Pinealon
Pinealon Peptide (EDR) – Neuroprotection, Cognitive & Cellular Aging Research
Glu–Asp–Arg Tripeptide for Neuronal Oxidative Stress, DNA–Peptide Interactions, Synaptic Plasticity & Experimental Neurobiology
Pinealon, also known as EDR peptide, is a synthetic tripeptide consisting of glutamic acid, aspartic acid and arginine.
It belongs to a group of short peptides investigated in bioregulation, neurobiology and experimental aging research.
Pinealon has attracted scientific interest because of its reported effects in selected laboratory models involving neuronal oxidative stress, cell survival, gene-associated signaling and synaptic structure.
Its principal research areas include:
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Neuronal cell biology
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Oxidative stress and reactive oxygen species
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Experimental neuroprotection
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DNA–peptide interactions
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Chromatin-associated molecular research
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Gene expression regulation
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Neuronal apoptosis and cell survival
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Synaptic plasticity
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Dendritic spine morphology
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Experimental cognitive research
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Neurodegeneration-related cellular models
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Age-associated neuronal changes
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Peptide bioregulation
Pinealon is a biologically interesting research compound, but its mechanism of action is not fully established.
Most directly relevant experimental evidence comes from cell-based studies and animal models.
Limited clinical observations have been described in the literature, but independently replicated, well-controlled human trials establishing efficacy and safety are lacking.
Pinealon is not an approved human therapeutic drug.
ICAME Pharmacy Pinealon is intended strictly for laboratory research and development purposes.
FOR RESEARCH USE ONLY — NOT FOR HUMAN OR VETERINARY USE.
What Is Pinealon?
Pinealon is an ultrashort synthetic peptide with the amino acid sequence:
Glu–Asp–Arg
The corresponding one-letter sequence is:
EDR
Its three constituent amino acids are:
Glutamic Acid (E)
Aspartic Acid (D)
Arginine (R)
Pinealon has been studied primarily within the short-peptide bioregulation research tradition associated with Vladimir Khavinson and collaborators.
This research investigates whether small peptides can influence cellular responses and gene-associated processes.
Pinealon has been examined in models involving neuronal injury, oxidative stress and cellular aging.
However, the biological effects reported for Pinealon are model-dependent.
A result observed in cultured neurons does not necessarily predict an effect in the human brain.
Pinealon Molecular Structure
Pinealon is a linear tripeptide composed of three amino acid residues joined by two peptide bonds.
Molecular Characteristics
| Property | Description |
|---|---|
| Compound Name | Pinealon |
| Alternative Names | EDR Peptide / Glu-Asp-Arg |
| Classification | Synthetic Linear Tripeptide |
| Peptide Length | 3 Amino Acids |
| Amino Acid Sequence | Glu–Asp–Arg |
| One-Letter Sequence | EDR |
| Standard Free-Acid Structure | H-Glu-Asp-Arg-OH |
| Molecular Formula | C₁₅H₂₆N₆O₈ |
| Molecular Weight | Approximately 418.40 g/mol |
| CAS Number | 175175-23-2 |
| PubChem CID | 10273502 |
| Principal Research Fields | Neurobiology / Oxidative Stress / Peptide Bioregulation |
| Human Clinical Efficacy | Not Established |
These molecular characteristics describe the unmodified free peptide.
Products containing counterions or other formulation components may have a different total material mass.
Pinealon Amino Acid Sequence
The amino acid sequence of Pinealon is:
H-Glu-Asp-Arg-OH
Amino Acid Composition
| Position | Amino Acid | Abbreviation | One-Letter Code |
|---|---|---|---|
| 1 | Glutamic Acid | Glu | E |
| 2 | Aspartic Acid | Asp | D |
| 3 | Arginine | Arg | R |
The N-terminal residue is glutamic acid.
Aspartic acid occupies the central position.
Arginine forms the C-terminal residue.
Structural Characteristics
Short linear peptide backbone
Two peptide bonds
Acidic side chains from glutamic acid and aspartic acid
Basic guanidinium group from arginine
Multiple hydrogen-bonding sites
Ionizable functional groups
These properties are relevant to investigations of molecular interactions and peptide behavior in aqueous biological systems.
Why Is the EDR Sequence Important?
