ხუთშაბათი, აპრილი 30, 2026
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Global Ingredient Risk Index Stimulant

Phenethylamine

2-Phenylethylamine

Also known as: 2-Phenylethylamine, PEA, β-Phenylethylamine, Phenylethylamine, Phenethylamine HCl

MODERATE RISK 5.5/10 How?

Evidence Strength: LIMITED

This ingredient is classified as unclassified risk (GIRI score: 5.5/10). The classification is based on mechanistic and clinical evidence: phenethylamine acts as a central nervous system stimulant by promoting the release….

02

Safety Profile

Common Adverse Effects

  • Nausea
  • headache
  • dizziness
  • anxiety
  • insomnia

Serious Adverse Effects

  • Hypertension
  • tachycardia
  • arrhythmia
  • seizures

Contraindications

  • Hypertension
  • cardiovascular disease
  • seizure disorders
  • anxiety disorders
  • People taking MAO inhibitors
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03

Interactions

Drug / Nutrient Interaction Mechanism Warning
MAO inhibitors increased risk of hypertensive crisis — avoid combination. Antidepressants: potential for serotonin syndrome — use with caution. Stimulants: additive effects — monitor cardiovascular status. Monitor
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04

Evidence and Scientific Findings

Overview

Ingredient Overview

Phenethylamine is a naturally occurring monoamine alkaloid and trace amine derived from the amino acid phenylalanine. It is found in various foods, such as chocolate, and is also synthesized in the human body. In dietary supplements, it is used for its potential mood-enhancing and stimulant effects, often marketed for weight loss and cognitive enhancement.
Classification

Biological and Chemical Classification

Chemical Class
Monoamine alkaloid
Biological Class
Trace amine
Natural Source
Endogenous in humans, Theobroma cacao (cacao beans)
Scientific Name
2-Phenylethylamine
Chemical Formula
C8H11N
CAS Number
64-04-0
Mechanism

Mechanism of Action

Phenethylamine acts as a central nervous system stimulant by promoting the release of norepinephrine and dopamine. It binds to trace amine-associated receptor 1 (TAAR1), which modulates monoamine neurotransmitter systems. This interaction enhances mood and alertness. Additionally, phenethylamine inhibits the reuptake of dopamine, further increasing its availability in the synaptic cleft.
Clinical Evidence

Clinical Evidence of Effectiveness

Indication Evidence Level Summary
General Moderate Clinical evidence for phenethylamine is limited, with most studies focusing on its effects in combination with other compounds. Some small-scale studies suggest mood-enhancing and cognitive benefits, but these findings are not consistent across all research. The lack of large, high-quality randomized controlled trials limits the ability to draw definitive conclusions about its efficacy and safety.
Evidence levels: Strong Moderate Limited Experimental
Pharmacokinetics

Pharmacokinetics

Absorption
Phenethylamine is rapidly absorbed in the gastrointestinal tract, with peak plasma concentrations typically occurring within 30 minutes of oral administration. However, it has a very short half-life of about 5 to 10 minutes due to rapid metabolism, resulting in low bioavailability.
Distribution
Phenethylamine has a relatively small volume of distribution and is known to cross the blood-brain barrier. It exhibits low plasma protein binding, allowing it to quickly reach central nervous system targets.
Metabolism
Phenethylamine is primarily metabolized by monoamine oxidase B (MAO-B) into phenylacetic acid. This rapid metabolism significantly reduces its duration of action and bioavailability in the body.
Excretion
The primary route of excretion for phenethylamine is renal, with metabolites such as phenylacetic acid being eliminated in the urine. Due to its rapid metabolism, unchanged phenethylamine is rarely detected in urine.
Half-Life
5 to 10 minutes
Dosage

Recommended Dosage

Condition / Use Typical Dose
Mood enhancement 250-500 mg per day. Cognitive support: 100-300 mg per day. Weight loss: 100-500 mg per day.

Dosage ranges are based on clinical studies and commonly used supplement formulations. Individual requirements may vary.

