Selank
Also known as: Selanc, TP-7
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Selank
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Key Facts: Selank
- Category
- Cognitive
- FDA Status
- Not FDA Approved
- Clinical Status
- Approved in Russia - Not FDA or EMA approved. FDA removed selank acetate from 503A Category 2 in Sept 2024 after the nominators withdrew it, and now lists it among nominated-but-withdrawn substances, noting it lacks key human safety information. It is not on the 503A bulks list, was not among the seven peptides reviewed at the July 2026 PCAC meeting, and has no announced review date.
- Banned in Sport (WADA)
- Not named on the WADA list. Because it is approved in Russia, the S0 catch-all arguably does not apply, but no other section clearly covers it, so its status is unclear; check with your anti-doping agency.
- Administration
- Intranasal spray (most common), subcutaneous injection
- Typical Dose
- 250-500 mcg 2-3x daily
- Frequency
- 2-3x daily
- Duration
- 14-21 days typical
How does Selank work?
Selank seems to work through several overlapping systems rather than one tidy target. It influences GABA signaling, the brain's main calming neurotransmitter system, which likely accounts for its anti-anxiety effect. It also slows the breakdown of enkephalins, the body's own opioid-like peptides involved in mood and stress, which is a mechanism entirely different from benzodiazepines or SSRIs. Animal work additionally points to effects on serotonin and dopamine balance and on BDNF, a growth factor tied to learning and neuron health. These pathways are well documented in rodents; the picture in humans is inferred rather than directly measured.
What does the research show?
Most of the rigorous data is preclinical and Russian. In rodents, Selank shows consistent anxiety-reducing and mild cognitive effects, and one PMC-indexed study found it enhanced diazepam's anti-anxiety effect under chronic stress. The main human clinical reference is a Russian comparative trial by Zozulia, Neznamov, and colleagues in patients with generalized anxiety disorder and neurasthenia, reporting that Selank's anxiolytic effect was comparable to the benzodiazepine medazepam on standard rating scales, with added anti-fatigue benefits and changes in enkephalin activity. The honest caveat: that trial was relatively small, the published English abstract gives qualitative results rather than hard effect sizes and p-values, and it has not been replicated by independent Western groups. So the evidence supports a real but modestly studied anxiolytic, mostly validated within the regulatory system that approved it.
What doses have been studied?
Typical Dosingⓘ
Community experience
250-500 mcg 2-3x daily
200-750 mcg per dose
2-3x daily
An anxiolytic nootropic. Reported effects build over days to weeks, and it is frequently reported alongside Semax.
Research Dosingⓘ
Scientific studies
Doses from clinical practice
Doses from Studies
250-500 mcg intranasal
Up to 3x daily
Duration
14-21 days typical
Administration
Intranasal spray (most common), subcutaneous injection
When and how is Selank taken?
Best Time to Take
Morning or as needed for anxiety
2-3 times daily as needed
Food Recommendation
With or without food
Why This Timing?
Selank has anxiolytic effects without sedation. Morning use helps manage daytime stress and anxiety.
What are the side effects of Selank?
Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.
- ●Generally well-tolerated
- ●Nasal irritation (spray)
- ●Headache
- ●Nausea
- ●Fatigue
- ●May enhance effects of benzodiazepines
References
- https://pubmed.ncbi.nlm.nih.gov/18577961/
- https://pmc.ncbi.nlm.nih.gov/articles/PMC5322660/
- https://pubmed.ncbi.nlm.nih.gov/18454096/
- https://www.fda.gov/drugs/human-drug-compounding/certain-bulk-drug-substances-use-compounding-may-present-significant-safety-risks
- https://www.fda.gov/media/94155/download
Research This Peptide Further
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Selank
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Frequently Asked Questions
What does Selank do?
Selank is a synthetic seven-amino-acid peptide (Thr-Lys-Pro-Arg-Pro-Gly-Pro) built from the natural immune peptide tuftsin, with a small chemical tweak to make it last longer in the body. It was developed in Russia as an anti-anxiety and nootropic agent and is approved there for generalized anxiety disorder, but it has no FDA or EMA approval and almost no Western clinical data. The pitch is calm and focus without the sedation, dependence, or withdrawal that come with benzodiazepines.
How does Selank work?
