KPV
α-MSH C-terminal tripeptide
Identifier graph
Cross-references to canonical chemistry knowledge graphs. Each binding is the same identity used in PubMed-indexed literature.
- CAS Registry Number
- 159492-07-6 · CAS Common Chemistry
- ChEMBL
- CHEMBL317974
- Molecular formula
Lys-Pro-Val- Molecular weight
- 329.43 g/mol
- Peptide sequence
Lys-Pro-Val
What is KPV?
KPV is the C-terminal tripeptide Lys-Pro-Val of α-melanocyte-stimulating hormone (α-MSH). Despite being only three residues — far shorter than the parent 13-residue hormone — KPV retains the anti-inflammatory activity of α-MSH while having essentially none of the melanocortin- receptor activity that drives pigmentation and central effects.
CAS 159492-07-6, molecular weight 329.43 g/mol. ChEMBL ID CHEMBL317974.
Mechanism of action
KPV's anti-inflammatory mechanism is independent of the melanocortin receptors that α-MSH activates. The peptide appears to act intracellularly, modulating NF-κB activation and reducing pro-inflammatory cytokine production (notably TNF-α, IL-1β, IL-6) in keratinocytes, intestinal epithelial cells and immune cells.
The intracellular action is consistent with KPV's ability to penetrate cell membranes — a property unusual for a small tripeptide and attributable to its non-polar valine residue.
Research context
Investigated in preclinical models of inflammatory bowel disease (notably DSS-induced colitis), atopic dermatitis, and other inflammatory skin and mucosal conditions. The absence of melanocortin-receptor side-effects (unlike full α-MSH or Melanotan-II) is the principal advantage of KPV as a research probe for the anti-inflammatory arm of α-MSH biology.
Analytical specifications
Every batch of KPV supplied by NMChem is characterised by reversed-phase HPLC for purity determination and by mass spectrometry for identity confirmation. Certificate of Analysis (COA) documents are issued per batch and made available on request.
Identity is confirmed by electrospray-ionisation mass spectrometry (ESI-MS); the observed mass falls within ±2 Da of the theoretical monoisotopic mass calculated from the residue sequence. Purity is determined by reversed-phase HPLC on a C18 column with a trifluoroacetic-acid-modified water/acetonitrile gradient and reported as the area-under-curve percentage of the main peak at 214 nm. NMChem specification is ≥99% main peak. Material ships as lyophilised powder and must be reconstituted in sterile water or bacteriostatic water immediately before use.
UK regulatory status
Supplied as a research-grade reference standard for laboratory use only. Not a licensed medicinal product in the United Kingdom and not approved by the MHRA for human or veterinary administration. Sale is restricted to researchers, institutions and laboratory professionals; the compound must be retained within research premises. End-user compliance with the Human Medicines Regulations 2012, the Misuse of Drugs Act 1971 (where applicable) and local institutional biosafety policy is the responsibility of the buyer.
Research literature
Selected peer-reviewed publications from PubMed referencing this compound.
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KPV and RAPA Self-Assembled into Carrier-Free Nanodrugs for Vascular Calcification Therapy.
Zhang L et al. · Advanced healthcare materials · 2024
PubMed PMID 39252648 -
A KPV-binding double-network hydrogel restores gut mucosal barrier in an inflamed colon.
Zhao Y et al. · Acta biomaterialia · 2022
PubMed PMID 35245681 -
International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy: A Consensus-Based Approach.
Engelen M et al. · Neurology · 2022
PubMed PMID 36175155
Related compounds
Other research compounds in adjacent mechanism classes or commonly used alongside KPV.
Frequently asked questions about KPV
Why use KPV instead of full α-MSH?
Get research-grade KPV from NMChem
UK supplier · HPLC and MS verified · Per-batch Certificate of Analysis · Tracked Royal Mail dispatch.