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About This Item
Empirical Formula (Hill Notation):
C22H22O10
CAS Number:
Molecular Weight:
446.40
UNSPSC Code:
12352201
NACRES:
NA.25
MDL number:
biological source
plant (Pueraria thunbergianaI)
Quality Level
assay
≥98% (HPLC)
form
powder
technique(s)
HPLC: suitable
color
white to faint beige
mp
203 - 204 °C ((397 - 399 °F ))
solubility
10 mg, clear, colorless to faintly yellow
storage temp.
room temp
SMILES string
O=C1C2=CC(OC)=C(O[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O3)C=C2OC=C1C4=CC=C(O)C=C4
InChI
1S/C22H22O10/c1-29-15-6-12-14(30-9-13(18(12)25)10-2-4-11(24)5-3-10)7-16(15)31-22-21(28)20(27)19(26)17(8-23)32-22/h2-7,9,17,19-24,26-28H,8H2,1H3/t17-,19-,20+,21-,22-/m1/s1
InChI key
OZBAVEKZGSOMOJ-MIUGBVLSSA-N
General description
Glycitin is an isoflavonoid recently found in flowers of Pueraria thunbergianaI. Glycitin can be modified into the metabolite glycitein which has anti-inflammatory properties.
Application
- The antioxidant Glycitin protects against intervertebral disc degeneration through antagonizing inflammation and oxidative stress in nucleus pulposus cells.: This study highlights Glycitin′s therapeutic potential in mitigating intervertebral disc degeneration by counteracting inflammatory and oxidative processes, demonstrating its viability as a bioactive compound for degenerative diseases (Zhao W et al., 2023).
- Spectrum-effect relationship study to reveal the pharmacodynamic substances in Flos Puerariae-Semen Hoveniae medicine pair for the treatment of alcohol-induced liver damage.: Analyzes the pharmacological effects of herbal components, including Glycitin, targeting liver damage recovery, illustrating the compound′s therapeutic relevance in traditional and modern medical applications (Zhang H et al., 2023).
Biochem/physiol Actions
Glycitin is a soy isoflavone in the glucoside form. A rat model study demonstrated glycitin to be effective in preventing bone loss and reversing the unfavorable changes of lipid metabolism in this model.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Isoflavone glycosides from the flowers of Pueraria thunbergiana.
Park HJ
Phytochemistry, 51, 147-151 (1999)
Kouya Yamaki et al.
Planta medica, 68(2), 97-100 (2002-02-23)
Previously, we reported that the isoflavones tectorigenin and tectoridin, a glycosylated tectorigenin, isolated from the rhizomes of Belamcanda chinensis have an activity to inhibit prostaglandin (PG) E2 production in 12-O-tetradecanoylphorbol 13-acetate (TPA)-stimulated rat peritoneal macrophages. The inhibitory effect of tectorigenin
Global Trade Item Number
| SKU | GTIN |
|---|---|
| G1296-5MG | 04061833628065 |
| G1296-25MG | 04061832389776 |