bioactivity-guided fractionation of the methanolic extract of Psorothamnus polydenius yielded the new chalcone 2,2',4'-trihydroxy-6'-methoxy-3',5'-dimethylchalcone (2), together with six other known compounds, 2',4'-dihydroxy-6'-methoxy-3',5'-dimethylchalcone (1), dalrubone (3), demethoxymatteucinol (4), eriodictyol (5), and photodalrubone (6a and 6b). This is the first report of
François Ngandeu et al.
Phytochemistry, 69(1), 258-263 (2007-07-21)
Three prenylated rotenoids, elliptol, 12-deoxo-12alpha-methoxyelliptone and 6-methoxy-6a,12a-dehydrodeguelin were isolated from the twigs of Millettia duchesnei, together with the known compounds, 6a,12a-dehydrodeguelin, 6-hydroxy-6a,12a-dehydrodeguelin, 6-oxo-6a,12a-dehydrodeguelin, elliptone, 12a-hydroxyelliptone and eriodictyol. Their structures were elucidated on the basis of spectral data and comparison with
B A 'T Hart et al.
Chemico-biological interactions, 73(2-3), 323-335 (1990-01-01)
The mechanism by which (a panel of) flanonoids inhibit the production of luminol-dependent chemiluminescence (CLlum) by activated human neutrophils is subject to this study. CLlum is frequently used as a bio-assay to quantify the effect of xenobiotics on the production
Defang Li et al.
Frontiers in pharmacology, 9, 33-33 (2018-02-15)
Myocardial ischemia-reperfusion (I/R) injury remains the leading risk factor of disability and mortality worldwide. In this study, the myocardial protective effect of eriodictyol (EDT) and the underlying mechanism in an
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