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Merck

17804

Sigma-Aldrich

Isovitexin

≥98.0% (HPLC)

別名:

6-C-Glucosylapigenin, Homovitexin, Saponaretin

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About This Item

実験式(ヒル表記法):
C21H20O10
CAS番号:
分子量:
432.38
Beilstein:
66651
MDL番号:
UNSPSCコード:
85151701
PubChem Substance ID:
NACRES:
NA.25

アッセイ

≥98.0% (HPLC)

形状

powder

white to light yellow

mp

220 -221  °C ((428 - 430 °F))

SMILES記法

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

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アプリケーション

Isovitexin can be used to study biochemicals found in plants and nutrition. Isovitexin has been used in a study to assess collagenase inhibitors from Viola yedoensis. Isovitexin has also been used in a study to investigate the inhibitory activity of Gentiana lutea extracts on the enzyme myeloperoxidase (MPO), as well as the antioxidant activity of these extracts and their correlation with the total polyphenol content.

生物化学的/生理学的作用

Phytochemical found in medicinal herbs. Antioxidant.

その他情報

To gain a comprehensive understanding of our extensive range of Disaccharides for your research, we encourage you to visit our Carbohydrates Category page.

保管分類コード

11 - Combustible Solids

WGK

WGK 3

引火点(°F)

Not applicable

引火点(℃)

Not applicable

個人用保護具 (PPE)

Eyeshields, Gloves, type N95 (US)


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

Jan Code

17804-BULK:
17804-VAR:
17804-1MG:


試験成績書(COA)

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ビテキシン phyproof® Reference Substance

PHL89290

ビテキシン

Vicenin 2 primary reference standard

03980585

Vicenin 2

Loganin analytical standard

Supelco

36483

Loganin

ヒペロシド primary reference standard

00180585

ヒペロシド

Branislav Nastasijević et al.
Journal of pharmaceutical and biomedical analysis, 66, 191-196 (2012-04-24)
The aim of this study was to investigate the inhibitory activity of Gentiana lutea extracts on the enzyme myeloperoxidase (MPO), as well as the antioxidant activity of these extracts and their correlation with the total polyphenol content. Extracts were prepared
Kazuki Kanazawa et al.
Journal of agricultural and food chemistry, 60(17), 4359-4368 (2012-04-18)
It is desirable to increase the flavonoid contents of postharvest vegetables since flavonoids play a beneficial role in human health promotion. In the present study, we show that postharvest vegetables increasingly produced flavonoids when irradiated with light near the absorption
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 &

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