Effect

Peptides for Cognitive Enhancement

The cognitive enhancement category on PeptScope collects compounds studied for memory, attention, and neuroprotection. Several were developed inside the Soviet and post-Soviet biomedical pipeline. None of the major members of this category currently hold FDA approval for a cognitive indication in the United States.

Peptides studied for Cognitive Enhancement

Cerebrolysin

Cerebrolysin (porcine brain hydrolysate)

Evidence: Approved

Porcine brain-derived peptide hydrolysate used in Europe and Asia for stroke and dementia; not FDA-approved.

Cognitive Enhancement

Cerluten

Cerluten — Khavinson Brain Cytomax

Khavinson Bioregulators
Evidence: Preclinical

Khavinson brain Cytomax peptide complex extracted from young calf brain tissue. Marketed for CNS support in cognitive aging and post-stroke recovery.

RecoveryCognitive Enhancement

Cortagen

Cortagen — Ala-Glu-Asp-Pro (AEDP) Khavinson Cortex Cytogen

Khavinson Bioregulators
Evidence: Preclinical

Synthetic Ala-Glu-Asp-Pro tetrapeptide derived by epitope mapping from Cortexin brain extract. Khavinson cortex Cytogen targeting central nervous system gene expression.

RecoveryCognitive Enhancement

Cortexin

Cortexin (porcine cerebral cortex polypeptide complex, 10 mg lyophilized)

Cognition & Nootropics
Evidence: Preclinical

A Russian-developed porcine cerebral cortex polypeptide complex from Geropharm. Not a single peptide. Used clinically in Russia and CIS for stroke, TBI, pediatric encephalopathy, and cognitive disorders. Standard course: 10 mg intramuscular daily for 10 days. Not FDA-approved.

Cognitive Enhancement

Dihexa

Dihexa (PNB-0408, N-hexanoic-Tyr-Ile-(6)-aminohexanoic amide)

Cognition & Nootropics
Evidence: Preclinical

A small peptidomimetic derived from angiotensin IV. Reportedly potentiates HGF/c-Met receptor signaling and promotes synaptogenesis. Preclinical rodent data only. Foundational biochemistry was retracted. No human evidence.

Cognitive Enhancement

FGL

FGL — NCAM-Derived FGFR1 Agonist Peptide

Cognition & Nootropics
Evidence: Preclinical

Synthetic 15-amino-acid peptide derived from neural cell adhesion molecule (NCAM) FG loop. Activates FGFR1, promotes synaptic plasticity in aged-rat models. No human trial.

Cognitive Enhancement

Klotho

Klotho (alpha-Klotho protein, KL gene product)

Longevity & Mitochondrial
Evidence: Phase 2

An endogenous human protein produced in kidneys and brain that declines with age. Mouse overexpression extends lifespan 20-30 percent. Two Phase 1 human trials were initiated in 2025 and 2026. Not approved for any indication.

RecoveryCognitive Enhancement

Methylene Blue

Methylthioninium Chloride

Experimental & Other
Evidence: Approved

A 150-year-old textile dye and the only FDA-approved treatment for methemoglobinemia. Repurposed as a mitochondrial electron carrier with off-label cognitive and longevity use that is not supported by Phase 3 data.

Cognitive Enhancement

N-Acetyl Selank Amidate

N-Acetyl Selank Amidate — Stabilized Selank Analog

Cognition & Nootropics
Evidence: Phase 1

Modified Selank analog with N-acetyl and C-terminal amide groups added for protease resistance. Russian research literature exists; no peer-reviewed RCT of the modified form. Not FDA-approved.

Cognitive Enhancement

N-Acetyl Semax Amidate

N-Acetyl Semax Amidate — Stabilized Semax Analog

Cognition & Nootropics
Evidence: Phase 1

N-terminally acetylated and C-terminally amidated analog of Semax, the Russian ACTH(4-10) heptapeptide nootropic. Modifications target protease resistance.

