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AZD5904

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Catalog No. T14379Cas No. 618913-30-7

AZD5904 is a potent and irreversible inhibitor of human Myeloperoxidase (MPO, IC50: 140 nM) which has similar potency in mouse and rat.

AZD5904

AZD5904

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🥰Excellent
Purity: 99.89%
Catalog No. T14379Cas No. 618913-30-7
AZD5904 is a potent and irreversible inhibitor of human Myeloperoxidase (MPO, IC50: 140 nM) which has similar potency in mouse and rat.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$30In StockIn Stock
5 mg$66In StockIn Stock
10 mg$123In StockIn Stock
25 mg$289In StockIn Stock
50 mg$513In StockIn Stock
100 mg$787In StockIn Stock
1 mL x 10 mM (in DMSO)$73In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.89%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
AZD5904 is a potent and irreversible inhibitor of human Myeloperoxidase (MPO, IC50: 140 nM) which has similar potency in mouse and rat.
Targets&IC50
MPO (human):140 nM
In vitro
In isolated human neutrophils, 1 μM AZD5904 inhibits PMA stimulated HOCl by >90%[1]. It is 10 to 19-fold selective compare to the closely related lactoperoxidase and thyroid peroxidase. For a broad panel of other enzymes, ion channels, and receptors, is higher than >70-fold.
Chemical Properties
Molecular Weight252.29
FormulaC10H12N4O2S
Cas No.618913-30-7
SmilesO=c1[nH]c(=S)n(C[C@H]2CCCO2)c2[nH]cnc12
Relative Density.1.54 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: 65 mg/mL (257.64 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+90% Saline: 2.5 mg/mL (9.91 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 mM3.9637 mL19.8185 mL39.6369 mL198.1846 mL
5 mM0.7927 mL3.9637 mL7.9274 mL39.6369 mL
10 mM0.3964 mL1.9818 mL3.9637 mL19.8185 mL
20 mM0.1982 mL0.9909 mL1.9818 mL9.9092 mL
50 mM0.0793 mL0.3964 mL0.7927 mL3.9637 mL
100 mM0.0396 mL0.1982 mL0.3964 mL1.9818 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

You can also refer to dose conversion for different animals. More Dose Conversion

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

Keywords

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