TB-500
TB-500 is a synthetic peptide corresponding to the N-terminal acetylated 17–23 amino acid fragment of thymosin beta-4 (Ac-LKKTETQ). Preliminary in vitro and animal data suggest roles in actin binding, cell migration, angiogenesis, and wound healing, but no human clinical trials have been conducted and no regulatory approval exists for any indication. It is classified as a prohibited substance by WADA.
20/28 claims verified by independent fact-checker.
1 claim pending coverage
- Src:f3d17e0f-08e8-4985-a22c-3096ca007f68 is titled 'Comparative effects of dietary sodium butyrate and tributyrin on broiler chickens' performance, gene expression, intestinal histomorphometry, blood indices, and litter.' This appears to be an entirely unrelated poultry nutrition study. The UUID exists in the packet but the source almost certainly does not support any claim about TB-500 structure. This is a critical citation mismatch — likely a wrong UUID assigned to this source slot. Claim fails: cited source does not plausibly support the claim.(1 claim)
Pepteligence regenerates entries quarterly and when new high-tier evidence appears.
Quick facts
Suggested labs for this peptide class — educational reference only; not medical advice.
TL;DR
- Half-life: — — dosed —.
- Administered via —.
- Evidence base: animal model studies.
- Primary goals: healing, recovery, inflammation.
Primarily animal data
How it works
TB-500 is a synthetic, N-terminal acetylated form of the 17–23 fragment of thymosin beta-4, with the sequence Ac-LKKTETQ [8][3][2][1]. In vitro and mechanistic studies indicate that this fragment may promote actin binding, cell migration, wound healing, angiogenesis, keratinocyte migration, and collagen deposition, while preliminary evidence suggests it may also reduce local inflammation [3][2]. Mechanistic reviews of therapeutic peptides in orthopaedics note that compounds in this class may engage signalling pathways including PI3K/Akt, mTOR, MAPK, TGF-β, and AMPK, though direct confirmation of these pathways for TB-500 in human tissue is not established [4]. In vitro metabolic studies demonstrate that TB-500 undergoes significant metabolic transformation in human kidney microsomes and related in vitro metabolic systems, suggesting rapid enzymatic degradation [7]. All mechanistic evidence is derived from in vitro or animal models; no human pharmacokinetic or pharmacodynamic data are available in the current research packet.
What the research says
Research summary content coming soon. Check the references section for indexed studies.
Protocol lifecycle
Before — Pre-cycle readiness
Readiness checklist
Evidence awareness
- Understand that all available mechanistic evidence for TB-500 is derived from in vitro and animal studies only — no human efficacy, safety, or pharmacokinetic data exist.
- Be aware that TB-500 is a WADA-prohibited substance; competitive athletes face career-affecting sanctions [5][6].
- Consult a licensed physician before considering any unapproved peptide; no prescribing-label or approved indication exists for TB-500.
Regulatory and legal
- Confirm the legal status of TB-500 in your jurisdiction — it is not approved by the FDA, EMA, or any identified regulatory body for human use.
- Verify that any supplier compound has undergone independent third-party purity and sterility testing.
- No evidence-based pre-cycle guidance exists for TB-500 in humans; the research packet contains no human clinical trial protocols.
During — Active protocol
After — Post-cycle
- No evidence-based post-cycle or washout guidance exists for TB-500 in humans.
Stacks it appears in
TB-500 is typically used as a standalone compound. Stack data coming soon.
Related peptides
Other compounds indexed on Pepteligence that share research tags with TB-500. Educational context only.
Safety
Common side effects
- ·[insufficient evidence in research packet — no human adverse event data identified]
Rare side effects
- ·[insufficient evidence in research packet]
- [insufficient evidence in research packet — the absence of human safety data means serious risks cannot be characterised or excluded]
Contraindications
- ·[insufficient evidence in research packet — no human contraindication data identified]
Community experiences
No community experiences yet for TB-500. Be the first to share yours.
Share your experience →Have you tried TB-500?
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TB-500 — at a glance
| Property | TB-500 | — |
|---|---|---|
| Half-life | — | — |
| Route | — | — |
| Typical dose | See research context | — |
| Mechanism | TB-500 is a synthetic, N-terminal acetylated form of the 17–23 fragment of thymosin beta-4, with the sequence Ac-LKKTETQ. In vitro and mechanistic studies indicate that this fragment may promote actin binding, cell migration, wound healing, angiogenesis, keratinocyte migration, and collagen deposition, while preliminary evidence suggests it may also reduce local inflammation. Mechanistic reviews of therapeutic peptides in orthopaedics note that compounds in this class may engage signalling pathways including PI3K/Akt, mTOR, MAPK, TGF-β, and AMPK, though direct confirmation of these pathways for TB-500 in human tissue is not established. In vitro metabolic studies demonstrate that TB-500 undergoes significant metabolic transformation in human kidney microsomes and related in vitro metabolic systems, suggesting rapid enzymatic degradation. All mechanistic evidence is derived from in vitro or animal models; no human pharmacokinetic or pharmacodynamic data are available in the current research packet. | — |
| Evidence strength | animal | anecdotal |
| Primary goal | healing | — |
Frequently asked questions
What is TB-500?
