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Prinoxodan (Synonyms: RGW2938)

Catalog No. T12720 Copy Product Info
Purity: 98.99%
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Prinoxodan is a potent phosphodiesterase 3 (PDE3) inhibitor. It exerts cardiotonic and vasodilatory effects by increasing intracellular cAMP levels, used for heart failure and cardiovascular research.

Prinoxodan

Copy Product Info
🥰Excellent
Catalog No. T12720
Synonyms RGW2938

Prinoxodan is a potent phosphodiesterase 3 (PDE3) inhibitor. It exerts cardiotonic and vasodilatory effects by increasing intracellular cAMP levels, used for heart failure and cardiovascular research.

Prinoxodan
Cas No. 111786-07-3
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$61-In Stock
5 mg$147-In Stock
10 mg$243-In Stock
25 mg$513-In Stock
50 mg$793-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:98.99%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Prinoxodan is a potent phosphodiesterase 3 (PDE3) inhibitor. It exerts cardiotonic and vasodilatory effects by increasing intracellular cAMP levels, used for heart failure and cardiovascular research.
In vitro
Prinoxodan dose-dependently (5 nmol-5 umol) increases myocardial contractility in isolated guinea pig hearts [1].
In vivo
Prinoxodan (30-300 ug/kg i.v. or 0.3 mg/kg p.o.) significantly enhances myocardial contractility and reduces peripheral resistance in dogs [2].
SynonymsRGW2938
Chemical Properties
Molecular Weight258.28
FormulaC13H14N4O2
Cas No.111786-07-3
SmilesO=C1NC=2C=CC(=CC2CN1C)C3=NNC(=O)CC3
Relative Density.1.47 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
Ethanol: < 1 mg/mL (insoluble)

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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:
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
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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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