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≥99% PurityKPV vial

KPV

Inflammation Pathway Studies

$60.00$30.00/vial with BOGO
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About this compound

KPV is a three amino acid peptide: lysine, proline, and valine. It is the tail end of a larger hormone called alpha-MSH. That tail carries the anti-inflammatory part of the sequence but not the part that affects skin color. Studies have measured its effect on NF-kB, a signaling pathway involved in inflammation. Its small size lets it enter cells through routes that larger peptides cannot use.

α-MSH-derived tripeptide (α-MSH 11–13)

Formula
C16H31N5O4
Molecular weight
342.43 g/mol
Form
Lyophilized powder
Sequence length
3 residues
Read the full KPV research monograph
0
Amino Acids
Lys-Pro-Val (α-MSH 11–13)
NF-κB
Pathway Target
Master inflammatory regulator
0
Research Areas
Intestinal Inflammation Models · α-MSH Signalling · Epithelial Wound Closure & more
How It Works

How KPV works

The pathways KPV acts on — and what each one does. The animation traces its signal outward from the compound to every target it engages.

Signalling pathways studied in preclinical models · illustrative
Inflammatory Pathway Suppression
NF-κB Inhibition

At nanomolar concentrations, lower NF-κB and MAP-kinase pathway activation is measured in vitro. NF-κB is a principal regulator of inflammatory gene expression, and reduced secretion of TNF-α, IL-6 and IL-1β is recorded alongside.

  • Inhibits NF-κB and MAP-kinase signaling at nanomolar levels
  • Lower TNF-α, IL-6, IL-1β and other pro-inflammatory cytokines measured
  • Acts on inflammatory output rather than on anti-inflammatory cytokines
Cellular Transport & Action
PepT1-Mediated Uptake

Research shows KPV is taken up by cells via the PepT1 di/tripeptide transporter, which is expressed on immune cells and intestinal epithelial cells. This transporter-mediated uptake allows KPV to act intracellularly on inflammatory signaling.

  • Enters cells through the PepT1 peptide transporter
  • PepT1 is expressed on immune and intestinal epithelial cells
  • Enables intracellular modulation of inflammatory pathways
Melanocortin Fragment
α-MSH-Derived Activity

KPV is the C-terminal tripeptide of alpha-melanocyte-stimulating hormone (α-MSH 11–13). Most of α-MSH's anti-inflammatory activity has been attributed to this fragment, which also shows antimicrobial activity in vitro.

  • C-terminal tripeptide of the melanocortin peptide α-MSH
  • Carries much of α-MSH's anti-inflammatory activity
  • Antimicrobial effects reported against S. aureus and C. albicans
Uses & Applications

What KPV is researched for

The main areas KPV is being studied for — and the study-reported figures behind them.

GASTROENTEROLOGY

Intestinal Inflammation Models

PepT1-mediated uptake of KPV was followed by lower intestinal inflammation scores in DSS- and TNBS-induced colitis models.

IMMUNOLOGY

α-MSH Anti-Inflammatory Signaling

KPV is studied as the C-terminal tripeptide that carries much of α-MSH's anti-inflammatory and immunomodulating activity.

DERMATOLOGY

Epithelial Wound Closure

In a rabbit corneal model, topical KPV produced complete re-epithelialization by 60 hours, with a mechanism that may involve nitric-oxide signaling.

MICROBIOLOGY

Antimicrobial Activity

KPV shows antimicrobial effects against Staphylococcus aureus and Candida albicans across a broad concentration range in published research.

Study-reported magnitudes

Representative figures from published research. Bars fill as you scroll.

NF-κB ActivationInhibited
Pro-inflammatory Cytokines (TNF-α, IL-6)Measured
Colitis Severity (DSS / TNBS models)Scored
Corneal Re-epithelialization (rabbit study, 60 h)100% vs. 0% placebo

Figures are representative of published research findings and shown for reference.

Molecular Structure

The KPV molecule

An interactive 3D model rendered from the compound record — rotate and explore its structure.

C16H31N5O4

Molecular formula
C16H31N5O4
Molecular weight
342.43 g/mol
Sequence length
3 residues
Physical form
Lyophilized powder
Documented purity
≥99% by HPLC
Compound Information

Full specification

Chemical NameKPV (Lys-Pro-Val)
SequenceL-Lysyl-L-Prolyl-L-Valine (α-MSH 11–13)
Molecular Weight342.43 g/mol
Molecular FormulaC₁₆H₃₁N₅O₄
Content10 mg per vial
FormLyophilized powder
Purity≥99% (HPLC verified)
TestingThird-party HPLC, Mass Spec, Endotoxin
Storage-20°C for long-term stability
SolubilityWater-soluble
COAIncluded with every order
FAQ

Common questions about KPV

KPV is a tripeptide composed of lysine, proline and valine. It is the C-terminal fragment of alpha-melanocyte-stimulating hormone (α-MSH 11–13), and much of α-MSH's anti-inflammatory and immunomodulating activity has been attributed to this fragment.

At nanomolar concentrations, KPV inhibits the NF-κB and MAP-kinase inflammatory signaling pathways. NF-κB is a master regulator of inflammatory gene expression, so suppressing it lowers production of pro-inflammatory cytokines such as TNF-α, IL-6 and IL-1β in research models.

PepT1 is a di/tripeptide transporter expressed on immune cells and intestinal epithelial cells. Research shows KPV enters cells through PepT1, which allows it to act intracellularly on inflammatory signaling — a mechanism considered central to its effects in intestinal-inflammation models.

In DSS- and TNBS-induced mouse colitis models, PepT1-mediated uptake of KPV was followed by lower intestinal inflammation scores and reduced expression of pro-inflammatory cytokines including IL-1β, IL-6, IL-12, TNF-α and IFN-γ.

No. Despite roughly two decades of preclinical research across multiple organ systems, KPV has not completed human clinical trials. Research-grade KPV sold here is intended strictly for in vitro laboratory research and is not for human or veterinary use.

Lyophilized KPV should be stored at -20°C, protected from light and moisture, to preserve peptide integrity.

Research Use Only.

Not for human or veterinary use. For in-vitro laboratory research only. These statements have not been evaluated by the FDA; this product is not intended to diagnose, treat, cure, or prevent any disease. Sold exclusively to qualified researchers and institutions.