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KPV

Lys-Pro-Valα-MSH (11-13)alpha-MSH fragment
Preclinical

Evidence

Preclinical

Half-life

1 h

Typical vial

5 mg

Route

3 routes

What it is

A three-amino-acid fragment of alpha-MSH studied for anti-inflammatory effects, largely in animal models of gut inflammation.

Reviewed 12 Aug 2026

KPV is the final three amino acids of alpha-melanocyte-stimulating hormone: lysine, proline, valine. The parent hormone has broad effects including on pigmentation; the KPV fragment appears to retain anti-inflammatory activity without them, which is the reason for interest in it specifically.

The published work is preclinical and concentrated on inflammatory bowel models in rodents, with some work on skin inflammation. No controlled human trial has been published. It is the newest and least-studied of the four compounds in a KLOW blend.

How it works

KPV appears to act inside the cell rather than at a surface receptor — interfering with NF-κB — a signalling pathway that switches on a large share of the body's inflammatory response. Blocking it upstream would reduce many inflammatory outputs at once. That is what the animal models report.

Because it is small and uncharged at physiological pH, it is thought to cross cell membranes readily. That is the proposed reason a three-amino-acid fragment can reach an intracellular target at all.

What it is studied for

Each entry states the evidence behind it. We do not rank indications by effectiveness — for most compounds here, that would be a claim nobody can support.

  • Gut inflammation

    Published review

    The main focus of published work.

    EvidenceRodent models of induced colitis. No human trials.

  • Skin inflammation

    Published review

    Studied topically for inflammatory skin conditions.

    EvidenceAnimal and in vitro work.

Regulatory status

Last reviewed 12 Aug 2026. Positions in this category change frequently, so we date the line.

United States

Not approved for human use in the United States. Sold only as a research chemical.

Identity and clearance

What the molecule is, and how long a dose stays measurable.

Published review

Molecule

Class
Tripeptide, C-terminal fragment of α-MSH
Molecular weight
342.4 Da
Length
3 amino acids

Sequence

Lys-Pro-Val

Pharmacokinetics

Published review
Half-life1 h
Substantially cleared6 h
100%50%25%0%half-life 1hdose2h3h5h6h
Modelled from the half-life above, assuming first-order elimination. Illustrative rather than measured — it shows the shape of clearance, not a prediction for any individual.

Not measured in humans. Short-peptide clearance is expected to be rapid.

Dose protocols reported in sources

Displayed for reference only. Every row says where it came from, and a trial protocol and a community convention are not the same kind of information. None of this is fed into the calculator, and none of it is a recommendation.

Mixed sources

A week-by-week progression is also reported for KPV. See it against a 5 mg vial, where the syringe units can be worked out.

Dose protocols reported in sources, with the source of each.
GoalDoseFrequencyRouteUnits, 5 mg vialSourceStart this protocol
Commonly described dose200 mcg – 500 mcgOnce dailySubcutaneous12–30 uCommunity practiceStart this
As delivered within a KLOW blend250 mcg – 400 mcgOnce dailySubcutaneousFixed by the vial's ratio rather than chosen independently.15–24 uCommunity practiceStart this

The doses above in syringe units, for the vial you have:

Start this copies a row into a protocol of your own, which you can then edit. Where a source gave a dose range or an ambiguous frequency, those fields arrive empty — we will not pick a number on your behalf.

CheckRows marked community practice describe what people commonly do, drawn from public discussion. They are not derived from any trial and are not evidence that a dose is safe or effective.

Work out what to draw

Pre-filled with a 10 mg vial as a worked example. These are not recommended values — change them to match the vial in front of you.

Tool
Dose unit
Your syringe
01020304050607080901005 units0.05 mL

Draw to 5 units on a 1 mL U-100 syringe. That is 0.05 mL, containing 250 mcg of KPV.

Concentration5mg / mL
Volume drawn0.05mL
Doses per vial40doses
Per unit50mcg / unit

Check5 units falls between the printed lines on a 1 mL U-100 syringe. Mixing with 1.6 mL of water instead would put this dose at 4 units.

BioAlmanac performs arithmetic on values you enter. It does not recommend doses, schedules or compounds, and nothing here is medical advice. Confirm every calculation against your vial and syringe before drawing, and speak with a licensed healthcare provider.

Open this calculation in the full calculator

Units, concentration, bacteriostatic water — the glossary defines the vocabulary, and a unit is not a fixed volume.

Safety

Reported effects, the situations that need care, and the ones that mean stop.

Read before dosing

Reported effects

  • Injection site reactionsCommunity practice

    Occasionally reported

    Reported less often than with several other peptides in this category, which is part of why it is added to blends.

