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Dipyridamole, Thermo Scientific Chemicals
An inhibitor of adenosine transport and phosphodiesterase
| Catalog Number | Quantity |
|---|---|
| ALFJ63329.06 | 5 g |
Catalog number ALFJ63329.06
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Quantity:
5 g
Chemical Identifiers
CAS532-31-0
IUPAC Namesilver(1+) benzoate
Molecular FormulaC7H5AgO2
InChI KeyCLDWGXZGFUNWKB-UHFFFAOYSA-M
SMILES[Ag+].[O-]C(=O)C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to beige to light grey
Infrared spectrumConforms
Silver (Ag)46.4 to 47.8 %
Appearance (Form)Powder or crystals and/or chunks
Dipyridamole prevents platelets sticking to the replacement heart valve and causing a blood clot on the valve. It is used to dilate blood vessels in people with peripheral arterial disease and coronary artery disease. This compound has been shown to suppress high glucose-induced osteopontin mRNA expression and protein secretion, as well as inhibit cAMP and cGMP hydrolysis. Research indicates that Dipyridamole is a non-specific nucleoside transport inhibitor with the ability to increase the effects of adenosine in sinoatrial and atrioventricular nodes. Dipyridamole is an inhibitor of ENT1 and ENT2.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Dipyridamole prevents platelets sticking to the replacement heart valve and causing a blood clot on the valve. It is used to dilate blood vessels in people with peripheral arterial disease and coronary artery disease. This compound has been shown to suppress high glucose-induced osteopontin mRNA expression and protein secretion, as well as inhibit cAMP and cGMP hydrolysis. Research indicates that Dipyridamole is a non-specific nucleoside transport inhibitor with the ability to increase the effects of adenosine in sinoatrial and atrioventricular nodes. Dipyridamole is an inhibitor of ENT1 and ENT2.
Solubility
Soluble in chloroform, methanol, dilute acids, ethanol. Slightly soluble in water.
Notes
Store in a cool dry place. Keep away from oxidizing agents.
Dipyridamole prevents platelets sticking to the replacement heart valve and causing a blood clot on the valve. It is used to dilate blood vessels in people with peripheral arterial disease and coronary artery disease. This compound has been shown to suppress high glucose-induced osteopontin mRNA expression and protein secretion, as well as inhibit cAMP and cGMP hydrolysis. Research indicates that Dipyridamole is a non-specific nucleoside transport inhibitor with the ability to increase the effects of adenosine in sinoatrial and atrioventricular nodes. Dipyridamole is an inhibitor of ENT1 and ENT2.
Solubility
Soluble in chloroform, methanol, dilute acids, ethanol. Slightly soluble in water.
Notes
Store in a cool dry place. Keep away from oxidizing agents.
RUO – Research Use Only
H.C. Diener.; L. Cunha.; C. Forbes.; J. Sivenius, P. Smets.; A. Lowenthal. European Stroke Prevention Study 2. Dipyridamole and acetylsalicylic acid in the secondary prevention of stroke.Journal of the Neurological Sciences. 1996, 143 (1-2),1-13 .