Noopept
Not FDA approvedSynthetic nootropic dipeptide
Also known as: omberacetam, GVS-111, Omberacetam, J759.455K, omberacetamum, ethyl (2-phenylacetyl)-L-prolylglycinate, ethyl 1-(phenylacetyl)-L-prolylglycinate
Very thin human evidence
- Regulatory standing. Sold as a research chemical, not approved
- Animal / preclinical only. Evidence is largely animal or in-vitro
- No registered human trials. Nothing registered on ClinicalTrials.gov
- 1 cited source. Includes primary / regulatory sources
Computed with the same four public criteria as every profile. The human-evidence grade on an indexed profile is set automatically and may change when it is hand-reviewed. It is not a safety score, not a purity rating, and not medical advice, and not a claim that this compound treats, cures, or prevents any condition.
What it is
Noopept, also called omberacetam or GVS-111, is a synthetic dipeptide-derived compound developed in Russia and often grouped with racetam-style nootropics. It is thought to act partly through its metabolite cycloprolylglycine and has been studied for effects on neurotrophic factors such as BDNF and NGF and on glutamate and acetylcholine signaling, mainly in laboratory and animal models.
What the evidence shows
It is not FDA-approved and has no registered human trials in the gathered data. Most of the roughly 86 published papers are preclinical, with only a few small clinical studies, mostly from Russia, so any cognitive benefit in humans is not established.
Key facts
Registered human trials
Live from ClinicalTrials.gov, refreshed daily.
Published literature
Live from Europe PMC. This is how much has been published, not how much is proven in humans.
GVS-111 prevents oxidative damage and apoptosis in normal and Down's syndrome human cortical neurons.
The nootropic and neuroprotective proline-containing dipeptide noopept restores spatial memory and increases immunoreactivity to amyloid in an Alzheimer's disease model.
Noopept Attenuates Diabetes-Mediated Neuropathic Pain and Oxidative Hippocampal Neurotoxicity via Inhibition of TRPV1 Channel in Rats.
Characterization and prebiotic potential of polysaccharides from Rosa roxburghii Tratt pomace by ultrasound-assisted extraction.
Sources
- PubChem compound record (CID 180496)
- Registered trials on ClinicalTrials.gov
- Published papers on Europe PMC
Risks, side effects and study doses are only published on hand-reviewed profiles. Want this one reviewed, or spotted something wrong? Tell us.