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Omni Peptides

P-21

Regular price Dhs. 1,100.00 AED
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Size
Quantity
Lyophilised & sealed vials
Independent COA · ≥99% purity
Cold-chain dispatch · same day Dubai
Discreet · unbranded outer packaging

P-21 (also known as P021, Peptide 021, or GLXC-21260) is a synthetic adamantane-modified tetrapeptide derived from a biologically active region (residues 148–151) of ciliary neurotrophic factor (CNTF). This research compound was rationally designed to capture the neurotrophic and neurogenic properties of full-length CNTF while overcoming its limitations (poor blood-brain barrier penetration, short half-life, and side effects such as anorexia and weight loss). The addition of an adamantylated glycine at the C-terminus enhances lipophilicity, metabolic stability, and CNS accessibility, enabling oral administration in research models.

Preliminary and advanced preclinical studies demonstrate that P21 promotes hippocampal neurogenesis, upregulates BDNF expression, competitively inhibits leukemia inhibitory factor (LIF) signaling, reduces tau hyperphosphorylation (via GSK-3β modulation), and improves cognitive performance in models of aging and Alzheimer’s disease. Researchers utilize P21 in laboratory and animal models to investigate mechanisms of adult neurogenesis, synaptic plasticity, tauopathy, and neurotrophic support. As a research-grade compound, P21 is intended exclusively for in vitro and animal studies. Scientists value its oral bioavailability, small size, dual BDNF/LIF mechanism, and consistent disease-modifying effects observed in 3xTg-AD and aged rodent models.

Molecular Formula
C₂₇H₄₂N₆O₈
Molecular Weight
578.7 g/mol
Sequence
Ac-DGGLAG-NH₂ (where the final “A” represents adamantylated glycine; N-terminal acetylation and C-terminal amidation; CAS 1246751-68-7)
01 Neurogenesis and Synaptic Plasticity
Preclinical studies show increased proliferation and survival of neural progenitor cells in the dentate gyrus, elevated BDNF levels, enhanced synaptic markers (e.g., synaptophysin, PSD-95), and improved long-term potentiation.
02 Cognitive Enhancement and Aging
Chronic oral administration rescues spatial learning and memory deficits in aged rats and restores performance to near wild-type levels in Alzheimer’s transgenic models.
03 Alzheimer’s Disease and Tau Pathology
In 3xTg-AD mice, P21 reduces hyperphosphorylated tau at multiple epitopes, decreases neurofibrillary pathology, and in some paradigms lowers amyloid burden, with benefits observed even when treatment is initiated after pathology onset.
04 Neuroprotection and Developmental Models
Early postnatal or prenatal-to-postnatal treatment prevents later Alzheimer-like behavioral and synaptic deficits. Additional work explores benefits in Down syndrome (Ts65Dn) models.
05 Mechanism-Focused Research
Dual action of LIF pathway inhibition (favoring neural stem cell proliferation) combined with BDNF upregulation provides a targeted tool for studying neurotrophic deficits in neurodegeneration and cognitive aging.
Storage & Handling

Lyophilised vials are stable at −20°C for up to 2 years unopened. Once reconstituted, refrigerate at 2–8°C and use within 28 days. Avoid repeated freeze-thaw cycles.

Beyond Use Date

Pre-filled formats (cartridge, pen, nasal) carry a beyond-use date of typically 4–8 weeks from receipt. ≥98% purity by HPLC. For in vitro and preclinical research use only — not for human or veterinary use.

Molecular Formula
C₂₇H₄₂N₆O₈
Molecular Weight
578.7 g/mol
Sequence
Ac-DGGLAG-NH₂ (where the final “A” represents adamantylated glycine; N-terminal acetylation and C-terminal amidation; CAS 1246751-68-7)

— About this compound

P-21 is a adamantylated CNTF-derived tetrapeptide.

