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BiologicalX

Comparison

Rapamycin vs TB-500

Side-by-side of Rapamycin and TB-500. 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

Rapamycin

  • Inhibits mTORC1 signaling by binding FKBP12, reducing protein synthesis and relieving autophagy suppression
  • ITP mouse program reproduced lifespan extension of ~10 to 25% across multiple genetic backgrounds and sexes
  • Mannick trials showed improved influenza vaccine response in elderly adults using analogs of rapamycin
  • PEARL human trial reported acceptable safety at 5 to 10 mg weekly with some functional and lean-mass signals
  • Common dose-limiting adverse effects include stomatitis, acne-like rash, and mildly elevated lipid markers
  • CYP3A4 substrate: grapefruit, ketoconazole, and clarithromycin substantially raise rapamycin exposure

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

Side-by-side

Attribute Rapamycin TB-500
Category pharmaceutical peptide
Also known as Sirolimus, Rapamune Thymosin Beta-4 fragment, TB4-Frag, Thymosin Beta 4
Half-life (hr) 62 2
Typical dose (mg) 6 2.5
Dosing frequency weekly (longevity protocols); daily for transplant indication 2x weekly (anecdotal protocols)
Routes oral subcutaneous, intramuscular
Onset (hr) 1 -
Peak (hr) 2 -
Molecular weight 914.17 4963.4
Molecular formula C51H79NO13 C212H350N56O78S
Mechanism Binds FKBP12, and the resulting complex inhibits mTORC1, reducing protein synthesis and autophagy suppression downstream of nutrient and growth-factor signaling. 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.
Legal status Prescription only (off-label for longevity) Not FDA approved; research-use-only grey market; banned by WADA
WADA status allowed banned
DEA / Rx Rx only (not a controlled substance) Not FDA approved; not scheduled; research-chemical status
Pregnancy Not recommended Insufficient data
CAS 53123-88-9 885340-08-9
PubChem CID 5284616 62707662
Wikidata Q410174 Q7799921

Safety profile

Rapamycin

Common side effects

  • mouth ulcers (stomatitis)
  • acne-like rash
  • GI upset
  • altered lipid panel
  • delayed wound healing

Contraindications

  • active infection
  • severe hepatic impairment
  • planned surgery (delayed wound healing)
  • pregnancy
  • live vaccines within dosing window

Interactions

  • strong CYP3A4 inhibitors (ketoconazole, clarithromycin, grapefruit): substantially raises rapamycin levels, toxicity risk(major)
  • strong CYP3A4 inducers (rifampin, St John's wort): lowers rapamycin levels, reduced effect(major)
  • ACE inhibitors: increased risk of angioedema(moderate)
  • live vaccines: reduced vaccine efficacy due to immunosuppression(major)

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)

Which Should You Take?

Rapamycin comes out ahead for most readers on the criteria we weight: 2 catalogued goals, prescription-only, oral dosing, with a Tier-A outcome catalogued. TB-500 is the right call when one of the conditionals below applies.

  • If your priority is healthspan extension, pick Rapamycin.
  • If your priority is immune support, pick Rapamycin.
  • If your priority is post-training recovery, pick TB-500.
  • If your priority is tendon repair, pick TB-500.

Edge case: If you cannot self-administer injections, Rapamycin is the only oral option in this pair.

Default choice: Rapamycin. 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 Rapamycin and TB-500?

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

Which has a longer half-life, Rapamycin or TB-500?

Rapamycin half-life is 62 hours; TB-500 half-life is 2 hours.

Can you stack Rapamycin with TB-500?

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

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