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74565

Sigma-Aldrich

Eriodictyol

≥95.0% (HPLC)

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C15H12O6
Numero CAS:
552-58-9
Peso molecolare:
288.25
Beilstein:
5104930
Numero CE:
209-016-4
Numero MDL:
MFCD00135890
Codice UNSPSC:
12352200
ID PubChem:
329764998
NACRES:
NA.25
Prezzi e disponibilità al momento non sono disponibili

Livello qualitativo

100

Saggio

≥95.0% (HPLC)

Stato

powder

Temperatura di conservazione

2-8°C

Stringa SMILE

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
SBHXYTNGIZCORC-ZDUSSCGKSA-N

Informazioni sul gene

mouse ... Hexa(15211)

Azioni biochim/fisiol

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]

Sostituito da

N° Catalogo
Descrizione
Determinazione del prezzo

94258

Eriodictyol, ≥95.0% (HPLC)

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCBX0041
BCBW5582
BCBW4677
BCBW1769

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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
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
Jakob P Ley et al.
Journal of agricultural and food chemistry, 53(15), 6061-6066 (2005-07-21)
Products made from Herba Santa (Eriodictyon californicum (H. & A.) Torr.) have been used as bitter remedies for some pharmaceutical applications for many years, but they are actually too aromatic to be useful for many food or pharmaceutical applications. In
M Clavin et al.
Journal of ethnopharmacology, 112(3), 585-589 (2007-06-16)
Three anti-inflammatory compounds: nepetin, jaceosidin and hispidulin have been isolated and identified from Eupatorium arnottianum Griseb. dichloromethane extract. Nepetin reduced the TPA mouse ear edema by 46.9% and jaceosidin by 23.2% (1mg/ear). Both compounds inhibited the NF kappaB induction by
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