ხუთშაბათი, აპრილი 30, 2026
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Global Ingredient Risk Index Stimulants

TeaCrine

Also known as: Theacrine, 1,3,7,9-tetramethyluric acid, Patented theacrine

MODERATE RISK 3.5/10 How?

This ingredient is classified as unclassified risk.

02

Safety Profile

Information not yet available for this ingredient profile.

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03

Interactions

Information not yet available for this ingredient profile.

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04

Evidence and Scientific Findings

Overview

Ingredient Overview

TeaCrine is a branded form of theacrine, a purine alkaloid structurally similar to caffeine. Produces stimulant-like effects with less rapid tolerance. Well tolerated up to 300 mg/day. May potentiate caffeine effects unpredictably. Insomnia, anxiety, and elevated heart rate possible at high doses. Avoid in pregnancy and cardiac conditions.

Classification

Biological and Chemical Classification

Information not yet available for this ingredient profile.

Mechanism

Mechanism of Action

Information not yet available for this ingredient profile.

Clinical Evidence

Clinical Evidence of Effectiveness

Information not yet available for this ingredient profile.

Pharmacokinetics

Pharmacokinetics

Information not yet available for this ingredient profile.

Dosage

Recommended Dosage

Information not yet available for this ingredient profile.

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05

SETI — Scientific Evidence Transparency Index

SETI Score 51/100
Risk Level High risk
Scientific Confidence Low
Evidence Strength Limited
Key Benefit Stimulants
Evidence Reviewed 9 PubMed studies
Scientific Confidence Low
Based on study quality, consistency, and recency

Executive Summary — Ingredient Assessment

SETI Score 51/100
Risk Level High risk
Evidence Strength Limited
Main Benefit Stimulants
Ingredient TeaCrine
Scientific Evidence Overview
  • 9 studies reviewed
  • 0 high-quality studies (meta-analysis or RCT)
  • Main clinical benefit observed: Stimulants
  • Evidence consistency: High consistency across studies (100%)
Safety Signals
  • No significant safety signals identified in the reviewed literature.
Evidence Strength Limited
Final Scientific Assessment

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

Ingredient TeaCrine
Evidence reviewed 9 peer-reviewed studies (last 10 years)
51 /100

Total SETI Score

High risk
Evidence quality 9/40
Evidence consistency 20/20
Safety signals 2/20
Study recency 10/10
Evidence transparency 10/10

Evidence Summary

  • 9 studies reviewed
  • 0 high-quality studies (meta-analysis or systematic review)
  • 0 studies identified benefits or no safety concern (GREEN)
  • 9 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 აპრ 2026, 12:12