The amino acid sequence of a peptide influences its chemical properties and potential molecular interactions.
Pinealon contains two acidic residues followed by one basic residue.
This combination produces a small, highly polar molecule with several ionizable groups.
Potential Molecular Research Areas
Hydrogen bonding
Electrostatic interactions
Peptide–protein interactions
DNA-associated binding models
Chromatin interaction studies
Cellular uptake investigations
Molecular docking
However, chemical plausibility does not establish that Pinealon reaches a particular intracellular target under physiological conditions.
Direct experimental evidence is required.
Scientific Background of Pinealon
Pinealon is associated with research into short synthetic peptide bioregulators.
This research program has examined small peptide sequences and their possible influence on cellular function.
Pinealon has been discussed in connection with peptide fractions identified during research involving complex tissue-derived preparations.
However, a purified synthetic EDR tripeptide is not equivalent to a complex tissue extract.
Biological findings involving multi-component preparations cannot automatically be attributed to Pinealon alone.
Main Research Themes
Neuronal survival
Oxidative stress responses
Cellular signaling
Gene-associated regulation
Age-related neuronal biology
Experimental learning and memory
Neurodegeneration-associated cellular models
The evidence supporting these areas varies considerably.
How Does Pinealon Work?
The precise molecular mechanism of Pinealon has not been conclusively established.
Researchers have proposed several possible mechanisms based on laboratory observations and computational models.
These include:
Interactions with DNA or chromatin-associated structures
Changes in cellular oxidative stress responses
Modulation of selected signaling pathways
Effects on neuronal survival
Changes in synaptic morphology
However, no single validated receptor-mediated mechanism has been established that explains all reported effects.
Proposed Experimental Framework
Pinealon (EDR)
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Cellular Exposure
↓
Potential Molecular Interactions
↓
Changes in Selected Cellular Signaling or Gene-Associated Processes
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Measured Responses in Experimental Models
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Oxidative Stress / Cell Survival / Synaptic Morphology Endpoints
This framework represents research hypotheses and observations.
It should not be interpreted as a confirmed therapeutic pathway.
Pinealon and DNA Interaction Research
One of the more distinctive aspects of Pinealon research involves proposed interactions between short peptides and DNA.
Some investigators have used molecular modeling to examine whether EDR can interact with particular DNA sequences.
These studies explore possible hydrogen bonding and electrostatic interactions.
Research Topics
Peptide–DNA binding
DNA minor-groove interaction models
Sequence-associated molecular recognition
Chromatin accessibility
Transcription-associated processes
Molecular docking
Gene expression regulation
However, computational docking does not demonstrate that Pinealon regulates the same genes in living human brain tissue.
Predicted molecular binding requires biochemical and cellular validation.
Pinealon and Histone Research
Histones are proteins involved in organizing DNA into chromatin.
Chromatin structure influences gene accessibility and transcription.
Short-peptide bioregulation research has proposed that some peptides may interact with chromatin-associated structures.
Pinealon has been investigated within this broader framework.
Potential Research Areas
Histone–peptide interactions
Chromatin organization
DNA accessibility
Transcriptional regulation
Nuclear localization
Peptide-mediated molecular recognition
However, a clinically meaningful epigenetic effect of Pinealon has not been demonstrated.
Claims that Pinealon directly reprograms human gene expression or reverses epigenetic aging are not established.
Pinealon and Neuronal Oxidative Stress
Oxidative stress occurs when the production of reactive species exceeds cellular antioxidant defenses.
Neurons can be vulnerable to oxidative injury because of their metabolic demands and cellular characteristics.
Pinealon has been investigated in experimental systems involving oxidative stress.
Some studies reported reduced accumulation of reactive oxygen species in selected cell models.
Experimental Endpoints
Reactive oxygen species (ROS)
Cell viability
Necrotic cell death
Oxidative damage
Cellular stress signaling
Antioxidant-associated responses
These findings suggest potential research relevance but do not establish clinical neuroprotection.
Pinealon and Reactive Oxygen Species
Reactive oxygen species are chemically reactive molecules involved in both normal cellular signaling and oxidative damage.
Common examples include:
Superoxide
Hydrogen peroxide
Hydroxyl radicals
Pinealon has been investigated for its effects on ROS-associated measurements.