Cognitive Enhancement

NAD+

Nicotinamide Adenine Dinucleotide

Longevity & Mitochondrial
Evidence: Approved

A redox cofactor required by over 500 enzymes. Declines with age in some tissues. Sold as oral precursors (NR, NMN) and as IV infusions in clinics. Longevity claims outpace controlled human evidence.

RecoveryCognitive Enhancement

NMN

β-Nicotinamide Mononucleotide

Longevity & Mitochondrial
Evidence: Approved

An NAD+ precursor that reliably raises blood NAD+ in human trials. Lived through three years of FDA regulatory uncertainty before being confirmed as a dietary supplement in September 2025.

RecoveryCognitive Enhancement

Noopept

Noopept (GVS-111, Omberacetam, N-phenylacetyl-L-prolylglycine ethyl ester)

Cognition & Nootropics
Evidence: Phase 1

A small-molecule prodrug of the endogenous dipeptide cycloprolylglycine. Approved as a prescription nootropic in Russia since 1996. Increases hippocampal BDNF and NGF. Limited Western trial validation.

Cognitive Enhancement

NR

Nicotinamide Riboside (NR, Niagen)

Longevity & Mitochondrial
Evidence: Approved

A vitamin B3 form and oral NAD+ precursor with NDI/GRAS regulatory status in the US. Reliably raises blood NAD+ by 22 to 150 percent depending on dose. Clinical endpoint benefits remain mixed.

RecoveryCognitive Enhancement

Oxytocin

Oxytocin (OT, OXT)

Cognition & Nootropics
Evidence: Approved

An endogenous 9-amino-acid neuropeptide. FDA-approved (Pitocin) for labor induction. Intranasal use widely studied for social cognition, autism, and bonding with inconsistent controlled trial results.

Cognitive Enhancement

P-21

P021 — CNTF-Derived Neurotrophic Tetrapeptide

Cognition & Nootropics
Evidence: Preclinical

Synthetic adamantylated tetrapeptide derived from CNTF by epitope mapping. Promotes hippocampal neurogenesis and BDNF expression in animal Alzheimer's models. No published human clinical trial.

Cognitive Enhancement

PE-22-28

PE-22-28 — Spadin Synthetic Peptide for TREK-1 Inhibition

Cognition & Nootropics
Evidence: Preclinical

Synthetic 7-amino-acid peptide derived from sortilin propeptide. Inhibits TREK-1 potassium channel, producing antidepressant-like effects in rodent models. No human trial.

Cognitive Enhancement

PHDP5

PHDP5 — Pleckstrin Homology Domain Peptide 5 from Dynamin 1

Experimental & Other
Evidence: Phase 2

Synthetic peptide derived from the pleckstrin homology domain of dynamin 1. Inhibits dynamin-microtubule binding and rescues synaptic transmission in tau-loaded models. Mouse Alzheimer's-model data only.

Cognitive Enhancement

Pinealon

Glu-Asp-Arg (EDR) — Khavinson Pineal Cytogen

Cognition & Nootropics
Evidence: Preclinical

Synthetic Glu-Asp-Arg tripeptide developed by the Khavinson group as the pineal-derived Cytogen for neural and cognitive bioregulation. Russian-network clinical observation data only.

Cognitive Enhancement

Pinealon

Pinealon (Glu-Asp-Arg, EDR tripeptide, Khavinson brain bioregulator)

Khavinson Bioregulators
Evidence: Preclinical

Khavinson tripeptide bioregulator (Glu-Asp-Arg) developed at the St. Petersburg Institute of Bioregulation and Gerontology. Brain-tissue-specific cytogen. Animal studies report neuroprotection and cognitive effects. No Western clinical trials.

Cognitive Enhancement

Selank

Selank (TP-7)

Cognition & Nootropics
Evidence: Phase 1

Russian-developed heptapeptide anxiolytic based on tuftsin sequence, approved in Russia, no FDA approval.

Cognitive Enhancement

Semax

Semax (Pro-Gly-Pro analog)

Cognition & Nootropics
Evidence: Phase 1

Russian heptapeptide nootropic derived from ACTH(4-7); approved in Russia for stroke and cognitive disorders.

