Vinpocetine
Discontinued Product
Chemical Name: (3α,16α)-Eburnamenine-14-carboxylic acid ethyl ester
Purity: ≥99%
Biological Activity
Vinpocetine is a phosphodiesterase inhibitor, selective for PDE1 (IC50 = 21 μM). Also blocks voltage-gated Na+ channels.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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High-throughput genotoxicity assay identifies antioxidants as inducers of DNA damage response and cell death.
Fox JT, Sakamuru S, Huang R
Proc. Natl. Acad. Sci. U.S.A., 2012;109(14):5423-8. -
Vinpocetine inhibits Streptococcus pneumoniae-induced upregulation of mucin MUC5AC expression via induction of MKP-1 phosphatase in the pathogenesis of otitis media.
Lee J, Komatsu K, Lee B, Miyata M, O'Neill Bohn A, Xu H, Yan C, Li J
J Immunol, 2015;194(12):5990-8. -
Effect of vinpocetine on cyclic nucleotide metabolism in vascular smooth muscle.
Hagiwara et al.
Biochem.Pharmacol., 1984;33:453 -
Vinpocetine is as potent as phen. to block voltage-gated Na+ channels in rat cortical neurons.
Molnar and Erdo
Eur.J.Pharmacol., 1995;273:303
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Citations for Vinpocetine
The citations listed below are publications that use Tocris products. Selected citations for Vinpocetine include:
2 Citations: Showing 1 - 2
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Vinpocetine inhibits Streptococcus pneumoniae-induced upregulation of mucin MUC5AC expression via induction of MKP-1 phosphatase in the pathogenesis of otitis media.
Authors: Lee Et al.
EMBO Mol Med 2015;194:5990
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Assessing the emetic potential of PDE4 inhibitors in rats.
Authors: Robichaud Et al.
Br J Pharmacol 2002;135:113
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