Skip to content
BiologicalX

Comparison

BPC-157 vs Urolithin A

Side-by-side of BPC-157 and Urolithin A. 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

Urolithin A

  • Gut-microbiome-derived metabolite of pomegranate and walnut ellagitannins
  • Roughly 40% of adults are 'urolithin producers' from dietary intake; ~60% are non-producers
  • Ryu 2016 (Nature Medicine) reported lifespan extension in C. elegans and muscle benefits in aged rodents
  • Andreux 2019 first-in-human trial (n=60) established safety and mitochondrial gene-expression upregulation
  • Singh 2022 (n=66, 4 months, 1000 mg/day) reported improved muscle endurance in older adults
  • Most human trial portfolio is Amazentis-funded; independent replication is thin

Side-by-side

Attribute BPC-157 Urolithin A
Category peptide supplement
Also known as Body Protection Compound-157, Pentadecapeptide BPC-157 UA, Mitopure, ellagitannin metabolite
Half-life (hr) 4 17
Typical dose (mg) 0.25 500
Dosing frequency daily (anecdotal protocols) daily, morning with food
Routes subcutaneous, intramuscular, oral oral
Onset (hr) - 2
Peak (hr) - 4
Molecular weight - 228.2
Molecular formula C62H98N16O22 C13H8O4
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. Induces mitophagy via potentiation of PINK1/Parkin signaling, leading to selective degradation of damaged mitochondria. Secondary anti-inflammatory effects via NF-kB modulation.
Legal status Not FDA approved; research-use-only grey market; banned by WADA (2022) OTC dietary supplement (US GRAS 2018; EFSA Novel Food 2021)
WADA status banned allowed
DEA / Rx Not FDA approved; not scheduled; research-chemical status OTC supplement (not scheduled)
Pregnancy Insufficient data Insufficient data; not routinely recommended
CAS 137525-51-0 1143-70-0
PubChem CID 9941957 5488186
Wikidata Q4835418 Q27101321

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

Urolithin A

Common side effects

  • mild GI upset (rare)
  • soft stools (rare)

Contraindications

  • pregnancy and lactation (insufficient data)
  • active chemotherapy (consult oncology)

Interactions

  • chemotherapy agents: theoretical interaction with mitochondrial-targeting agents; consult oncologist(moderate)

Which Should You Take?

Urolithin A comes out ahead for most readers on the criteria we weight: 3 catalogued goals, OTC dietary supplement, oral dosing, with a Tier-A 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 Urolithin A.
  • If your priority is muscle hypertrophy, pick Urolithin A.

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

Default choice: Urolithin A. Lower friction to source, a Tier-A evidence outcome catalogued, 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 Urolithin A?

BPC-157 and Urolithin A 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 Urolithin A?

BPC-157 half-life is 4 hours; Urolithin A half-life is 17 hours.

Can you stack BPC-157 with Urolithin A?

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

Go deeper