Is TB-500 the same as thymosin beta-4?
No — it is a short fragment of it. The human safety data belong to the full protein.
Actin Regulation & Cell Migration Pathways (Preclinical)
Thymosin Beta-4 Synthetic Fragment (Ac-LKKTETQ)
Last reviewed: August 2026
TB-500 is a synthetic version of a small fragment of a protein your body already produces naturally, called Thymosin Beta-4. This protein is found in virtually every cell in your body and plays a key role in how cells move and organize themselves during repair.
TB-500's main job in research models is enabling cells to move. Specifically, it interacts with actin — the internal scaffolding protein that gives cells their shape and allows them to crawl. By regulating actin dynamics, TB-500 appears to help repair cells migrate from where they're stored to where they're needed. Imagine a city after a storm: TB-500 is studied for its potential role in clearing the roads so repair crews can actually reach the damage.
Many tissues fail to heal properly not because the body lacks repair cells, but because those cells can't efficiently navigate to the injury site. TB-500's actin-regulating mechanism is particularly interesting to researchers because it works systemically — meaning it may influence cell movement throughout the body, not just at a specific local site. This distinguishes it from more locally-acting compounds like BPC-157.
TB-500 has a stronger clinical research foundation than most peptides in this category — its parent molecule (full-length Thymosin Beta-4) entered human trials for wound healing and dry eye. TB-500 itself is a shorter, more targeted fragment. All current TB-500 research is preclinical; it is a research compound only.
TB-500 (also referenced in research literature as TB500, tb-500 peptide, or Thymosin Beta-4 fragment) is a synthetic heptapeptide corresponding to the N-acetylated active fragment (amino acids 17–23) of thymosin beta-4 (Tβ4), a naturally occurring 43-amino-acid protein found ubiquitously in human and animal tissues. Thymosin beta-4 was first isolated from thymic tissue in the 1960s and has since been recognized as a master regulator of actin dynamics — the cytoskeletal processes that govern cell shape, movement, and division.
The TB-500 fragment (Ac-LKKTETQ) retains the actin-binding domain of the full-length thymosin beta-4 molecule, which is responsible for the peptide's primary biological activities in preclinical research models.
TB-500 consists of seven amino acids: Leucine-Lysine-Lysine-Threonine-Glutamate-Threonine-Glutamine, with an N-terminal acetyl group (Ac-LKKTETQ). This acetylation is functionally significant — it protects the peptide from aminopeptidase degradation and is required for full actin-sequestering activity.
The compound has a molecular weight of approximately 889.0 Daltons. Despite its reduced size compared to the full thymosin beta-4 molecule, TB-500 retains the critical WH2 (Wiskott-Homology 2) actin-binding motif, which is the structural basis for its primary mechanism of action.
TB-500 promotes healing by sequestering actin monomers to regulate cell migration and stimulate new blood vessel growth at injury sites.
The central mechanism of TB-500 revolves around its capacity to bind monomeric G-actin (globular actin) and thereby regulate the equilibrium between G-actin and filamentous F-actin. Actin dynamics are essential for virtually every aspect of cell motility, including the directed migration of repair cells to sites of tissue injury.
By sequestering G-actin, TB-500 reduces the pool available for F-actin polymerization in a spatially controlled manner, effectively enabling cells to extend lamellipodia and migrate toward chemotactic gradients. This mechanism is particularly relevant to wound healing, where fibroblasts, endothelial cells, and keratinocytes must migrate into the wound bed to initiate repair.
Beyond actin regulation, preclinical research has identified additional activities of TB-500, including promotion of endothelial cell differentiation and angiogenesis, inhibition of inflammatory cytokine expression (notably IL-1β and TNF-α), and activation of the Akt survival signaling pathway, which confers cytoprotective effects in ischemic tissue models.

Binds monomeric G-actin via the WH2 domain, regulating cytoskeletal dynamics and enabling directed cell migration.
Activates the Akt pathway, promoting cellular survival and providing cytoprotection in ischemic and inflammatory conditions.
Promotes endothelial cell differentiation and new vessel formation through mechanisms partially independent of classical VEGF signaling.
Downregulates pro-inflammatory cytokines including IL-1β and TNF-α, reducing inflammatory burden at sites of tissue injury.
Each outcome rated by the highest level of evidence available. Tiers follow our 5-tier methodology.
