Also known as P021 / CNTF-derived peptidergic compound
P21 is a small peptidergic compound derived from an active region of ciliary neurotrophic factor (CNTF), studied in research for neurogenic and synaptogenic signaling.
Supplied strictly for laboratory research use within Canada. Not for human or veterinary use.
$154.95CAD
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Research Use Only
This product is intended strictly for laboratory research use within Canada. It is not approved by Health Canada for the diagnosis, treatment, cure, or prevention of any disease. Not for human or veterinary use.
By purchasing, you confirm the material will be used solely for lawful research purposes in accordance with applicable Canadian regulations.
P21 is a small peptidergic compound derived from an active region of ciliary neurotrophic factor (CNTF), studied in research for neurogenic and synaptogenic signaling.
Experimental models examine its effect on hippocampal neurogenesis, BDNF expression and synaptic plasticity endpoints.
P21 (P021) was developed from an active fragment of ciliary neurotrophic factor and chemically modified to improve stability and brain penetration relative to the parent peptide. That modification is what allows it to be dosed in whole-animal work rather than only in cell culture.
Research frameworks use it to probe neurotrophic signaling: adult hippocampal neurogenesis in the dentate gyrus, BDNF-associated pathways, dendritic and synaptic markers, and tau-related endpoints in aged and transgenic rodent models.
History
Neurotrophic factors such as CNTF showed activity in neurodegeneration models but were poor drug candidates — large, unstable, and unable to cross the blood-brain barrier in useful amounts. That motivated a search for small-molecule and peptide mimetics reproducing the signaling without the delivery problem.
P021 emerged from that work as an adamantylated tetrapeptide derived from a CNTF active region. It was subsequently characterized in a triple-transgenic Alzheimer model, in aged rats where cerebrospinal-fluid tau was measured, and in the Ts65Dn mouse model of Down syndrome, including treatment initiated during early postnatal development.
Key Research Areas
Laboratory investigations into P21 focus on neurotrophic signaling and its structural correlates. Research frameworks evaluate adult hippocampal neurogenesis, BDNF expression and downstream plasticity pathways, dendritic and synaptic markers, and tau-related endpoints in transgenic and aged rodent models under controlled conditions.
2 of the 4 areas below are addressed directly by a paper cited on this page.
CNTF-derived neurotrophic signaling models
Addressed on this page by Kazim SF et al. 2014, Khatoon S et al. 2015, Kazim SF et al. 2017. Each is linked to its source record in the references below, so what was measured — and in what system — can be read rather than taken on trust.
Kazim SF et al. (2014) — Disease modifying effect of chronic oral treatment with a neurotrophic peptidergic compound in a triple transgenic mouse model of Alzheimer’s disease
Khatoon S et al. (2015) — Elevated Tau Level in Aged Rat Cerebrospinal Fluid Reduced by Treatment with a Neurotrophic Compound
Kazim SF et al. (2017) — Early neurotrophic pharmacotherapy rescues developmental delay and Alzheimer’s-like memory deficits in the Ts65Dn mouse model of Down syndrome
Adult hippocampal neurogenesis research
No paper cited on this page reports on adult, hippocampal or neurogenesis. This heading marks where P21 is discussed in the category rather than a question the cited literature answers, and it is worth knowing which of these areas has work behind it and which does not.
Synaptic plasticity and BDNF pathway studies
Addressed on this page by Kazim 2016. Each is linked to its source record in the references below, so what was measured — and in what system — can be read rather than taken on trust.
Kazim SF, Iqbal K (2016) — Neurotrophic factor small-molecule mimetics mediated neuroregeneration and synaptic repair: emerging therapeutic modality for Alzheimer’s disease
Tau and neurodevelopmental rodent-model frameworks
No paper cited on this page reports on neurodevelopmental or rodent. This heading marks where P21 is discussed in the category rather than a question the cited literature answers, and it is worth knowing which of these areas has work behind it and which does not.
The references section of this page cites 4 primary papers published between 2014 and 2017 — a limited but non-trivial record. Every citation is linked to its PubMed or DOI record so it can be read rather than taken on trust, and the summaries above describe what those papers report rather than what the compound is claimed to do.
Worth noting when weighing that record: roughly 50% of the citations here list Kazim SF et al. as lead author. A literature concentrated in one research group has not been independently replicated to the same degree as one drawn from many, and that is a real limitation on how far the findings can be generalised — regardless of how consistent the individual results look.
