For laboratory and research use only. Not for human or animal consumption.

How it works

KPV is the C-terminal tripeptide (lysine-proline-valine) of α-melanocyte-stimulating hormone. It retains the anti-inflammatory activity of the parent hormone while lacking its melanocortin-receptor pigmentation effects. Published research suggests KPV acts intracellularly — entering cells partly via the PepT1 transporter — to inhibit pro-inflammatory signaling cascades such as NF-κB and downstream cytokine production. It is studied in models of colitis, wound healing, and mucosal repair for effects on inflammation and tissue recovery.

Learn more about the science →
α-MSH 11-13 fragmentPepT1-mediated uptake
↓ NF-κB signaling↓ pro-inflammatory cytokines
mucosal modelstissue repair · healing
Certificate of Analysis+

LC-MS identity, HPLC purity (≥99%), mass spec confirmation, endotoxin by LAL, appearance. Third-party ISO-17025 verified.

View full certificate →Lot KPV-2607-P · Jul 2026 · printable
Purity (HPLC)99.2%✓ Pass
Mass spec (MW)342.43✓ Pass
Endotoxin (LAL)<0.5 EU/mg✓ Pass
Certificate metadata
Lot
KPV-2607-P
Released
Jul 2026
Tested by
Janus Analytical (ISO-17025)
Method
RP-HPLC · LC-MS · LAL · KF
Specifications+
CompoundLys-Pro-Val (α-MSH 11-13)
FormLyophilized
Purity≥99% by HPLC
Endotoxin<0.5 EU/mg
Storage & handling+

Lyophilized: −20°C, 24 months. Reconstituted: 2–8°C, use within 30 days. Reconstitute with bacteriostatic water; swirl gently, protect from light.

We ship in insulated parcels with phase-change cooling and a tamper-evident seal.

FAQs+
What is KPV derived from?+

It is the C-terminal tripeptide (Lys-Pro-Val) of α-MSH. It keeps the parent hormone's anti-inflammatory activity but not its melanocortin-receptor pigmentation effects.

Why is KPV in Longevity Research?+

Longevity Research covers broad-spectrum compounds studied for systemic effects. KPV is the C-terminal tripeptide of α-MSH, and its anti-inflammatory and mucosal-healing research context runs across tissues rather than sitting within one system.

How is KPV thought to act?+

Research suggests an intracellular anti-inflammatory mechanism — uptake partly via the PepT1 transporter and inhibition of NF-κB signaling — rather than a classical melanocortin-receptor route.

What's a typical reconstitution concentration?+

Investigator-dependent. A common preparation is 2 mL bacteriostatic water per 10mg vial, yielding 5 mg/mL.

How is KPV quality verified?+

LC-MS identity and HPLC purity per lot, mass spec against the theoretical mass, and a third-party ISO-17025 repeat assay.

Is KPV subscription-eligible?+

Yes. 15% off on a 60-day cycle once it returns to stock.

The research behind this compound, cited in full.

Provided for context only. None of the studies cited below evaluate hábit material specifically; they document the published literature on the compound and its mechanism. Research-use claims are not therapeutic claims.

  1. [01] Luger TA. & Brzoska T. Ann Rheum Dis 66 (2007): iii52–iii55.
  2. [02] Kannengiesser K. et al. Inflamm Bowel Dis 14 (2008): 324–331.
  3. [03] Dalmasso G. et al. Gastroenterology 134 (2008): 166–178.
  4. [04] PepT1-Mediated Tripeptide KPV Uptake Reduces Intestinal InflammationGastroenterology · 2008 · Dalmasso G, et al.DOI 10.1053/j.gastro.2007.10.026

Verified buyer notes

Initials only — every quote is verified against an order record. We don’t ghost-write reviews.

COA matched what we ran in-house. Powder reconstituted clean, no haze. Did exactly what we needed it to.
M.O.Boston, MAApril 2026
Switched after two bad lots from a previous source. Three orders in, zero issues.
J.K.Austin, TXMarch 2026
Asked support a purity question and got the raw HPLC trace back within the hour. That transparency is why we reorder.
S.L.Chicago, ILFebruary 2026