16733
Quercetin 3-O-(6″-O-malonyl)-β-D-glucoside
≥85% (HPLC)
Synonym(s):
Quercetin 3-O-malonylglucoside
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About This Item
Empirical Formula (Hill Notation):
C24H22O15
CAS Number:
Molecular Weight:
550.42
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
6625918
Quality Segment
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
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.
signalword
Danger
hcodes
pcodes
Hazard Classifications
Acute Tox. 3 Oral
Storage Class
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
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Global Trade Item Number
| SKU | GTIN |
|---|---|
| D120405-25G | 04061833558966 |
| 16733-1MG | 04061838749536 |