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Comparison

TB-500 vs Thymosin Alpha-1

Side-by-side of TB-500 and Thymosin Alpha-1. Every row below is pulled from the compound schema and will update as our data grows. For deeper reads, follow through to each compound page.

Effects at a glance

TB-500

  • 17-amino-acid fragment of endogenous Thymosin Beta-4, an actin-sequestering peptide
  • Preclinical models show accelerated tendon, ligament, and dermal wound healing
  • Equine veterinary use for soft-tissue injury is the most documented real-world application
  • Anecdotal human protocols use 2 to 5 mg twice weekly subcutaneously for 4 to 6 weeks
  • WADA banned under S2 (peptide hormones, growth factors) since 2018
  • No completed phase II or III human RCTs as of 2026; long-term safety unestablished

Thymosin Alpha-1

  • 28-amino-acid synthetic peptide identical to thymic-derived immunomodulator
  • Approved in over 35 countries as Zadaxin for hepatitis B, hepatitis C adjunct, and immune support
  • Not FDA approved in US; compounded by 503A/503B pharmacies for off-label immune support
  • Modulates T-cell maturation, NK activity, and Th1 polarization in immunocompromised states
  • Standard label dose: 1.6 mg subcutaneously twice weekly
  • Cleanest safety profile in the peptide class with hundreds of regulated trials behind it

Side-by-side

Attribute TB-500 Thymosin Alpha-1
Category peptide peptide
Also known as Thymosin Beta-4 fragment, TB4-Frag, Thymosin Beta 4 Talpha1, Ta1, Zadaxin, Thymalfasin
Half-life (hr) 2 2
Typical dose (mg) 2.5 1.6
Dosing frequency 2x weekly (anecdotal protocols) 2x weekly
Routes subcutaneous, intramuscular subcutaneous, intramuscular
Onset (hr) - 24
Peak (hr) - 168
Molecular weight 4963.4 3108.32
Molecular formula C212H350N56O78S C129H215N33O55
Mechanism Sequesters G-actin monomers, modulates cell migration and angiogenesis, and upregulates VEGF and myosin transcription. Promotes endothelial differentiation and stem-cell migration to injury sites in preclinical models. Synthetic peptide modulator of innate and adaptive immunity. Promotes T-cell maturation and CD4/CD8 production, modulates Th1/Th2 balance, stimulates NK cell activity, and modulates TLR2/TLR9 signaling in dendritic cells.
Legal status Not FDA approved; research-use-only grey market; banned by WADA Approved in 35+ countries as Zadaxin (hepatitis B, hepatitis C adjunct, immune support); not FDA approved in US; compounded by 503A/503B pharmacies for off-label use; not on WADA Prohibited List
WADA status banned unknown
DEA / Rx Not FDA approved; not scheduled; research-chemical status Rx only via international approval or US compounding (no controlled-substance schedule)
Pregnancy Insufficient data Not recommended; insufficient data
CAS 885340-08-9 62304-98-7
PubChem CID 62707662 16130571
Wikidata Q7799921 Q913854

Safety profile

TB-500

Common side effects

  • injection-site irritation
  • fatigue (anecdotal)
  • lethargy in early dosing (anecdotal)

Contraindications

  • pregnancy
  • active malignancy (theoretical angiogenic concern)
  • no established human safety profile

Interactions

  • BPC-157: Frequently co-administered in anecdotal healing protocols; no controlled interaction data(minor)

Thymosin Alpha-1

Common side effects

  • mild injection-site irritation (rare)
  • transient mild fatigue (rare)
  • occasional headache (rare)

Contraindications

  • pregnancy
  • lactation
  • active organ transplant rejection therapy
  • systemic immunosuppression for autoimmune disease (relative)
  • severe active autoimmune disease (caution)

Interactions

  • interferon-alpha: additive immune effect; used clinically in approved combination protocols(minor)
  • calcineurin inhibitors (cyclosporine, tacrolimus): theoretical destabilization of immunosuppression; avoid(major)
  • antimetabolites (azathioprine, mycophenolate): theoretical destabilization of immunosuppression; avoid(major)
  • vaccine administration: may augment vaccine response in elderly or immunocompromised; coordinate with clinician(minor)

Which Should You Take?

Thymosin Alpha-1 comes out ahead for most readers on the criteria we weight: 3 catalogued goals, Approved in 35+ countries as Zadaxin (hepatitis B, hepatitis C adjunct, immune support); not FDA approved in US; compounded by 503A/503B pharmacies for off-label use; not on WADA Prohibited List, with a Tier-A outcome catalogued. TB-500 is the right call when one of the conditionals below applies.

  • If your priority is tendon repair, pick TB-500.
  • If your priority is wound healing, pick TB-500.
  • If your priority is immune support, pick Thymosin Alpha-1.
  • If your priority is antiviral action, pick Thymosin Alpha-1.

Default choice: Thymosin Alpha-1. Wider use case, a Tier-A evidence outcome catalogued, and broader goal coverage. Reach for TB-500 only if your priority sits squarely in the goals it owns above.

This verdict is generated from each compound's schema (goals, legal status, evidence outcomes, dosing route). It updates automatically as our compound data evolves; the deeper read sits on each individual compound page.

Common questions

What is the difference between TB-500 and Thymosin Alpha-1?

TB-500 and Thymosin Alpha-1 differ in category (peptide vs peptide), mechanism, and typical dosing. See the side-by-side table for full details.

Which has a longer half-life, TB-500 or Thymosin Alpha-1?

TB-500 half-life is 2 hours; Thymosin Alpha-1 half-life is 2 hours.

Can you stack TB-500 with Thymosin Alpha-1?

Stack compatibility depends on mechanism overlap, legal status, and individual response. Check each compound page for specific interactions and contraindications before combining.

Go deeper