Noopept
Omberacetam · N-phenylacetyl-L-prolylglycine ethyl ester · GVS-111
Noopept is a small molecule built from a dipeptide backbone, which is why it is filed with peptides and why that filing is misleading. It is not injected, not reconstituted, and behaves like a conventional oral drug.
It has been a registered prescription medicine in Russia since 1996, prescribed for cognitive impairment after stroke or injury and for age-related decline. That is a genuine regulatory status with a clinical programme behind it. It is also a Russian programme, carrying the reporting and replication limits this site describes for that body of work generally.
Outside Russia it is unapproved and sold as a supplement or research chemical. In the United Kingdom it is a controlled substance under the Psychoactive Substances Act, which is a distinction worth knowing before ordering it.
How it works
Noopept is metabolised to cycloprolylglycine, an endogenous dipeptide, which is thought to be the active form. That relationship to a naturally occurring molecule is the basis of the mechanistic argument for it.
It is described as raising BDNF and nerve growth factor in the hippocampus in animal work, and as modulating glutamate receptor signalling. Both are plausible routes to the cognitive effects claimed, and neither is established in humans outside the Russian programme.
It is often described as a racetam, and structurally it is not one. The resemblance is functional rather than chemical, which matters if you are reasoning about interactions from drug class.
Regulatory status — Russia and United States
A registered prescription medicine in Russia since 1996 for cognitive impairment following stroke or injury. Not approved in the United States or the European Union, and controlled in the United Kingdom under the Psychoactive Substances Act.
Last reviewed 18 Aug 2026. Regulatory positions in this category change frequently; we date this line so you can see how current it is.
What it is studied for
Each entry states the evidence behind it. We do not rank indications by effectiveness — for most compounds here, that would be a claim nobody can support.
Cognitive impairment after stroke or injury
Published reviewThe registered Russian indication.
EvidenceRussian clinical work supporting registration since 1996. Not replicated to contemporary standards outside that programme.
Cognitive enhancement in healthy people
Community practiceWhy it is bought outside Russia.
EvidenceNo trial has studied it in healthy people for cognitive enhancement. The registered indication involves existing impairment.
Identity and clearance
Molecule
- Class
- Small molecule derived from a dipeptide, not a peptide drug
- Molecular weight
- 318.4 Da
Taken orally. Nothing here is reconstituted, and the calculator on this site does not apply.
Dose protocols reported in sources
Displayed for reference only. Every row says where it came from, and a trial protocol and a community convention are not the same kind of information. None of this is fed into the calculator, and none of it is a recommendation.
| Goal | Dose | Frequency | Route | Units, 10 mg vial | Source | Start this protocol |
|---|---|---|---|---|---|---|
| Registered Russian dosing | 10 mg – 30 mg | 10 mg two or three times daily, in courses of 6 to 8 weeks | OralThe registered protocol is a course rather than continuous use. Note the doses are milligrams, unlike most of what surrounds it on this site. A 10 mg figure here is not comparable to a 10 mg peptide dose. | from 100 u | Published review | Start this |
Start this copies a row into a protocol of your own, which you can then edit. Where a source gave a dose range or an ambiguous frequency, those fields arrive empty — we will not pick a number on your behalf.
Cycling
Published review6 to 8 weeks on, At least a month between courses off.
The course structure comes from the registered Russian protocol rather than from community convention.
Safety
Reported effects
- Irritability and disturbed sleepCommunity practice
Commonly reported
The most frequent complaint, and the reason the registered protocol avoids evening doses.
- HeadacheCommunity practice
Commonly reported
- Raised blood pressurePublished review
Reported in the Russian literature
Noted in the registered product information, particularly in older patients.
- Long-term effects outside a course structurePublished review
Unknown
The registered use is a 6 to 8 week course. Continuous use has not been studied.
When to stop
- Irritability, agitation or sleep disturbance that does not settle.
- Raised blood pressure. Measure it rather than guessing.
- Persistent headache.
