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Merck

75759

Sigma-Aldrich

Quercetin 3-O-α-L-arabinopyranoside

≥95% (HPLC)

Sinónimos:

3′,4′,5,7-Tetrahydroxyflavone 3-O-α-L-arabinoside, 3-(α-L-Arabinopyranosyloxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one, Feniculin, Foeniculin, Guaijaverin, Quercetin 3-O-α-L-arabinoside

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About This Item

Fórmula empírica (notación de Hill):
C20H18O11
Número de CAS:
Peso molecular:
434.35
Número MDL:
Código UNSPSC:
12352201
ID de la sustancia en PubChem:
NACRES:
NA.25

Nivel de calidad

Ensayo

≥95% (HPLC)

Formulario

powder

temp. de almacenamiento

room temp

cadena SMILES

O[C@H]1CO[C@@H](OC2=C(Oc3cc(O)cc(O)c3C2=O)c4ccc(O)c(O)c4)[C@H](O)[C@H]1O

InChI

1S/C20H18O11/c21-8-4-11(24)14-13(5-8)30-18(7-1-2-9(22)10(23)3-7)19(16(14)27)31-20-17(28)15(26)12(25)6-29-20/h1-5,12,15,17,20-26,28H,6H2/t12-,15-,17+,20-/m0/s1

Clave InChI

PZZRDJXEMZMZFD-IEGSVRCHSA-N

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Descripción general

Quercetin 3-O-α-L-arabinopyranoside was isolated from the leaves of the Ruprechtia polystachya tree.

Acciones bioquímicas o fisiológicas

Plant flavonoid which exhibits antibacterial and antioxidant activities. It shows significantly strong ABTS radical scavenging activity, inhibitory activity against urease of quercetin glycosides isolated from Allium cepa and Psidium guajava. It is a potential antiplaque agent against Streptococcus mutans.
quercetin 3-O-α-L-arabinopyranoside was shown to inhibit the activity of glucose-6-phosphatase.

Envase

Bottomless glass bottle. Contents are inside inserted fused cone.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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1 of 4

Maryan Bruzual De Abreu et al.
Chemistry & biodiversity, 8(11), 2126-2134 (2011-11-16)
Two new compounds, 5-methyl-2-(2-methylbutanoyl)phloroglucinol 1-O-(6-O-β-D-apiofuranosyl)-β-D-glucopyranoside (1) and trans-2,3-dihydrokaempferol 3-O-(4-O-sulfo)-α-L-arabinopyranoside (2), together with 14 known flavonoids, trans-dihydrokaempferol 3-O-α-L-arabinopyranoside (3), trans-taxifolin 3-O-α-L-arabinofuranoside (4), quercetin 3-O-α-L-rhamnopyranoside (5), quercetin 3'-O-α-L-arabinofuranoside (6), catechin 3-O-α-L-rhamnopyranoside (7), trans-taxifolin 3-O-α-L-arabinopyranoside (8), cis-dihydrokaempferol 3-O-α-L-arabinopyranoside (9), catechin (10), myricetin 3-O-α-L-rhamnopyranoside
G R Prabu et al.
Journal of applied microbiology, 101(2), 487-495 (2006-08-03)
The aim of the present study was to investigate the anti-Streptococcus mutans activity and the in vitro effects of subminimal inhibitory concentrations of guaijaverin isolated from Psidium guajava Linn. on cariogenic properties of Strep. mutans. Bioautography-directed chromatographic fractionation, yield biologically
Huaguo Chen et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 35(10), 1284-1286 (2010-08-17)
The aim of the paper was to develop a HPLC method for the quality control of Periploca forrestii Schltr. The 18 samples were analyzed on a Hypersil C18 column. The mobile phase was methanol-water (33:67) and the flow rate was
Samah Shabana et al.
Bioscience, biotechnology, and biochemistry, 74(4), 878-880 (2010-04-10)
Methanolic extracts of edible plants and seaweeds were tested for their inhibitory activity against Jack bean urease. Quercetin-4'-O-beta-D-glucopyranoside was isolated from Allium cepa as a urease inhibitor with an IC(50) value of 190 microM-. Quercetin and two quercetin glycosides, avicularin
X Lozoya et al.
Archives of medical research, 25(1), 11-15 (1994-01-01)
The traditional herbal remedy from Psidium guajava leaves has been medically proposed in Mexico as effective treatment of acute diarrhea. A methanolic leaf extract was subjected to a bioassay-guided isolation of spasmolytic constituents. Six fractions were separated on a polyvinylpolypyrrolidine

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