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Merck
CN

89948

鸢尾苷

analytical standard

别名:

D-Glucopyranosyloxy)-5-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one, Shekanin, Tectorigenin 7-O-β-D-glucopyranoside

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关于此项目

经验公式（希尔记法）:
C22H22O11
化学文摘社编号:
611-40-5
分子量:
462.40
NACRES:
NA.24
PubChem Substance ID:
329769568
UNSPSC Code:
85151701
MDL number:
MFCD04039835

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产品名称

鸢尾苷, analytical standard

InChI

1S/C22H22O11/c1-30-21-14(32-22-20(29)19(28)17(26)15(8-23)33-22)7-13-16(18(21)27)11(25)6-12(31-13)9-2-4-10(24)5-3-9/h2-7,15,17,19-20,22-24,26-29H,8H2,1H3/t15-,17-,19+,20-,22-/m1/s1

SMILES string

O[C@@H]1[C@@H](O)[C@H](OC2=CC(OC(C3=CC=C(O)C=C3)=CC4=O)=C4C(O)=C2OC)O[C@H](CO)[C@H]1O

InChI key

GCLAFEGUXXHIFT-IWLDQSELSA-N

grade

analytical standard

assay

≥98% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

food and beverages

format

neat

storage temp.

2-8°C

Quality Level

100

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCH6407
BCCF0989
BCCB8093
BCBV2408
BCBS7355V

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Kyoung Ah Kang et al.
European journal of pharmacology, 519(1-2), 16-23 (2005-08-17)
In the present study, the antioxidative properties of tectorigenin, a metabolite formed by transformation of tectoridin by intestinal microflora, were investigated. Tectorigenin was found to scavenge intracellular reactive oxygen species, and 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical, and thus prevented lipid peroxidation. The
JangJa Hong et al.
Inflammation & allergy drug targets, 7(3), 195-202 (2008-09-11)
Effects of compounds isolated from medicinal plants in Korea on prostaglandin E2 (PGE2) production in rat peritoneal macrophages were examined, and mechanism of action of the active constituents was analyzed. The active constituents were as follows; tectorigenin and tectoridin isolated
Yong Chen et al.
The Journal of pharmacy and pharmacology, 60(6), 709-716 (2008-05-24)
In this work, liquid chromatography-electrospray ionization tandem ion-trap mass spectrometry (LC-MS(n)) was used to investigate the in-vivo and in-vitro metabolism of tectoridin. After oral administration of a single dose (100 mg kg(-1)) of tectoridin to healthy rats, faeces and urine
Cheng-Feng Luo et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(19), 1497-1501 (2011-04-23)
A highly sensitive and specific method of rapid resolution liquid chromatography tandem mass spectrometry (RRLC-MS/MS) in positive ionization mode has been developed and validated for pharmacokinetic study of puerarin in rat plasma. Chromatography was carried out on a Zorbax XDB
Kyungsu Kang et al.
Molecules and cells, 27(3), 351-357 (2009-03-28)
Phytoestrogens are the natural compounds isolated from plants, which are structurally similar to animal estrogen, 17beta-estradiol. Tectoridin, a major isoflavone isolated from the rhizome of Belamcanda chinensis. Tectoridin is known as a phytoestrogen, however, the molecular mechanisms underlying its estrogenic
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