Peptuno
Cognitive & Neuropeptides
HOT

Product details

P21 (also designated P021 or Peptide 6c in some publications) is a synthetic tetrapeptide derivative inspired by ciliary neurotrophic factor (CNTF), specifically a capped hexapeptide (Ac-Asp-Gly-Gly-Leu-Ala-Gly-NH2, Ac-DGGLAG-NH2) whose Asp-Gly-Gly-Leu (DGGL) N-terminal segment is the active core pharmacophore, with an adamantane moiety carried on the molecule that provides oral bioavailability and blood-brain-barrier penetration. The molecule was developed at the New York State Institute for Basic Research as a small-molecule mimetic of CNTF's neurogenic and BDNF-upregulating effects without CNTF's known dose-limiting side-effect profile. P21 is studied in research contexts for adult hippocampal neurogenesis, BDNF expression, and Alzheimer's disease and aging-related cognitive decline models.

Peptuno supplies P21 as a lyophilized powder at ≥99.0% HPLC purity. The adamantane modification creates analytical challenges similar to other lipidated peptides, the modified molecule is substantially more hydrophobic than the unmodified DGGLAG hexapeptide and requires modified RP-HPLC conditions for adequate resolution. The release packet covers peak-integration HPLC under appropriate conditions, mass spec confirming the adamantane-modified mass, and water content. The 5 mg fill size matches typical neuroscience-research aliquot scales.

Regulatory note: Research peptide derivative; CAS is not consistently registered across suppliers. Sold for research use only.

FAQ

Why does P21 need the adamantane modification?
The unmodified DGGLAG peptide is too polar for both oral absorption and blood-brain-barrier penetration, properties that would make it useless for CNS research. The adamantane group provides three things: (1) increased overall hydrophobicity that supports passive membrane diffusion, (2) protection against aminopeptidase cleavage, and (3) sufficient blood-brain-barrier permeability that systemic administration produces meaningful CNS exposure. The adamantane is a delivery vehicle rather than a pharmacophore, the biological activity comes from the DGGL core sequence, but the modification is essential for the molecule to reach its target tissue at functional concentrations.
What is CNTF and why is P21 derived from a CNTF-mimetic design?
CNTF (Ciliary Neurotrophic Factor) is a 200-amino-acid cytokine in the IL-6 family with strong neurotrophic and neurogenic activity in CNS research models. Native CNTF advanced through clinical trials for ALS in the 1990s and was discontinued due to severe off-target side effects (weight loss, fever, antibody formation) that came from the cytokine's broad receptor-binding profile. The P21 design strategy isolated a short active core (DGGL, presented within the Ac-DGGLAG-NH2 hexapeptide) from a specific region of CNTF hypothesized to drive the neurogenic activity, then added the adamantane group for delivery, producing a small molecule that retains some of CNTF's neurogenic effects without the cytokine's full receptor-binding profile and associated side effects. P21 is therefore a research tool for studying CNTF-mimetic biology in isolation from the broader cytokine pharmacology.

Certificate of Analysis (COA)

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