Glycitin

Glycitin
  • CAS No.:40246-10-4
Other grades of this product :
Glycitin Basic information
Product Name:Glycitin
Synonyms:Glycitin, froM GlycineMax (L.) Merr.;4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-;Glycitin, >99%;Glycitin, >=98%;Daidzin/Glycitin;Glycitein-7-.beta.-O-glucoside;Glycitin, 98%, from Glycinemax (L.) merr.;4H-1-Benzopyran-4-one 7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-Glycitein Glycitein 7-O-β-glucoside
CAS:40246-10-4
MF:C22H22O10
MW:446.41
EINECS:
Product Categories:The group of Daidzin;Intermediates & Fine Chemicals;Miscellaneous Natural Products;Pharmaceuticals;Aromatics;Glucuronides;Heterocycles;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;inhibitor;Inhibitors
Mol File:40246-10-4.mol
Glycitin Chemical Properties
Melting point 2100C
Boiling point 751.1±60.0 °C(Predicted)
density 1.545
storage temp. room temp
solubility DMSO (Slightly, Sonicated), Methanol (Slightly, Heated)
pka9.62±0.30(Predicted)
form Solid
color White to Off-White
Stability:Hygroscopic
CAS DataBase Reference40246-10-4(CAS DataBase Reference)
Safety Information
Safety Statements 24/25
WGK Germany 3
HS Code 29389090
MSDS Information
Glycitin Usage And Synthesis
Chemical PropertiesWhite Solid
UsesA derivative of Glycitein. Inhibitor
UsesA metabolite of isoflavone derivatives.
UsesA metabolite of isoflavone derivatives. A derivative of Glycitein. Inhibitor.
DefinitionChEBI: A glycosyloxyisoflavone that is isoflavone substituted by a methoxy group at position 6, a hydroxy group at position 4' and a beta-D-glucopyranosyloxy group at position 7.
General DescriptionGlycitin is an isoflavonoid recently found in flowers of Pueraria thunbergianaI. Glycitin can be modified into the metabolite glycitein which has anti-inflammatory properties.
Biochem/physiol ActionsGlycitin 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.

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