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Peptide Protocol Index
Anti-Inflammatory / GutCommunity-derived

KPV

Lys-Pro-Val · alpha-MSH(11-13)

Tripeptide C-terminal fragment of alpha-MSH studied for anti-inflammatory activity (preclinical)

View Partner ProductsLast reviewed 2026-06-19
01

Overview

KPV is a tripeptide consisting of lysine, proline, and valine — the C-terminal three residues (11–13) of alpha-melanocyte-stimulating hormone (alpha-MSH). Unlike the full alpha-MSH molecule, KPV lacks the sequence required for melanocortin-receptor-driven pigmentation, yet preclinical work suggests it retains much of the parent hormone's anti-inflammatory signaling.

Interest in KPV centers on intestinal and skin inflammation. Cell and rodent studies report that the peptide can be taken up by intestinal epithelial and immune cells and may dampen pro-inflammatory signaling (for example, NF-kB and MAPK pathways), which is the rationale behind its community use for gut-related complaints and inflamed skin. It is sometimes combined with BPC-157 in gut-focused protocols.

Human clinical evidence specific to KPV is limited, and the dosing summarized here is derived from community practice rather than controlled trials. All figures are provided strictly as a research reference and should be verified against primary sources.

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Key parameters

Dose range
200–500 mcg daily (community)
Frequency
1–2× daily
Half-life
Short (small tripeptide, rapidly cleared)
Route
Subcutaneous (also oral for gut)
Vial sizes
10 mg
Regulatory status
Not approved; research use only. KPV is a research peptide and is not an approved drug product in any jurisdiction; supplied material is labeled for laboratory use only.
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Mechanism of action

  • NF-kB pathway modulation

    Preclinical models indicate KPV can reduce activation of NF-kB, a transcription factor that drives expression of many pro-inflammatory cytokines, lowering the downstream inflammatory response.

  • Pro-inflammatory cytokine reduction

    Associated in cell and animal studies with decreased production of inflammatory mediators such as TNF-alpha and certain interleukins.

  • Intracellular uptake via PepT1

    Reported to enter intestinal epithelial and immune cells partly through the peptide transporter PepT1, allowing it to act locally within gut tissue — one basis for oral interest in gut applications.

  • Melanocortin-related anti-inflammatory signaling

    As a C-terminal fragment of alpha-MSH, KPV is thought to retain anti-inflammatory activity associated with the parent hormone while lacking the residues responsible for pigmentation.

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Dosing protocol & phases

PhaseWeeksDoseNotes
Standard (community)Ongoing200–500 mcg dailyCommunity-derived range; not clinically established. Often split into 1–2 administrations.
Gut-focused (community)OngoingOral 250–500 mcg dailySome protocols use an oral route for local intestinal effect; the rationale is PepT1-mediated uptake, though oral absorption and stability are not well characterized.
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Reconstitution guide

For educational and research reference only. Not intended for human consumption, not medical advice. Compounds discussed are sold and used for laboratory research purposes only.

10 mg vial + 2 mL bacteriostatic water

Concentration5,000 mcg/mL · 5 mg/mL

Target doseDraw volumeU-100 units
200 mcg0.04 mL4
350 mcg0.07 mL7
500 mcg0.1 mL10

Higher-strength mix that keeps daily draws very small.

10 mg vial + 5 mL bacteriostatic water

Concentration2,000 mcg/mL · 2 mg/mL

Target doseDraw volumeU-100 units
200 mcg0.1 mL10
400 mcg0.2 mL20
500 mcg0.25 mL25

More dilute mix for easier measurement of small doses.

06

Reconstitution calculator

Pre-filled with KPV's vial sizes. Adjust the water volume and target dose to see the exact draw, with warnings for doses that are hard to measure or won't fit a syringe.

KPV vial sizes
mg
mL
mcg
Concentration
5,000mcg/mL
Draw volume
0.04mL
Syringe units
4U-100
Doses / vial
50

At 5,000 micrograms per millilitre, a 200 microgram dose is 0.04 millilitres, or 4 units on a U-100 syringe, giving 50 doses per vial.

This draw is only 4 units — small volumes are hard to measure accurately. Consider using less bacteriostatic water to make each dose a larger, easier-to-read draw.

07

Supplies needed

Affiliate disclosure: we may earn a commission from supplier links, at no extra cost to you. For research and educational use only.

Recommended supply

KPV research vial

KPV — research vial

From our verified partner Dynotides, with a third-party certificate of analysis per batch.

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Injection supplies

  • Bacteriostatic water

    Diluent for reconstituting lyophilized vials.

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  • Insulin syringes (U-100)

    0.3–0.5 mL, 29–31 G for accurate small draws.

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  • Alcohol prep pads

    Sterile swabs for the vial stopper and site.

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  • Sharps container

    Safe disposal of used needles.