P-21 (also known as P021, Peptide 021, or GLXC-21260) is a synthetic adamantane-modified tetrapeptide derived from a biologically active region (residues 148–151) of ciliary neurotrophic factor (CNTF). This research compound was rationally designed to capture the neurotrophic and neurogenic properties of full-length CNTF while overcoming its limitations (poor blood-brain barrier penetration, short half-life, and side effects such as anorexia and weight loss). The addition of an adamantylated glycine at the C-terminus enhances lipophilicity, metabolic stability, and CNS accessibility, enabling oral administration in research models.

Preliminary and advanced preclinical studies demonstrate that P21 promotes hippocampal neurogenesis, upregulates BDNF expression, competitively inhibits leukemia inhibitory factor (LIF) signaling, reduces tau hyperphosphorylation (via GSK-3β modulation), and improves cognitive performance in models of aging and Alzheimer’s disease. Researchers utilize P21 in laboratory and animal models to investigate mechanisms of adult neurogenesis, synaptic plasticity, tauopathy, and neurotrophic support. As a research-grade compound, P21 is intended exclusively for in vitro and animal studies. Scientists value its oral bioavailability, small size, dual BDNF/LIF mechanism, and consistent disease-modifying effects observed in 3xTg-AD and aged rodent models.

VIAL ANATOMY
LYOPHILISED VIAL
Flip-off cap
Tamper-evident seal
Rubber stopper
Bacteriostatic-water compatible
Batch-labelled body
Lot & expiry printed
USP Type I glass
Borosilicate, sealed
P-21 vial
P-21
10 MG
DUBAI PEPTIDES
RESEARCH USE ONLY
BLACK RESEARCH SERIES

Research Applications

Where researchers apply it.

01 Neurogenesis and Synaptic Plasticity
Preclinical studies show increased proliferation and survival of neural progenitor cells in the dentate gyrus, elevated BDNF levels, enhanced synaptic markers (e.g., synaptophysin, PSD-95), and improved long-term potentiation.
02 Cognitive Enhancement and Aging
Chronic oral administration rescues spatial learning and memory deficits in aged rats and restores performance to near wild-type levels in Alzheimer’s transgenic models.
03 Alzheimer’s Disease and Tau Pathology
In 3xTg-AD mice, P21 reduces hyperphosphorylated tau at multiple epitopes, decreases neurofibrillary pathology, and in some paradigms lowers amyloid burden, with benefits observed even when treatment is initiated after pathology onset.
04 Neuroprotection and Developmental Models
Early postnatal or prenatal-to-postnatal treatment prevents later Alzheimer-like behavioral and synaptic deficits. Additional work explores benefits in Down syndrome (Ts65Dn) models.
05 Mechanism-Focused Research
Dual action of LIF pathway inhibition (favoring neural stem cell proliferation) combined with BDNF upregulation provides a targeted tool for studying neurotrophic deficits in neurodegeneration and cognitive aging.

— Verified & Documented

Every vial is backed by a Certificate of Analysis.

Each lot is independently characterised by HPLC and mass spectrometry, with identity, mass and purity documented per batch and available on request.

Additional quality-control testing, including sterility, endotoxin and heavy metals, is conducted periodically across our product range.

>99%
HPLC Purity
MS
Identity Confirmed
Certificate of Analysis
P-21 · QC RELEASE
PASS
IdentityConfirmed
Mass—
Purity>99%
AppearanceWhite Lyophilised
LabJanoshik Analytical (Independant)
Date

Storage & Handling

Storage & Handling

Lyophilised vials are stable at −20°C for up to 2 years unopened. Once reconstituted, refrigerate at 2–8°C and use within 28 days. Avoid repeated freeze-thaw cycles.

Beyond Use Date

Pre-filled formats (cartridge, pen, nasal) carry a beyond-use date of typically 4–8 weeks from receipt. ≥98% purity by HPLC. For in vitro and preclinical research use only — not for human or veterinary use.