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74284

Sigma-Aldrich

Luteolin 7-O-β-D-Glucosid

≥98.0% (HPLC)

Synonym(e):

3′,4′,5,7-Tetrahydroxyflavon-7-glucosid, Cynarosid, Glucoluteolin, Glucosylluteolin, Luteolosid

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About This Item

Empirische Formel (Hill-System):
C21H20O11
CAS-Nummer:
5373-11-5
Molekulargewicht:
448.38
EG-Nummer:
226-365-8
MDL-Nummer:
MFCD06799436
UNSPSC-Code:
12352202
PubChem Substanz-ID:
329765596
NACRES:
NA.28

Assay

≥98.0% (HPLC)

Form

powder or crystals

Anwendung(en)

metabolomics
vitamins, nutraceuticals, and natural products

SMILES String

OC[C@H]1O[C@@H](Oc2cc(O)c3C(=O)C=C(Oc3c2)c4ccc(O)c(O)c4)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)30-9-4-12(25)17-13(26)6-14(31-15(17)5-9)8-1-2-10(23)11(24)3-8/h1-6,16,18-25,27-29H,7H2/t16-,18-,19+,20-,21-/m1/s1

InChIKey

PEFNSGRTCBGNAN-QNDFHXLGSA-N

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Allgemeine Beschreibung

Luteolin 7-O-β-D-glucoside (LUT-7G) is a flavonoid recently isolated from the Bidens parviflora Wild plant. It is a glycosylated form of luteolin present in many plants.

Biochem./physiol. Wirkung

Luteolin 7-O-β-D-glucoside possesses antioxidant, antiviral, and antibacterial properties. It is a hexokinase 2 (HEK2) inhibitor with anti-inflammatory and anti-proliferative activities. LUT-7G also exerts cardioprotective effects against H9c2 cells injury induced by oxidative stress.

Verpackung

Bottomless glass bottle. Contents are inside inserted fused cone.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Luteolin analytical standard

Supelco

72511

Luteolin

Isoverbascosid phyproof® Reference Substance

PHL89232

Isoverbascosid

Isoorientin ≥98% (HPLC)

Sigma-Aldrich

I1536

Isoorientin

Luteolin-7-diglucuronid phyproof® Reference Substance

PHL83412

Luteolin-7-diglucuronid

Apigenin-7-glucosid analytical standard

Supelco

44692

Apigenin-7-glucosid

Luteolin primary reference standard

03880590

Luteolin

Aucubin primary reference standard

00090590

Aucubin

Oleuropein ≥80% (HPLC)

Sigma-Aldrich

O8889

Oleuropein

Apigenin-7-O-glucuronid primary reference standard

04490590

Apigenin-7-O-glucuronid

Yu-Lan Li et al.
Molecules (Basel, Switzerland), 13(8), 1931-1941 (2008-09-17)
Fifteen flavonoids, 1-7 and 9-16, and a polyacetylene, 8, were isolated from the ethanol extract of the dried whole plant of Bidens parviflora Willd. by various chromatographic techniques. Their structures have been elucidated on the basis of spectroscopic analyses and
Ramona Palombo et al.
International journal of molecular sciences, 20(11) (2019-06-05)
Flavonoids have been demonstrated to affect the activity of many mammalian enzyme systems. Their functional phenolic groups are able to mediate antioxidant effects by scavenging free radicals. Molecules of this class have been found able to modulate the activity of
Meng-Na Wang et al.
Natural product research, 1-6 (2021-01-13)
A new flavonoid, saffloflavone , along with six known compounds, kaempferol-3-O-rutinoside, kaempferol-3-O-sophoroside, quercetin-3-O-β-d-glucoside, quercetin-7-O-β-d-glucoside, luteolin-7-O-β-d-glucoside and kaempferol 3-O-β-d-glucoside were isolated from the flowers of Carthamus tinctorius L. All the structures were determined by interpretation of their spectroscopic data. The cardioprotective
Yihui Yang et al.
Lipids in health and disease, 11, 38-38 (2012-03-15)
In folklore, some people take the decoction of Calyx seu Fructus Physalis (CSFP) for lowering blood lipids. The present study is designed to evaluate the lipid-lowering activities of CSFP, and search for its pharmacodynamical material. CSFP was extracted by water
Nadine Backhouse et al.
Journal of ethnopharmacology, 119(1), 160-165 (2008-07-22)
Leaf extracts of Buddleja globosa (Buddlejaceae) are used in Chilean folk medicine for wound healing. The anti-inflammatory (topic and per os), analgesic (per os) effects and the antioxidant activity of Buddleja globosa were for the first time reported by us.
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