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Trade names | Noopept |
Other names | omberacetam; GVS-111; DVD-111; SGS-111; benzylcarbonyl-Pro-Gly-OEt |
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Chemical and physical data | |
Formula | C17H22N2O4 |
Molar mass | 318.373 g·mol−1 |
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N-Phenylacetyl-l-prolylglycine ethyl ester is promoted as a nootropic and is a prodrug of cyclic glycine-proline.[a][2] Other names include the brand name Noopept (Russian: Ноопепт), developmental code GVS-111, and proposed INN omberacetam.[2][3][4]
Its synthesis was first reported in 1996.[2] It is orally available. As of 2017, its metabolism and elimination half-life were not well understood, and cycloprolylglycine has not been measured in humans following administration.[2] In cell culture, cycloprolylglycine increases brain derived neurotrophic factor (BDNF).[5]
It has been evaluated for neuroprotective effects in treating brain injuries and stroke.[6]
One oft-cited study (originally published in Russian) conducted on rats, suggests that Noopept works via the "antioxidant effect, the anti-inflammatory action, and the ability to inhibit the neurotoxicity of excess calcium and glutamate, and to improve the blood rheology".[6]
Some studies suggest that the pharmacological properties of Noopept are derived from its action as an activator of Hypoxia-inducible factor (HIF-1).[7][8]
Most of the effects of Noopept could be explained by its action as an activator of HIF-1.[8]
Noopept is frequently dosed at 10–30 mg per day. However, there is no solid evidence indicating that any dose of Noopept is optimal. Few human trials have ever been carried out on Noopept, and as one meta-analysis notes, animal studies have used doses ranging from 0.1 mg/kg bodyweight to 10 mg/kg bodyweight.[unreliable medical source?][9] Furthermore, no long-term studies have been done to evaluate the lasting effects of chronic use at any given dose; the longest human study lasted for 56 days.[10] There is, therefore, no dose of Noopept which may be called "safe".