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Biolivon publishes the science.

Investigational compound

N-Acetyl Selank

Also known as NA-Selank, N-Acetyl Selank Amidate

An acetylated variant of Selank sold on the research market.

Human studies
0
Trials tracked
0
Preclinical
0
Safety signals
1
Last reviewed
11 Aug 2026
Reviewed by
Not yet reviewed

Same position as N-Acetyl Semax. The clinical history belongs to Selank; this variant borrows the reputation without the evidence, and the modification that is supposed to make it better is also what makes the borrowing invalid.

This dossier has not been reviewed yet. Our editorial board is not appointed. Every page is supposed to carry a named scientific and medical reviewer with declared conflicts, and until that is true this page has had no expert check — treat it accordingly. We would rather say so than print a name-shaped placeholder where a person should be.
N-Acetyl Selank is not an approved medicine for human use in the jurisdictions listed below. This page summarises research. It is not a recommendation, and it contains no dosing or administration guidance. If you are considering anything described here, discuss it with a qualified clinician.
On this page

What it is

Selank with an acetyl group at the N-terminus, sold as a research chemical.

How it is proposed to work

Marketed as longer-acting through resistance to aminopeptidase cleavage. The chemistry is plausible; the human consequence is uncharacterised.

Approved medical uses

None. N-Acetyl Selank has no approved human medical indication in the jurisdictions we track. Any use is outside an approved label.

Human research

Each entry states what the study found and, separately, what it cannot show.

No adequate published human research. This absence is the reason for the evidence grade above — it is not a gap we can fill with animal data.

Preclinical research

Animal and laboratory work. Useful for generating hypotheses; it cannot establish that something works in people.

No preclinical studies catalogued.

Potential safety concerns

  • CautionInsufficient

    No clinical data for this variant. Selank's use history does not transfer to a modified molecule.

Known interactions and contraindication considerations

  • Uncharacterised.

This list is not exhaustive and is not a substitute for a clinician reviewing your full medication history.

Regulatory status

Status is shown per jurisdiction and is accurate only as of the date stated. Where a compound is approved, the approval is bound to a specific formulation, manufacturer and indication — shown in the detail column.

United States
FDA
Unapproved / investigational
as of 11 Aug 2026

No marketing authorisation. The FDA has not evaluated this compound — that is an absence of any opinion, not a negative finding.

European Union
EMA
Unapproved / investigational
as of 11 Aug 2026

No marketing authorisation.

India
CDSCO
Unapproved / investigational
as of 11 Aug 2026

Not approved for human use. A first-time synthetically manufactured peptide falls under the new-drug pathway.

Russian Federation
Ministry of Health / Roszdravnadzor
Unapproved / investigational
as of 11 Aug 2026

The registered Russian medicine is Selank. This variant is not that product.

How it is being used

What the grey community actually runs, the reasoning they give, and our read on whether it follows from known biology. This is observation, not evidence, and not a recommendation.

No community use documented for this compound yet. Absence here means our editorial team has not reviewed and verified a pattern — not that none exists.

Active clinical trials

No registered trials currently tracked for N-Acetyl Selank.

Search all tracked trials

What remains unknown

The questions that would change our assessment if they were answered.

  • Does it differ from Selank in any way a person would notice?

References

    Editorial change history

    When we change a grade or a regulatory note, we log it here rather than editing quietly.

    • Dossier created.

    Spotted something wrong? Tell us — we publish corrections.