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Evidence-rated reference Updated August 2026
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Research Use Only Immune & Anti-inflammatory Evidence 1/5 · Minimal

KPV

Also known as Lysine-Proline-Valine · α-MSH (11-13)

C-terminal tripeptide fragment of alpha-melanocyte-stimulating hormone

Overview

The smallest active piece of alpha-MSH, retaining the anti-inflammatory activity while dropping the pigmentation effects. The preclinical inflammatory bowel data is genuinely interesting. Human data does not exist.

Not approved for human use anywhereNo approval anywhere for human use. Sold under research-use labelling. Not approved for human use.

At a glance
Regulatory statusNot approved. Preclinical anti-inflammatory research compound; increasingly marketed for gut and skin inflammation.
Drug classC-terminal tripeptide fragment of alpha-melanocyte-stimulating hormone
RouteOral, topical, or subcutaneous (research)
Half-lifeShort; not well characterised
Evidence rating
1/5 Minimal Evidence rating 1 out of 5: Minimal
Animal or laboratory data only. No human efficacy evidence.
Studied inRodent colitis models, in-vitro immune cell work, and topical dermatology models. No completed human trials.

How it works

Enters cells and inhibits NF-κB nuclear translocation and downstream pro-inflammatory cytokine production (TNF-α, IL-6, IL-1β), apparently without requiring melanocortin receptor binding. Also shows direct antimicrobial activity against some organisms in vitro.

Evidence base

Rated 1 of 5 — Minimal. Animal or laboratory data only. No human efficacy evidence.

  • Promising preclinical anti-inflammatory data; the human translation step has not been attempted.

Benefits & potential uses

Bars indicate how well each claim is supported: three = strong human evidence, two = moderate, one = preliminary or preclinical.

  • Anti-inflammatory without pigmentation Preliminary

    Retains alpha-MSH anti-inflammatory activity while lacking the melanocortin pigmentation effect — a clean pharmacological separation.

  • Colitis improvement in rodents Preliminary

    Oral and rectal delivery reduce colonic inflammation in animal models of inflammatory bowel disease.

  • Antimicrobial activity in vitro Preliminary

    Activity against Candida and some bacteria in laboratory models.

  • Favourable preclinical safety Preliminary

    Small tripeptides with endogenous origins generally show low toxicity in animal work.

Risks, cons & cautions

Bars indicate seriousness: three = serious or common, two = moderate, one = minor.

  • No human trials Serious

    All efficacy claims are preclinical extrapolation.

  • Immune modulation is not inherently benign Moderate evidence

    Suppressing NF-κB signalling long-term has implications for infection surveillance and tumour immunity that have not been studied.

  • Unapproved and unregulated Serious

    Research-chemical supply chain.

  • Delivery and stability poorly characterised Moderate evidence

    How much survives oral administration in humans is unknown.

Who should avoid it

  • Immunosuppressed patients
  • Pregnancy
  • Active infection

If used under medical supervision, monitor

  • No validated monitoring exists

Not approved for human use.

Infographic

KPV — benefits & risks at a glance Download SVG
Infographic summarising the benefits and risks of KPV, from pepteyes.com

Where to read further

We link to live literature searches rather than a frozen citation list, so you always see current results — including anything published after our last review.

inflammationgut healthskinresearch chemical

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Terms used on this page

Preclinical Study and Animal Model
Preclinical studies are the laboratory, cell and animal experiments done before any human exposure, establishing mechanism, target engagement and the toxicology package that permits a first trial.
Melanocortin System
The melanocortin system is the POMC-derived signalling network in which alpha-MSH and ACTH act on five receptors to control pigmentation, adrenal steroid output, appetite and energy balance.
Cytokine
Cytokines are small secreted signalling proteins acting at picomolar concentrations over short distances to coordinate immune cells, characterised by pleiotropy and extensive functional redundancy.
Nuclear Factor Kappa B (NF-kB)
Nuclear factor kappa B is a family of transcription factors held inactive in the cytoplasm until an inflammatory signal frees them to switch on genes for cytokines, adhesion molecules and survival.
Tumour Necrosis Factor Alpha (TNF-alpha)
Tumour necrosis factor alpha is a pro-inflammatory cytokine central to acute inflammation and to several autoimmune diseases, and the target of the most widely used class of biologic drugs.
Oral Peptide Delivery
Oral peptide delivery is the formulation of a peptide into a swallowed dosage form, a route that fights gastric acid, gut proteases and an epithelium built to exclude large molecules.

This page is educational information, not medical advice. It cannot account for your medical history, medications, or risk factors. Do not start, stop or change any treatment based on it. Speak to a qualified healthcare professional who knows your case.