Direkt zum Inhalt
Merck
Alle Fotos(1)

Wichtige Dokumente

Gesamtdokumentation anzeigen

74565

Sigma-Aldrich

Eriodictyol

≥95.0% (HPLC)

Synonym(e):

(S)-3′,4′,5,7-Tetrahydroxy-flavanon, Eriodictiol, Huazhongilexon

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)

About This Item

Empirische Formel (Hill-System):
C15H12O6
CAS-Nummer:
552-58-9
Molekulargewicht:
288.25
Beilstein:
5104930
EG-Nummer:
209-016-4
MDL-Nummer:
MFCD00135890
UNSPSC-Code:
12352200
PubChem Substanz-ID:
329764998
NACRES:
NA.25

Qualitätsniveau

100

Assay

≥95.0% (HPLC)

Form

powder

Lagertemp.

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

InChIKey

SBHXYTNGIZCORC-ZDUSSCGKSA-N

Angaben zum Gen

mouse ... Hexa(15211)

Biochem./physiol. Wirkung

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

Ersetzt durch

Produkt-Nr.
Beschreibung
Preisangaben

94258

Eriodictyol, ≥95.0% (HPLC)

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCBX0041
BCBW5582
BCBW4677
BCBW1769

Die passende Version wird nicht angezeigt?

Wenn Sie eine bestimmte Version benötigen, können Sie anhand der Lot- oder Chargennummer nach einem spezifischen Zertifikat suchen.

Suche nach COA

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

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
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
Jennifer Johnson et al.
Investigative ophthalmology & visual science, 50(5), 2398-2406 (2009-01-02)
Eriodictyol, a flavonoid found in citrus fruits, is among the most potent compounds reported to protect human RPE cells from oxidative stress-induced cell death. The present study sought to determine whether eriodictyol-induced phase 2 protein expression further enhances the resistance
Alle zugehörigen Dokumente anzeigen

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.