Glycitin

CAS : 40246-10-4

Ref. 3D-MG08014

Informations sur le produit

• Nom: Glycitin
• Synonymes: 7-(β-D-Glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-oneGlycitein-7-O-β-D-glucoside, 3-(4-Hydroxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one, 3-(4-hydroxyphenyl)-6-methoxy-4-oxo-4H-chromen-7-yl beta-D-glucopyranoside, 4H-1-Benzopyran-4-one, 7-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-, 7-(β-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one, Glycitein 7-O-glucoside, Glycitein 7-O-β-glucoside, Glycitein-7-β-O-glucoside, 4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-, 7-(β-D-Glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one

Description

Glycitin is a plant extract that has been shown to have a variety of biological properties, including antioxidant, anti-inflammatory, and antitumor effects. It has been found to inhibit the synthesis of cholesterol and promote the production of bile acids in liver cells. Glycitin also inhibits growth by binding to DNA and inhibiting the activity of transcription factors. This compound can be isolated from plants such as Pueraria lobata, which contains high levels of isoflavones. Glycitin has been found to have an effect on cell proliferation in vitro assays with HL-60 cells at concentrations between 10 and 50 μg/mL but not at higher concentrations. The matrix effect may also play a role in its biological properties.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 446.4 g/mol
• Formule: C₂₂H₂₂O₁₀
• Degré de pureté: Min. 98 Area-%
• Couleur/Forme: White Powder
• InChI: 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
• Code InChI: InChIKey=OZBAVEKZGSOMOJ-MIUGBVLSSA-N
• SMILES: COc1cc2c(=O)c(-c3ccc(O)cc3)coc2cc1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O