Basic information Safety Supplier Related

Vitexia-glucoside

Basic information Safety Supplier Related

Vitexia-glucoside Basic information

Product Name:
Vitexia-glucoside
Synonyms:
  • Vitexia-glucoside
  • Vitexin 4'-glucoside
  • 4H-1-Benzopyran-4-one, 8-β-D-glucopyranosyl-2-[4-(β-D-glucopyranosyloxy)phenyl]-5,7-dihydroxy-
  • 4'-O-Glucosylvitexin
  • Glucosylvitexin/Vitexin -4''-O-glucoside
CAS:
38950-94-6
MF:
C27H30O15
MW:
594.52
Mol File:
38950-94-6.mol
More
Less

Vitexia-glucoside Chemical Properties

Boiling point:
937.3±65.0 °C(Predicted)
Density 
1.723±0.06 g/cm3 (20 ºC 760 Torr)
form 
Solid
pka
6.25±0.40(Predicted)
color 
Light yellow to yellow
More
Less

Vitexia-glucoside Usage And Synthesis

Chemical Properties

Light yellow crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, derived from hawthorn.

Uses

Vitexia-glucoside has the effects of treating ischemic heart disease, lowering blood lipids and resisting cancer.

Definition

ChEBI: 4'-O-Glucosylvitexin is a member of flavonoids and a glycoside.

Biological Activity

Vitexin 4'-glucoside is a leaf flavonoid identified from Briza stricta.

Synthesis

60g of crude extract of hawthorn leaf was dissolved by adding 500mL of distilled water with ultrasonication, and the insoluble material was filtered out, and the filtrate flowed through the HPD-400 macroporous resin column at a flow rate of 3BV/h. After the adsorption was completed, the HPD-400 macroporous resin column was first fully eluted with distilled water at 5BV, and the first-stage eluent was collected, and after concentrated and lyophilized, 5.49g of chlorogenic acid analogs with a purity of 70.3% was obtained; The HPD- 400 macroporous resin column was then fully eluted with 5BV 50% ethanol aqueous solution, and the second stage eluent was collected, and the solvent was recovered by reduced-pressure distillation to obtain 19.32 g of total hawthorn leaf flavonoids with a purity of 59.7%; the total flavonoids of hawthorn leaf were solubilized with 50 mL of methanol, and purified by preparative chromatography using a {C18 column (50??250 mm, 10 ??m), 35/65 ( V/V) of 0.1% aqueous acetic acid/methanol}, the monomer eluent was collected separately, and after distillation under reduced pressure, 0.29 g of pungitin glucoside with 96.2% purity and 1.29 g of pungitin rhamnoside with 96.3% purity were obtained.

Vitexia-glucosideSupplier

Shanghai Tauto Biotech Co., Ltd.
Tel
021-51320588
Email
tauto@tautobiotech.com
Wuhan ChemFaces Biochemical Co., Ltd.
Tel
18607101326 15172504745
Email
aileen@chemfaces.com
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Email
3008007409@qq.com
Chengdu Alfa Biotechnology Co.,Ltd.
Tel
028-85142057, 18030712385
Email
sales@alfabiotech.com
Shanghai Innovative Reseach Center Of Traditional
Tel
86-21-50801717-301
Email
wangjh@sirc-tcm.sh.cn
More
Less