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Research compoundRecovery & Tissue ResearchIn stock

KPV

Also known as: Lys-Pro-Val

KPV (Lys-Pro-Val) is a tripeptide corresponding to the C-terminal end of alpha-melanocyte-stimulating hormone (α-MSH 11-13). Research consists of mouse intestinal (DSS, TNBS, T-cell transfer) models, cell studies and nanoparticle-delivery work; no human trials were identified.

Evidence: preclinical · Rodent and cell studies only

At a glance

Class
α-MSH C-terminal tripeptide
Developer
No pharmaceutical developer
FDA status
Not FDA-approved
Human data
None identified
Animal / lab data
Mouse colitis models (DSS, TNBS, T-cell transfer); intestinal epithelial, macrophage and T-cell lines

Where it’s been studied

123
  • 1GutColitis models (DSS, TNBS, transfer), mouse (2008, 2017, 2024)
  • 2Immune cellsJurkat T cells, RAW 264.7 macrophages (2008, 2017)
  • 3Cell studiesCaco2-BBE and HT29 intestinal epithelial cells (2008, 2017)

Mechanism studied

Established in cell studies: KPV is taken up into intestinal epithelial and immune cells by the peptide transporter PepT1, and nanomolar concentrations reduced NF-κB and MAP kinase signaling and inflammatory cytokine release [1]. Proposed: KPV's effects in mouse colitis models appear at least partly independent of the melanocortin-1 receptor, since effects persisted in mice with non-functional MC1R [2]. Its short half-life has led researchers to package it in targeted nanoparticles [3][4].

What the research shows

StudyModelReported resultSource
PepT1-mediated KPV uptake [1]Cell
Human intestinal epithelial cells (Caco2-BBE, HT29) and Jurkat T cells with cytokine stimulation; mouse DSS and TNBS colitis models
Nanomolar KPV reduced NF-κB and MAP kinase activation and cytokine secretion via PepT1; researchers measured colonic cytokine expression in mouse DSS and TNBS models.Peer-reviewed
Gastroenterology 2008
KPV in two mouse colitis models [2]Mouse
Colitis models (DSS and CD45RBhi T-cell transfer), plus MC1R-deficient mice given DSS; n=5 per group
Researchers measured faster weight regain (significant from day 10), lower colonic MPO activity and fewer inflammatory infiltrates.Peer-reviewed
Inflammatory Bowel Diseases 2008
Hyaluronic acid-coated KPV nanoparticles [3]Mouse
Colitis model (DSS), oral nanoparticles in a hydrogel; plus Colon-26, RAW 264.7 and Caco2-BBE cells
Targeted particles (~272 nm) increased cell uptake, lowered macrophage TNF-α, and reduced weight loss, colonic MPO and TNF-α in mice versus untargeted particles.Peer-reviewed
Molecular Therapy 2017
KPV co-assembled with FK506 [4]Mouse
Acute (4% DSS) and chronic (2.5% DSS) colitis models; KPV alone as a comparison arm
In the acute model, survival was 80% with KPV alone versus 60% with DSS only; combined nanoparticles outperformed KPV alone.Peer-reviewed
Frontiers in Pharmacology 2024

Human trials are listed for research context only; outcomes are reported in the linked publications. Animal and lab results do not establish effects in humans.

Verified by third-party testing

CertificatePosted on the product page
TestingIndependent, third-party

Research-grade supply

PureLab supplies KPV for laboratory research. Lot-specific certificates of analysis are posted on the product page as they are issued.

View research-grade KPV

More in Recovery & Tissue Research

Sources

  1. Dalmasso G et al. (2008) Source
  2. Kannengiesser K et al. (2008). doi:10.1002/ibd.20334 Source
  3. Xiao B et al. (2017). doi:10.1016/j.ymthe.2016.11.020 Source
  4. Zhang D et al. (2024). doi:10.3389/fphar.2024.1442876 Source
For research use only. Not for human or veterinary use. Not a drug, food or cosmetic, and not intended to diagnose, treat, cure or prevent any disease. This library summarizes published research for educational purposes. PureLab Performance Inc.