Some experimental studies reported changes in oxidative stress markers after exposure to the peptide.
However, these results depend on the model, conditions and measured endpoint.
A reduction in laboratory ROS measurements does not establish prevention of neurological disease.
Pinealon and Cellular Antioxidant Research
Cells contain multiple systems for regulating oxidative stress.
These include:
Superoxide dismutase
Catalase
Glutathione-associated enzymes
Redox-sensitive signaling pathways
DNA repair systems
Mitochondrial quality-control mechanisms
Pinealon-related research may examine whether exposure alters oxidative stress responses.
However, Pinealon has not been established as a clinically effective antioxidant treatment.
Its effects on individual antioxidant enzymes require direct experimental verification.
Pinealon and Neuronal Cell Survival
Neuronal survival depends on multiple cellular processes.
These include energy metabolism, calcium regulation, membrane integrity and responses to injury.
Pinealon has been investigated in selected neuronal cell models.
Some experiments reported improved cell viability or reduced cell death under specific stress conditions.
Research Areas
Cell viability
Necrotic cell death
Apoptosis-associated signaling
Oxidative injury
Stress-related protein activity
Neuronal morphology
Experimental injury models
These findings should be interpreted as preclinical observations.
They do not establish that Pinealon prevents neuronal loss in humans.
Pinealon and Apoptosis Research
Apoptosis is a regulated form of cell death.
It involves multiple signaling pathways and molecular regulators.
Important research markers include:
Caspase activity
Mitochondrial signaling
DNA fragmentation
Cell survival proteins
Stress-associated signaling pathways
Pinealon has been examined in research involving apoptosis-associated endpoints.
However, its effects are not sufficiently established to define it as a clinically validated anti-apoptotic treatment.
Pinealon and ERK1/2 Signaling
ERK1/2 proteins participate in the mitogen-activated protein kinase signaling network.
They are involved in cellular responses to extracellular signals.
Some Pinealon experiments have examined changes in ERK1/2-associated signaling.
Research Topics
ERK phosphorylation
Cell survival responses
Cell cycle-associated regulation
Stress signaling
Neuronal responses
Temporal signaling patterns
Changes in ERK1/2 activity may reflect complex cellular processes.
They should not automatically be interpreted as beneficial.
Pinealon and Synaptic Plasticity Research
Synaptic plasticity refers to changes in the strength and structure of connections between neurons.
It is important for learning and memory.
Researchers have investigated Pinealon in cellular models involving synaptic structure.
One experimental study examined the effects of EDR on dendritic spine morphology in cultured hippocampal neurons exposed to amyloid-related stress.
The investigators reported changes in the proportion of mature, mushroom-shaped dendritic spines.
Research Areas
Dendritic spine morphology
Synaptic structure
Hippocampal neuronal cultures
Amyloid-associated cellular stress
Neuronal connectivity
Structural plasticity
However, improvements in dendritic spine measurements do not establish improved memory in humans.
Pinealon and Dendritic Spine Research
Dendritic spines are small protrusions from neuronal dendrites.
Many excitatory synapses are located on these structures.
Spine morphology is associated with aspects of synaptic function.
Common Experimental Measurements
Spine density
Spine head size
Mushroom-shaped spine proportion
Thin spine proportion
Synaptic protein markers
Dendritic branching
Neuronal morphology
Pinealon has been studied using some of these structural endpoints.
The findings are relevant to experimental neurobiology but are not proof of clinical cognitive enhancement.
Pinealon and Hippocampal Research
The hippocampus participates in learning and memory.
It is also important in research involving synaptic plasticity and neurodegeneration.
Pinealon has been investigated in hippocampal neuronal culture models.
Research Topics
Synaptic morphology
Amyloid-associated cellular stress
Dendritic spine changes
Neuronal survival
Plasticity-associated processes
Experimental neurodegeneration
However, effects in cultured hippocampal neurons cannot be directly extrapolated to whole-brain function.
Pinealon and Learning Research
Learning involves changes in neural activity and synaptic networks.
Some animal studies have investigated Pinealon in experimental models involving learning-related behavioral tasks.
For example, research involving offspring of rats exposed to prenatal hyperhomocysteinemia reported changes in learning and spatial orientation measures.
