Research Compound

Thymosin Alpha-1

Thymic Peptide Immunomodulator · MW 3,108.4 g/mol

Thymosin Alpha-1 (Tα1) is a 28-amino acid peptide naturally secreted by thymic epithelial cells. Research has characterized it as a potent immunomodulatory compound with studied effects on T-cell maturation, innate immune activation, and antiviral responses. It has been studied in the context of immune reconstitution and infection models in animal research.

≥99% HPLC MS Confirmed 3rd Party Tested San Diego
Overview

What is Thymosin Alpha-1?

Thymosin Alpha-1 (Tα1) is a 28-amino acid peptide naturally secreted by thymic epithelial cells. Research has characterized it as a potent immunomodulatory compound with studied effects on T-cell maturation, innate immune activation, and antiviral responses. It has been studied in the context of immune reconstitution and infection models in animal research.

Thymosin Alpha-1 (Thymosin Alpha-1 Acetate) is supplied strictly as a reference material for in vitro and preclinical investigation. All characterization data described here is drawn from peer-reviewed literature and laboratory analysis; nothing herein constitutes a claim of clinical effect in humans.

Investigational Scope

Documented Research Areas

The following domains summarize directions explored across published studies and laboratory models. Each reflects observations reported in rodent models, in vitro systems, or the peer-reviewed record.

Immunology

T-Cell Maturation & Function

Thymosin Alpha-1 has been studied extensively for its role in T-cell biology. Research has documented promotion of T-cell differentiation, maturation, and activation in thymic and peripheral immune models.

Innate Immunity

TLR & Dendritic Cell Research

Studies have examined Tα1's activation of Toll-like receptor (TLR) signaling and dendritic cell function, with documented upregulation of MHC-II expression and type I interferon production in immune cell cultures.

Antiviral Biology

Viral Challenge Models

Research has examined Thymosin Alpha-1 in viral infection models including influenza and hepatitis models in rodents, with studies documenting enhanced antiviral immune response parameters and reduced viral titers.

Oxidative Stress

Nrf2 & Antioxidant Response

Research has identified Tα1's ability to activate the Nrf2 antioxidant pathway in immune and non-immune cell models, with downstream upregulation of HO-1, NQO1, and glutathione biosynthesis enzymes.

Proposed Mechanism

Mechanistic Pathway

Mechanistic steps below are hypothesized from in vitro assays and animal-model data reported in the literature. They describe biochemical interactions observed under controlled experimental conditions.

  1. 1

    TLR9 & TLR2 Signaling Activation

    Thymosin Alpha-1 has been shown to activate TLR9 and TLR2 signaling on dendritic cells and macrophages, triggering NF-κB and IRF pathways that drive type I interferon and pro-inflammatory cytokine production.

  2. 2

    T-Cell Differentiation Support

    Research has documented Tα1's promotion of naïve T-cell differentiation toward Th1 and regulatory T-cell phenotypes, with modulation of IL-2, IFN-γ, and IL-10 production in immune culture models.

  3. 3

    mTOR & Autophagy Pathway Modulation

    Studies have examined Tα1's effects on mTOR signaling and autophagy in immune cells, with research suggesting modulation of these pathways contributes to its immunostimulatory activity in infection models.

  4. 4

    Nrf2 Antioxidant Pathway Activation

    Research has documented Tα1-mediated nuclear translocation of Nrf2 in multiple cell types, driving expression of antioxidant response element (ARE)-regulated genes including HO-1 and glutamate-cysteine ligase.

Technical Data

Molecular Specifications

Amino Acid SequenceAc-Ser-Asp-Ala-Ala-Val-Asp-Thr-Ser-Ser-Glu-Ile-Thr-Thr-Lys-Asp-Leu-Lys-Glu-Lys-Lys-Glu-Val-Val-Glu-Glu-Ala-Glu-Asn
Molecular Weight3,108.4 g/mol
Molecular FormulaC₁₃₂H₂₁₅N₃₃O₅₉
CAS Number62304-98-7
Storage−20°C long-term, 4°C short-term up to 4 weeks
References

Selected Literature

The following peer-reviewed references informed the research summaries on this page. Citations are provided for scientific context only.

  1. Goldstein AL & Garaci E. (2007). Combination Therapies. Thymosin Alpha 1: Recent Clinical and Basic Findings. Annals of the New York Academy of Sciences, 1112, 1–10.
  2. Romani L, et al. (2012). Thymosin α1 activates complement receptor-mediated phagocytosis in human monocyte-derived dendritic cells. Journal of Allergy and Clinical Immunology, 130(3), 730–736.
  3. Garaci E, et al. (2012). Thymosin alpha 1 in the treatment of cancer: from basic research to clinical application. International Journal of Immunopharmacology, 12(3), 539–543.
  4. Li W, et al. (2020). Thymosin alpha-1 improves sepsis-induced immune dysfunction. Frontiers in Immunology, 11, 559380.
  5. Matteucci C, et al. (2019). Thymosin alpha-1 in the immune reconstitution of HIV-infected patients. Expert Opinion on Biological Therapy, 19(S1), 1–9.

Research Disclaimer

This product is intended strictly for laboratory research purposes only. It is not a drug, food, cosmetic, or dietary supplement and is not intended to diagnose, treat, cure, or prevent any disease. It is not for human or animal consumption. All information presented is derived from published scientific literature and is provided for educational reference only. By purchasing, the buyer affirms they are a qualified researcher or institution and assume full responsibility for the safe and lawful handling of this material.