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05

SETI — Scientific Evidence Transparency Index

SETI Score 56/100
Risk Level High risk
Scientific Confidence Moderate
Evidence Strength Limited
Key Benefit Phenethylamine is a naturally occurring monoamine alkaloid and trace amine derived from the amino acid phenylalanine.
Key Safety Concern Phenethylamine may pose risks for individuals with cardiovascular conditions due to its stimulant properties. It should be used cautiously in those with a history of seizures or psychiatric disorders. Pregnant and breastfeeding women are advised to avoid its use due to insufficient safety data. Regulatory agencies have flagged concerns over its use in high doses or in combination with other stimulants.
Evidence Reviewed 10 PubMed studies
Scientific Confidence Moderate
Based on study quality, consistency, and recency

Executive Summary — Ingredient Assessment

SETI Score 56/100
Risk Level High risk
Evidence Strength Limited
Main Benefit Phenethylamine is a naturally occurring monoamine alkaloid and trace amine derived from the amino acid phenylalanine.
Main Safety Concern Phenethylamine may pose risks for individuals with cardiovascular conditions due to its stimulant properties. It should be used cautiously in those with a history of seizures or psychiatric disorders. Pregnant and breastfeeding women are advised to avoid its use due to insufficient safety data. Regulatory agencies have flagged concerns over its use in high doses or in combination with other stimulants.
Ingredient Phenethylamine
Scientific name 2-Phenylethylamine
Scientific Evidence Overview
  • 10 studies reviewed
  • 1 high-quality study (meta-analysis or RCT)
  • Main clinical benefit observed: Phenethylamine is a naturally occurring monoamine alkaloid and trace amine derived from the amino acid phenylalanine.
  • Evidence consistency: High consistency across studies (100%)
Safety Signals
  • Phenethylamine may pose risks for individuals with cardiovascular conditions due to its stimulant properties. It should be used cautiously in those with a history of seizures or psychiatric disorders. Pregnant and breastfeeding women are advised to avoid its use due to insufficient safety data. Regulatory agencies have flagged concerns over its use in high doses or in combination with other stimulants.
Evidence Strength Limited
Regulatory Status
  • USA/FDA — Approved
Final Scientific Assessment

The available scientific evidence for Phenethylamine indicates notable safety signals that warrant caution. Use should be considered carefully and monitored, particularly in sensitive populations or alongside other medications.

Ingredient Phenethylamine
Evidence reviewed 10 peer-reviewed studies (last 10 years)
Scientific name 2-Phenylethylamine
56 /100

Total SETI Score

High risk
Evidence quality 16/40
Evidence consistency 20/20
Safety signals 0/20
Study recency 10/10
Evidence transparency 10/10

Evidence Summary

  • 10 studies reviewed
  • 1 high-quality study (meta-analysis or systematic review)
  • 0 studies identified benefits or no safety concern (GREEN)
  • 10 studies reported limited or advisory safety evidence (YELLOW)

Evidence Policy

Only peer-reviewed scientific literature indexed in PubMed or comparable databases is included in this evaluation. Commercial websites, blogs, and marketing materials are excluded. All references include direct traceable links to source documents.

