Compare Peptides

Select any two compounds for a side-by-side comparison of mechanism, uses, risks, and FDA regulatory status.

Popular comparisons

KPV

Lys-Pro-Val, α-MSH C-terminal tripeptide

Pending PCAC
Anti-Inflammatory & Healing

TB-500

Thymosin Beta-4 Fragment, TB4-Frag

Pending PCAC
Healing & Recovery
Overview

A tripeptide (Lysine-Proline-Valine) derived from the C-terminus of alpha-MSH (melanocyte-stimulating hormone). Has potent anti-inflammatory properties and is being studied for inflammatory bowel conditions and wound healing.

A synthetic fragment of thymosin beta-4, a naturally occurring peptide involved in tissue repair and regeneration. Widely used in the biohacking community for injury recovery.

Mechanism of Action

Inhibits NF-κB signaling and pro-inflammatory cytokine production. Crosses the intestinal epithelium to directly suppress inflammation locally. Anti-microbial properties have also been demonstrated in vitro.

Promotes cell migration, blood vessel formation, and reduces inflammation. Upregulates actin, a cell-building protein critical for healing and cell migration to injury sites.

Common Uses
  • Inflammatory bowel disease (IBD) support
  • Wound healing and skin conditions
  • General anti-inflammatory protocols
  • Gut health optimization
  • Muscle and tendon repair
  • Wound healing
  • Reducing inflammation
  • Hair regrowth (emerging research)
  • Cardiac tissue repair
Known Risks
  • Very limited human clinical data
  • Optimal delivery method not established
  • Injection vs. oral bioavailability differences not fully characterized
  • Long-term safety unknown
  • Limited human clinical data
  • Potential tumor growth concerns (theoretical)
  • Injection site reactions
  • Headaches reported anecdotally
Regulatory Status
Pending PCAC

Removed from FDA 503A Category 2 effective April 22, 2026. Scheduled for PCAC review on July 23, 2026 for wound healing and inflammatory conditions. Compounding not yet authorized — status is in regulatory gray zone pending PCAC recommendation.

PCAC: July 23, 2026

Pending PCAC

On April 15, 2026, the FDA announced TB-500 will be removed from the Category 2 'significant safety risks' list effective April 22, 2026. Scheduled for PCAC review on July 23, 2026 to determine eligibility for the 503A bulk drug substances list. Compounding pharmacies should exercise caution until PCAC takes action.

PCAC: July 23, 2026

This comparison is for educational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional before starting any peptide therapy.