  • Long-term effectsCommunity practice

    Unknown

    No human safety data of any duration.

When to stop

  • Signs of infection at an injection site.
  • Any allergic response: rash, hives, swelling, or difficulty breathing. Seek urgent care.
  • New or worsening gastrointestinal symptoms, given that the gut is where its studied activity lies.

Interactions and situations that need care

  • Immunosuppressant therapyUse caution

    KPV's proposed mechanism is suppression of an inflammatory signalling pathway. Adding it to prescribed immunosuppression compounds the same direction of effect, and no study has examined the combination.

  • Active infectionUse caution

    Inflammation is part of how the body clears infection. Damping it while fighting one is not obviously desirable, and has not been studied.

  • Pregnancy and breastfeedingAvoid

    No reproductive or developmental safety data.

What to expect

What the sources describe over time, and how confident anyone can be about it.

No human efficacy data

HonestlyThere is no human efficacy data for this compound, so there is no evidence-based timeline to give. Any site publishing a week-by-week schedule of expected effects has invented it.

  • No human trial has been published, so there is no evidence-based timeline for effects.
  • The published animal work concerns gut inflammation specifically; general anti-inflammatory claims extend beyond what those models tested.
  • It is the least-studied component of a KLOW blend, and the newest to this market.

Storage and combinations

How to keep it, and what it does and does not go with.

Storage and handling

Freeze-dried powder
Refrigerated at 2–8 °C, protected from light.
After mixing
Refrigerated at 2–8 °C. Do not freeze once mixed.
Long-term, frozen
Unopened powder is stable at −20 °C or colder.

Printable one-pagerHow to reconstitute a vial, step by step

Stacks with KPV in them

Documented combinations and plans people have published, with full schedules.

Published by people running it. Their plans, not ours — one person doing something is not evidence that it works.

Checking your vial

Research chemicals carry no manufacturing standard, so what the vial looks like is often the only quality signal available before you use it.

  • White cake, clear solution

    Standard appearance for a correctly lyophilised short peptide.

  • Collapsed cake or cloudy solution

    Suggests heat damage in transit or degraded material.

Vocabulary on this page

Duration of action
How long an effect lasts. This is not the same as half-life and often much longer.
Blend
One vial containing several peptides at a fixed ratio, reconstituted and drawn together.
Vial
The small sealed glass container a peptide is sold in, holding a stated mass of freeze-dried powder under a rubber stopper.
Evidence level
The category of human evidence behind a compound, from preclinical through to approved. Stated on every profile here as a category, not an adjective.
Stack
Several separate compounds run at the same time, each in its own vial and on its own schedule.
Injection site
Where on the body an injection is given. Rotating between sites is standard practice for anything given repeatedly.

The whole glossary →

Questions

Reader questions
How is KPV different from alpha-MSH?
KPV is the last three amino acids of alpha-MSH. The interest in the fragment, not the whole hormone, is that it appears to keep the anti-inflammatory activity without the parent hormone's other effects, including on pigmentation.
Why is KPV added to peptide blends?
It is usually described as being included for anti-inflammatory effect and because it is reported to cause fewer injection site reactions than the other components. Both are community observations rather than trial findings.

References

Everything on this page that came from a source, with the source.

  1. The Tripeptide KPV: Anti-inflammatory Activity and Therapeutic Potential

    Peptides / review literature, 2018 · Review of preclinical work

    Rodent colitis models and cultured cells

    Summarises reported suppression of NF-κB signalling and reduced inflammatory markers in animal models of intestinal inflammation.

  2. Commonly reported community protocols

    BioAlmanac editorial summary of public community sources, 2026 · Not a study

    Summarises the dose ranges most consistently described in public discussion. Carries no evidential weight about safety or effect.

  3. Compiled community protocols

    BioAlmanac editorial summary of a public protocol compilation, 2026 · Not a study

    Records a week-by-week progression described on a vendor-adjacent protocol site, retrieved August 2026. Only the doses are taken from it. Its own syringe-unit conversions were checked against the vial sizes it states and several understate the volume by half, so nothing computed by that source is reproduced here — the units on this site are worked out from the vial in front of you. Carries no evidential weight about safety or effect.

KPV compared with

Also compared with BPC-157, TB-500, GHK-Cu, LL-37, ARA-290, Thymulin.

Keep this page honest

If something here is wrong, out of date, or missing a source, tell us and we will fix it and say that we did.

Suggest a correction

This page is educational. It describes what published research reports, not what you should do. Peptides discussed here are largely not approved for human use, and nothing on BioAlmanac is medical advice. No clinician reviews these pages.

Page last updated 12 Aug 2026