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Semax

IntranasalEvidence B

What to know about Semax

Semax is a synthetic ACTH(4-7)-related heptapeptide developed in Russia and studied through intranasal administration. English-language human evidence is limited.

How it may work
Proposed mechanisms include changes in neurotrophin expression, oxidative-stress responses, and neurotransmitter systems. Much of this work is preclinical.
What research found
A small study of 30 adults after ischemic stroke reported short-term neurologic and laboratory differences. The size, setting, and older evidence base limit certainty.
What is not settled
Large, independently replicated safety studies and long-term surveillance are missing. FDA flags immune-reaction and peptide-impurity concerns for compounded Semax.
Research and product status
Semax is not a licensed U.S. medicine. Authorization in another country does not establish U.S. product quality or claims.

Research reference

Research amount range
200–600 mcg per administration — not a starting amount
Reference frequency
Every day — catalogue input, not a personal schedule
Evidence route
Intranasal in the cited evidence; formulation matters.
Reported timing context
Daytime dosing is typical; the peptide is short-acting so it's often split.
What people report
Focus and mood contexts are discussed acutely to within days.
Model accumulation timescale
~3 hours — about five half-lives with regular repeated exposure; not time to a result
Storage
Storage and in-use limits depend on the exact formulation and packaging. A compound name alone cannot establish temperature, diluent, or shelf life. Details
Reported course context
2–4 weeks
Reported break context
1–2 weeks Why

A research and community reference, not medical advice. Figures are descriptive, vary between sources, and are not a recommendation for use.

When results may show

When change was measured
The cited human report involved only 30 adults in an acute neurologic setting. It cannot establish when a healthy user should expect focus, mood, memory, or productivity changes.
When to assess
No modern, adequately controlled program supplies a reliable day or week for general cognitive goals. An immediate subjective sensation is not proof of a durable cognitive outcome.
Conditions and limitations
No robust evidence establishes a required time of day, work task, fasting state, cycle pattern, or companion compound for the commonly marketed use.
When to stop
No validated target, course length, maintenance phase, or quit rule exists for general cognitive use. Do not prolong exposure solely because a hoped-for focus effect is absent.

Research timing is descriptive, not a promise or personal instruction. A severe or persistent reaction needs prompt clinical review. This is not medical advice.

Combination evidence and cautions

What is known and unknown about Semax alongside other compounds or medicines.

Key properties

Formula
C37H51N9O10S
Mol. weight
813.9 Da
CAS
80714-61-0
PubChem CID
9811102

Sequence (one-letter)

MEHFPGP

Structure note

A diagram is a reference representation of the named chemical structure. It does not establish the composition, purity, or identity of any particular vial.

Loading the structure…

Degrades fast in plasma; estimates are rough.

Used intranasally where it is licensed; no Western dose-ranging trial fixes an injected schedule, so no schedule table is shown.

Modelled level — every day

1× is the peak after a single dose.

Steady-state peak
1.00× single dose

Read off the modelled curve, not an even-interval formula

Time to steady state
3hours

About five half-lives

Administrations
7/ week

Where these numbers come from

  • Russian Semax neuropeptide literatureMost Semax evidence is Russian-language clinical and preclinical work.

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