Important Limitation
These findings were obtained in a specific animal model.
They do not establish that Pinealon improves learning in healthy humans or people with cognitive disorders.
Pinealon and Memory Research
Pinealon is frequently discussed in connection with memory and cognitive performance.
However, the evidence requires careful interpretation.
Preclinical Research
Some animal experiments reported changes in learning-related outcomes.
Human Observations
Small clinical reports have described possible cognitive improvements.
However, study quality, control groups, independent replication and product-specific details remain important limitations.
Scientific Conclusion
Pinealon has not been established as an effective memory-enhancing treatment.
Claims of reliable improvements in recall, concentration or learning are not supported by strong clinical evidence.
Pinealon and Alzheimer's Disease Research
Alzheimer's disease involves complex pathological processes.
These include:
Amyloid-associated pathology
Tau-associated pathology
Synaptic dysfunction
Neuroinflammation
Oxidative stress
Neuronal loss
Network-level dysfunction
Pinealon has been investigated in selected experimental models relevant to Alzheimer's disease research.
Experimental Research Areas
Amyloid-associated neuronal stress
Synaptic structure
Dendritic spine morphology
Oxidative damage
Gene-associated molecular models
Cell survival
These findings remain preliminary.
Pinealon has not been demonstrated to prevent, slow or treat Alzheimer's disease in humans.
Pinealon and Amyloid-Associated Cellular Models
Amyloid-related experimental models are commonly used to investigate neuronal stress.
They can help researchers study changes in synaptic morphology and cellular signaling.
Pinealon has been evaluated in cultured neurons exposed to amyloid-associated conditions.
Some findings suggest changes in selected structural endpoints.
However, cell culture models cannot reproduce the full complexity of Alzheimer's disease.
A favorable laboratory result is not equivalent to clinical disease modification.
Pinealon and Neurodegeneration Research
Neurodegenerative diseases involve progressive changes in neuronal function and survival.
Pinealon-related research has explored cellular processes relevant to neurodegeneration.
Potential experimental areas include:
Oxidative stress
Neuronal apoptosis
Synaptic dysfunction
Cellular aging
Gene-associated regulation
Neuronal morphology
Stress-response pathways
However, Pinealon has not been established as an effective treatment for any neurodegenerative disease.
Pinealon and Parkinson's Disease Research
Parkinson's disease involves degeneration of specific neuronal populations and complex molecular pathology.
Oxidative stress and mitochondrial dysfunction are relevant research topics.
Because Pinealon has been investigated in oxidative stress models, it may be of exploratory interest in neurodegeneration research.
However, direct evidence establishing beneficial effects in Parkinson's disease is insufficient.
Pinealon should not be described as a proven Parkinson's disease treatment.
Pinealon and Brain Injury Research
Pinealon has been discussed in research involving brain injury and neurological recovery.
Some small human reports describe its use alongside other treatments.
However, these reports have important methodological limitations.
Research Questions
Does Pinealon alter neuronal stress responses?
Can it influence cell survival in injury models?
Are reported effects reproducible?
What are its pharmacokinetic properties?
Can any laboratory effect translate into a clinical outcome?
These questions remain unresolved.
Pinealon is not an established treatment for traumatic brain injury or stroke.
Pinealon and Cellular Aging Research
Cellular aging involves changes in gene expression, stress responses and tissue function.
Pinealon has been investigated in the context of experimental gerontology.
Research Areas
Age-associated neuronal changes
Cellular oxidative stress
Gene-associated regulation
Neuronal morphology
Cell survival
Stress adaptation
Neurobiological aging
However, no adequate human clinical evidence establishes that Pinealon slows biological aging or extends lifespan.
Pinealon and Senescence Research
Cellular senescence involves changes in cellular function that can occur in response to stress and aging.
Researchers study markers such as:
p16-associated signaling
DNA damage
Mitochondrial activity
Lysosomal activity
Cellular morphology
Inflammatory signaling
A 2024 study using induced cortical neurons derived from older human donors investigated several short peptides, including EDR.
Some measurements suggested changes in neuronal branching and oxidative DNA damage.
However, the same study did not demonstrate improvements across all tested aging-associated cellular endpoints.
These findings do not establish reversal of cellular aging.
