peppercalc.com · research use only
Peptide Protocol

KPV: α-MSH C-terminus — anti-inflammatory without the tan.

Tripeptide C-terminal fragment of α-MSH. Potent anti-inflammatory via NF-κB inhibition. Oral, SubQ, or topical.

Open Calculator All Protocols →
peppercalc.com · research use only
0.5–5 mg
Daily Dose
4–8 weeks
Cycle
Oral / SubQ / Topical
Route
1–2× daily
Frequency
Overview

What is KPV?

KPV is derived from the C-terminus of α-MSH — a melanocortin peptide produced from POMC (pro-opiomelanocortin) that has broad anti-inflammatory effects across many tissues. Research identified KPV as the biologically active anti-inflammatory core of the molecule, separating it from the melanogenic (MC1R-activating) properties of the full sequence.

KPV exerts its anti-inflammatory effects primarily by inhibiting NF-κB nuclear translocation and reducing production of pro-inflammatory cytokines (TNF-α, IL-1β, IL-6, IL-8). Its small size enables excellent tissue penetration and it has been studied as an oral agent for inflammatory bowel disease, a topical agent for skin inflammation, and a SubQ agent for systemic inflammatory conditions.

NF-κB Inhibition
Prevents NF-κB nuclear translocation in macrophages, epithelial cells, and mast cells — blocking transcription of pro-inflammatory genes.
Cytokine Reduction
Reduces production of TNF-α, IL-1β, IL-6, and IL-8 in activated immune cells through receptor-dependent and independent mechanisms.
Mucosal Protection
Studied orally for IBD/Crohn's — penetrates gut epithelium and reduces local mucosal inflammation without systemic immunosuppression.
No Melanogenic Activity
Unlike full α-MSH, KPV does not activate MC1R and does not stimulate melanin production — isolated anti-inflammatory mechanism.
Dosing Protocol

Dosing Schedule

Parameters documented in published preclinical and clinical research.

Research use only. The following documents parameters from published preclinical and clinical research. Not medical advice. Not for human consumption. Consult a licensed healthcare professional before any use.
PhaseDoseFrequencyDurationNotes
Starting dose200 mcg SubQOnce dailyDays 1–7Begin conservatively to assess response before escalating.
Oral0.5–2 mg1–2× daily oral4–8 weeksFor gut and systemic inflammation. Taken with or without food.
SubQ working dose500 mcg–1 mgDaily SubQ4–8 weeksFor systemic anti-inflammatory effect. Abdomen or thigh injection.
Topical0.1–1%Apply 1–2× dailyPer indicationFor skin inflammation, psoriasis, or wound healing research.
High dose5 mg oralDailyShort coursesHigher oral doses in acute IBD-related research protocols.
Safety Profile

Safety & Side Effects

Generally Well Tolerated
Selective anti-inflammatory without immunosuppression
No melanogenic activity — safe for longer protocols
Multiple delivery routes including oral for gut-targeting
Well tolerated in preclinical models across multiple indications
Potential Concerns
Limited human RCT data — primarily preclinical evidence
Oral bioavailability can be variable
Long-term safety profile not well characterized
Optimal human dose not clinically established
Research use onlyThis page is an educational reference. None of this constitutes medical advice. Consult a qualified professional before any use. All compounds are for research purposes only.
Evidence Base

Academic References

  1. [1]
    Gatti S, et al. (2002). Effect of peripheral and central melanocortins on fever and inflammation. Neuroendocrinology. 75(6):364–72. PubMed ↗
  2. [2]
    Luger TA, et al. (2003). Neuropeptide-mediated immunomodulation. J Invest Dermatol. 121(4):688–701. PubMed ↗
  3. [3]
    Catania A, et al. (2004). The melanocortin system in control of inflammation. ScientificWorldJournal. 4:890–5. PubMed ↗
  4. [4]
    Rajora N, et al. (1997). Alpha-MSH modulates local and circulating tumor necrosis factor. J Clin Invest. 99(6):1526–32. PubMed ↗
Recommended Source
Source your compounds at White Market Peptides
Use code PEPPERCALC10 for 10% off + free 2-day shipping over $200
Shop Now →