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Taxifolin (Dihydroquercetin) VEGFR inhibitor

Cat.No.S2366

Taxifolin (Dihydroquercetin), a flavonoid in many plants such as Taxus chinensis, Siberian larch, Cedrus deodara and so on, is a type I inhibitor for VEGFR-2 kinase.
Taxifolin (Dihydroquercetin) VEGFR inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 304.25

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 304.25 Formula

C15H12O7

Storage (From the date of receipt)
CAS No. 480-18-2 Download SDF Storage of Stock Solutions

Synonyms N/A Smiles C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O

Solubility

In vitro
Batch:

DMSO : 61 mg/mL (200.49 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 61 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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mg/kg g μL

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% DMSO % % Tween 80 % ddH2O
%DMSO %

Calculation results:

Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Mechanism of Action

Targets/IC50/Ki
VEGFR2 kinase [4]
In vitro
Taxifolin (Dihydroquercetin) is not mutagenic and low toxic compared to Qercetin. [1] It acts as a potential chemopreventive agent by regulating genes via an ARE-dependent mechanism. [2] This compound has shown to inhibit the ovarian cancer cell growth in a dose-dependent manner. [3]
References

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