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Recovery peptide◔ Preclinical

TB-500

TB-500 is a synthetic heptapeptide (Ac-LKKTETQ-OH) modeled on the actin-binding domain of Thymosin beta-4 (Tβ4), a 43-amino-acid protein studied preclinically for roles in cell migration, wound healing, and angiogenesis.

Molecular weight
~889 g/mol (LKKTETQ fragment)
g/mol
Half-life
short (minutes, animal PK)
estimated
Form
Lyophilized powder
FDA status
Not approved / research; WADA-banned

TB-500 reconstitution calculator

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Typical dosing

GoalRangeRouteFrequency
Validated human dosing for the TB-500 fragmentNone establishedn/aNo completed, published human trial of Ac-LKKTETQ-OH — every circulating figure is informal
Community protocol (no trial basis)2-2.5 mgSubQ2x weekly loading phase, then weekly maintenance
Full-length Thymosin beta-4 — Phase 1 safety study in 40 healthy volunteers (Ruff et al. 2010)42, 140, 420 or 1260 mg (ascending cohorts)IVSingle dose, then the same dose daily for 14 days; no dose-limiting toxicity — note this is the 43-aa protein, not TB-500
Full-length Thymosin beta-4 — topical ophthalmic (RGN-259), dry eye and neurotrophic keratopathy trials0.1% ophthalmic solutionTopical eye drops5-6x daily for ~28 days in published trials
Anti-doping statusAny amountAny routeProhibited by WADA at all times, in and out of competition

Ranges compiled from research literature — not a prescription.

How it works

Thymosin beta-4 (Tβ4) is a naturally occurring 43-amino-acid, G-actin-sequestering protein present in nearly all mammalian tissue and cell types. Its actin-binding region spans roughly residues 17-22, where it reversibly binds monomeric G-actin and modulates the equilibrium between G-actin and filamentous F-actin, a process central to cytoskeletal remodeling, cell shape change, and cell migration.

TB-500 is a synthetic peptide fragment, Ac-LKKTETQ-OH, corresponding to residues 17-23 of Tβ4 and encompassing its actin-binding motif. It is marketed as a smaller, more stable stand-in for the full protein that is intended to reproduce Tβ4's actin-regulating activity in a lab-synthesizable form.

In animal and cell-culture studies, full-length Tβ4 has been reported to accelerate dermal re-epithelialization and wound contraction, increase capillary ingrowth and collagen deposition, support corneal epithelial healing and reduce inflammation in keratitis models, and promote cardiomyocyte migration and survival after simulated myocardial infarction via an integrin-linked-kinase/Akt signaling pathway, alongside stimulation of epicardial-derived neovascularization in rodent and ex vivo heart tissue.

A key honesty point: the large majority of this mechanistic and efficacy evidence — the wound-healing, cardiac-repair, and corneal studies cited below — was conducted with the full 43-amino-acid Tβ4 protein or engineered variants, not with the isolated 7-residue TB-500 fragment sold under that name. A 2026 scoping review found no completed, published human clinical trials specifically evaluating TB-500. Whether the short fragment reproduces the full protein's pharmacology, pharmacokinetics, or safety profile in humans has not been established; extrapolation from full-length Tβ4 animal data to the synthetic TB-500 fragment used in research/gray-market settings remains unproven.

Side effects & safety

  • No published human clinical trials exist for the TB-500 fragment specifically; human safety and efficacy are unknown and are extrapolated only from full-length Tβ4 animal studies.
  • Preclinical tolerability data come from rodent and ex vivo/in vitro models; long-term effects, immunogenicity, and carcinogenic or proliferative risk in humans have not been studied.
  • Product purity and sourcing vary widely in the unregulated research-chemical market; contamination, incorrect concentration, and mislabeling are documented risks since these products are not pharmaceutical-grade or FDA-inspected.
  • TB-500/thymosin beta-4 is prohibited by the World Anti-Doping Agency (WADA) at all times; competitive athletes risk sanctions from any detectable use.
  • TB-500 is not FDA-approved for any human indication. Its compounding status has been under active FDA/Pharmacy Compounding Advisory Committee review in 2026, leaving it in a regulatory gray zone.
  • This is not medical advice; consult a licensed clinician before considering use, especially given the absence of human dosing, interaction, or safety data.

Research

Primary sources — PubMed.

  1. Bock-Marquette I, et al. Thymosin beta4 activates integrin-linked kinase and promotes cardiac cell migration, survival and cardiac repair. Nature. 2004. https://pubmed.ncbi.nlm.nih.gov/15565145/
  2. Smart N, et al. Thymosin beta-4 is essential for coronary vessel development and promotes neovascularization via adult epicardium. Ann N Y Acad Sci. 2007. https://pubmed.ncbi.nlm.nih.gov/17495252/
  3. Sosne G, et al. Thymosin beta 4: a novel corneal wound healing and anti-inflammatory agent. Clin Ophthalmol. 2007. https://pmc.ncbi.nlm.nih.gov/articles/PMC2701135/
  4. Progress on the Function and Application of Thymosin β4 (review). Front Endocrinol. 2021. https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2021.767785/full
  5. Thymosin Beta-4 and TB-500 in Tissue Healing, Regeneration, and Musculoskeletal Repair: A Scoping Review. Appl Sci. 2026. https://www.mdpi.com/2076-3417/16/12/6202
  6. U.S. FDA. Bulk Drug Substances Used in Compounding Under Section 503A of the FD&C Act. https://www.fda.gov/drugs/human-drug-compounding/bulk-drug-substances-used-compounding-under-section-503a-fdc-act
⚠︎TB-500 may be a research chemical not approved for human use in your country. This page is educational information only — not medical advice, and not an endorsement to use it.
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TB-500 FAQ

No, and the distinction matters. Thymosin beta-4 is a naturally occurring 43-amino-acid protein; TB-500 is a synthetic 7-residue fragment, Ac-LKKTETQ-OH, corresponding to its actin-binding region. Almost all of the wound-healing, cardiac, and corneal research attributed to TB-500 was actually performed with the full-length protein. Whether the short fragment reproduces its pharmacology, pharmacokinetics, or safety in humans is unestablished.
Not the fragment itself. A 2026 scoping review found no completed, published human clinical trials specifically evaluating TB-500. Full-length Thymosin beta-4 has human data: a Phase 1 study gave 40 healthy volunteers ascending intravenous doses of 42 to 1,260 mg, then the same dose daily for 14 days, reporting no dose-limiting toxicity. That safety finding applies to the full protein, not TB-500.
Yes. TB-500 and thymosin beta-4 are prohibited by the World Anti-Doping Agency at all times, both in and out of competition, and detection methods exist. Any competitive athlete subject to WADA-code testing risks sanctions from detectable use, regardless of whether it was taken for injury recovery rather than performance enhancement.
No validated human dose exists. Because no human trial of the fragment has been completed, every dosing figure circulating online originates from informal community protocols rather than clinical research, commonly a loading phase followed by weekly maintenance. Those numbers have no trial basis, and unregulated research-chemical suppliers introduce additional uncertainty about what a given vial actually contains.

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