PeptideNot FDA-approved as TB-500; often marketed as a thymosin beta-4 fragment.

TB-500

A peptide commonly associated with thymosin beta-4 discussions and recovery claims, where evidence must be separated by exact molecule and model.

Last reviewed:

Studies
0
Tracked suppliers
0
Identifiers
3
Updated
Jul 28, 2026

Identity

Overview

Aliases
Thymosin beta-4 fragment, TB500
Topics
mobility, peptide, recovery, tissue repair
Formula
C38H68N10O14
Sequence
Ac-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln
Regulatory and product note
Separate approved-product evidence, research evidence, and supplier product claims.

Proposed mechanism

Proposed mechanism

Often discussed around actin binding, cell migration, inflammation models, and tissue-remodeling hypotheses.

Evidence

Evidence and limitations

This record keeps mechanisms, animal studies, human biomarkers, controlled clinical outcomes, safety data, and supplier documentation separate so claims are not flattened into one misleading score.

Research questions tracked

  • What exact molecule, route, formulation, and outcome were studied?
  • Is the evidence mechanistic, animal, early human, or controlled clinical evidence?
  • Does the commercial product match the studied material and documentation?

Key findings and boundaries

  • Evidence strength changes by outcome and study type.
  • Mechanism is useful context but not proof of clinical benefit.
  • Supplier claims require separate documentation review.

Important gaps

  • Long-term human safety and real-world product quality are often incomplete.
  • Claims can exceed the route, formulation, and population studied.

Safety and unknowns

Safety and unknowns

Research information, not medical advice.

Public products and research discussions may not refer to identical material. Documentation and exact identity matter.

  • Known and plausible adverse effects must be separated from product-quality risks.
  • Injectable or research-use products add sterility, endotoxin, impurity, and handling concerns.

Testing & COAs

Testing and COAs

An observed COA may support specific laboratory findings. It does not by itself prove clinical benefit, safety, legality, sterility or suitability.

  • Identity, assay/purity, batch matching, lab identity, and test date should be visible.
  • COAs do not prove clinical effectiveness, legal status, or suitability for use.