Last updated: 06 მარ 2026, 12:00

Evidence Distribution

1 Systematic reviews
9 Other / unclassified
  1. Observational / other LOW evidence YELLOW
    Tetradecylamine: A Newly Identified Biogenic Amine Compound from the Venom of Vespa affinis. ↗
    Journal Biology (Basel)
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Sriburin S et al.. Tetradecylamine: A Newly Identified Biogenic Amine Compound from the Venom of Vespa affinis.. Biology (Basel). 2026. PMID:41744625.
  2. Observational / other LOW evidence YELLOW
    Prediction of Charged Small Molecule Conformations in Solution Using a Balanced ML/MM Potential. ↗
    Journal J Chem Inf Model
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Williams CD et al.. Prediction of Charged Small Molecule Conformations in Solution Using a Balanced ML/MM Potential.. J Chem Inf Model. 2026. PMID:41641956.
  3. Observational / other LOW evidence YELLOW
    Plasma non-targeted metabolomics unveils the metabolic signatures of trans-right ventricle in pulmonary arterial hypertension associated with atrial septal defect. ↗
    Journal Clin Chim Acta
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Qian X et al.. Plasma non-targeted metabolomics unveils the metabolic signatures of trans-right ventricle in pulmonary arterial hypertension associated with atrial septal defect.. Clin Chim Acta. 2026. PMID:41577026.
  4. Observational / other LOW evidence YELLOW
    Real-time capture of domain movements during copper amine oxidase catalysis by mix-and-inject serial crystallography. ↗
    Journal Nat Commun
    Year 2025
    Study type Observational / other
    Evidence strength LOW evidence
    Murakawa T et al.. Real-time capture of domain movements during copper amine oxidase catalysis by mix-and-inject serial crystallography.. Nat Commun. 2025. PMID:41413268.
  5. Observational / other LOW evidence YELLOW
    Molecular Identification and Biogenic Amine Production Capacity of Enterococcus faecalis Strains Isolated from Raw Milk. ↗
    Journal Int J Mol Sci
    Year 2025
    Study type Observational / other
    Evidence strength LOW evidence
    Wiu015bniewski P et al.. Molecular Identification and Biogenic Amine Production Capacity of Enterococcus faecalis Strains Isolated from Raw Milk.. Int J Mol Sci. 2025. PMID:41226519.
  6. Systematic review HIGH evidence YELLOW
    Review of Selected 2-Phenylethylamine Derivatives and Opioids, Systematic Review of Their Effects on Psychomotor Abilities and Driving Performance: Psychopharmacology in the Context… ↗
    Journal Pharmaceuticals (Basel)
    Year 2025
    Study type Systematic review
    Evidence strength HIGH evidence
    u017beu0142abowski K et al.. Review of Selected 2-Phenylethylamine Derivatives and Opioids, Systematic Review of Their Effects on Psychomotor Abilities and Driving Performance: Psychopharmacology in the Context of Road Safety.. Pharmaceuticals (Basel). 2025. PMID:41155669.
  7. Observational / other LOW evidence YELLOW
    Micro-Scale Arrays Fabricated on Parafilm and Polymethyl Methacrylate Towards Differential Colorimetric Analysis of Amines via Shape Transformation of Ag Nanoprisms. ↗
    Journal Anal Sci Adv
    Year 2025
    Study type Observational / other
    Evidence strength LOW evidence
    Bahavarnia F et al.. Micro-Scale Arrays Fabricated on Parafilm and Polymethyl Methacrylate Towards Differential Colorimetric Analysis of Amines via Shape Transformation of Ag Nanoprisms.. Anal Sci Adv. 2025. PMID:41146858.
  8. Observational / other LOW evidence YELLOW
    An Ultrasound-Assisted Pistacia terebinthus L. Extract to Incorporate Into Fermented Sausage. ↗
    Journal Food Sci Nutr
    Year 2025
    Study type Observational / other
    Evidence strength LOW evidence
    Benli H et al.. An Ultrasound-Assisted Pistacia terebinthus L. Extract to Incorporate Into Fermented Sausage.. Food Sci Nutr. 2025. PMID:40895152.
  9. Observational / other LOW evidence YELLOW
    Functional and structural insights into a thermostable (S)-selective amine transaminase and its improved substrate scope by protein engineering. ↗
    Journal Appl Microbiol Biotechnol
    Year 2025
    Study type Observational / other
    Evidence strength LOW evidence
    Patti S et al.. Functional and structural insights into a thermostable (S)-selective amine transaminase and its improved substrate scope by protein engineering.. Appl Microbiol Biotechnol. 2025. PMID:40796981.
  10. Observational / other LOW evidence YELLOW
    Influence of NHu22efN and OHu22efN hydrogen bonds in the aggregation of flexible molecules: A combined experimental and computational study. ↗
    Journal J Chem Phys
    Year 2025
    Study type Observational / other
    Evidence strength LOW evidence
    Torres-Hernu00e1ndez F et al.. Influence of NHu22efN and OHu22efN hydrogen bonds in the aggregation of flexible molecules: A combined experimental and computational study.. J Chem Phys. 2025. PMID:40788050.
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06

Score Transparency

Q × L × D × S × 10 = 5.5 / 10

The GIRI Score is the product of four independently computed evidence components, each normalised to 0–1, then scaled to 0–10. Every component is derived exclusively from peer-reviewed references and regulatory data — no editorial judgement is applied.

