G1296
Glycitin
≥98% (HPLC)
Synonym(s):
4′,7-Dihydroxy 6-methoxyisoflavone 7-O-glucoside, 4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-, Glycitein 7-O-β-glucoside
About This Item
Recommended Products
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
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General description
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
Packaging
Other Notes
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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