Evidence Distribution

9 Other / unclassified
  1. Observational / other LOW evidence YELLOW
    A Combination of Caffeine, TeaCrine, and Dynamine Improves the Neurophysiological and Performance Measures of Electronic (E)-Gamers. ↗
    Journal Cureus
    Year 2023
    Study type Observational / other
    Evidence strength LOW evidence
    Evans C et al.. A Combination of Caffeine, TeaCrine, and Dynamine Improves the Neurophysiological and Performance Measures of Electronic (E)-Gamers.. Cureus. 2023. PMID:37772230.
  2. Observational / other LOW evidence YELLOW
    A Combination of Caffeine, TeaCrineu00ae (Theacrine), and Dynamineu00ae (Methylliberine) Increases Cognitive Performance and Reaction Time Without Interfering With Mood in Adult Male… ↗
    Journal Cureus
    Year 2021
    Study type Observational / other
    Evidence strength LOW evidence
    Tartar JL et al.. A Combination of Caffeine, TeaCrineu00ae (Theacrine), and Dynamineu00ae (Methylliberine) Increases Cognitive Performance and Reaction Time Without Interfering With Mood in Adult Male Egamers.. Cureus. 2021. PMID:35103121.
  3. Observational / other LOW evidence YELLOW
    Development of a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for characterizing caffeine, methylliberine, and theacrine pharmacokinetics in humans. ↗
    Journal J Chromatogr B Analyt Technol Biomed Life Sci
    Year 2020
    Study type Observational / other
    Evidence strength LOW evidence
    Wang YH et al.. Development of a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for characterizing caffeine, methylliberine, and theacrine pharmacokinetics in humans.. J Chromatogr B Analyt Technol Biomed Life Sci. 2020. PMID:32829142.
  4. Observational / other LOW evidence YELLOW
    Safety of Short-Term Supplementation with Methylliberine (Dynamine(u00ae)) Alone and in Combination with TeaCrine(u00ae) in Young Adults. ↗
    Journal Nutrients
    Year 2020
    Study type Observational / other
    Evidence strength LOW evidence
    VanDusseldorp TA et al.. Safety of Short-Term Supplementation with Methylliberine (Dynamine(u00ae)) Alone and in Combination with TeaCrine(u00ae) in Young Adults.. Nutrients. 2020. PMID:32121218.
  5. Observational / other LOW evidence YELLOW
    The effects of a caffeine-like supplement, TeaCrineu00ae, on muscular strength, endurance and power performance in resistance-trained men. ↗
    Journal J Int Soc Sports Nutr
    Year 2019
    Study type Observational / other
    Evidence strength LOW evidence
    Cesareo KR et al.. The effects of a caffeine-like supplement, TeaCrineu00ae, on muscular strength, endurance and power performance in resistance-trained men.. J Int Soc Sports Nutr. 2019. PMID:31660991.
  6. Observational / other LOW evidence YELLOW
    The effects of TeaCrineu00ae and caffeine on endurance and cognitive performance during a simulated match in high-level soccer players. ↗
    Journal J Int Soc Sports Nutr
    Year 2019
    Study type Observational / other
    Evidence strength LOW evidence
    Bello ML et al.. The effects of TeaCrineu00ae and caffeine on endurance and cognitive performance during a simulated match in high-level soccer players.. J Int Soc Sports Nutr. 2019. PMID:30999897.
  7. Observational / other LOW evidence YELLOW
    Assessment of the Drug-Drug Interaction Potential Between Theacrine and Caffeine in Humans. ↗
    Journal J Caffeine Res
    Year 2017
    Study type Observational / other
    Evidence strength LOW evidence
    He H et al.. Assessment of the Drug-Drug Interaction Potential Between Theacrine and Caffeine in Humans.. J Caffeine Res. 2017. PMID:28875060.
  8. Observational / other LOW evidence YELLOW
    A Two-Part Approach to Examine the Effects of Theacrine (TeaCrineu00ae) Supplementation on Oxygen Consumption, Hemodynamic Responses, and Subjective Measures of Cognitive and… ↗
    Journal J Diet Suppl
    Year 2017
    Study type Observational / other
    Evidence strength LOW evidence
    Ziegenfuss TN et al.. A Two-Part Approach to Examine the Effects of Theacrine (TeaCrineu00ae) Supplementation on Oxygen Consumption, Hemodynamic Responses, and Subjective Measures of Cognitive and Psychometric Parameters.. J Diet Suppl. 2017. PMID:27164220.
  9. Observational / other LOW evidence YELLOW
    Safety of TeaCrineu00ae, a non-habituating, naturally-occurring purine alkaloid over eight weeks of continuous use. ↗
    Journal J Int Soc Sports Nutr
    Year 2016
    Study type Observational / other
    Evidence strength LOW evidence
    Taylor L et al.. Safety of TeaCrineu00ae, a non-habituating, naturally-occurring purine alkaloid over eight weeks of continuous use.. J Int Soc Sports Nutr. 2016. PMID:26766930.
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06

Score Transparency

Q × L × D × S × 10 = 3.5 / 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 = 3.5 / 10

Final GIRI Score for TeaCrine. 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 3.5/10

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
3.5

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

What drove the Moderate classification for TeaCrine

GIRI Score 3.5 / 10

A score of 3.5 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 No restrictions found

No major regulatory restrictions or advisories recorded across monitored jurisdictions (FDA, EMA, Health Canada, TGA, and others).

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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