Pinealon and DNA Damage Research
DNA damage can result from oxidative stress and other cellular processes.
Neurons require mechanisms for maintaining genomic integrity.
Pinealon-related studies have investigated oxidative DNA damage in selected experimental systems.
Research Topics
Oxidative DNA lesions
Cellular stress
DNA repair-associated pathways
Neuronal viability
Aging-associated molecular changes
These findings remain preclinical.
They do not establish that Pinealon prevents DNA damage in humans.
Pinealon and Mitochondrial Research
Mitochondria play important roles in cellular energy metabolism and signaling.
Mitochondrial dysfunction is relevant to neuronal stress and aging.
Pinealon has been included in experimental studies assessing neuronal cell health.
However, the evidence does not establish consistent improvements in mitochondrial function.
Research Areas
Mitochondrial activity
Cellular energy metabolism
Oxidative stress
Cell survival
Mitochondrial-associated signaling
Age-related neuronal biology
Pinealon should not be described as a proven mitochondrial enhancer.
Pinealon and Neuroinflammation Research
Neuroinflammation involves interactions among neurons, microglia, astrocytes and immune signaling molecules.
Oxidative stress and inflammatory signaling can interact in experimental neural injury models.
Pinealon has been investigated in some research involving inflammatory or stress-associated markers.
However, evidence for direct and reproducible anti-inflammatory activity in the human central nervous system remains insufficient.
Potential Research Endpoints
Inflammatory cytokines
Cellular stress responses
Neuronal viability
Glial signaling
Oxidative damage
Inflammation-associated gene expression
These are exploratory research topics, not established therapeutic benefits.
Pinealon and Sleep Research
Pinealon is sometimes promoted in connection with sleep, circadian rhythms and REM sleep.
However, strong clinical evidence supporting these claims is lacking.
Scientific Questions
Does EDR influence circadian gene expression?
Does it affect pineal gland signaling?
Does it alter melatonin-associated pathways?
Can it change sleep architecture?
Are any reported changes reproducible?
These questions require appropriately controlled studies.
Anecdotal reports of improved REM sleep do not establish efficacy.
Pinealon has not been clinically established as a treatment for insomnia or sleep disorders.
Pinealon and Melatonin Research
Melatonin is a hormone associated with circadian timing.
It is produced primarily by the pineal gland.
Pinealon and melatonin are distinct molecules.
Despite Pinealon's name, it should not automatically be assumed to increase melatonin production.
Research into gene-associated signaling does not establish a direct or clinically meaningful melatonin-enhancing effect.
Pinealon and Neuroplasticity Research
Neuroplasticity describes the nervous system's capacity to change in response to experience, activity and injury.
Pinealon has attracted interest because of findings involving neuronal morphology and synaptic structure.
Experimental Research Areas
Dendritic branching
Synaptic morphology
Neuronal connectivity
Cell survival
Plasticity-associated signaling
Stress-related neuronal responses
However, these observations do not establish that Pinealon enhances overall brain plasticity in humans.
Pinealon and Cognitive Aging Research
Cognitive aging involves changes in memory, attention and processing speed.
These changes vary substantially between individuals.
Pinealon has been investigated in experimental research related to neuronal aging.
Some small human observations have also been reported.
However, available clinical evidence is insufficient to establish a reliable effect on cognitive aging.
Pinealon should not be marketed as a clinically proven cognitive rejuvenation treatment.
Pinealon vs. Epitalon
Pinealon and Epitalon are distinct synthetic peptides associated with short-peptide bioregulation research.
Pinealon: Glu–Asp–Arg
Epitalon: Ala–Glu–Asp–Gly
| Characteristic | Pinealon | Epitalon |
|---|---|---|
| Alternative Name | EDR | AEDG |
| Peptide Length | 3 Amino Acids | 4 Amino Acids |
| Sequence | Glu–Asp–Arg | Ala–Glu–Asp–Gly |
| Main Research Association | Neurobiology and cellular stress | Experimental aging and telomere-associated research |
| Structure | Linear | Linear |
| Established Human Clinical Efficacy | No | No |
| Approved Human Therapeutic Drug | No | No |
Results involving Epitalon cannot be assumed to apply to Pinealon.
Pinealon vs. Cortexin
Cortexin is a complex polypeptide preparation.