Study counts reflect peer-reviewed publications in the evidence database below. "Theoretical" outcomes have mechanistic rationale only. Learn about our evidence tiers →
2 cited studies — model, sample size, outcome, and effect size from published literature.
| Study | Model | Sample | Outcome | Effect Size | Level |
|---|---|---|---|---|---|
Goldstein AL, et al. (2012) Thymosin β4: a multi-functional regenerative peptide PubMed | Rodent + human cardiac (Phase II) | Phase II: n=44 | Improved cardiac function post-MI; reduced fibrosis; stem cell mobilization | Significant improvement in ejection fraction vs. placebo (Phase II) | Phase II |
Huff T, et al. (2001) Thymosin β4 is released from human blood platelets and attached to actin filamen… PubMed | Human platelet — in vitro | In vitro | Confirmed Tβ4 sequestration of G-actin; mechanism of actin polymerization modulation | Quantitative G-actin binding demonstrated | In Vitro |
TB-500 (Thymosin Beta-4 Fragment) — half-life, bioavailability, onset, and duration data
| Parameter | Value | Source |
|---|---|---|
| Half-Life (t½) | ~4–6 hours (estimated) Preclinical data; no published human PK studies for the fragment | Preclinical Data |
| Time to Peak (Tmax) | ~30–90 minutes Subcutaneous injection; preclinical estimates | Preclinical Data |
| Bioavailability (F) | Estimated >75% (SC/IM) No direct human bioavailability data | Preclinical Data |
| Onset of Action | Days to weeks Tissue repair and anti-inflammatory effects | — |
| Duration of Action | Variable Tissue-level effects persist beyond plasma half-life | — |
TB-500 is a synthetic fragment of Thymosin Beta-4 (Tβ4). Full-length Tβ4 has a half-life of ~2–4 hours in plasma. The fragment's PK profile is estimated from preclinical data. No human pharmacokinetic studies have been published.
References:
• Goldstein AL et al. Ann N Y Acad Sci 2012
• Huff T et al. Int J Biochem Cell Biol 2001
Peer-reviewed literature supporting the research profile of TB-500
The following peer-reviewed studies form the primary evidence base for TB-500's research profile. All references are sourced from PubMed, NCBI, and peer-reviewed scientific journals. Published research is available through PubMed, NCBI, and peer-reviewed biomedical journals.
Goldstein AL, Hannappel E, Kleinman HK. Thymosin beta4: actin-sequestering protein moonlights to repair injured tissues. Trends in Molecular Medicine. 2005.PMID: 16099219
Established Thymosin β4's dual role as actin-sequestering protein and tissue repair mediator.
Bock-Marquette I, et al. Thymosin beta4 activates integrin-linked kinase and promotes cardiac cell migration, survival and cardiac repair. Nature. 2004.PMID: 15565145
Thymosin β4 activates ILK signaling to promote cardiac cell survival and migration in repair models.
Sosne G, et al. Thymosin beta 4 promotes corneal wound healing and decreases inflammation in vivo following alkali injury. Experimental Eye Research. 2002.PMID: 11950239
Anti-inflammatory and wound-healing effects confirmed in corneal injury model.
Huff T, et al. Beta-thymosins, small acidic peptides with multiple functions. International Journal of Biochemistry & Cell Biology. 2001.PMID: 11311852
Comprehensive review of beta-thymosin family functions including actin dynamics and cell motility.
Recovery Research
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15 documented interactions for TB-500
BPC-157 promotes angiogenesis while TB-500 modulates actin. Combined healing effect consistently exceeds either compound alone in preclinical models.
Both support tissue remodeling and wound healing via different mechanisms — TB-500 via actin modulation, GHK-Cu via collagen synthesis.
IGF-1 LR3 for muscle growth and hypertrophy; TB-500 for accelerated tissue repair and recovery.
Thymosin Alpha-1 immune modulation may complement TB-500 tissue repair in post-injury recovery protocols.
Interaction data is based on published research, known pharmacological mechanisms, and clinical practitioner experience. Evidence tiers: Clinical = human data; Emerging = preclinical/case reports; Theoretical = mechanism-based inference. Always consult a qualified healthcare provider before combining compounds.
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No human data for the fragment; the parent protein (thymosin β4) has been through human trials
TB-500 is a synthetic fragment of thymosin β4. Full-length thymosin β4 has been studied in people (eye drops for dry eye and corneal healing; intravenous in cardiac trials) with an acceptable safety profile. The fragment sold as TB-500 has no human trial of its own, so its tolerability is assumed from the parent, not shown.
