Mechanism overviews · 29 papers
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TB-500

También conocido como: Thymosin Beta-4 fragment · TB4

A synthetic fragment related to Thymosin Beta-4, used in actin-regulation and tissue-repair research.

Written by Peptidoteca Research Desk·Reviewed by Peptidoteca Research Desk·Last reviewed 2026-06-14·4 sources

§ In brief

TB-500 (also known as Thymosin Beta-4 fragment, TB4) is a synthetic fragment related to Thymosin Beta-4, used in actin-regulation and tissue-repair research. It is supplied for laboratory research use only and is not approved for human or veterinary use. Its 27-residue amino-acid sequence is LKKTETQEKNPLPSKETIEQEKQAGES.

What is TB-500?

A synthetic fragment related to Thymosin Beta-4, used in actin-regulation and tissue-repair research.

TB-500 is catalogued here as a reference compound for tissue-repair and regenerative research. The entry covers its chemical identity and the public databases that describe it; it is not a usage guide.

How is TB-500 studied?

TB-500 appears in the tissue-repair and regenerative literature, primarily in in-vitro and preclinical (animal) models. This page indexes 4 primary papers on TB-500, each tagged with its study type below. Peptidoteca summarizes the proposed mechanism class and the primary sources rather than human outcomes; for the wider library, see the research library.

Is TB-500 approved for human use?

No. TB-500 is supplied for laboratory (in-vitro) research use only. It is not approved by the FDA or any comparable regulator for human or veterinary use, and nothing on this page constitutes medical advice, dosing guidance or a treatment recommendation.

What are the research limitations?

Most available evidence for TB-500 is preclinical — in-vitro and animal models — and findings in those models do not establish efficacy or safety in humans. Human clinical data is limited or absent, and TB-500 is not an approved drug. Treat the literature as mechanistic research, not clinical guidance.

§ Primary literature

  1. 1.Rahaman KA (2024). 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. Journal of Chromatography B.Rodent studyUsing in-vitro incubations and rat samples, this analytical study describes a UHPLC-Q-Exactive orbitrap MS/MS method for the simultaneous quantification of TB-500 and its metabolites, and reports in-vitro screening of associated wound-healing activities.
  2. 2.Wang Y (2024). Activation of pro-resolving pathways mediate the therapeutic effects of thymosin beta-4 during Pseudomonas aeruginosa-induced keratitis. Frontiers in Immunology.Rodent studyIn a mouse model of Pseudomonas aeruginosa-induced bacterial keratitis, with in-vitro validation in LPS-stimulated murine RAW 264.7 cells, the study reports that thymosin beta-4 (Tβ4) was associated with activation of pro-resolving inflammatory pathways during the resolution of infection and inflammation. Findings are limited to animal and cell-culture models.
  3. 3.He S (2026). Low-Temperature Fabrication of Thymosin β4-Loaded Soluble Microneedles to Promote Wound Healing by Specific Binding to Downregulated Immune Regulators Vsig4 and IL22rα2. Advanced Healthcare Materials.Rodent studyIn a mouse wound-healing model with in-vitro binding assays, Thymosin β4 (TB4/TB-500)-loaded soluble microneedles were associated with enhanced wound closure, an effect the authors attribute to specific binding to the downregulated immune regulators Vsig4 and IL22rα2. These are preclinical (rodent and in-vitro) findings only.
  4. 4.Di H (2026). Thymosin beta 4: An emerging therapeutic candidate for kidney diseases. Peptides.ReviewThis review synthesizes reported mechanisms of thymosin beta-4 (the peptide also known as TB-500), including actin regulation and anti-inflammatory signaling, as described across preclinical models of acute and chronic kidney injury.
Compound spec
Sequence
LKKTETQEKNPLPSKETIEQEKQAGES
Length27 aa
ClassRecovery
CAS885340-08-9
Research vial5 / 10 mg

Solo para investigación in-vitro. No es consejo médico, clínico ni de dosificación.