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Peptide · Research use only

KPV

$75CAD

A three-amino-acid peptide fragment explored in early inflammation, immune-signalling and gut models.

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KPV$75

Product information

KPV, clearly explained.

A three-amino-acid peptide fragment explored in early inflammation, immune-signalling and gut models.

Overview

Most KPV research comes from laboratory systems and mouse models of intestinal inflammation. Human benefit and safety have not been established, and regulators report little to no human exposure data for administered KPV products.

KPV (Lys-Pro-Val) is the C-terminal tripeptide of alpha-melanocyte-stimulating hormone. Published research focuses on inflammatory signalling in cells and experimental colitis in mice.
Format
Vial
Available strengths
10mg
Batch
KPV 003-026
Purity
99.1%
Research at a glanceCell and animal evidence; administered human-drug evidence absent
Reviewed 23 July 2026View research context

Specifications

Product details

Sequence / identity
Lys-Pro-Val
Molecular formula
Confirm in batch record
Molecular weight
342.44 g/mol
Storage and handling
Store and handle according to the verified batch record.
Batch documentationVerified record available

Review the analytical record connected to this exact batch.

Batch
KPV 003-026
Purity
99.1%
View batch record
Important research-use boundary

Health Canada lists the named compound or components among unauthorized injectable drugs identified in the Canadian market. A research-use label does not make an unauthorized product suitable or legal for personal use.

Explore the research

What has been studied?

Keep the context attached

Check what was studied, what researchers observed, and the limitation attached to each finding.

Question 01

Intestinal inflammation models

Murine colitis studies report changes in histology, inflammatory markers and recovery under experimental conditions.

Evidence so far: Animal evidence
Question 02

Epithelial inflammatory signalling

Human-derived cell-line studies examine NF-κB signalling, chemokine secretion and cellular uptake.

Evidence so far: In-vitro mechanistic evidence
Question 03

Human administration

FDA reports no identified human exposure data for drug products containing KPV.

Evidence so far: Direct human evidence gap

Proposed mechanism

How researchers are investigating the mechanism.

Cell studies report effects on NF-κB-related signalling and cytokine release. Intestinal models also examine uptake through the PepT1 transporter. These findings describe experimental pathways, not established clinical outcomes.

Study records

What was studied—and what was not.

See what researchers tested, what they observed and the limitation attached to each result.

Study 01Two mouse models of inflammatory bowel disease
What researchers saw
Investigators reported reduced inflammatory measures and earlier recovery in KPV-treated animals.
Why that is not the whole story
Animal colitis models cannot establish human efficacy, dose, route or safety.
Read the original source
Study 02Immortalized human bronchial epithelial cell experiments
What researchers saw
The study reported inhibition of NF-κB-related signalling and chemokine secretion.
Why that is not the whole story
A cell-line mechanism is not a clinical respiratory or anti-inflammatory outcome.
Read the original source

Evidence gaps

What remains unknown?

  • No adequately controlled human efficacy or safety trials were identified.
  • Human pharmacokinetics, route-specific tolerability and immunogenicity remain uncharacterized.
  • Cell and mouse findings cannot support a personalized treatment or dosing protocol.