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01120590

Isovitexin

primary reference standard

Sinónimos:

6-C-Glucosylapigenin, Homovitexin, Saponaretin

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About This Item

Fórmula empírica (notación de Hill):
C21H20O10
Número de CAS:
38953-85-4
Peso molecular:
432.38
Beilstein:
66651
Número MDL:
MFCD00076044
Código UNSPSC:
85151701
ID de la sustancia en PubChem:
329747213
NACRES:
NA.24

grado

primary reference standard

caducidad

limited shelf life, expiry date on the label

fabricante / nombre comercial

HWI

aplicaciones

food and beverages

cadena SMILES

OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c2c(O)cc3OC(=CC(=O)c3c2O)c4ccc(O)cc4

InChI

1S/C21H20O10/c22-7-14-17(26)19(28)20(29)21(31-14)16-11(25)6-13-15(18(16)27)10(24)5-12(30-13)8-1-3-9(23)4-2-8/h1-6,14,17,19-23,25-29H,7H2/t14-,17-,19+,20-,21+/m1/s1

Clave InChI

MYXNWGACZJSMBT-VJXVFPJBSA-N

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Descripción general

Produced and qualified by HWI pharma services GmbH.
Exact content by quantitative NMR can be found on the certificate.

Acciones bioquímicas o fisiológicas

Phytochemical found in medicinal herbs. Antioxidant.

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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Certificados de análisis (COA)

Lot/Batch Number
HWI02820-1
HWI02820
HWI02131-1
HWI02131
HWI01807-2

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Rose bengal ≥96% (HPLC), Dye content 95 %

Sigma-Aldrich

330000

Rose bengal

Lipopolysaccharides from Escherichia coli O55:B5 γ-irradiated, BioXtra, suitable for cell culture

Sigma-Aldrich

L6529

Lipopolysaccharides from Escherichia coli O55:B5

Jong Min Kim et al.
Chemistry & biodiversity, 5(2), 352-356 (2008-02-23)
Ellagic acid (1), 3,3'-di-O-methylellagic acid (2), 3,3',4-tri-O-methylellagic acid (3), isovitexin (4), kaempferol 3-O-beta-D-glucuronide methyl ester (5), quercetin 3-O-alpha-L-arabinopyranosyl-(1-->6)-beta-D-galactopyranoside (6), ursolic acid, pomolic acid, tormentic acid, euscaphic acid, euscaphic acid 28-O-beta-D-glucopyranoside, and maslinic acid were isolated from the AcOEt- and BuOH-soluble
C Y Choo et al.
Journal of ethnopharmacology, 142(3), 776-781 (2012-06-12)
The leaves of Ficus deltoidea are used as a traditional medicine by diabetes patients in Malaysia. The objective of the study is to identify and evaluate bioactive constituents with in vivo α-glucosidase inhibition. The partitioned extracts, subfractions and pure bioactive
Yujie Fu et al.
Journal of separation science, 31(2), 268-275 (2008-01-16)
A method based on ultrasonic extraction (USE) followed by LC-MS is presented for the determination of vitexin and isovitexin in pigeonpea extracts in this study. The influential parameters of the USE procedure were optimized, and the optimal conditions were as
Yujie Fu et al.
Journal of chromatography. A, 1139(2), 206-213 (2006-12-05)
Vitexin and isovitexin are a pair of isomeric compounds known as the major constituents in pigeonpea leaves and possess various pharmacological activities. In the present study, the preparative separation of vitexin and isovitexin with macroporous resins (Nankai Hecheng S &
Tie-Jun Ling et al.
Molecules (Basel, Switzerland), 15(11), 8469-8477 (2010-11-23)
Four phenolics, salviaplebeiaside (1), γ-tocopherol (2), chrysosplenol-D (4), and isovitexin (5), along with α-tocoquinone (3) and β-sitosterol (6) were isolated from the aerial parts of Vitex negundo var. cannabifolia. The isolation was performed using bio-assay tracking experiments. The structures of
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