Peptide library
RecoveryImmune Research

KPV

Tripeptide fragment of α-MSH studied for inflammatory modulation.

Emerging Research

Evidence Level

Emerging

Mechanism6/10
Safety Clarity5/10
Research Popularity5/10

Research Type

AnimalIn vitro

/ System Mapping

Where this compound appears in research pathways

Research-only note: This mapping is educational and does not represent a treatment protocol.

/ 01

Overview

Tripeptide fragment of α-MSH studied for inflammatory modulation.

/ 02

Mechanism of Action

Studied for melanocortin receptor signaling and intracellular anti-inflammatory effects.

/ 03

Research Applications

Immune signaling and gut inflammation models.

Studied for, research explores, preclinical models suggest, clinical studies have investigated.

/ 04

Studied Research Contexts

AnimalIn vitro

/ 05

Studied Research Dosing Ranges

Limited public data on dosing ranges across research models.

Dosing varies by study design and is not a recommendation for human use.

/ 06

Potential Adverse Effects Reported in Research

Adverse effect data is limited. Many compounds in this database lack human safety profiles.

/ 07

Mechanism Deep Dive

KPV is the C-terminal tripeptide (Lys-Pro-Val) of alpha-MSH. Research describes anti-inflammatory signaling associated with NF-κB modulation, antimicrobial activity in cell models, and broader immune-modulatory behavior in inflammatory disease models.

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Pathway Role

Sits within inflammatory signaling pathways, with reported activity at the NF-κB and innate immune signaling layer.

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Biological Targets

NF-κB signaling (modulation)Pro-inflammatory cytokine outputMicrobial membrane interactions (in vitro)Melanocortin-related signaling (indirect)

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Research Applications

  • Inflammatory bowel disease preclinical models
  • Skin inflammation research
  • Antimicrobial activity in vitro studies
  • General inflammation modulation research

/ 11

Evidence Summary

Mechanistic anti-inflammatory data is reasonably developed in cell and animal models, with limited controlled human outcome studies.

Evidence Level Rationale

Rated emerging-to-moderate based on consistency of preclinical mechanistic signals across multiple inflammation models.

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Research Observation Timeline

Early Signal Window

Cytokine and signaling shifts in cell models within hours

Primary Study Window

Days to weeks in animal inflammation models

Endpoint Type

Inflammatory biomarker and histological endpoints

Evidence Strength

Emerging mechanistic preclinical

Human timing is not established. Inflammatory signaling endpoints are studied in cell and animal models.

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Safety & Unknowns

Human safety profile is not extensively characterized. Long-term systemic effects are not established.

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Research Limitations

Translation from animal inflammation models to human outcomes is not established.

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References

References are being curated from peer-reviewed literature.

/ 07

Evidence Score

Mechanism Confidence6/10
Safety Clarity5/10
Research Popularity5/10

Overall Research Confidence

Emerging

Reflects breadth of mechanism, study type, and reproducibility across research literature.

For research and educational purposes only.

Not medical advice. Not intended to diagnose, treat, cure, or prevent disease. Compounds discussed may not be approved for human use. Any dosing information shown describes ranges studied in research settings — never a recommendation.