P21-Adamantane, product photo
Cognition

P21-Adamantane

P21-Adamantane - stabilized P21 variant with adamantane modification. Better lipophilicity and half-life.

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At a glance

P21-Adamantane by the numbers

The key figures from our lexicon.

Full lexicon entry
Class
CNTF-derived neurogenic peptide

stabilized

Half-life
longer than P21

adamantylated

Use
Subcutaneous

in mcg

Sizes
10 mg

1 size in the shop

For research and educational purposes only. Values from the TPD lexicon, sources linked there.

There is no lab analysis for P21-Adamantane yet. Vote for itAll lab analyses

Knowledge

Everything about P21-Adamantane

Description

P21-Adamantane is a chemically modified variant of the CNTF mimetic peptide P21 with attached adamantane group. The adamantane modification is an established strategy in medicinal chemistry for raising lipophilicity and improving blood-brain barrier penetration.

Per study reports the adamantane group brings three theoretical advantages over pure P21:

  • Increased lipophilicity with better CNS penetration
  • Extended half-life through protection from enzymatic degradation
  • Improved membrane permeability

The action mechanism remains identical to P21: activation of the CNTF receptor pathway with stimulation of neurogenesis in the hippocampus and subventricular zone. Direct comparison data between P21 and P21-Adamantane are however very limited - the adamantane variant is newer and less well characterized.

Typical application is subcutaneous or intranasal, possibly also oral with better bioavailability than the unmodified P21.

You can order P21-Adamantane as lyophilized peptide in 10-pack at 10mg per vial.

This information is for research and educational purposes only. No medical recommendations.

Risks & Safety

P21-Adamantane is described as well tolerated per study reports. The profile follows the parent compound P21, though the adamantane variant itself is newer and less well characterized.

Observed in research and user reports:

  • Application site: with subcutaneous or intranasal use, mild redness or irritation at the application site is the most common observation.
  • Neurogenic action: the compound activates CNTF receptor pathways and stimulates neurogenesis in animal models, a biologically active intervention in central plasticity pathways.
  • Adamantane modification: the adamantane group increases lipophilicity and CNS penetration, which may amplify the effect but makes additional data on the modified form very limited.
  • No human data: direct comparison studies against P21 are very limited. Robust human studies and long-term data do not exist.

This classification does not replace medical advice. Risk and responsibility for any actual use lie entirely with the buyer.

Studies

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FAQ

Frequently asked

Sources for every answer: lexicon entry

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Is P21-Adamantane approved or studied in humans?

No. There is no approval and as of 26 October 2026 ClinicalTrials.gov lists no trial with P021. All data come from cells and animals.

How does P21-Adamantane differ from P21?

According to the literature, nothing that has been shown. The very first paper from 2010 described P21 as a peptide with adamantane. Later papers call it P021: a tetrapeptide from CNTF plus a glycine with an adamantane group at the end. A further, longer-acting adamantane variant is not described in any study.

What is the adamantane for?

It is meant to get the peptide through the blood-brain barrier more easily and protect it from enzymes that cut peptides from the end. In old rats P021 did reach the brain.

What did the Alzheimer models show?

Mice with three Alzheimer genes received P021 with their food for twelve months. Abnormal tau declined clearly, soluble amyloid fell, memory and the formation of new nerve cells improved. When dosing started early, the changes largely did not appear.

What did old rats show?

Rats aged 22 to 24 months lost less learning and memory performance with P021 and made more BDNF. The tau level in the cerebrospinal fluid fell to that of young rats.

Which side effects are known?

There are no solid data because P021 has never been tested in humans. In old rats it caused no detectable immune reaction. That cannot be transferred to humans.

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