16733

Quercetin 3-O-(6″-O-malonyl)-β-D-glucoside

≥85% (HPLC)

• Synonyme(s) : Quercetin 3-O-malonylglucoside
• Formule empirique (notation de Hill) : C₂₄H₂₂O₁₅
• Numéro CAS: 96862-01-0
• Poids moléculaire : 550.42
• UNSPSC Code: 12352201
• NACRES: NA.25
• PubChem Substance ID: 329751366
• MDL number: MFCD20527305
• Beilstein/REAXYS Number: 6625918

Propriétés

• Quality Segment: 100
• assay: ≥85% (HPLC)
• form: powder
• storage temp.: −20°C
• SMILES string: O[C@H]1[C@H](O)[C@@H](COC(=O)CC(O)=O)O[C@@H](OC2=C(Oc3cc(O)cc(O)c3C2=O)c4ccc(O)c(O)c4)[C@@H]1O
• InChI: 1S/C24H22O15/c25-9-4-12(28)17-13(5-9)37-22(8-1-2-10(26)11(27)3-8)23(19(17)33)39-24-21(35)20(34)18(32)14(38-24)7-36-16(31)6-15(29)30/h1-5,14,18,20-21,24-28,32,34-35H,6-7H2,(H,29,30)/t14-,18-,20+,21-,24+/m1/s1
• InChI key: NBQPHANHNTWDML-UJKBSQBPSA-N

Description

General description

The flavonoid quercetin 3-O-(6-O-malonyl)glucoside, a conjugate of quercetin, was identified in the green-leafed lettuce Lactuca sativum.

Biochem/physiol Actions

Metabolite in flavone and flavonol biosynthesis, is found in plants like the fruit peel of Sicana odorifera and mulberry leaves, shows antioxidant activity. Q3MG also potentially has antiatherogenic protective effects; and found to improve hyperglycemia in obese mice and reduced oxidative stress in the liver.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Informations sur la sécurité

• pictograms: GHS06
• signalword: Danger
• hcodes: H301
• pcodes: P301 + P310
• Hazard Classifications: Acute Tox. 3 Oral
• Classe de stockage: 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable