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CAS: | 157115-85-0 | MF: | C17H22N2O4 |
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MW: | 318.37 | Source: | Synthetic |
Purity: | 99%min. | Properties: | Powder |
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Nootropic Raws Noopept CAS 157115-85-0 for Health Supplement
Product Name: ethyl 2-[[(2S)-1-(2-phenylacetyl)pyrrolidine-2-carbonyl]amino]acetate
Synonyms: ethyl 2-[[(2S)-1-(2-phenylacetyl)pyrrolidine-2-carbonyl]amino]acetate;N-(1-(Phenylacetyl)-L-prolyl)glycine ethyl ester;Noopept;(S)-ethyl 2-(1-(2-phenylacetyl)pyrrolidine-2-carboxaMido)acetate;SGS 111;SGS111;SGS-111;1-(2-Phenylacetyl)-L-prolylglycine Ethyl Ester
CAS: 157115-85-0
MF: C17H22N2O4
MW: 318.37
Noopept (Russian: Ноопепт; GVS-111, N-phenylacetyl-L-prolylglycine ethyl ester) is a peptide promoted and prescribed in Russia and neighbouring countries as a nootropic. The registered brand name Noopept (Ноопепт) is trademarked by the manufacturer JSC LEKKO Pharmaceuticals. The compound is patented in both the US and Russia with patent of Russian Federation number 2119496, U.S. Patent 5,439,930 issued 8/8/1995.[1] It is sold as a dietary supplement in the US[citation needed] and as a medication in other countries.
Noopept Mechanism of action
Noopept Box Front
Noopept blister pack
Noopept is not a racetam (due to not having a 2-oxo-pyrrolidine skeleton),[2] but is generally grouped together in the same category because it shares similar mechanisms of action with the racetam family, mainly modulation of the acetylcholine system, as well as modulation of AMPA receptors.[3] When compared to traditional racetams, it has been found to be, according to studies, 1000 times more potent than the prototypical racetam drug, piracetam.[4] Noopept is a prodrug for the endogenous peptide cycloprolylglycine,[5] which means that Noopept isn't active until metabolized into cycloprolylglycine.
Noopept Pharmacokinetics
Peak plasma noopept concentrations of 13-33 μg/L are reached within one hour after a single 20 mg oral dose. The half-life averages about 1 hour in healthy individuals. It is mainly cleared renally as a series of metabolites produced by amide and ester hydrolysis, deacylation and aromatic hydroxylation. Noopept may be quantitated in biofluids by liquid chromatography with one of several different detection techniques.
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