★ Tissue Repair

KPV

Tissue Repair · 5mg × 10 vials

Anti-inflammatory tripeptide (the C-terminus of alpha-MSH). Studied in gut and skin inflammation models.

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Pricing
$85from · 10-vial kit
Shipping: $40 US · $60 international (10-vial kits only) · single vials $20, US only · free over $1,000
5mg × 10 vials$85
10mg × 10 vials$110
Order / Consult on Telegram →
~hours (short, sub-day)
Half-life
healing
Class
Overview

What Is KPV?

KPV is the C-terminal tripeptide of alpha-melanocyte-stimulating hormone (alpha-MSH 11-13): lysine, proline, valine. Alpha-MSH is a well-characterised endogenous anti-inflammatory hormone, and the published work established that most of its anti-inflammatory activity resides in this three-residue tail, without the pigmentary or melanocortin-receptor-driven effects of the full peptide.

The proposed primary mechanism is intracellular. KPV enters cells, likely via the PepT1 oligopeptide transporter, and directly inhibits the NF-kB pathway by interfering with IkB phosphorylation and p65 nuclear translocation. Downstream, production of TNF-alpha, IL-1beta, IL-6, IL-8, and other pro-inflammatory cytokines falls. KPV also appears to inhibit mast cell degranulation and reduce neutrophil chemotaxis, which is why skin-inflammation models (atopic dermatitis, psoriasis, acne) respond alongside the gut models. PepT1 is overexpressed in inflamed colonic tissue, so KPV concentrates preferentially in the tissue where inflammation is active, an effect documented in the Merlin laboratory's colitis work at Georgia State University.

Published Safety Data

What the published studies measured.

What the studies show
Measured in clinical trials
  • No human RCTs of pure KPV at scale. Preclinical (mouse/rat) IBD and dermatitis models report no observed adverse effects at therapeutic doses
  • Small open-label dermatology / cosmetic studies (atopic dermatitis topical) report no irritation or sensitization above vehicle
  • Theoretical: alpha-MSH is the parent peptide and is well-tolerated in humans, the tripeptide tail lacks the MC1/MC4 receptor activity that drives the full peptide's pigmentation/appetite signals, so the tripeptide profile is cleaner than the parent
The Research

Peer-reviewed studies and clinical guidelines - tap any to read the source.

PubMedKannengiesser et al, KPV in inflammatory bowel disease, Inflamm Bowel Dis 2008

oral KPV reduces colitis severity in DSS mouse model via PepT1

Read study ↗
PubMedDalmasso et al, PepT1-mediated tripeptide KPV uptake reduces intestinal inflammation, Gastroenterology 2008

mechanism paper on PepT1 transport in inflamed colon

Read study ↗
PubMedBrzoska et al, Alpha-MSH and related tripeptides: biochemistry, anti-inflammatory and protective effects, Endocrine Reviews 2008

definitive review of the alpha-MSH / KPV anti-inflammatory axis

Read study ↗
PubMedMastrofrancesco et al, KPV modulates inflammation in human keratinocytes, J Invest Dermatol

skin/dermatology mechanism, NF-kB inhibition in keratinocytes

Read study ↗
PubMedBettenworth et al, Nanoparticle-based delivery of KPV in colitis

targeted delivery research, validates oral/colon route

Read study ↗
PubMedLuger et al, Alpha-MSH-related peptides in immune regulation

broader immune/cytokine context

Read study ↗
+ 3 more studies & references

Reconstitution & Storage

Storage: Refrigerated, 4-6 weeks once reconstituted. Lyophilized vials stable at room temp for shipping; refrigerate on arrival. Short half-life in solution means fresher recon is meaningfully better than month-old recon for skin/gut work.

All products sold for research purposes only. Not for human or animal consumption. Must be 21 or older to purchase. By placing an order you confirm compliance with all applicable local laws and regulations.