Dypyridamole
CAS No. 58-32-2
Dypyridamole( NSC 515776 | NSC 619103 )
Catalog No. M15141 CAS No. 58-32-2
Dipyridamole (Persantine) is a phosphodiesterase inhibitor that blocks uptake and metabolism of adenosine by erythrocytes and vascular endothelial cells.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 29 | In Stock |
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| 50MG | 35 | In Stock |
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| 100MG | 47 | In Stock |
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| 200MG | 54 | In Stock |
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| 500MG | 62 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameDypyridamole
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NoteResearch use only, not for human use.
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Brief DescriptionDipyridamole (Persantine) is a phosphodiesterase inhibitor that blocks uptake and metabolism of adenosine by erythrocytes and vascular endothelial cells.
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DescriptionDipyridamole (Persantine) is a phosphodiesterase inhibitor that blocks uptake and metabolism of adenosine by erythrocytes and vascular endothelial cells.(In Vitro):Dipyridamole (5 μM; 15 min) results in a 2.5-fold increase in intracellular cAMP levels in OCI-AML-3 cells.Dipyridamole (5 μM; 48 h) with the statin combination induces apoptosis in primary AML cells.Dipyridamole (5 μM; 48 h) possesse cAMP/PKA-independent activity against statininduced SREBP2 activation.(In Vivo):Dipyridamole (10 mg/kg; p.o. once daily for 18 d) mitigates tumor growth, ameliorated concurrent alterations in blood circulation and tumor tissues, and platelet infiltration in tumor tissues.
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In VitroDipyridamole (5 μM; 15 min) results in a 2.5-fold increase in intracellular cAMP levels in OCI-AML-3 cells.Dipyridamole (5 μM; 48 h) with the statin combination induces apoptosis in primary AML cells.Dipyridamole (5 μM; 48 h) possesse cAMP/PKA-independent activity against statininduced SREBP2 activation. Apoptosis Analysis Cell Line:AML (OCI-AML-2, OCI-AML-3) cell line Concentration:5 μM Incubation Time:48 h Result:Induced apoptosis with the combination of fluvastatin and dipyridamole, cilostazol, forskolin, or dbcAMP in OCI-AML-2 and OCI-AML-3 cells.RT-PCRCell Line:LP1 cell line Concentration:5 μM Incubation Time:16 h Result:Increased the sensibility of cancer cells to statin-induced apoptosis.
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In VivoDipyridamole (10 mg/kg; p.o. once daily for 18 d) mitigates tumor growth, ameliorated concurrent alterations in blood circulation and tumor tissues, and platelet infiltration in tumor tissues. Animal Model:C57BL/6-LLC tumor-bearing mice models Dosage:10 mg/kg Administration:Oral gavage; 10 mg/kg; once daily for 18 days Result:Mitigated tumor growth in tumor-bearing mice.
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SynonymsNSC 515776 | NSC 619103
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PathwayAngiogenesis
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TargetPDE
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RecptorPDE| PDE
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Research AreaCardiovascular Disease
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Indication——
Chemical Information
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CAS Number58-32-2
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Formula Weight504.63
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Molecular FormulaC24H40N8O4
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Purity>98% (HPLC)
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SolubilityEthanol: 50 mg/mL (99.08 mM); DMSO: 101 mg/mL (200.14 mM)
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SMILESOCCN(CCO)C1=NC(N2CCCCC2)=C(N=C(N(CCO)CCO)N=C3N4CCCCC4)C3=N1
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Chemical Name2,2',2'',2'''-((4,8-di(piperidin-1-yl)pyrimido[5,4-d]pyrimidine-2,6-diyl)bis(azanetriyl))tetraethanol
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Fujishige K, et al. J Biol Chem. 1999 Jun 25;274(26):18438-45.
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