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Semax: doses reported in published research

Sources checked 2026-10-07 · 3 cited studies (1 human, 2 animal, 0 cell culture)

Semax (Met-Glu-His-Phe-Pro-Gly-Pro) is a synthetic analog of the ACTH(4-10) fragment developed in Russia. Human data come from small Russian clinical studies; animal data mainly from rat brain ischaemia models.

Human data: one small Russian clinical study in acute ischaemic stroke (30 treated, 80 controls; 1997). Other Russian clinical reports do not state amounts in their abstracts.

Studies in people (1)

Human 30 adults in the acute period of ischaemic stroke (80 controls on conventional care), non-randomized comparison

Dose as reported
12 mg per day (moderate stroke) or 18 mg per day (severe stroke)
Route
Not stated in the abstract
Frequency / duration
Courses of 5 and 10 days

Source wording: daily doses were 12 mg for patients with strokes of moderate severity and 18 mg for patients with severe strokes (treatment course--5 and 10 days) was studied in 30 patients in acute period of hemispherical ischemic stroke. Control group consisted of 80 patients

Gusev EI, Skvortsova VI, Miasoedov NF et al.. [Effectiveness of semax in acute period of hemispheric ischemic stroke (a clinical and electrophysiological study)]. Zh Nevrol Psikhiatr Im S S Korsakova 1997. PubMed PMID 11517472 ↗

Animal studies (2)

Animal doses are listed exactly as the studies report them. They are not converted to human amounts here; doses do not translate between species by body weight.

Animal Rats (basal forebrain BDNF levels)

Dose as reported
50 or 250 µg/kg
Route
Intranasal
Frequency / duration
Single dose; measured after 3 h

Source wording: Semax applied intranasally at 50 and 250 microg/kg bodyweight resulted in a rapid increase in BDNF levels after 3 h

Dolotov OV, Karpenko EA, Seredenina TS et al.. Semax, an analogue of adrenocorticotropin (4-10), binds specifically and increases levels of brain-derived neurotrophic factor protein in rat basal forebrain. J Neurochem 2006. PubMed PMID 16635254 ↗

Animal Rats (permanent middle cerebral artery occlusion)

Dose as reported
100 µg/kg
Route
Intraperitoneal
Frequency / duration
15 min, 1 h, 4 h and 8 h after occlusion

Source wording: ischemia + Semax animals were given intraperitoneal injections of Semax (100 μg/kg) The injections of Semax or saline were performed 15 min, 1, 4 and 8 h after pMCAO.

Medvedeva EV, Dmitrieva VG, Povarova OV et al.. The peptide semax affects the expression of genes related to the immune and vascular systems in rat brain focal ischemia: genome-wide transcriptional analysis. BMC Genomics 2014. PubMed PMID 24661604 ↗ · full text PMC3987924 ↗

Half-life

No half-life value was found in the sources reviewed for this page.

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See also: Semax research profile · lab-tested lots (COA lookup) · all compounds in this section.