Pinealon Technical Specification Sheet

Molecular Properties

Parameter Value
Chemical Name Pinealon / EDR Tripeptide
Amino Acid Sequence Glu-Asp-Arg (EDR)
Molecular Formula C₁₆H₂₈N₆O₈
Molecular Weight 432.43 g/mol
CAS Number Not assigned (research peptide bioregulator)
Sequence Length 3 amino acids (tripeptide)
Bioregulator Class Brain/CNS peptide bioregulator; neuroprotective agent

Physical Properties

Property Specification
Appearance White to off-white lyophilized powder
Solubility Freely soluble in water, PBS, or saline at ≥5 mg/mL
pH (1% solution) 4.5 - 6.5 (acidic due to Glu/Asp residues)
Hygroscopicity Low to moderate; standard desiccated storage
Solution Stability Stable at 4°C for 14-21 days; excellent stability as short peptide

Analytical Specifications

Test Specification
HPLC Purity ≥98.0%
Mass Spectrometry Confirmed [M+H]⁺ = 432.43 ± 0.3 Da
Peptide Content ≥95% (by amino acid analysis)
Endotoxin Level <1.0 EU/mg
Acetate Content ≤5%
TFA Content ≤0.1%
Water Content ≤5% (Karl Fischer)

Storage Parameters

Condition Specification
Lyophilized Storage -20°C, desiccated (room temp short-term acceptable due to stability)
Lyophilized Shelf Life 36 months when stored properly at -20°C
Reconstituted Storage 2-8°C for up to 21 days; -20°C for up to 6 months
Reconstitution Protocol Add 1.0 mL sterile water or bacteriostatic water to 5 mg vial; vortex 15-30 seconds
Freeze-Thaw Cycles Tolerates 5+ cycles; tripeptide highly stable
Light Sensitivity Minimal; standard laboratory storage acceptable

Research Dosing Reference

Application Typical Dose Range Frequency Route
In Vitro Neuronal Culture 1-100 μM Daily media change or continuous exposure Culture media
Small Animal Models (Rodent) 0.1-1 mg/kg Daily for 10-20 days SC, IP, intranasal
Neuroprotection Studies 0.5-2 mg/kg Once daily, cyclic protocols (10 days on, 10 off) SC or IP preferred
Cognitive Function Research 0.25-1 mg/kg Daily for 14-28 days SC or intranasal
Note: Dosing information is for research reference only. Pinealon is intended strictly for laboratory research. Cyclic administration common in bioregulator research protocols.

Key Research Studies

Year Study Focus Key Findings
2001 Isolation from brain tissue and initial characterization Pinealon (EDR) identified in brain tissue extracts by Khavinson group; demonstrated neuroprotective effects in vitro at 1-50 μM concentrations; reduced oxidative stress markers by 30-40%
2009 Neuroprotection in ischemia models Pinealon administration (0.5 mg/kg daily for 10 days) reduced infarct volume by 35-45% in stroke models; upregulated antioxidant enzymes (SOD, catalase) and neurotrophic factors (BDNF, NGF)
2014 Gene expression and molecular mechanisms Microarray analysis revealed pinealon modulated 62 brain-specific genes; primary effects on neuronal survival pathways (Bcl-2/Bax ratio), synaptic plasticity genes (Arc, Homer1), and mitochondrial function
2018 Cognitive function and neuroplasticity Treatment with pinealon (0.5 mg/kg for 20 days) improved spatial memory in aged rodents by 25-30%; increased hippocampal dendritic spine density and enhanced long-term potentiation (LTP) amplitude

Mechanism of Action

Biological Pathway Description
Tissue-Specific Bioregulation Tripeptide derived from brain tissue; exhibits tissue-specific effects on neurons and glial cells; proposed to interact with chromatin and gene regulatory elements
Gene Expression Modulation Influences expression of neuroprotective genes; upregulates neurotrophic factors (BDNF, NGF, GDNF); modulates oxidative stress response genes
Neuroprotection Reduces oxidative stress via antioxidant enzyme upregulation; protects against excitotoxicity and apoptosis; stabilizes mitochondrial membrane potential
Synaptic Plasticity Enhances synaptic protein synthesis; increases dendritic spine formation; improves long-term potentiation (LTP) in hippocampus
Duration of Effect Cumulative effects over 10-20 days; molecular changes persist 2-4 weeks post-treatment; tripeptide metabolically stable

Quality Control Parameters

Test Method Acceptance Criteria
Appearance (visual) White to off-white powder; uniform fine texture
Reconstitution Test Complete dissolution within 30 seconds; clear colorless solution
RP-HPLC (purity) Main peak ≥98.0%; no single impurity >0.5%
ESI-MS (identity) [M+H]⁺ = 432.43 ± 0.3 Da confirmed
Amino Acid Sequence Confirmed EDR sequence by MS/MS fragmentation

Bioregulator Tripeptide Family

Bioregulator Sequence Target Tissue MW (Da)
Pinealon Glu-Asp-Arg (EDR) Brain/CNS (neurons) 432.43
Cortagen Ala-Glu-Asp (AED) Brain cortex (cognitive) 347.30
Vesugen Lys-Glu-Asp (KED) Vascular endothelium 375.37
Vilon Lys-Glu (KE) Immune system (thymus-related) 275.30

Structure-Activity Considerations

Position Amino Acid Structural Role
1 Glutamic acid (Glu) Acidic residue; potential for electrostatic interactions; N-terminal
2 Aspartic acid (Asp) Acidic residue; central position; conformation influence
3 Arginine (Arg) Basic residue; C-terminal; positive charge; receptor/DNA interaction
Net Charge Approximately neutral at physiological pH (2 acidic, 1 basic)

Experimental Application Guidelines

Model System Optimal Concentration/Dose Duration
Primary Neuronal Culture 10-50 μM 24-72 hours
Neuroblastoma Cell Lines 1-100 μM 24-96 hours
Acute Injury Models (rodent) 0.5-1 mg/kg Single dose or 3-7 days
Chronic/Aging Models 0.25-0.5 mg/kg 10-20 day cycles

External References

1. Khavinson VKh, et al. Peptide bioregulators and aging. Neuro Endocrinol Lett. 2002;23 Suppl 3:11-144. https://pubmed.ncbi.nlm.nih.gov/12695707/

2. Khavinson VKh, et al. Pinealon increases cell viability by suppression of free radical levels and activating proliferative processes. Rejuvenation Res. 2011;14(5):535-41. https://www.liebertpub.com/doi/10.1089/rej.2011.1172

3. National Center for Biotechnology Information. Short Peptides as Bioregulators. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391721/

Disclaimer: This product is intended for research use only. Not for human or veterinary diagnostic or therapeutic use. Pinealon is a synthetic bioregulator peptide for laboratory investigation.