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Dipyridamole

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Catalog No. T1618Cas No. 58-32-2
Alias Persantin, NSC-515776, Dypyridamole, Dipyudamine, Dipyridamol

Dipyridamole (Persantin) is a Platelet Aggregation Inhibitor. The physiologic effect of dipyridamole is by means of Decreased Platelet Aggregation.

Dipyridamole

Dipyridamole

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Purity: 99.84%
Catalog No. T1618Alias Persantin, NSC-515776, Dypyridamole, Dipyudamine, DipyridamolCas No. 58-32-2
Dipyridamole (Persantin) is a Platelet Aggregation Inhibitor. The physiologic effect of dipyridamole is by means of Decreased Platelet Aggregation.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
50 mg$38In StockIn Stock
100 mg$50In StockIn Stock
200 mg$58In StockIn Stock
500 mg$67In 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]
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:99.84%
Appearance:Solid
Color:Yellow
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Product Introduction

Dipyridamole AI Summary
Dipyridamole is a multifunctional inhibitor displaying significant bioactivity across a range of targets. It primarily inhibits Phosphodiesterase 4 (PDE4) from guinea pig macrophages with an IC50 value of 500.0 nM and exhibits a range of inhibitory effects on [3H]thymidine uptake in L1210 cells, showing 80.0%-99.0% inhibition at both 1 μM and 10 μM concentrations, and retains significant activity even in the presence of alpha1-acid glycoprotein (AGP). Additionally, Dipyridamole demonstrates notable inhibitory action on several human phosphodiesterases (PDEs) with mixed potencies: it is most effective against PDE1, PDE2, PDE3, PDE4, and PDE5, with varying IC50 values. It also shows significant inhibition of nucleoside transporters, particularly human ENT1 and ENT2, with IC50 values as low as 8.1 nM for ENT1. In terms of antithrombosis, Dipyridamole has effective doses (ED50) of 142.69 μmol/kg and 72.0 mg/kg in mice. It shows mild inhibition of Batrachotoxinin [3H]BTX-B binding to sodium channels in guinea pig cerebral cortex. Furthermore, Dipyridamole has bioactivity against several malaria strains, especially Plasmodium falciparum 7G8, with IC50 values indicating substantial antiplasmodial effects. In viral studies, it has demonstrated limited antiviral activity against SARS-CoV-2. The compound exhibits transporter inhibition, demonstrating influence on P-glycoprotein, MRP, and various organic cation transporters (OCTs), and shows multidrug resistance modulation properties. It also affects hepatic and renal function markers, suggesting a moderate risk for liver toxicity. Finally, Dipyridamole indicates cytotoxicity towards certain cancer cell lines and exhibits potential in reducing cell proliferation and inducing autophagy. Overall, Dipyridamole is a potent and versatile compound with broad pharmacological profiles, making it a promising candidate for therapeutic applications..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Dipyridamole (Persantin) is a Platelet Aggregation Inhibitor. The physiologic effect of dipyridamole is by means of Decreased Platelet Aggregation.
SynonymsPersantin, NSC-515776, Dypyridamole, Dipyudamine, Dipyridamol
Chemical Properties
Molecular Weight504.63
FormulaC24H40N8O4
Cas No.58-32-2
SmilesN(CCO)(CCO)C1=NC2=C(C(=N1)N3CCCCC3)N=C(N(CCO)CCO)N=C2N4CCCCC4
Relative Density.1.352 g/cm3
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 250 mg/mL (495.41 mM), Sonication is recommended.
Ethanol: 47 mg/mL (93.14 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 3.3 mg/mL (6.54 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
Ethanol/DMSO
1mg5mg10mg50mg
1 mM1.9816 mL9.9082 mL19.8165 mL99.0825 mL
5 mM0.3963 mL1.9816 mL3.9633 mL19.8165 mL
10 mM0.1982 mL0.9908 mL1.9816 mL9.9082 mL
20 mM0.0991 mL0.4954 mL0.9908 mL4.9541 mL
50 mM0.0396 mL0.1982 mL0.3963 mL1.9816 mL
DMSO
1mg5mg10mg50mg
100 mM0.0198 mL0.0991 mL0.1982 mL0.9908 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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