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Ligustrazine

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Catalog No. T2722Cas No. 1124-11-4
Alias Tetramethylpyrazine

Ligustrazine (Tetramethylpyrazine), a natural compound isolated from Chinese herbal medicine Ligusticum wallichii (Chuan Xiong) shows anti-inflammation, antioxidant, antiplatelet, and antiapoptosis activities.

Ligustrazine

Ligustrazine

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Purity: 99.91%
Catalog No. T2722Alias TetramethylpyrazineCas No. 1124-11-4
Ligustrazine (Tetramethylpyrazine), a natural compound isolated from Chinese herbal medicine Ligusticum wallichii (Chuan Xiong) shows anti-inflammation, antioxidant, antiplatelet, and antiapoptosis activities.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
100 mg$42In StockIn Stock
1 mL x 10 mM (in DMSO)$30In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.91%
Color:White
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Product Introduction

Ligustrazine AI Summary
Ligustrazine exhibits a diverse range of bioactivities. It stimulates the proliferation rate of human umbilical vascular endothelial cells (HUVECs) by a maximum of 20.66% at a concentration of 0.6 mM. Additionally, it provides protection against hydrogen peroxide-induced damage in various cell types such as ECV304 and SH-SY5Y cells, with EC50 values ranging between 15,180.0 nM to 600,000.0 nM. The compound demonstrates significant anti-platelet activity, inhibiting ADP-induced platelet aggregation in rabbit plasma by up to 42.9%, and also shows antithrombotic activity, with inhibition rates of thrombus formation at 71.2% in Sprague-Dawley rats at 2 mg/kg. It also exhibits neuroprotective activity in various models, including protection against focal cerebral ischemia and spinal cord injury, and has shown neuroprotective effects in assays utilizing t-BHP against rat cerebellar granule neurons. Moreover, Ligustrazine displays antiviral activity against SARS-CoV-2, with inhibition of viral-induced cytotoxicity in VERO-6 and Caco-2 cells, although its IC50 values vary widely from low effectiveness to moderate. The compound also exhibits weak inhibition of human HDAC6 enzyme, antioxidant properties, and moderate solubility and lipophilicity with a LogP of 1.26. Furthermore, it shows anticoagulant activity in rabbit platelet poor plasma and has moderate antitumor activity against various human cancer cell lines, such as K562, A549, HCT116, and U87MG, with IC50 values in the micromolar range. However, it has demonstrated less significant antiproliferative activity against other cell lines, such as Bel7402 and HT-29, indicating varied effectiveness across different cancer types..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Ligustrazine (Tetramethylpyrazine), a natural compound isolated from Chinese herbal medicine Ligusticum wallichii (Chuan Xiong) shows anti-inflammation, antioxidant, antiplatelet, and antiapoptosis activities.
SynonymsTetramethylpyrazine
Chemical Properties
Molecular Weight136.19
FormulaC8H12N2
Cas No.1124-11-4
SmilesCC1=NC(C)=C(C)N=C1C
Relative Density.1.08 g/cm3
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 51.05 mg/mL (374.84 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (14.69 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM7.3427 mL36.7134 mL73.4268 mL367.1342 mL
5 mM1.4685 mL7.3427 mL14.6854 mL73.4268 mL
10 mM0.7343 mL3.6713 mL7.3427 mL36.7134 mL
20 mM0.3671 mL1.8357 mL3.6713 mL18.3567 mL
50 mM0.1469 mL0.7343 mL1.4685 mL7.3427 mL
100 mM0.0734 mL0.3671 mL0.7343 mL3.6713 mL

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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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Tech Support

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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