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Item: KPV·Reference Standard

KPV

98.49% HPLC VerifiedLot #KRSKPV-10-260908-01
Third-Party HPLC Tested·Batch-Linked COA Enclosed

From $33.25to $1087.50

Tripeptide KPV (Lys-Pro-Val, α-MSH 11-13), lyophilized reference standard for in vitro laboratory research.

KPV 50 mg research compound vial from KAM Research
KPV
50 mg
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  • Third-party HPLC tested. Every lot ships with a batch-linked certificate of analysis naming the laboratory, the method and the measured result. Browse certificates
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Analytical Verification · Independent Testing

Certificate of Analysis & Specifications

Released Batch

HPLC Purity

98.49% HPLC

Area Normalization

Assay Content

10.43mg

Quantitative Target

Testing Lab

KMD Analytical

Lot Number

KRSKPV-10-260908-01

Tested Sep 22, 2026

Storage

36°F to 46°F

Retest Date

Sep 18, 2028

Download COA (PDF)Verify this lotQR link
Batch Archive

Released COA Library

Published Certificates of Analysis for KPV. All released analytical records are preserved here. Pending and in-testing lots are reachable only through the QR printed on the vial.

10mg1 released lot
  • Lot KRSKPV-10-260908-01

    Tested Sep 22, 2026 · KMD Analytical · HPLC 98.49% · Assay 10.43

    View COA
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Research Data

Chemical & Structural Identifiers

2D chemical structure of (2S)-1-[(2S)-2,6-diaminohexanoyl]-N-[(2S)-1-hydroxy-3-methylbutan-2-yl]pyrrolidine-2-carboxamide (L-lysyl-L-prolyl-L-valine)
Chemical Name (IUPAC)
(2S)-1-[(2S)-2,6-diaminohexanoyl]-N-[(2S)-1-hydroxy-3-methylbutan-2-yl]pyrrolidine-2-carboxamide (L-lysyl-L-prolyl-L-valine)
CAS Registry Number
67727-97-3
PubChem CID
125564
Molecular Formula
C16H31N5O4
Molecular Weight
357.24 Da (357.45 g/mol average)
Sequence
H-Lys-Pro-Val-OH (Single-letter: KPV)
SMILES
CC(C)[C@@H](C(=O)O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCCN)N
InChIKey
ODHQKDOEXFUXNQ-YWTDRTNVSA-N
Salt / Counter-Ion
Supplied as a high-purity lyophilized acetate (CH3COO-) or trifluoroacetate (CF3COO-) salt.
Synonyms
KPV, KPV Tripeptide, α-MSH(11--13), Lys-Pro-Val, ACTH(11-13)

Analytical & COA Specifications

Analytical Purity (RP-HPLC)
≥ 98.5% by area normalization under UV detection at λ = 214 nm and 220 nm.
Identity Confirmation (RP-HPLC RT + UV vs. reference)
Main peak retention time and UV spectrum conform to the reference standard.
Physical Characterization
Dense, white to off-white lyophilized crystalline powder/cake.

Handling & Stability

Storage. Store dry solid desiccated at -20°C to -80°C, protected from atmospheric moisture and direct light.

Solubility. Highly hydrophilic; freely soluble in sterile laboratory-grade deionized water (≥ 25 mg/mL) and sterile Phosphate-Buffered Saline (PBS, pH 7.4, ≥ 20 mg/mL) for in vitro assay application.

  • Membrane Transporter Specificity & Handling: Exhibits high aqueous stability; transported across cellular membranes via the oligopeptide transporter PepT1 (SLC15A1); prepare concentrated working stocks freshly or aliquot into single-use fractions at -20°C to eliminate degradation from repeated freeze-thaw cycles.

Mechanism & Literature

Biochemical Target & Classification: Synthetic linear tripeptide corresponding to the carboxy-terminal residues 11–13 of α-melanocyte-stimulating hormone (α-MSH). Exhibits zero melanotropic pigmentation activity (does not bind MC1R to stimulate melanogenesis) while retaining specific non-pigmentary cellular signaling pathways.

Cellular Pathways Investigated: Extensively documented in in vitro intestinal epithelial cell models (Caco-2, HT-29) and macrophage cultures (RAW 264.7) to evaluate PepT1-mediated cellular uptake, cytoplasmic interaction with downstream signaling proteins, inhibition of Nuclear Factor-κB (NF-κB) p65 nuclear translocation, suppression of IκBα phosphorylation, and downregulation of proinflammatory cytokine gene transcription (TNF-α, IL-1β, IL-6, IL-8).

References (3)
  1. Luger, T. A., et al. (2003). The C-terminal tripeptide of alpha-MSH (KPV) inhibits NF-kappaB activation in vitro. Annals of the New York Academy of Sciences, 994(1), 133–140.
  2. Dalmasso, G., et al. (2008). PepT1-mediated transport of the tripeptide KPV modulates cellular inflammatory signaling in intestinal epithelial cells in vitro. Gastroenterology, 134(1), 166–178.
  3. Land, S. C. (2012). Cellular mechanism of alpha-MSH and its C-terminal tripeptide KPV in cell culture and oxidative stress models. Peptides, 34(2), 405–412.

Technical Laboratory FAQs

What is the sequence and origin of the KPV tripeptide?

KPV is a synthetic tripeptide with the sequence Lys-Pro-Val, derived from the C-terminal sequence of α-melanocyte-stimulating hormone (α-MSH11--13), possessing selective signaling properties without inducing melanocortin-1 receptor (MC1R) melanogenic activation.

How does KPV cross cellular membranes in epithelial cell culture assays?

KPV is actively transported across epithelial cell membranes via the proton-coupled oligopeptide transporter 1 (PepT1 / SLC15A1), facilitating rapid intracellular accumulation in cell-based assays.

What solvent conditions are recommended for preparing in vitro KPV stock solutions?

Sterile deionized water or sterile PBS (pH 7.4) dissolves KPV rapidly at concentrations ≥ 20 mg/mL, creating a neutral delivery carrier suitable for cell culture and biochemical receptor assays.

For Research Use Only. Not for human or animal administration. Not intended to diagnose, treat, cure, or prevent any disease. Sold for laboratory research purposes only.

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