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  • Storage fridge

    Keeps reconstituted vials at 2–8 °C.

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  • Insulated travel case

    Cooled, TSA-friendly case for travel.

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08

Missed-dose guidance

No approved-label guidance exists, as KPV is a research peptide. With a short-acting daily peptide, a common community approach is to take the missed dose when remembered the same day, or otherwise skip it and resume the normal schedule the next day rather than doubling up.

09

Side effects & safety

CategoryEffectTrial incidence
GeneralGenerally reported as well toleratedBased on community reports; no controlled-trial incidence data exists for KPV in humans.
Injection siteLocal reactions (redness, irritation)
GeneralEffects on melanocortin-mediated pigmentation not expectedKPV lacks the alpha-MSH core residues responsible for MC1R-driven pigmentation.
10

Clinical trials & evidence

  • Preclinical anti-inflammatory studies

    Preclinical (animal/cell)

    Varies · Rodent / in vitro (including colitis models)

    Reduced markers of intestinal and systemic inflammation reported; no large human efficacy trials specific to KPV.

    Trial identifier needs verification

11

Storage & handling

Lyophilized
Refrigerate lyophilized powder at 2–8 °C, protected from light; for longer-term storage, freeze at −20 °C.
Reconstituted
Refrigerate at 2–8 °C and use within ~28 days; do not freeze.
12

Comparisons

Vs.TargetHalf-lifeDosingEfficacyStatus
BPC-157Anti-inflammatory (alpha-MSH fragment) vs reparative/cytoprotectiveShort vs short200–500 mcg daily vs ~200–500 mcg daily (community)Often combined for gut/inflammation; complementary mechanismsBoth research-only / not approved
Thymosin Alpha-1Anti-inflammatory peptide vs immune-modulating peptideShort vs ~2 hDaily vs ~2× weeklyDifferent roles (local anti-inflammatory vs broad immune modulation)Research-only vs approved in some countries
13

Featured in these stacks

Tissue RepairCommunity-derived

KLOW (KPV + BPC-157 + TB-500 + GHK-Cu)

KPVBPC-157TB-500GHK-Cu

KLOW adds KPV — a tripeptide fragment of alpha-MSH with anti-inflammatory properties — to the GLOW stack, aiming to pair tissue/skin repair with an inflammation- and gut-oriented signal.

4 compoundsView stack →
14

Sources & references

  1. [1]Dalmasso G et al. PepT1-mediated tripeptide KPV uptake reduces intestinal inflammation. Gastroenterology 2008. ↗ source
  2. [2]Kannengiesser K et al. Melanocortin-derived tripeptide KPV has anti-inflammatory potential in murine models of inflammatory bowel disease. Inflamm Bowel Dis 2008. ↗ source
15

Frequently asked questions

What is KPV derived from?

KPV is the C-terminal tripeptide (residues 11–13: lysine-proline-valine) of alpha-MSH. It is studied for the anti-inflammatory activity associated with the parent hormone while lacking the part of the molecule responsible for pigmentation.

Why is KPV taken orally for gut issues?

Preclinical work suggests KPV can be absorbed into intestinal cells via the PepT1 transporter and act locally on gut inflammation, which is the rationale some community protocols give for an oral route. Oral absorption and stability in humans are not well characterized.

Is KPV approved for any use?

No. KPV is a research peptide and is not an approved drug product in any jurisdiction. The dosing here reflects community practice, not controlled clinical trials.

Related protocols

Tissue RepairCommunity-derived

BPC-157

Body Protection Compound 157

Broad tissue-repair effects in rodent models; no human efficacy trials

Dose
250–500 mcg daily
Frequency
1–2× daily
Half-life
Very short in plasma (~15 min IV in rats; undetectable by ~4 h)
Subcutaneous (also studied oral)View protocol →
Anti-Inflammatory / GutCommunity-derived

VIP

Vasoactive Intestinal Peptide

28-amino-acid neuropeptide; the definitive aviptadil COVID-19 trial (TESICO) showed no benefit

Dose
50 mcg/nostril intranasal (community); 50–200 mcg SC; IV aviptadil in trials
Frequency
Intranasal up to 4× daily, or SC 1–2× daily (community)
Half-life
Very short (~1–2 minutes in plasma)
Intranasal (community); intravenous as aviptadil in trialsView protocol →
Anti-Inflammatory / GutCommunity-derived

Thymosin Alpha-1

Tα1

Immune-modulating thymic peptide; 1.6 mg twice weekly is the typical Zadaxin regimen

Dose
1.6 mg per dose (typical Zadaxin)
Frequency
2× weekly (typical)
Half-life
~2 hours
SubcutaneousView protocol →

Looking to match this protocol to a verified research vial? Our partner supplier publishes a certificate of analysis per batch.

Research use only

For educational and research reference only. Not intended for human consumption, not medical advice. Compounds discussed are sold and used for laboratory research purposes only.