Pinealon is a defined synthetic tripeptide.
Important Differences
Pinealon
A chemically defined molecule containing three amino acids.
Cortexin
A multi-component peptide preparation containing numerous molecular species.
Research involving Cortexin cannot automatically establish the activity of isolated Pinealon.
Similarly, safety or clinical observations involving Cortexin do not establish the safety of synthetic EDR.
Pinealon vs. Semax
Semax is a synthetic peptide investigated in neuropharmacological research.
It is structurally distinct from Pinealon.
| Characteristic | Pinealon | Semax |
|---|---|---|
| Peptide Length | 3 Amino Acids | 7 Amino Acids |
| Sequence | Glu–Asp–Arg | Met–Glu–His–Phe–Pro–Gly–Pro |
| Research Background | Short-peptide bioregulation | ACTH-derived peptide research |
| Principal Research Areas | Cellular stress and neurobiology | Neuropharmacology and neuronal signaling |
| Mechanism | Not conclusively established | Multiple proposed pathways |
| Human Clinical Evidence | Limited and methodologically weak | Context-dependent regional research |
The two peptides should not be treated as interchangeable.
Pinealon vs. Selank
Selank is a synthetic heptapeptide investigated in neurobehavioral and pharmacological research.
Pinealon is a three-amino-acid peptide.
Main Differences
Pinealon: Primarily associated with cellular neurobiology, oxidative stress and short-peptide bioregulation research.
Selank: Primarily associated with experimental neurobehavioral and anxiety-related research.
Neither compound should be assigned the other's reported effects.
Pinealon vs. KPV
Pinealon and KPV are both tripeptides, but their sequences and research backgrounds differ.
| Characteristic | Pinealon | KPV |
|---|---|---|
| Sequence | Glu–Asp–Arg | Lys–Pro–Val |
| One-Letter Code | EDR | KPV |
| Peptide Length | 3 | 3 |
| Research Focus | Neuronal oxidative stress and bioregulation | Inflammatory and epithelial signaling |
| Principal Established Receptor | Not identified | No single established classical receptor |
| Approved Human Treatment | No | No |
Their equal peptide length does not imply similar biological activity.
Pinealon Human Clinical Research
The human evidence for Pinealon is limited.
Some publications discuss small clinical observations involving neurological symptoms or cognitive outcomes.
However, these reports require careful evaluation.
Major Limitations
Small sample sizes
Unclear or insufficient randomization
Limited placebo-controlled evidence
Potential co-interventions
Incomplete product characterization
Limited independent replication
Uncertain long-term safety
Limited pharmacokinetic data
The existence of a published human observation does not establish clinical efficacy.
Scientific Interpretation
Pinealon has not been adequately demonstrated to improve memory, prevent dementia, treat neurological injury or slow aging in humans.
Pinealon Safety Considerations
The safety profile of Pinealon has not been adequately established.
Unknown Long-Term Safety
There are insufficient controlled human data evaluating repeated exposure.
Unknown Pharmacokinetics
Absorption, distribution, metabolism and elimination have not been fully characterized.
Uncertain Central Nervous System Exposure
Claims that Pinealon reliably crosses the human blood–brain barrier require direct pharmacokinetic evidence.
Potential Off-Target Effects
The compound's molecular targets are not conclusively established.
Uncertain Gene-Associated Effects
Proposed interactions with DNA or chromatin require further validation.
Product Quality Risks
Research products may contain impurities, incorrect peptide quantities or unverified formulation components.
Unknown Clinical Benefit
Claims involving cognition, sleep, neuroprotection and anti-aging are not supported by strong clinical evidence.
Research-Grade Limitations
Research-grade peptide preparations are not automatically sterile, pharmaceutical-grade or suitable for human administration.
Pinealon and Blood–Brain Barrier Research
The blood–brain barrier regulates movement of substances between the bloodstream and central nervous system.
Pinealon is a small peptide, but small molecular size alone does not establish effective brain penetration.
Transport depends on several factors, including:
Molecular polarity
Transporter interactions
Peptide degradation
Membrane permeability
Efflux mechanisms
Physiological conditions
Some cellular studies have examined intracellular localization.