Research-use information only. Research-grade TB-500 is not an approved medicine; where trial or label figures appear below they belong to the pharmaceutical product studied, not to any research vial. This section does not give dosing or medical advice.
Every rate carries its source. Where no source exists, no rate is printed.
| Effect | Rate (sourced) | Detail | Source |
|---|---|---|---|
| Thymosin β4 (parent) in human trials | not quantified | Topical and intravenous Tβ4 were well tolerated in phase 2 studies; adverse events were similar to placebo. | RGN-259 / RGN-352 trial reports |
| Injection-site reactions | not quantified | Expected from any injected peptide; unquantified for TB-500. | General |
Regulatory status: Not approved anywhere.
Everything above describes TB-500 the molecule. The risk specific to a research vial is different: it may not contain TB-500 at the labelled amount, and it may contain what the synthesis left behind. Identity (mass spectrometry), purity (HPLC), measured net content and an endotoxin result are the four lines on a certificate that bear on adverse effects, and only a certificate you can check at the laboratory tells you any of them. This is what we have verified for TB-500 so far.
72 of the 105 vendors on our scoreboard list TB-500 with a price we read on the product page (5 Sep 2026–1 Nov 2026). Of those, 64 name their testing laboratory, 48 publish certificates that resolve on the lab's own site, and 60 publish measured milligrams against the label. The full ranking, with every dated price, is on Best TB-500 Vendors.
| Vendor | Rubric | Lab named | Price read |
|---|---|---|---|
| Idun Peptides | 10/10 | Kovera Labs (named in certificate captions only) | $44.99 · 10mg · 5 Sep 2026 |
| MyPurePeptidepartner | 10/10 | Janoshik Analytical | $25.00 · 10mg · 1 Nov 2026 |
| Oneday Compoundspartner | 10/10 | ILS Laboratories (San Diego, CA) | $29.99 · 10mg · 29 Oct 2026 |
| Panda Peptides | 10/10 | Janoshik Analytical · ILS Labs (per batch) | $24.99 · 5mg · 25 Oct 2026 |
| Peptide Giantspartner | 10/10 | Janoshik Analytical · Vanguard Laboratory | $29.99 · 5mg · 1 Nov 2026 |
Top 5 by rubric score; 67 more on the ranking page.
5 certificates for TB-500 in the COA library: 3 checkable on the laboratory's own site, 5 stating measured mass against the label, 4 carrying a flag.
No — it is a short fragment of it. The human safety data belong to the full protein.
Side-effect section last reviewed 2026-09-12. Moved from the standalone side-effects page on 10 October 2026; text unchanged.
TB-500 (a synthetic fragment of Thymosin Beta-4) is legal to purchase and possess in the United States as a research chemical. It is not a controlled substance and is not FDA-approved for human use.
| Jurisdiction | Status as stated |
|---|---|
| United States | Legal as a research chemical. Not a scheduled substance under the DEA Controlled Substances Act. Not FDA-approved for human use. |
| Canada | Not a scheduled substance. Available for research purposes. Not approved by Health Canada for human use. |
| United Kingdom | Not listed under the Misuse of Drugs Act. Available for research purposes. Not licensed by the MHRA. |
| Australia | Not currently scheduled by the TGA. Available for research purposes. Regulatory status may change. |
| European Union | Generally available for research purposes across most member states. Not approved as a medicinal product by the EMA. |
Statements above are as our legal-status page for TB-500 stated them in 2025; they were moved here on 10 October 2026 and were not re-verified in the move. Regulations change. This is general information, not legal advice; check the current position with your own jurisdiction's regulator before relying on it.
No. TB-500 is not listed as a controlled substance under the US DEA Controlled Substances Act.
Yes. TB-500 can be legally purchased as a research chemical in the United States for legitimate laboratory research purposes.
Yes. TB-500 (Thymosin Beta-4 and its fragments) is prohibited by WADA under the category of peptide hormones and related substances.
TB-500 is a synthetic fragment of Thymosin Beta-4, specifically the actin-binding domain (amino acids 17-23). It is not identical to full TB-4 but shares many studied properties.
TB-500 is not currently scheduled by the TGA in Australia, but regulations can change. Always verify current status with a qualified legal or medical professional.
TB-500 is a synthetic fragment of thymosin beta-4. The regenerative evidence is preclinical (animal/in vitro). There are no human efficacy RCTs for TB-500 as used in the research-peptide market. Distinguish clearly between thymosin beta-4 in animal studies and TB-500 in humans — the latter has no clinical trials.
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