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α-MSH C-Terminal Tripeptide · Melanocortin Research

KPV Research Compound

KPV (Lys-Pro-Val) is the C-terminal tripeptide of alpha-melanocyte-stimulating hormone (α-MSH). Available in 10mg research-grade vials, independently tested by Krause Analytical via HPLC and mass spectrometry. For research use only. Not for human use.

10mg Research Vial COA — Krause Analytical Sabrina Runbeck, PA-C Finnrick Pulse Verified

Compound Overview

What Is KPV?

KPV is a synthetic tripeptide composed of three amino acids in sequence: Lysine (Lys), Proline (Pro), and Valine (Val). It represents the C-terminal fragment of alpha-melanocyte-stimulating hormone (α-MSH) — the last three residues of that 13-amino-acid neuropeptide.

Published research has examined whether this minimal C-terminal fragment retains meaningful melanocortin receptor binding activity. Studies in cell models have evaluated KPV's interaction with MC1R and MC3R receptor subtypes — the same melanocortin receptor targets engaged by the full α-MSH peptide — at significantly reduced molecular weight.

At approximately 342 Da, KPV is among the smallest peptide fragments that have been examined in melanocortin receptor research contexts. Its compact size has made it a subject of preclinical models investigating mucosal tissue and intestinal epithelial barrier cell systems.

For research use only. Not for human use. Not for clinical or diagnostic application.

Technical Specifications

  • Compound KPV
  • Full Name Lys-Pro-Val
  • Source α-MSH C-terminal
  • Molecular Formula C16H30N4O4
  • Molecular Weight ~342 Da
  • CAS Number 83702-02-7
  • Classification Tripeptide
  • Research Grade ≥98% purity
  • SL Vial Size 10 mg
  • Form Lyophilized powder
For Research Use Only · Not for Human Use

Published Research Areas

Research Background

The following research areas represent contexts in which published literature has examined KPV or closely related α-MSH C-terminal sequences in preclinical and cell-model settings.

01
MC1R / MC3R Receptor Mechanism Research
Published research has examined KPV's binding activity at melanocortin receptor subtypes MC1R and MC3R. These G-protein-coupled receptors are implicated in a range of signaling cascades, and KPV's compact structure has made it a subject of mechanistic receptor research in cell-free and cell-based assay systems.
02
Intestinal Epithelial Barrier Research in Cell Models
Published research has examined KPV's effects on intestinal epithelial cell lines in vitro. Researchers have investigated tight junction protein expression and barrier integrity markers in cell model systems. These findings remain confined to controlled laboratory cell culture models.
03
NF-κB Pathway Modulation Research in Preclinical Models
Published research has examined KPV's relationship to NF-κB signaling pathway activity in preclinical model systems. The NF-κB pathway is a transcription factor system studied extensively in the context of cellular stress and immune signaling. Observations have been noted in rodent model contexts.
04
Cytokine Signaling Research in Cell Models
Published research has examined KPV's influence on cytokine-related signaling in isolated cell model systems. Research has focused on interleukin and related signaling markers measured in vitro. These studies were conducted under controlled laboratory conditions and do not reflect outcomes in living organisms.
05
Mucosal Tissue Research in Animal Models
Published research has examined KPV in rodent mucosal tissue models. Studies have evaluated delivery method parameters and tissue-level markers in gastrointestinal mucosal preparations. Findings derive entirely from preclinical animal model research and have not been validated in human subjects.
Browse KPV / α-MSH Publications on PubMed →

Research Context

KPV vs BPC-157 — Different Receptor Mechanisms, Overlapping GI Research Models

KPV
  • C-terminal tripeptide of α-MSH (Lys-Pro-Val)
  • Melanocortin receptor mechanism: MC1R / MC3R
  • ~342 Da — one of the smallest melanocortin research fragments
  • Research in intestinal epithelial barrier cell models
  • NF-κB and cytokine pathway research in preclinical models
  • Mucosal tissue research in rodent model systems
vs
BPC-157
  • 15-amino-acid pentadecapeptide derived from gastric protein
  • Nitric oxide (NO) and growth factor pathway research
  • ~1,419 Da — larger peptide structure
  • Research in gastrointestinal mucosal and tissue models
  • VEGF and angiogenesis pathway research in preclinical models
  • Musculoskeletal tissue research in rodent model systems

Both KPV and BPC-157 have been studied in preclinical and cell model contexts relevant to gastrointestinal research, but their proposed mechanisms of action are distinct. KPV research focuses on melanocortin receptor signaling (MC1R/MC3R), while BPC-157 research centers on NO/growth factor-related pathways. Neither compound is approved for human use. All comparisons reflect published preclinical and cell-model research only. For research use only. Not for human use.

Sequence Labs Supply

KPV — 10mg Research Vial

~$45 per 10mg vial
  • 10mg lyophilized powder — research-grade KPV, CAS 83702-02-7
  • HPLC + Mass Spectrometry — dual verification by Krause Analytical
  • COA included — batch-level certificate of analysis on every vial
  • ≥98% purity — verified by independent third-party laboratory
  • Catalog reviewed by Sabrina Runbeck, PA-C for research integrity
  • Finnrick Pulse verified — quality checkpoint documentation
  • Ships within 1–2 business days. Research use only. Not for human use.
Independent Testing Laboratory
Krause Analytical
Every KPV batch is independently tested using both high-performance liquid chromatography (HPLC) and mass spectrometry (MS). Full COA documentation available on the COA Library page.
Catalog Medical Review
Sabrina Runbeck, PA-C
Licensed physician assistant reviewing the Sequence Labs compound catalog for research classification integrity and regulatory compliance framing.
Quality Verification
Finnrick Pulse
Third-party quality checkpoint documentation providing an additional verification layer for Sequence Labs research compound batches.

Laboratory Reference

Reconstitution Reference

Standard laboratory protocol for preparing a KPV research sample from lyophilized powder. For research use only. Not for human use.

1
Gather materials
Ensure you have the KPV research vial (lyophilized powder), bacteriostatic water (most common laboratory solvent), a sterile syringe, and appropriate laboratory PPE. Work in a clean environment consistent with your laboratory SOP.
2
Introduce solvent
Draw the appropriate volume of bacteriostatic water into the syringe. Introduce solvent into the vial by directing it along the inner glass wall — avoid directing the stream directly onto the lyophilized powder cake. The volume introduced determines the resulting research sample concentration.
3
Swirl gently
Gently swirl the vial in a circular motion until the powder is fully dissolved. Do not shake vigorously — this can compromise peptide integrity in some formulations. Allow time for complete solubilization before drawing a research sample.
4
Store per SOP
Reconstituted research samples should be stored according to your laboratory's standard operating procedure. Refrigeration at 2–8°C is standard practice for short-term storage. Refer to the COA for compound-specific stability data.
Research Use Only. This reference is provided for qualified researchers following established laboratory protocols. KPV from Sequence Labs is not for human use, human consumption, or clinical application. All reconstitution procedures should be conducted within a compliant research environment. These statements have not been evaluated by the Food and Drug Administration.

Frequently Asked Questions

Order KPV or Explore Related Research Compounds

10mg vials, HPLC + MS tested by Krause Analytical, reviewed by Sabrina Runbeck PA-C. Browse the full catalog or view the related BPC-157 research page.