Vinpocetine | PDE1 inhibitor
NMR (Conforms)
Available Options
| Size : | Price | Quantity | |
|---|---|---|---|
| 20 mg | $30.00 | ||
| 100 mg | $65.00 |
Vinpocetine (42971-09-5) is a phosphodiesterase PDE1 inhibitor (IC50=21 μM).1 Also blocks voltage-gated Na+ channels, IC50=44.2 μM (potency similar to phenytoin), a mechanism which may contribute to its neuroprotective and anticonvulsant activity.2 It reduces inflammatory IL-1β and TNF-α expression in rat hippocampus.3 Displays beneficial effects in a rat model of cerebral ischemia-reperfusion injury.4 Vinpocetine exerts neuroprotective effects by suppressing microglial inflammation.5
References/Citations:
1) Hagiwara et al. (1984), Effects of vinpocetine on cyclic nucleotide metabolism in vascular smooth muscle; Biochem. Pharmacol., 33 453
2) Molnar and Erdo (1995), Vinpocetine is as potent as phenytoin to block voltage-gated Na+ channels in rat cortical neurons; Eur. J. Pharmacol., 273 303
3) Gomez et al. (2014), The anti-seizure drugs vinpocetine and carbamazepine, but not valproic acid, reduced inflammatory IL1β and TNF-α expression in rat hippocampus; J. Neurochem., 130 770
4) Wang et al. (2014), Anti-inflammatory effects of vinpocetine on the functional expression of nuclear factor-kappa B and tumor necrosis factor-alpha in a rat model of cerebral ischemia-reperfusion injury; Neuro. Sci. Lett., 566 247
5) Zhao et al. (2011), TSPO-specific ligand vinpocetine exerts a neuroprotective effect by suppressing microglial inflammation; Glia Biol., 7 187
NMR (Conforms)
Safety Data Sheet:
Product Data Sheet:
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Vinpocetine (42971-09-5) is a phosphodiesterase PDE1 inhibitor (IC50=21 μM).1 Also blocks voltage-gated Na+ channels, IC50=44.2 μM (potency similar to phenytoin), a mechanism which may contribute to its neuroprotective and anticonvulsant activity.2 It reduces inflammatory IL-1β and TNF-α expression in rat hippocampus.3 Displays beneficial effects in a rat model of cerebral ischemia-reperfusion injury.4 Vinpocetine exerts neuroprotective effects by suppressing microglial inflammation.5
References/Citations:
1) Hagiwara et al. (1984), Effects of vinpocetine on cyclic nucleotide metabolism in vascular smooth muscle; Biochem. Pharmacol., 33 453
2) Molnar and Erdo (1995), Vinpocetine is as potent as phenytoin to block voltage-gated Na+ channels in rat cortical neurons; Eur. J. Pharmacol., 273 303
3) Gomez et al. (2014), The anti-seizure drugs vinpocetine and carbamazepine, but not valproic acid, reduced inflammatory IL1β and TNF-α expression in rat hippocampus; J. Neurochem., 130 770
4) Wang et al. (2014), Anti-inflammatory effects of vinpocetine on the functional expression of nuclear factor-kappa B and tumor necrosis factor-alpha in a rat model of cerebral ischemia-reperfusion injury; Neuro. Sci. Lett., 566 247
5) Zhao et al. (2011), TSPO-specific ligand vinpocetine exerts a neuroprotective effect by suppressing microglial inflammation; Glia Biol., 7 187
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