How does TB-500 work?
Is TB-500 the same as Thymosin Beta-4?
What is TB-500 used for?
Is TB-500 FDA-approved?
What are common dosages of TB-500?
How is TB-500 administered?
What are common side effects of TB-500?
Are there safety concerns with TB-500?
Is TB-500 legal?
Can TB-500 be combined with other peptides?
What does the research on TB-500 show overall?
References
- [1]
Synthesis and characterization of the N-terminal acetylated 17-23 fragment of thymosin beta 4 identified in TB-500, a product suspected to possess doping potential.
Esposito Simone, Deventer Koen, Goeman Jan et al.
Drug testing and analysis · 2012 · PMID 22962027
- [2]
Doping control analysis of TB-500, a synthetic version of an active region of thymosin β₄, in equine urine and plasma by liquid chromatography-mass spectrometry.
Ho Emmie N M, Kwok W H, Lau M Y et al.
Journal of chromatography. A · 2012 · PMID 23084823
- [3]
Simultaneous quantification of TB-500 and its metabolites in in-vitro experiments and rats by UHPLC-Q-Exactive orbitrap MS/MS and their screening by wound healing activities in-vitro.
Rahaman Khandoker Asiqur, Muresan Anca Raluca, Min Hophil et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences · 2024 · PMID 38382158
- [4]
Therapeutic Peptides in Orthopaedics: Applications, Challenges, and Future Directions.
Rahman Omar F, Lee Steven J, Seeds William A
Journal of the American Academy of Orthopaedic Surgeons. Global research & reviews · 2026 · PMID 41490200
- [5]
Simplifying and expanding the screening for peptides <2 kDa by direct urine injection, liquid chromatography, and ion mobility mass spectrometry.
Thomas Andreas, Görgens Christian, Guddat Sven et al.
Journal of separation science · 2016 · PMID 26578461
- [6]
Detecting peptidic drugs, drug candidates and analogs in sports doping: current status and future directions.
Thevis Mario, Thomas Andreas, Schänzer Wilhelm
Expert review of proteomics · 2014 · PMID 25382550
- [7]
Comparison of various in vitro model systems of the metabolism of synthetic doping peptides: Proteolytic enzymes, human blood serum, liver and kidney microsomes and liver S9 fraction.
Zvereva Irina, Semenistaya Ekaterina, Krotov Grigory et al.
Journal of proteomics · 2016 · PMID 27569051
- [8]
Comparative effects of dietary sodium butyrate and tributyrin on broiler chickens' performance, gene expression, intestinal histomorphometry, blood indices, and litter.
Ismael Elshaimaa, Kamel Shaimaa, Elleithy Ebtihal M M et al.
Scientific reports · 2025 · PMID 40681595
- [?]
Therapeutic peptides in gerontology: mechanisms and applications for healthy aging.
Mavrych Volodymyr, Shypilova Inna, Bolgova Olena
Frontiers in aging · 2026 · PMID 42021992
- [?]
Safety and Efficacy of Approved and Unapproved Peptide Therapies for Musculoskeletal Injuries and Athletic Performance.
Mendias Christopher L, Awan Tariq M
Sports medicine (Auckland, N.Z.) · 2026 · PMID 41966639
- [?]
Injectable Peptide Therapy: A Primer for Orthopaedic and Sports Medicine Physicians.
Mayfield Cory K, Bolia Ioanna K, Feingold Cailan L et al.
The American journal of sports medicine · 2026 · PMID 41476424
- [?]
Adsorption effects of the doping relevant peptides Insulin Lispro, Synachten, TB-500 and GHRP 5.
Judák Péter, Van Eenoo Peter, Deventer Koen
Analytical biochemistry · 2017 · PMID 28887173
- [?]
Solid-phase extraction of small biologically active peptides on cartridges and microelution 96-well plates from human urine.
Semenistaya Ekaterina, Zvereva Irina, Krotov Grigory et al.
Drug testing and analysis · 2016 · PMID 26472487
- [?]
In vitro models for metabolic studies of small peptide hormones in sport drug testing.
Esposito Simone, Deventer Koen, Geldof Lore et al.
Journal of peptide science : an official publication of the European Peptide Society · 2015 · PMID 25469748
- [?]
Analytical approaches for the detection of emerging therapeutics and non-approved drugs in human doping controls.
Thevis Mario, Schänzer Wilhelm
Journal of pharmaceutical and biomedical analysis · 2014 · PMID 24906629
- [?]
Doping control analysis of seven bioactive peptides in horse plasma by liquid chromatography-mass spectrometry.
Kwok Wai Him, Ho Emmie N M, Lau Ming Yip et al.
Analytical and bioanalytical chemistry · 2013 · PMID 23318763