TB-500
Also known as: Thymosin Beta-4 Fragment 17–23, Ac-LKKTETQ
Molecular Formula
Molecular Weight
889.01 Da (Free Base; Acetate salt ~949.1 Da)
Half-Life
Unknown in humans (human pharmacokinetics and elimination half-life have not been established; equine SC peak ~1–2 hours)
Sequence
Ac-LKKTETQ-OH (Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH)
Clinical Applications & Evidence
Mechanism of Action
TB-500 contains the central actin-binding sequence (LKKTET) of Thymosin Beta-4. In preclinical models, it is hypothesized to sequester G-actin and influence cell migration and tissue remodeling. A 2024 metabolic study indicated that the N-terminal metabolite Ac-LKKTE contributes to fibroblast scratch-wound closure in vitro. Direct equivalence to full-length Tβ4 signaling cascades (VEGF upregulation, NF-κB modulation) in humans remains unconfirmed.
Investigated Uses
- Muscle & tendon injury repair (Preclinical models & research interest; no human clinical trials for Ac-LKKTETQ-OH)
- Post-infarction cardiac repair (Preclinical animal models of full-length Tβ4; unstudied clinically for TB-500)
- Corneal & dermal wound healing (Mouse models & non-acetylated fragment research; human trials RGN-259 evaluated full-length 43-residue Tβ4)
- Anti-inflammatory & anti-fibrotic research (Preclinical cell & animal models; metabolic activity under investigation)
Regulatory & Safety Status
FDA Status
Research OnlyWADA / Athletic Status
Prohibited at All Times (WADA S4.4.1)Known Side Effects
Contraindications
- WADA-tested athletes (Prohibited at all times under S2 Peptide Hormones and Mimetics)
- Active malignancy or history of cancer (Precautionary exclusion due to theoretical angiogenesis/cell migration concerns)
- Pregnancy and lactation (Unstudied safety profile)
Drug Interactions
- No formal clinical drug-interaction studies exist for TB-500
- Unregulated gray-market injectable preparations carry risks of peptide impurities, endotoxins, or inconsistent dosing