Selank seems to work through several overlapping systems rather than one tidy target. It influences GABA signaling, the brain's main calming neurotransmitter system, which likely accounts for its anti-anxiety effect. It also slows the breakdown of enkephalins, the body's own opioid-like peptides involved in mood and stress, which is a mechanism entirely different from benzodiazepines or SSRIs. Animal work additionally points to effects on serotonin and dopamine balance and on BDNF, a growth factor tied to learning and neuron health. These pathways are well documented in rodents; the picture in humans is inferred rather than directly measured.
Is Selank FDA approved?
No, Selank is not currently FDA approved. Current status: Approved in Russia - Not FDA or EMA approved. FDA removed selank acetate from 503A Category 2 in Sept 2024 after the nominators withdrew it, and now lists it among nominated-but-withdrawn substances, noting it lacks key human safety information. It is not on the 503A bulks list, was not among the seven peptides reviewed at the July 2026 PCAC meeting, and has no announced review date.
Is Selank banned in sport?
Not named on the WADA list. Because it is approved in Russia, the S0 catch-all arguably does not apply, but no other section clearly covers it, so its status is unclear; check with your anti-doping agency.
What are the side effects of Selank?
Reported side effects include: Generally well-tolerated, Nasal irritation (spray), Headache, Nausea, Fatigue. Individual responses vary based on dosage, duration, and personal health factors.
What is the typical dose of Selank?
Community-reported common dose: 250-500 mcg 2-3x daily (2-3x daily). Range: 200-750 mcg per dose. Administration: Intranasal spray (most common), subcutaneous injection. Community-reported doses. Not medical advice. Consult healthcare provider.
Related Peptides
Peptides commonly compared with Selank or used in similar applications.
Semax
Clinical TrialsSemax is a synthetic heptapeptide (Met-Glu-His-Phe-Pro-Gly-Pro) developed in Russia in the 1980s as an analog of the ACTH(4-10) fragment, with a Pro-Gly-Pro tail added to resist breakdown. It is researched and used as a neuroprotective and nootropic agent, typically intranasally, and keeps the cognitive and neurotrophic effects of the ACTH fragment without the parent hormone's cortisol-raising activity. It is used clinically and registered in Russia (including for ischemic stroke and cognitive disorders) but is not approved by the FDA or EMA, and Western evidence is limited.
CognitiveCerebrolysin
Clinical TrialsCerebrolysin is not a single peptide but a mixture: a preparation of small peptides and free amino acids made by enzymatically breaking down purified porcine (pig) brain protein, manufactured by EVER Neuro Pharma in Austria. It is given by injection and is approved as a prescription drug in dozens of countries for stroke, traumatic brain injury, and dementia, but it is not FDA-approved in the United States. Despite decades of use abroad, the human evidence remains genuinely contested.
CognitiveDihexa
PreclinicalDihexa (N-hexanoic-Tyr-Ile-(6) aminohexanoic amide) is a small synthetic peptide built from angiotensin IV, engineered at Washington State University to be orally active and to cross into the brain. The pitch is bold: it is studied as a procognitive compound that may rebuild synaptic connections, and lab claims of extreme potency made it a darling of the nootropic underground. The reality check: every supporting study is in cells or rodents, there are zero human clinical trials, and in April 2025 the journal retracted two of the key papers behind its proposed mechanism (2012 and 2014) after a university investigation.
CognitiveP21
PreclinicalP21 (also written P021) is a small synthetic peptide reverse-engineered from the most active region of ciliary neurotrophic factor (CNTF), with an adamantane group bolted on to help it survive in the body and reach the brain. It is studied as a neurogenic and neurotrophic compound for Alzheimer's disease and other memory disorders, with the appeal of getting CNTF-like benefits in a small, orally available molecule. The honest status: it looks genuinely promising in mouse models, but the entire evidence base comes from a single research group and there are no human trials.
CognitiveGB-115
Clinical TrialsGB-115 is a synthetic dipeptide anxiolytic developed in Russia, chemically the amide of N-phenylhexanoyl-glycyl-L-tryptophan and described as a retro-analogue of cholecystokinin-4. Rather than acting like a benzodiazepine, it blocks cholecystokinin receptors, a different anti-anxiety route. It has been studied in animals and in a small pilot human study, but it is not an approved or widely available medication.
CognitiveAdamax
PreclinicalAdamax is sold widely as an enhanced Semax derivative, and it is one of the clearest examples of a compound where availability has run far ahead of information. Vendors list it, forums discuss it, and there is essentially no peer-reviewed literature under this name. This page tells you what is actually known, what is inferred from its parent compound, and where the honest gaps are, because pretending otherwise would not help you.
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