For laboratory and research use only. Not for human or animal consumption. Sold to qualified researchers and licensed laboratories.
Home › Learn › P-21 guide
Nootropics & Neuro · Research guide · Updated 2 October 2026

What is P-21, and what is it studied for?

P-21, written P021 in the literature, is a small peptide derived from ciliary neurotrophic factor, built on the tetrapeptide Asp-Gly-Gly-Leu with an N-terminal acetyl, a C-terminal amide and an adamantyl group added for metabolic stability. It is studied in rodent models of neurodegeneration as a neurotrophic mimetic. No CAS number or PubChem record is on file here, and the product page says so.

What is the structure of P-21?

The core is the CNTF-derived sequence Asp-Gly-Gly-Leu, acetylated at the N-terminus and amidated at the C-terminus, with an adamantylated glycine appended; the adamantane cage is the modification the adamantane post describes. Because no public registry record has been confirmed, the formula and mass fields on the product page are blank rather than estimated, and the certificate's identity line is the reference for this material's mass.

IdentifierValue
Molecular formulanot recorded
Molecular weightnot recorded
Residuesnot recorded
CAS numbernot recorded
PubChem CIDnot recorded
Current lotP21-5-0318

How is P-21 thought to work?

Designed to mimic the active region of ciliary neurotrophic factor; the reported mechanism in rodent work is an increase in brain-derived neurotrophic factor and downstream neurogenesis and synaptic markers. A receptor-level interaction has not been established; the compound is a peptidergic mimetic rather than a receptor ligand with a defined binding site.

Which research areas use P-21?

AreaTypical models and endpoints
Neurotrophic signallingBDNF and synaptic-marker readouts in rodent brain.
Neurodegeneration modelsTransgenic mouse models in the Iqbal laboratory's work.
Peptide designAdamantylation as a stability strategy; comparison with the parent CNTF fragment.
Analytical chemistryA modified tetrapeptide whose identity depends on the certificate's measured mass.

What does the published literature show?

Kazim and colleagues reported chronic oral treatment with the compound in a triple-transgenic mouse model in Neurobiology of Disease in 2014, and Kazim and Iqbal reviewed neurotrophic mimetics in Molecular Neurodegeneration in 2016. The work is from one laboratory group, in mice. There is no clinical programme; research use is in-vitro and preclinical.

How is P-21 handled in the laboratory?

Dissolves in water with swirling; the adamantyl group adds hydrophobicity, so a small fraction of organic co-solvent may be needed at high concentration. Store lyophilized at minus 20 °C; aliquot and freeze solutions; use low-binding tubes. The concentration table covers volumes and syringe units; the storage guide covers stability by compound class.

What does the current certificate show?

Lot P21-5-0318 tested at 99.8% purity by RP-HPLC (214 nm), identity confirmed by MALDI-MS, endotoxin <0.05 EU/mL. The certificate is in the COA library and the lot number on the vial matches it. Sold as 5 mg per vial at $120, for laboratory research only.

Certificate history for P-21

Every certificate the library holds for this compound, newest first. A replaced lot stays listed so the history can be read; the certificate dataset reads all 114 together.

LotIssuedSizeIdentityPurityContentStatus
P21-5-0318Jun 17, 20265 mgMALDI-MS99.8%5.25 mgCurrent
P21-5-0318Apr 3, 20265 mgMALDI-MS99.6%5.42 mgCurrent

Frequently asked questions

Why are the formula and CAS fields blank?

Because no public registry record has been confirmed for this material, and the editorial policy is to leave a field blank rather than fill it with a plausible number. The certificate's identity line is the mass reference.

What does the current certificate show?

Lot P21-5-0318: identity by MALDI-MS, purity 99.8% by RP-HPLC at 214 nm, content 5.25 mg, endotoxin below 0.05 EU/mL, sterility not detected. Issued 17 June 2026.

What does the adamantyl group do?

It is a rigid hydrocarbon cage attached to improve stability against enzymatic breakdown and alter how the peptide crosses membranes. The adamantane post covers the chemistry.

References

  1. Kazim SF, Blanchard J, Dai CL, et al. Disease modifying effect of chronic oral treatment with a neurotrophic peptidergic compound in a triple transgenic mouse model of Alzheimer's disease. Neurobiol Dis. 2014;71:110-130.
  2. Kazim SF, Iqbal K. Neurotrophic factor small-molecule mimetics mediated neuroregeneration and synaptic repair: emerging therapeutic modality for Alzheimer's disease. Mol Neurodegener. 2016;11:50.

Clinical results cited above describe regulated trials of pharmaceutical products and are given as context for research interest only. Nothing on this page describes or recommends use of the material sold here in humans or animals.

COA on every lotPublished before listing
≥99% purityHPLC and LC-MS verified
Same-day shippingOrders before 2pm ET
Secure checkoutCard details are entered on our payment partner's own encrypted page
USA-basedSynthesized and shipped domestically
Discreet packagingPlain box, no product names

Restock alerts and new lot reports, by email

One email when a new certificate is published, when a sold-out compound is back, or when a new compound is added. About twice a month, nothing else.