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Cilostazol is a potent cyclic nucleotide phosphodiesterase type 3 (PDE3) inhibitor with IC50 of 0.2 μM and inhibitor of adenosine uptake. It can be used to construct animal models of deep vein thrombosis.
| Molecular Weight | 369.46 |
| Formula | C20H27N5O2 |
| CAS Number | 73963-72-1 |
| Solubility (25°C) | 74 mg/mL in DMSO |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
[1] Bedenis R, et al. Cochrane Database Syst Rev. Cilostazol for intermittent claudication.
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