Select Strength — 80mg
For in vitro laboratory research use only. Not for human consumption, diagnostic, or therapeutic use.
Research Data
Mechanisms of Action
Data presented from peer-reviewed in vitro studies. All findings are laboratory observations only.
KPV (Lys-Pro-Val) is the C-terminal tripeptide of alpha-MSH, an endogenous anti-inflammatory neuropeptide. KPV inhibits NF-κB activation and downstream cytokine production in colonic epithelial and immune cell models — with particular efficacy in gut inflammation research (IBD models).
The KLOW formulation combines GHK-Cu (gene modulation, collagen synthesis), KPV (NF-κB anti-inflammatory), BPC-157 (VEGF, FAK-paxillin localised repair), and TB-500 (actin sequestration, systemic wound healing) — providing full-spectrum coverage from upstream inflammation control to systemic tissue regeneration.
KLOW combines four research peptides targeting the complete recovery pathway: GHK-Cu for gene modulation and collagen synthesis; KPV for upstream NF-κB anti-inflammatory signalling; BPC-157 for localised tissue repair via VEGF and FAK-paxillin; TB-500 for systemic actin-mediated healing.
Analytical Data
| Specification | Value |
|---|---|
| CAS Number | 89030-95-5 / 79561-22-1 / 137525-51-0 / 77591-33-4 |
| Molecular Formula | GHK-Cu C₁₄H₂₃CuN₆O₄ · KPV C₁₃H₂₅N₃O₄ · BPC-157 C₆₂H₉₈N₁₆O₂₂ · TB-500 C₂₁₂H₃₅₀N₅₆O₇₈S |
| Molecular Weight | 403.91 / 287.36 / 1419.56 / 4963.44 g/mol |
| Purity (HPLC) | 99.0% |
| Appearance | White/light blue lyophilised powder |
| Solubility | Soluble in water (1 mg/mL per component) |
| Storage | −20°C long-term / 2–8°C short-term |
| Shelf Life | 24 months from production date |
| Research Grade | Yes — For In Vitro Use Only |
What Research Has Shown
Component Pathway Analysis — Syntra Research Formulation
Synergistic Repair Pathways — Full-Spectrum Coverage vs. Single-Peptide Protocols
Comparative Activity Profile
In Vitro Safety Data
All four KLOW components (GHK-Cu, KPV, BPC-157, TB-500) have independent safety data from separate research programs. No receptor competition or known antagonism between components has been identified in published literature.
Observed Adverse Indicators
Cytotoxicity (any component)
NoneComponent antagonism
NoneCombined angiogenic activity
ExpectedNF-κB pathway inhibition
Expected⚠️ Theoretical Concern
Both BPC-157 (VEGF pathway) and TB-500 (eNOS/SDF-1) promote angiogenesis through independent mechanisms. Combined, this angiogenic activity is additive. Researchers using angiogenesis-sensitive models should account for this combined effect.
Researcher Reference
Each component targets a distinct recovery pathway: GHK-Cu modulates 4,000+ genes and drives collagen synthesis; KPV inhibits NF-κB for upstream anti-inflammatory action; BPC-157 targets localised tissue repair via VEGF and FAK-paxillin; TB-500 provides systemic healing through actin sequestration. Together they cover the full spectrum from systemic inflammation to site-specific repair.
KPV (Lys-Pro-Val, CAS: 79561-22-1, MW: 287.36 g/mol) is a tripeptide derived from the C-terminal of alpha-MSH. It inhibits NF-κB signalling independently of its melanocortin receptor activity, producing anti-inflammatory effects in gut, skin, and immune cell models — particularly relevant in intestinal inflammation research.
Lyophilised: −20°C up to 24 months. Reconstituted: 4°C, use within 14 days. Protect from light.
Peer-Reviewed Literature
All citations refer to published peer-reviewed in vitro research. Data presented for scientific reference only. No claims made regarding human therapeutic use.
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