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Homoeriodictyol 7-O-β-D-glucoside

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Catalog No. TN4222Cas No. 14982-11-7
Alias Homoeriodictyol 7-O-glucoside

Homoeriodictyol 7-O-β-D-glucoside (Homoeriodictyol 7-O-glucoside) is a natural product derived from Viscum coloratum (Kom.) Nakai and acts as an antagonist of platelet-activating factor (PAF).

Homoeriodictyol 7-O-β-D-glucoside

Homoeriodictyol 7-O-β-D-glucoside

😃Good
Catalog No. TN4222Alias Homoeriodictyol 7-O-glucosideCas No. 14982-11-7
Homoeriodictyol 7-O-β-D-glucoside (Homoeriodictyol 7-O-glucoside) is a natural product derived from Viscum coloratum (Kom.) Nakai and acts as an antagonist of platelet-activating factor (PAF).
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Product Introduction

Bioactivity
Description
Homoeriodictyol 7-O-β-D-glucoside (Homoeriodictyol 7-O-glucoside) is a natural product derived from Viscum coloratum (Kom.) Nakai and acts as an antagonist of platelet-activating factor (PAF).
In vitro
Homoeriodictyol 7-O-β-D-glucoside exhibits no inhibitory effect on ADP-induced platelet aggregation [1].
SynonymsHomoeriodictyol 7-O-glucoside
Chemical Properties
Molecular Weight464.42
FormulaC22H24O11
Cas No.14982-11-7
SmilesOC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O1)OC2=CC(O)=C(C(C[C@H]3C4=CC(OC)=C(O)C=C4)=O)C(O3)=C2
Relative Density.1.569 g/cm3 (Predicted)
ColorYellow
AppearanceSolid
Storage & Solubility Information
Storagestore at low temperature,keep away from direct sunlight,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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Keywords

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