Cognitive Enhancement

Tesofensine

Tesofensine (NS2330)

GLP-1 / Metabolic
Evidence: Phase 3

An oral triple monoamine reuptake inhibitor with approximately 10 percent weight loss in Phase 3. Originally developed for Alzheimer's and Parkinson's. Not approved in any major jurisdiction as of 2026.

Cognitive EnhancementWeight Loss

Compounds in this category

Semax and Selank are the two most documented compounds here. Both came out of the Russian Academy of Sciences in the 1980s and 1990s. Semax is registered in Russia for ischemic stroke and cognitive dysfunction. Selank is registered for generalized anxiety. The published trial base is largely Russian-language and clinically smaller than Western Phase 3 standards. Independent replication outside Russia is thin. That is the honest evidence picture, not a marketing failure.

Cerebrolysin is a different case. It is a porcine-brain-derived peptide mixture sold in more than 50 countries for Alzheimer's disease and post-stroke recovery. Multiple Phase 3 trials and Cochrane reviews exist. Effect sizes are modest. The compound is not FDA-approved in the United States and is regulated as a drug, not a supplement, in the markets that allow it.

Dihexa sits in a different evidence tier. It is an angiotensin IV analog developed by Joseph Harding's lab at Washington State University. Preclinical work suggests strong hepatocyte growth factor activity in rat hippocampal cultures. Zero human trials have been published. Anything written about Dihexa in human cognition is extrapolation from rodents.

Methylene blue belongs in its own awkward subcategory. It is an FDA-approved drug for methemoglobinemia, used clinically since the 1890s. The cognitive use case is off-label, built on mitochondrial electron transport effects observed in rodent studies and a few small human imaging studies. Pharmacy-grade methylene blue differs sharply from industrial methylene blue, which carries heavy-metal contamination.

Khavinson bioregulators like Cortexin, Cerluten, and Pinealon are short peptides developed by Vladimir Khavinson's group in St. Petersburg starting in the 1970s. Animal data is published in volume. Western peer-reviewed clinical replication is sparse. The compounds are sold as supplements in Russia and as research chemicals elsewhere. Research Use Only (RUO) labeling applies in the United States and the European Union.

Mechanism overlap

Most cognitive peptides in this category act on one of four systems. Some target BDNF and neurotrophic signaling (Cerebrolysin, Semax, Dihexa indirectly via HGF). Some modulate serotonergic and GABAergic tone (Selank). Methylene blue affects mitochondrial electron transport. The Khavinson family is proposed to act through short-peptide regulation of gene expression. Different mechanism, different tier of evidence, different regulatory status. They are not interchangeable, and stacking them does not multiply effect sizes in any controlled human trial.

Cognitive screening: what the evidence does not cover

No peptide in this category currently has Phase 3 efficacy data for cognitive enhancement in healthy adults. The clinical literature that does exist tests these compounds in stroke recovery, age-related cognitive decline, post-concussion syndrome, or specific anxiety disorders. Extrapolating efficacy to a healthy 30-year-old executive is not supported by the trial design or patient populations enrolled.

What this category is not. It is not a curated list of compounds that reliably make people smarter. Published effect sizes range from "statistically detectable in a Russian Phase 2" to "rat-only and unconfirmed." Where dosing appears in each compound page, it is reported as it appears in the cited literature. PeptScope does not frame dosing as personal advice.

What is missing from cognitive enhancement research is also worth flagging. Long-term safety data beyond 12 months is rare for the off-label members of this category. Mechanism is often plausible. Translation to humans remains the open question for the preclinical-only compounds. Readers screening this category for usable evidence should start with the trial-stage compounds and treat the rest as unverified.

Educational content only

This information is provided for research and educational purposes. It is not medical advice, diagnosis, or treatment. Many peptides described are not approved for human use outside clinical trials. Always consult a qualified healthcare professional before using any compound.