PubMed
Semax, an analog of ACTH(4-7), regulates expression of immune response genes
Dmitrieva et al., 2013
ACTH(4-10)-Pro-Gly-Pro
Semax is a synthetic heptapeptide analog of the ACTH 4-7 fragment extended with Pro-Gly-Pro (PGP) to increase CNS stability and activity. Developed in Russia and approved there for stroke treatment, cognitive enhancement, and neuroprotection. Administered intranasally for direct CNS delivery. Robust Russian clinical literature; not FDA-approved in the US. Widely used as a research nootropic.
Overall check-ins
Trackers & reports
Overview
Semax is a synthetic heptapeptide analog of the ACTH 4-7 fragment extended with Pro-Gly-Pro (PGP) to increase CNS stability and activity. Developed in Russia and approved there for stroke treatment, cognitive enhancement, and neuroprotection. Administered intranasally for direct CNS delivery. Robust Russian clinical literature; not FDA-approved in the US. Widely used as a research nootropic.
Community
From check-in ratings — separate from side effects logged below. Side effects are logged separately from overall experience. A favorable check-in can still include nausea, fatigue, or injection-site reactions.
Favorable 97% · Mixed 3% · Unfavorable overall 0%
Benefits users selected when logging a favorable or mixed check-in.
Side effects are logged separately from overall experience. A favorable check-in can still include nausea, fatigue, or injection-site reactions.
Median bucket: 0.2–0.4 mg · Most common: 0.2–0.4 mg
Reports span 0.1 to ≥ 5 mg (open-ended top bucket)
Anonymized self-reports from PeptIQ users — not prescribing guidance. Buckets group similar logged amounts; open-ended top buckets mean “at least” that dose.
Among repeat reporters, 92% said they felt similar to their last entry, 8% more positive, and 0% more negative.
Overall, repeat reporters leaned more positive than their previous entry.
Median gap between entries: 46 days · Based on 37 repeat reporters
Research
PubMed
Dmitrieva et al., 2013
PubMed
Ashmarin et al., 2006
PubMed
Dolotov et al., 2008
ClinicalTrials.gov
ClinicalTrials.gov, 2024
PubMed
Giri et al., 2025
PubMed
Gusev et al., 2018
Tools
More ways to learn about Semax from observational PeptIQ data.
Help
This page summarizes 74 anonymized self-reports from PeptIQ users who track Semax, including commonly reported effects and co-tracked peptides. These are observational patterns, not clinical outcomes.
PeptIQ separates overall check-in ratings (favorable, mixed, or unfavorable) from logged side effects like nausea or fatigue. Users often report benefits and side effects in the same check-in — a high experience score does not mean zero side effects were noted.
6 sources are linked on this page, including PubMed articles, clinical trial registries, and FDA labels where applicable. Citations describe published research — not recommendations.
This wiki does not assess safety or recommend use. Semax is listed as Intl. Approved (Russia). Consult a licensed clinician for personal medical decisions.
Research, primarily in animal models, suggests Semax may have a wide range of therapeutic potentials due to its ability to promote angiogenesis (formation of new blood vessels), stimulate collagen synthesis, and modulate inflammatory responses.
SourceSemax is not approved by the FDA for any human use. There is no legal basis for selling it as a drug, food, or dietary supplement in the United States. The FDA has classified Semax as a Category 2 bulk drug substance, which explicitly prohibits licensed compounding pharmacies from using it in compounded medications.
SourceThe safety and effectiveness of Semax have not been thoroughly evaluated in humans through rigorous clinical trials. This lack of human data means that safe dosages, short-term side effects, and long-term health consequences are largely unknown.
SourceWhile there are over 200 published studies on Semax, the vast majority are animal or in vitro (cell) studies. These preclinical studies consistently show positive results across various tissue types. However, there is a significant lack of comprehensive human clinical trial data.
Source