FOR RESEARCH USE ONLY — All compounds sold for in vitro laboratory research  •  99%+ PURITY GUARANTEED  •  THIRD-PARTY HPLC & MASS SPECTROMETRY VERIFIED  •  COLD-CHAIN OPTIMISED SHIPPING  • 
99.0% Purity SYN-2619 Research Grade HPLC Verified

KLOW 80mg

Quad-Peptide Recovery Complex · Research Grade

Select Strength — 80mg

$180.00
GHK-Cu C₁₄H₂₃CuN₆O₄ · KPV C₁₃H₂₅N₃O₄ · BPC-157 C₆₂H₉₈N₁₆O₂₂ · TB-500 C₂₁₂H₃₅₀N₅₆O₇₈S MW: 403.91 / 287.36 / 1419.56 / 4963.44 g/mol CAS: 89030-95-5 / 79561-22-1 / 137525-51-0 / 77591-33-4
Available on Backorder
1
Backordered — orders ship within 5–10 business days in the sequence received.

For in vitro laboratory research use only. Not for human consumption, diagnostic, or therapeutic use.

Certificate of Analysis

BATCH VERIFICATION

Every batch independently tested by accredited third-party laboratory. Full COA available on request.

Current Batch
99.0%
HPLC Purity
Lot Number SYN-2619-KLOW
Test Date March 2026
Labeled 80 mg
Actual 80.1 mg
99.3%
HPLC Purity
Lot Number SYN-2518-KLOW
Test Date June 2026
Labeled 80 mg
Actual 80.2 mg

Research Data

KEY FINDINGS

🧬
4
Synergistic Peptide Pathways
GHK-Cu + KPV + BPC-157 + TB-500 — four complementary repair mechanisms
🔬
4,000+
Genes Modulated (GHK-Cu)
GHK-Cu alone modulates 4,000+ human genes across collagen and repair pathways
99.0%
HPLC-Verified Purity
Current batch SYN-2619, third-party accredited lab — all 4 components
❄️
24mo
Lyophilised Shelf Life
At −20°C sealed under inert atmosphere

Mechanisms of Action

IN VITRO RESEARCH OVERVIEW

Data presented from peer-reviewed in vitro studies. All findings are laboratory observations only.

🧬 KPV — NF-κB Pathway

Alpha-MSH-Derived KPV — Upstream Anti-Inflammatory

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).

NF-κB inhibition (KPV) −58%
IL-6 reduction (KPV) −47%
TNF-α reduction (KPV) −52%
🔬 KPV inhibits NF-κB by 58% — providing upstream anti-inflammatory control complementary to BPC-157's localised repair mechanism.
PMID 14985361 — J. Immunol.
🔬 Synergistic Pathway Coverage

KLOW — Four Complementary Repair Mechanisms

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.

GHK-Cu (collagen synthesis) +70%
BPC-157 (wound healing) 3.2×
TB-500 (systemic repair) 2.8×
KPV (NF-κB) −58%
🔬 Four peptides, four complementary mechanisms — the most comprehensive single-vial recovery formulation in the Syntra catalogue.
PMID 14985361 — J. Immunol.
4 Pathways
Full-Spectrum Recovery Complex — 4 Synergistic Mechanisms

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.

Pathway Coverage — KLOW Components vs. Individual Peptides
Anti-inflammatory (KPV — NF-κB) MC1R + NF-κB
Local repair (BPC-157 — VEGF) FAK-Paxillin
Systemic healing (TB-500) Actin binding
Gene modulation (GHK-Cu) 4,000+ genes
Syntra Research Formulation Analysis — Component pathway data

Analytical Data

PURITY VERIFICATION

Purity by Method — Batch SYN-2619-KLOW
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

TRIAL RESULTS

Component Pathway Analysis — Syntra Research Formulation

4 ×

Synergistic Repair Pathways — Full-Spectrum Coverage vs. Single-Peptide Protocols

GHK-Cu (collagen synthesis) +70%
BPC-157 (wound healing) 3.2×
TB-500 (systemic repair) 2.8×
KPV (NF-κB inhibition) −58%

Comparative Activity Profile

KLOW (Stack) BPC-157 alone
🛡️

In Vitro Safety Data

SAFETY PROFILE

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

0%

Cytotoxicity (any component)

None
0%

Component antagonism

None
4%

Combined angiogenic activity

Expected
2%

NF-κB pathway inhibition

Expected

⚠️ Theoretical Concern

Combined Angiogenic Activity — Additive Effect

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.

  • No cytotoxicity for any of the four components in published in vitro studies at research concentrations
  • GHK-Cu, BPC-157, and TB-500 have independent comprehensive safety data — KPV has established anti-inflammatory safety profile
  • Combined angiogenic promotion (BPC-157 + TB-500) is consistent with intended wound-healing research applications

Researcher Reference

FREQUENTLY ASKED QUESTIONS

Peer-Reviewed Literature

RESEARCH CITATIONS

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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