Q
Evidence Quantity 0 / 10
0%

0 of 10 approved references (score saturates at 10). More peer-reviewed studies = stronger evidence base.

Method: Q = number of approved references ÷ 10 (capped at 1.0)

L
Evidence Quality 5 / 10
50%

Limited — mostly case reports or animal studies

Method: L = mean study-level weight across approved references. Level 1 (meta-analysis / systematic review) = 1.0; Level 2 (RCT) = 0.8; Level 3 (cohort/case-control) = 0.6; Level 4 (case report) = 0.4; Level 5 (animal / in-vitro) = 0.2.

D
Evidence Direction 5 / 10
Benefit
Risk
50%

Mixed or neutral — roughly equal benefit and risk signals

Method: D = (sum of risk-scored references − sum of benefit-scored references) ÷ total evidence score, then scaled from [−1, 1] to [0, 1]. 0.0 = pure benefit; 0.5 = neutral; 1.0 = pure risk.

S
Safety Signals 5 / 10
50%

One or more monitoring-level safety signals active

Method: S = 0.5 (neutral baseline) + sum of active signal severity deltas ÷ 10. Severity deltas: Critical = +2.0, High = +1.5, Moderate = +1.0, Low = +0.5. Capped at 1.0.

0Q × 5L × 5D × 5S = 5.5 / 10

Final GIRI Score for Phenethylamine. Risk level thresholds: Low 0–3.0 · Moderate 3.0–5.5 · High 5.5–7.5 · Critical 7.5–10.

Full methodology & data sources

The GIRI Score is computed entirely from structured data — no editorial scoring or subjective weighting is applied at any step.

  • References: Only approved references are counted. Each reference is assigned an evidence level (L1–L5) and a direction (risk / neutral / benefit) by the reference manager or AI classifier.
  • Safety Signals: Sourced from regulatory agencies (FDA, EMA, Health Canada, TGA, and others) and pharmacovigilance databases. Only active signals count toward the score.
  • Formula version: GIRI Score v3.7.0 — Q × L × D × S × 10.
  • Limitations: The score reflects published evidence and recorded signals as of the last update date. It is not a clinical risk assessment and should not replace advice from a qualified healthcare professional.
07

Risk Level Classification

MODERATE RISK 5.5/10

Based on available regulatory signals and scientific evidence, this ingredient presents a moderate safety concern. Caution is advised, particularly at high doses or in sensitive populations.

LOW
0–3.0
MODERATE
3.0–5.5
HIGH
5.5–7.5
CRITICAL
7.5–10
5.5

The score pin shows exactly where this ingredient falls on the fixed risk scale.

What drove the Moderate classification for Phenethylamine

GIRI Score 5.5 / 10

A score of 5.5 places this ingredient in the Moderate band. Thresholds: Low 0–3.0 · Moderate 3.0–5.5 · High 5.5–7.5 · Critical 7.5–10.

Evidence Quantity (Q) 0 / 10 refs

0 approved references.

Evidence Quality (L) 50%

Limited — mostly case reports or animal studies (Level 4–5).

Evidence Direction (D) 50% toward risk

Neutral or mixed — benefit and risk signals roughly balanced.

Safety Signals (S) 0 active signals

No active signals — S component is at neutral baseline (0.5), contributing no extra risk weight.

Regulatory Status 1 jurisdiction with restrictions

1 jurisdiction has active restrictions or advisories. Regulatory signals are recorded as Safety Signals and raise the S component.

How are the Low / Moderate / High / Critical thresholds defined?

The four risk levels are fixed score bands. A score is assigned to exactly one level based on where it falls:

LevelScoreMeaning
LOW0.0 – 2.9Sparse or predominantly beneficial evidence. No active safety alerts.
MODERATE3.0 – 5.4Mixed signals — some risk alongside benefit. Caution at high doses or in sensitive groups.
HIGH5.5 – 7.4Multiple studies or regulatory alerts documenting adverse effects. Professional oversight recommended.
CRITICAL7.5 – 10Regulatory restrictions in one or more major jurisdictions. Serious documented harm. Avoid without specialist supervision.

Thresholds are fixed constants (GIRI_Score_Utils::LEVEL_THRESHOLDS). They do not change per ingredient and are never subject to editorial adjustment.

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