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Comparison

BPC-157 vs Fisetin

Side-by-side of BPC-157 and Fisetin. 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

BPC-157

  • Preclinical models show accelerated tendon-to-bone and ligament healing after surgical or chemical injury
  • Rodent studies report mucosal protection and faster recovery from NSAID-induced and colitis-induced gut damage
  • Anecdotal human protocols use 250 to 500 mcg twice daily subcutaneously near the injury site
  • No completed phase II or III human RCTs as of 2026, so efficacy and long-term safety remain unestablished
  • Banned by WADA since 2022 under the S0 non-approved substances category for competitive athletes
  • Theoretical angiogenic concern means avoidance is prudent in active malignancy until human data exists

Fisetin

  • Flavonoid found in strawberries; most potent natural senolytic in screening assays (Yousefzadeh 2018)
  • Hickson 2019 confirmed reduced senescent-cell burden in human adipose tissue at 20 mg/kg pulsed for 2 days
  • Pulsed Mayo protocol (20 mg/kg/day x 2 days monthly) is the only dose with human biomarker evidence
  • Daily low-dose (100-500 mg) is mechanistically weaker but commonly used
  • Low oral bioavailability; with-fat dosing modestly improves absorption
  • Active cancer is a relative contraindication pending clearer polyphenol-treatment data

Side-by-side

Attribute BPC-157 Fisetin
Category peptide supplement
Also known as Body Protection Compound-157, Pentadecapeptide BPC-157 3,7,3',4'-tetrahydroxyflavone
Half-life (hr) 4 2
Typical dose (mg) 0.25 500
Dosing frequency daily (anecdotal protocols) pulsed 2 days/month (Mayo protocol) or daily continuous (empirical)
Routes subcutaneous, intramuscular, oral oral
Onset (hr) - 1
Peak (hr) - 4
Molecular weight - 286.24
Molecular formula C62H98N16O22 C15H10O6
Mechanism Proposed upregulation of VEGFR2 and nitric oxide pathways, modulation of growth-hormone receptor expression, and stabilization of gut-brain axis signaling. Mechanism remains largely preclinical. Senolytic via Bcl-2 family inhibition (Bcl-xL, Bcl-w); broad polyphenol with Nrf2 activation, mTOR inhibition at high concentrations, and antioxidant effects.
Legal status Not FDA approved; research-use-only grey market; banned by WADA (2022) OTC dietary supplement
WADA status banned allowed
DEA / Rx Not FDA approved; not scheduled; research-chemical status OTC supplement
Pregnancy Insufficient data Insufficient data
CAS 137525-51-0 528-48-3
PubChem CID 9941957 5281614
Wikidata Q4835418 Q230614

Safety profile

BPC-157

Common side effects

  • injection-site irritation
  • nausea
  • headache (anecdotal)

Contraindications

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

Fisetin

Common side effects

  • mild GI upset
  • headache (rare)

Contraindications

  • active cancer (theoretical, polyphenol interactions)
  • pregnancy and lactation (insufficient data)
  • concurrent CYP3A4-sensitive medications

Interactions

  • statins (CYP3A4 substrates): theoretical reduction in statin clearance at high fisetin doses(minor)
  • warfarin: theoretical CYP-mediated interaction; monitor INR if combining(moderate)
  • other senolytics (rapamycin, dasatinib + quercetin): additive senolytic effect; pairing is investigational(minor)

Which Should You Take?

Fisetin comes out ahead for most readers on the criteria we weight: 2 catalogued goals, OTC dietary supplement, oral dosing, with a Tier-B outcome catalogued. BPC-157 is the right call when one of the conditionals below applies.

  • If your priority is post-training recovery, pick BPC-157.
  • If your priority is gut barrier and microbiome health, pick BPC-157.
  • If your priority is healthspan extension, pick Fisetin.
  • If your priority is focus or working memory, pick Fisetin.

Edge case: If you want to avoid research-only / gray-market sourcing, Fisetin is the more accessible choice.

Default choice: Fisetin. Lower friction to source, and broader goal coverage. Reach for BPC-157 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 BPC-157 and Fisetin?

BPC-157 and Fisetin differ in category (peptide vs supplement), mechanism, and typical dosing. See the side-by-side table for full details.

Which has a longer half-life, BPC-157 or Fisetin?

BPC-157 half-life is 4 hours; Fisetin half-life is 2 hours.

Can you stack BPC-157 with Fisetin?

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

Go deeper