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Chrysotoxine (Synonyms: Phenol, 4-[2-(3,4-dimethoxyphenyl)ethyl]-2,6-dimethoxy-, 4-[2-(3,4-Dimethoxyphenyl)ethy...)

Catalog No. T27012 Copy Product Info
Purity: 99.34%
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Chrysotoxine (Phenol, 4-[2-(3,4-dimethoxyphenyl)ethyl]-2,6-dimethoxy-) inhibits 6-hydroxydopamine induced apoptosis in SH-SY5Y cells via NF-κB modulation and mitochondria protection.

Chrysotoxine

Copy Product Info
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Catalog No. T27012
Synonyms Phenol, 4-[2-(3,4-dimethoxyphenyl)ethyl]-2,6-dimethoxy-, 4-[2-(3,4-Dimethoxyphenyl)ethyl]-2,6-dimethoxyphenol

Chrysotoxine (Phenol, 4-[2-(3,4-dimethoxyphenyl)ethyl]-2,6-dimethoxy-) inhibits 6-hydroxydopamine induced apoptosis in SH-SY5Y cells via NF-κB modulation and mitochondria protection.

Chrysotoxine
Cas No. 156951-82-5
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$133In StockIn Stock
5 mg$298In StockIn Stock
10 mg$453In StockIn Stock
25 mg$747In StockIn Stock
50 mg$1,050In StockIn Stock
1 mL x 10 mM (in DMSO)$297In StockIn Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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Purity:99.34%
Appearance:Solid
Color:White
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Product Introduction

Chrysotoxine AI Summary
Chrysotoxine exhibits multiple bioactivities. It shows significant antioxidant activity with an IC50 value of 14000.0 nM in the DPPH radical scavenging assay. Additionally, it has demonstrated anti-cancer properties against human NCI-H23 cells (IC50 value of 145470.0 nM) and cytotoxicity against human NCI-H460 cells (IC50 value of 127340.0 nM). The compound also provides neuroprotective effects against Amyloid beta (25 to 35)-induced toxicity in rat PC-12 cells, where it increases cell viability at concentrations of 50 μM, 25 μM, and 10 μM, with activity percentages ranging from 52.72% to 58.89%. Furthermore, its permeability is evaluated by the PAMPA-BBB assay, with a measured rate of 4.1 x 10^-6 cm/s..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Chrysotoxine (Phenol, 4-[2-(3,4-dimethoxyphenyl)ethyl]-2,6-dimethoxy-) inhibits 6-hydroxydopamine induced apoptosis in SH-SY5Y cells via NF-κB modulation and mitochondria protection.
SynonymsPhenol, 4-[2-(3,4-dimethoxyphenyl)ethyl]-2,6-dimethoxy-, 4-[2-(3,4-Dimethoxyphenyl)ethyl]-2,6-dimethoxyphenol
Chemical Properties
Molecular Weight318.36
FormulaC18H22O5
Cas No.156951-82-5
SmilesC(CC1=CC(OC)=C(OC)C=C1)C2=CC(OC)=C(O)C(OC)=C2
Relative Density.1.147 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 55 mg/mL (172.76 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.1411 mL15.7055 mL31.4110 mL157.0549 mL
5 mM0.6282 mL3.1411 mL6.2822 mL31.4110 mL
10 mM0.3141 mL1.5705 mL3.1411 mL15.7055 mL
20 mM0.1571 mL0.7853 mL1.5705 mL7.8527 mL
50 mM0.0628 mL0.3141 mL0.6282 mL3.1411 mL
100 mM0.0314 mL0.1571 mL0.3141 mL1.5705 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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