However, nuclear localization in cultured cells is not equivalent to demonstrated blood–brain barrier penetration in humans.
Pinealon Research Quality and Analytical Characterization
Accurate molecular identification is essential for peptide research.
Important Specifications
Peptide sequence
Molecular identity
Terminal chemistry
Peptide purity
Peptide content
Counterion composition
Residual reagents
Impurity profile
Degradation products
Batch-specific documentation
High-Performance Liquid Chromatography
HPLC can help evaluate peptide purity and chromatographic impurities.
The reported purity depends on the analytical method.
A high purity percentage does not establish biological efficacy or suitability for human administration.
Liquid Chromatography–Mass Spectrometry
LC-MS can support molecular identity verification.
For Pinealon, the expected molecular mass should be consistent with the unmodified EDR peptide.
The presence of counterions or formulation components should be considered separately.
Peptide Content Analysis
Peptide content analysis helps distinguish the actual amount of peptide from the total mass of material.
This is important for products containing residual water or counterions.
Certificate of Analysis
A batch-specific COA should include appropriate identity and quality data.
Relevant information may include:
Batch number
Peptide identity
Analytical methods
Purity
Peptide content
Impurity profile
Counterion information
Stability-related documentation
A COA does not establish clinical safety or therapeutic efficacy.
Scientific Evidence and Research Limitations
Established Molecular Facts
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Pinealon is a synthetic tripeptide.
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Its amino acid sequence is Glu–Asp–Arg.
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Its molecular formula is C₁₅H₂₆N₆O₈.
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Its molecular weight is approximately 418.40 g/mol.
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It has been investigated in neuronal and oxidative stress models.
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Some cell studies reported changes in ROS and cell survival.
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Animal studies have investigated learning-related outcomes.
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Molecular modeling has examined potential DNA interactions.
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Experimental research has examined synaptic morphology.
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Its precise molecular mechanism remains uncertain.
Important Limitations
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Human clinical efficacy is not established.
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Long-term human safety is unknown.
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No approved human therapeutic indication exists.
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Reliable cognitive enhancement has not been demonstrated.
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Alzheimer's disease prevention or treatment has not been established.
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Sleep and REM sleep benefits are unproven.
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Anti-aging and lifespan extension claims are unproven.
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Blood–brain barrier penetration in humans is not adequately established.
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Proposed gene-regulatory effects require further validation.
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Preclinical findings may not translate into clinical benefits.
Potential Pinealon Research Applications
Pinealon may be relevant to appropriately controlled laboratory investigations involving:
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Neuronal cell biology
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Oxidative stress
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Reactive oxygen species
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Experimental neuroprotection
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Cell viability
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Neuronal apoptosis
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ERK1/2 signaling
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DNA–peptide interaction models
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Chromatin-associated research
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Gene expression studies
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Molecular docking
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Hippocampal neuronal cultures
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Dendritic spine morphology
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Synaptic plasticity
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Experimental amyloid-associated stress
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Neuronal aging
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DNA damage
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Cellular senescence
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Mitochondrial activity
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Experimental learning models
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Neurodegeneration-related research
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Peptide stability
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Analytical peptide characterization
These are scientific research applications, not established therapeutic benefits.
Pinealon Research Overview
Compound Name: Pinealon
Alternative Names: EDR Peptide / Glu-Asp-Arg
Classification: Synthetic Linear Tripeptide
Peptide Length: 3 Amino Acids
Sequence: H-Glu-Asp-Arg-OH
One-Letter Sequence: EDR
Molecular Formula: C₁₅H₂₆N₆O₈
Molecular Weight: Approximately 418.40 g/mol
CAS Number: 175175-23-2
PubChem CID: 10273502
Principal Research Areas: Neuronal Oxidative Stress / Synaptic Biology / Peptide Bioregulation
Established Molecular Receptor: Not Identified
Human Clinical Efficacy: Not Established
Long-Term Human Safety: Unknown
Intended Use: Laboratory Research Only
ICAME Pharmacy Product Information
Product Name: Pinealon
Alternative Name: EDR Peptide
Brand: ICAME Pharmacy
Product Category: Research Peptide
Research Classification: Synthetic Tripeptide
Research Areas: Neurobiology / Oxidative Stress / Cellular Aging / Molecular Signaling
Intended Use: Laboratory Research & Development Only
Product identity and specifications should be verified using batch-specific analytical documentation.
