KPV (Lys-Pro-Val)
C-terminal tripeptide fragment (Lys-Pro-Val) of alpha-melanocyte-stimulating hormone (alpha-MSH). Potent anti-inflammatory at nanomolar concentrations via NF-kB and MAPK pathway inhibition. Very short plasma half-life typical of tripeptides (~15 min). Taken orally, SC, or intranasally for gut inflammation and systemic anti-inflammatory effects.
Projected serum levels — 500 mcg (≈ 0.50 mg), once daily
Maintenance schedule: 500 mcg (≈ 0.50 mg) once daily (oral).
Modeled steady state after ~1 days: peak ≈ 0.073 mg, trough ≈ 0.000 mg body load. Population-based estimate over 15 days for a reference dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.
Key facts
- Category
- Peptide
- Route modeled
- Oral
- Model confidence
- inferred
- Half-life
- 14 min
- Common dose
- 500 mcg (≈ 0.50 mg)
- Suggested maximum
- 1.5k mcg/day
- Reference dose range
- 250–1.5k mcg (single dose)
- Suggested cadence
- once daily
Documented interactions
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moderate
Melanotan II + KPV (Lys-Pro-Val)
KPV (Lys-Pro-Val) and Melanotan II both push the mc1r and mc3r in the same direction.
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moderate
PT-141 (Bremelanotide) + KPV (Lys-Pro-Val)
KPV (Lys-Pro-Val) and PT-141 (Bremelanotide) both push the mc1r and mc3r in the same direction.
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watch
Mesalamine / 5-ASA (Lialda/Apriso/Pentasa) + KPV (Lys-Pro-Val)
KPV (Lys-Pro-Val) and Mesalamine / 5-ASA (Lialda/Apriso/Pentasa) both push the nfkb signaling in the same direction.
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watch
Milk Thistle (Silymarin / Silybin) + KPV (Lys-Pro-Val)
KPV (Lys-Pro-Val) and Milk Thistle (Silymarin / Silybin) both push the nfkb signaling in the same direction.
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watch
MSM (Methylsulfonylmethane) + KPV (Lys-Pro-Val)
KPV (Lys-Pro-Val) and MSM (Methylsulfonylmethane) both push the nfkb signaling in the same direction.
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watch
Sulfasalazine (Azulfidine) + KPV (Lys-Pro-Val)
KPV (Lys-Pro-Val) and Sulfasalazine (Azulfidine) both push the nfkb signaling in the same direction.
Serum checks 7 modeled interaction pairings for kpv (lys-pro-val) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.
Research behind this entry
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PepT1-Mediated Tripeptide KPV Uptake Reduces Intestinal Inflammation
Demonstrated KPV is transported into colonocytes via PepT1 transporter, where it inhibits NF-kB activation and reduces intestinal inflammation in colitis models at nanomolar concentrations.
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Orally Targeted Delivery of Tripeptide KPV via Hyaluronic Acid-Functionalized Nanoparticles Efficiently Alleviates Ulcerative Colitis
Developed HA-functionalized nanoparticles for oral KPV delivery that efficiently targeted inflamed colonic tissue and alleviated ulcerative colitis in mouse models.
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Inhibition of cellular and systemic inflammation cues in human bronchial epithelial cells by melanocortin-related peptides: mechanism of KPV action and a role for MC3R agonists
Elucidated KPV mechanism showing dose-dependent inhibition of NF-kB via IkappaBalpha stabilization and nuclear import blockade, with anti-inflammatory effects in bronchial epithelium.
3 published studies referenced in the app, each with a plain-language summary.