- Any allergic response: rash, hives, facial swelling or difficulty breathing. Seek urgent care.
Interactions and situations that need care
- Uncontrolled hypertensionAvoid
Raised blood pressure is noted in the registered product information, particularly in older patients, who are the population most likely to be taking it for its registered indication.
- Pregnancy and breastfeedingAvoid
No reproductive or developmental safety data.
- Severe kidney or liver impairmentAvoid
Listed as a contraindication in the registered Russian product information.
- Ordering it into the United KingdomUse caution
It is controlled there under the Psychoactive Substances Act. That is a legal fact — not a safety one — and it applies regardless of what the compound does.
What to expect
- It is a registered prescription medicine in Russia, which is a real status, and one resting on a body of work nobody has replicated to contemporary standards elsewhere.
- It is not a peptide. It is a small molecule taken as a tablet, and it appears alongside peptides only because of where it is sold.
- The registered indication is cognitive impairment after stroke or injury. Nobody has studied it in healthy people for enhancement.
- The registered protocol is a 6 to 8 week course, not continuous use.
- It is controlled in the UK.
Storage and handling
- Freeze-dried powder
- Tablets or powder at room temperature, dry and out of light.
- After mixing
- Not applicable. This is taken orally.
Checking your vial
Research chemicals carry no manufacturing standard, so what the vial looks like is often the only quality signal available before you use it. More on assessing quality and COAs.
You cannot assess a powder by looking at it
No visual check distinguishes this from any other white powder, and it is active at milligram doses where a measuring error matters.
Questions
- Is Noopept a peptide?
- No. It is built from a dipeptide backbone, which is where the name and the filing come from, but it is a small molecule taken as a tablet. Nothing about it is reconstituted or injected.
- Is it a racetam?
- Not structurally. It is often described as one because the effects are compared to piracetam, but it is a different kind of molecule, and that matters if you are reasoning about interactions from drug class.
- Is it legal?
- It is a prescription medicine in Russia, unapproved in the US and EU, and controlled in the UK under the Psychoactive Substances Act. Those are three different situations.
References
Russian clinical literature on regulatory peptides and nootropics: scope and limits
Russian pharmacology and psychiatry literature, 2015 · Body of clinical work, largely unregistered and not blinded to contemporary standards
Humans
Reports anxiolytic, nootropic and neuroprotective effects supporting registration of several of these compounds in Russia. Methodology, reporting standards and the absence of independent replication limit how much weight the findings carry elsewhere.
Commonly reported community protocols
Bioalmanac editorial summary of public community sources, 2026 · Not a study
Records dose and route patterns described in public discussion. Carries no evidential weight about safety or effect.
Related compounds
GHK-Cu
A naturally occurring copper-binding tripeptide with a long history in topical skincare research. Injected use is not what the research studied.
Ipamorelin
A selective growth hormone secretagogue that prompts a short pulse of GH release. Widely used, and supported almost entirely by early pharmacology rather than outcome trials.
CJC-1295
A GHRH analogue that raises growth hormone by amplifying the body's own release signal. Sold in two forms whose durations differ by two orders of magnitude.
Tesamorelin
A GHRH analogue approved by the FDA for reducing excess visceral fat in HIV-associated lipodystrophy. The only compound in this category with completed phase 3 trials.
Next
What to do with Noopept
- Keep a record of itTurn a dose and a schedule into a protocol, then log what you actually take. Noopept is filled in for you.
- See what it costsPer-milligram prices read from vendor sites and confirmed by a person, so vial sizes compare.
- Check a combinationWhat our profiles record about Noopept alongside each other compound — including the pairs where nothing is recorded.
Keep this page honest
If something here is wrong, out of date, or missing a source, tell us and we will fix it and say that we did.
This page is educational. It describes what published research reports, not what you should do. Peptides discussed here are largely not approved for human use, and nothing on Bioalmanac is medical advice. No clinician reviews these pages.
Page last updated 18 Aug 2026