Relevant quality information includes:
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Verified amino acid sequence
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Molecular identity
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Peptide purity
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Peptide content
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Counterion composition
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Impurity profile
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Analytical methodology
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Certificate of Analysis (COA)
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Batch or lot identification
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Validated stability and storage conditions
No claims of pharmaceutical quality, sterility, injectable suitability or clinical efficacy should be made without appropriate supporting documentation.
Important Research Use Notice
FOR RESEARCH USE ONLY (RUO)
This ICAME Pharmacy product is intended exclusively for legitimate laboratory, analytical and scientific research purposes.
Not for human or veterinary use. Not for diagnostic, therapeutic, cognitive enhancement, sleep improvement, anti-aging, neurodegenerative disease treatment or other clinical purposes. Not for direct administration to humans or animals.
Pinealon is an experimental tripeptide investigated in preclinical models of neuronal stress and cellular signaling.
Its precise mechanism, human pharmacokinetics, clinical efficacy and long-term safety have not been adequately established.
Experimental findings involving neuronal viability, synaptic morphology or oxidative stress do not establish treatment benefits for neurological diseases.
Information presented on this page is intended solely for scientific and educational purposes and does not constitute medical advice, prescribing information, dosage guidance or instructions for human use.
About ICAME Pharmacy
ICAME Pharmacy provides specialized research products for professional laboratory and scientific applications.
Our portfolio focuses on compounds relevant to peptide science, molecular signaling, neurobiology, cellular stress research and analytical chemistry.
We emphasize accurate product identification, responsible research use, scientific transparency and clear communication of evidence limitations.
For batch-specific analytical documentation and product inquiries, please contact ICAME Pharmacy.
Frequently Asked Questions About Pinealon
What is Pinealon?
Pinealon is a synthetic three-amino-acid peptide investigated in neuronal cell biology, oxidative stress and experimental peptide bioregulation.
Is Pinealon the same as EDR peptide?
Yes. Pinealon and EDR peptide refer to the Glu–Asp–Arg tripeptide.
How many amino acids does Pinealon contain?
Three amino acids.
What is the Pinealon amino acid sequence?
Glu–Asp–Arg, abbreviated EDR.
What is the molecular formula of Pinealon?
C₁₅H₂₆N₆O₈.
What is the molecular weight of Pinealon?
Approximately 418.40 g/mol.
What is the CAS number of Pinealon?
175175-23-2.
Is Pinealon a cyclic peptide?
No. Standard Pinealon is a linear tripeptide.
What is the mechanism of action of Pinealon?
Its precise mechanism has not been conclusively established. Research has examined possible DNA interactions, oxidative stress responses and neuronal signaling.
Does Pinealon cross the blood–brain barrier?
Reliable human pharmacokinetic evidence establishing blood–brain barrier penetration is lacking.
Has Pinealon been studied in neurons?
Yes. Several laboratory studies have investigated Pinealon in neuronal cell models.
Does Pinealon reduce oxidative stress?
Some experimental studies reported changes in oxidative stress markers, but human clinical benefits have not been established.
Does Pinealon improve memory?
Adequate controlled human clinical evidence does not establish Pinealon as an effective memory enhancer.
Does Pinealon treat Alzheimer's disease?
No. Pinealon has not been established as a treatment for Alzheimer's disease.
Does Pinealon improve REM sleep?
Reliable controlled clinical evidence supporting REM sleep benefits is lacking.
Is Pinealon an anti-aging peptide?
Pinealon has been investigated in aging-related experimental research, but human anti-aging benefits have not been demonstrated.
Is Pinealon the same as Epitalon?
No. Pinealon is EDR, while Epitalon is AEDG.
Is Pinealon the same as Cortexin?
No. Pinealon is a defined synthetic tripeptide, while Cortexin is a complex polypeptide preparation.
Is Pinealon approved by the FDA?
No. Pinealon is not an FDA-approved human therapeutic drug.
Is Pinealon safe for human use?
Its human safety has not been adequately established.
Is ICAME Pharmacy Pinealon intended for human use?
No. ICAME Pharmacy Pinealon is intended strictly for laboratory research and development purposes.