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Merck
모든 사진(1)

문서

01120590

Isovitexin

primary reference standard

동의어(들):

6-C-Glucosylapigenin, Homovitexin, Saponaretin

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모든 사진(1)

About This Item

실험식(Hill 표기법):
C21H20O10
CAS Number:
38953-85-4
Molecular Weight:
432.38
Beilstein:
66651
MDL number:
MFCD00076044
UNSPSC 코드:
85151701
PubChem Substance ID:
329747213
NACRES:
NA.24

Grade

primary reference standard

유통기한

limited shelf life, expiry date on the label

제조업체/상표

HWI

응용 분야

food and beverages

SMILES string

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

InChI key

MYXNWGACZJSMBT-VJXVFPJBSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

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

생화학적/생리학적 작용

Phytochemical found in medicinal herbs. Antioxidant.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

Choose from one of the most recent versions:

시험 성적서(COA)

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

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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

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
María Inés Ragone et al.
Journal of ethnopharmacology, 113(2), 258-266 (2007-07-21)
The spasmolytic effects of an acqueous extract of cedrón (AEC) were studied on rat isolated duodenums. This plant (Aloysia citriodora Palau, Verbenaceae) is widely used for gastrointestinal disorders and as eupeptic in South America. AEC non-competitively inhibited the dose-response curve
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 &
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
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