17793

Quercetin 3-β-D-glucoside

≥90% (HPLC)

• Sinónimos: 3,3′,4′,5,7-Pentahydroxyflavone 3-β-glucoside, Isoquercitrin
• Fórmula empírica (notación de Hill): C₂₁H₂₀O₁₂
• Número de CAS: 482-35-9
• Peso molecular: 464.38
• Beilstein: 100989
• Número MDL: MFCD00017746
• Código UNSPSC: 12352205
• ID de la sustancia en PubChem: 57647673
• NACRES: NA.25

Propiedades

• Nivel de calidad: 100
• Ensayo: ≥90% (HPLC)
• aplicaciones: metabolomics; vitamins, nutraceuticals, and natural products
• temp. de almacenamiento: −20°C
• cadena SMILES: OC[C@H]1O[C@@H](OC2=C(Oc3cc(O)cc(O)c3C2=O)c4ccc(O)c(O)c4)[C@H](O)[C@@H](O)[C@@H]1O
• InChI: 1S/C21H20O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-18,21-27,29-30H,6H2/t13-,15-,17+,18-,21+/m1/s1
• Clave InChI: OVSQVDMCBVZWGM-QSOFNFLRSA-N
• Información sobre el gen: mouse ... Hexa(15211)

Descripción

Descripción general

Quercetin 3-β-D-glucoside (Q3G), also known as isoquercitrin, is one of the major glycosidic forms of quercetin.[1] It is a mono-glucoside, first isolated from the seed pods of Cercis canadensis L., it is also found in various plants, vegetables, and fruits.[1] Q3G has the basic chemical structure of a flavonoid, with a glucose molecule attached to the C-3 of quercetin.[1]

Aplicación

Quercetin 3-β-D-glucoside has been used:

• as a dietary flavonoid supplement to check its binding capacity with human small ubiquitin-related modifier 1 (SUMO1) protein using surface plasmon resonance (SPR)[2]
• as an inhibitor for Escherichia coli adenosine triphosphate (ATP) synthase[3]
• as an anti-aggregation agent to test its activity against β-amyloid, green fluorescent protein (GFP), and chymotrypsinogen proteins[4]

Acciones bioquímicas o fisiológicas

Quercetin 3-β-D-glucoside possesses strong antioxidant and anti-inflammatory activities.[1] Being a potent oxygen-radical scavenger, it is a neuroprotective agent that improves Alzheimer′s disease (AD) condition in mice models.[5] It has shown antiproliferative activity against colon, lung, and hepatocellular cell lines[6] and MCF-7 human breast cancer cells in combination with apple extracts.[7]

Envase

Bottomless glass bottle. Contents are inside inserted fused cone.

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Equipo de protección personal: Eyeshields, Gloves, type N95 (US)