Default mode network study
A 2018 randomised fMRI study in 24 participants reported increased default mode network volume in the medial frontal cortex against placebo after dosing. Reported in the cited paper.
SourceResearch Use Only. Products listed are not for human or animal consumption. Statements have not been evaluated by the FDA.View full disclaimers →
Semax is a synthetic heptapeptide based on a fragment of ACTH with modifications that improve stability and brain penetration. Developed in Russia and registered there for stroke and cognitive disorders, it is not approved in the United States or Europe.
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Overview
Semax is a synthetic heptapeptide based on a fragment of ACTH with modifications that improve stability and brain penetration. Developed in Russia and registered there for stroke and cognitive disorders, it is not approved in the United States or Europe.
What the research reports
Outcomes described across the published Semax literature and ongoing study. Read each as research context rather than a promised personal result.
Cognitive research interest
Studied in Russia for cognitive disorders and stroke recovery, where it is a registered medicine rather than an unapproved compound. Reported in research settings.
Brain connectivity changes
A 2018 randomised fMRI study reported increased default mode network volume in the medial frontal cortex against placebo. Reported in research settings.
Neuroprotection study record
Animal work describes reduced ischemic damage, which underpins the stroke recovery indication in its country of registration. Reported in research settings.
Neurogenesis signalling work
Published work describes effects on neurogenesis and progenitor cell proliferation, alongside modulation of neurotransmitter systems. Reported in research settings.
Rapid onset by nasal route
Intranasal administration is reported to produce effects within 15 to 30 minutes, which shapes how protocols are timed. Reported in research settings.
Dosage and protocol
Protocols use 200 to 600 mcg daily intranasally, split across one or two doses, for 10 to 20 days before a break. Figures describe study protocols, not a personal regimen.
Clinical evidence
The published Semax record, labeled by strength so you can see what is settled and what is still emerging.
A 2018 randomised fMRI study in 24 participants reported increased default mode network volume in the medial frontal cortex against placebo after dosing. Reported in the cited paper.
SourceA randomised study in 52 participants reported distinct functional connectivity changes in amygdala and prefrontal regions for semax against selank. Reported in the cited paper.
SourceA Russian randomised trial in 60 patients reported 83 to 94 percent efficacy for visual field and light sensitivity, with semax inside a combined protocol. Reported in the cited paper.
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