KPV
Also known as: Lys-Pro-Val, Alpha-MSH fragment
At a glance
PeptiGuide dataset · reviewed Aug 2026
What it is
Alpha-MSH-derived tripeptide studied in preclinical anti-inflammatory models
Status
Preclinical
Typical dose
200–500mcg
Researched for
Gut inflammation, IBD, skin conditions and anti-inflammatory activity
Trial progress
- PrePreclinical
- IPhase I
- IIPhase II
- IIIPhase III
- IVPhase IV
- FDAFDA approved
Preclinical - Promising animal research, limited human data
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In plain language
- KPV is a single tripeptide composed of lysine, proline and valine and is described as an alpha-MSH fragment.
- The supplied evidence frames KPV as an anti-inflammatory research , mainly in gut inflammation, IBD-related models and skin-condition contexts.
- Evidence status is , with animal and cell-culture findings and no provided randomized human efficacy trials.
- Reported community dosing is 200-500 mcg daily, commonly 1-2 times daily, by injection or oral capsules.
How it's thought to work
KPV is described as a short alpha-MSH-derived with a proposed anti-inflammatory mechanism. In the supplied evidence, KPV uptake is linked to PepT1 transport, particularly in inflamed intestinal tissue. After cellular entry, laboratory findings associate KPV with dampened NF-kB activity and reduced production of inflammatory mediators such as TNF-alpha, IL-1beta and IL-6. The source also states that KPV does not appear to act through the classic melanocortin receptors used by alpha-MSH, so the mechanism remains a working model rather than a confirmed clinical pathway.
What the research shows
Where the research stands
The supplied research summary places KPV in a evidence tier. It cites Dalmasso and colleagues in Gastroenterology in 2008 for PepT1-dependent uptake and reduced intestinal inflammation in experimental colitis models, including DSS and TNBS mouse models, alongside lower pro-inflammatory cytokine signals. A 2016 PMC-listed study is described as showing fewer tumors in a mouse model of colitis-associated cancer when KPV activity depended on PepT1. The source emphasizes that these are animal and findings and does not provide published randomized human trials for inflammatory bowel disease, eczema or other promoted uses.
What it shows
✓ Animal studies
Promising animal research, limited human data
△ Limitations
Animal study doses may not translate directly to humans.
Bottom line: Preclinical research ongoing; no human clinical-trial benefit evidence was provided Not FDA approved
Typical dosing
CommunityCommunity dataset200–500 mcg
daily
Community-reported dosing for anti-inflammatory research contexts involving gut and skin topics; not established clinical dosing.
Research dosing
Animal studies onlyAnimal studies only - may not translate to humans
Timing & administration
Best time to take
Morning, or as directed in the source context
Once daily
Food recommendation
With or without food
Why this timing?
The source favors morning timing in the context of daytime inflammation-related research use; this is a reported timing preference, not a validated clinical requirement.
Possible side effects
Not everyone experiences these. Individual responses vary with dose, duration, and personal factors.
- Generally well tolerated
- Injection-site reactions
- Transient mild flu-like symptoms
- Mild gastrointestinal effects
- Possible histamine release
- Does not cause immunosuppression
- Cancer-history contraindication claim
Not everyone experiences side effects, and severity can vary by context, purity, route, and individual health factors.
Frequently asked questions
Sequence
H-Lys-Pro-Val-OH (KPV)
One open dataset
Every fact on this page - doses, side effects, references - comes from the same PeptiGuide dataset that powers the Tracker, Compare, and the Lab.
Browse the datasetEducational resource, not medical advice. Talk to your clinician before acting on anything here.
Community discussion
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