P21 is frequently listed as a peptide by suppliers in this market. It is not one. The structure published on this page is the compound's actual chemistry, and research on it should be read against its own class rather than against peptide literature.
Research compounds attract claims that outrun their evidence. Below are the ones most often encountered for P21, set against what the papers cited on this page actually report. Where the record is thin or contested, that is stated rather than smoothed over.
Preclinical only
P21 is commonly described online in connection with sharper focus, better memory and improved mood. In the research literature the same compound is filed under CNTF-derived neurotrophic signaling models, adult hippocampal neurogenesis research and synaptic plasticity and BDNF pathway studies.
The 4 papers cited on this page, published between 2014 and 2017 (3 in animal models) describe laboratory and animal work. None reports a controlled trial in humans. Findings in cell culture or in a rodent model describe what happened in that system; they do not establish that the same occurs in humans, and this compound is not approved for human use.
Contested
Presented as having independent scientific backing.
Around 50% of the papers cited here list Kazim SF et al. as lead author. A literature concentrated in one research group has not been independently replicated to the degree its volume suggests, and that is a real limit on how far the findings generalise — however consistent the individual results appear.
Nothing above is a statement of what this material does. It is a summary of what has been published and what has not. Eppix Labs supplies research materials only and provides no dosing, administration or protocol guidance.
Verification for P21 is per lot, not per product. The current 10mg lot P21-CA-26H-10 returned 99.339% purity, 12.24 mg measured, 122.4% of the labelled 10 mg, assayed by Janoshik. Those figures are the laboratory's, published in full rather than reduced to a badge.
Purity is half the number. It states what fraction of the material in the vial is P21; it says nothing about how much material is in the vial, and a short-filled vial can return a purity result that is entirely accurate. The figure that answers the second question is measured mass against expected content — for P21, this lot measured 122.4% of its labelled 10 mg. Both numbers are published for every lot, whichever way they fall.
The lot code printed on the vial matches the code on the certificate for P21. Matching the two is what confirms the unit in hand came from the batch that was tested — a certificate not tied to a lot code proves nothing about any particular unit.
Researchers who buy P21 in Canada through Eppix Labs receive the lot described by the certificate above: the code printed on the vial label is the code on the certificate, and both are searchable on the batch verification page.
−20 °C long-term; stable at room temperature in transit
After reconstitution
2–8 °C
Light
Protect from UV and direct light
Freeze-thaw
Avoid repeated cycles
Vehicle
Solvent selection depends on the compound; consult the published literature
Format
Lyophilized powder
P21 is supplied as lyophilized powder. It is not a peptide, and solvent behaviour follows from its own chemistry rather than from the aqueous-vehicle conventions that apply to peptide material — the published literature for this compound is the reference for solvent selection, not a general peptide protocol.
Dry storage below freezing and protection from light are the general controls. As with any lyophilized material, the powder frequently sits as a thin film at the base of the vial and is easy to mistake for an empty vial before inspection.
Vials may appear empty on arrival. Lyophilized material collects at the base of the vial and is often not visible until the vial is inspected under direct light.
1 × sealed glass vial in the strength selected (10mg / Single Vial, 10mg / 5-Pack, 10mg / 10-Pack available), batch-labelled
The batch-linked Certificate of Analysis for the exact lot shipped
Discreet outer packaging with no product names on the exterior
Canada Post Xpresspost, tracked, typically 1–2 business days from Canadian stock
Not included
Bacteriostatic water or any other reconstitution vehicle
Syringes, needles or filters
Dosing, administration or protocol guidance of any kind
Reconstitution materials are sourced separately. The reconstitution calculator on this site works out concentrations for a given volume, but it is an arithmetic tool for laboratory record-keeping and not a protocol.
No. Eppix Labs products are supplied exclusively for laboratory research. We do not provide dosing, administration, or usage guidance.
Each unit contains the labeled quantity of P21. Independent third-party analysis verifies purity, identity, and net content per batch.
The unit contains only the research compound. Any laboratory materials required for reconstitution or experimental procedures must be sourced separately.
Duration depends entirely on research design, storage conditions, and laboratory protocol.
Kazim SF et al.(2014)
Disease modifying effect of chronic oral treatment with a neurotrophic peptidergic compound in a triple transgenic mouse model of Alzheimer’s disease
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Have questions about batch verification, documentation, or research specifications? Our team is available to assist with product and compliance inquiries.