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01120590

Isovitexin

primary reference standard

Synonyme(s) :

6-C-Glucosylapigenin, Homovitexin, Saponaretin

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About This Item

Formule empirique (notation de Hill):
C21H20O10
Numéro CAS:
38953-85-4
Poids moléculaire :
432.38
Numéro Beilstein :
66651
Numéro MDL:
MFCD00076044
Code UNSPSC :
85151701
ID de substance PubChem :
329747213
Nomenclature NACRES :
NA.24

Qualité

primary reference standard

Durée de conservation

limited shelf life, expiry date on the label

Fabricant/nom de marque

HWI

Application(s)

food and beverages

Chaîne 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

Clé InChI

MYXNWGACZJSMBT-VJXVFPJBSA-N

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Description générale

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

Actions biochimiques/physiologiques

Phytochemical found in medicinal herbs. Antioxidant.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

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

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Sigma-Aldrich

330000

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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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