Vialox (Pentapeptide-3V) 200mg – Research Peptide

Here’s the straight data on Vialox. This is a synthetic pentapeptide (Gly-Pro-Arg-Pro-Ala) modeled after a compound found in snake venom. Its primary observed mechanism in research settings is the temporary inhibition of muscle contraction. Think of it like a research-grade, localized muscle signal blocker. It targets the neuromuscular junction, specifically the nicotinic acetylcholine receptors, which may prevent the signal for contraction from being received.

In lab studies, this has been shown to lead to a significant and rapid reduction in muscle contraction frequency and intensity. The data points to a potential 71% reduction within one minute of application in experimental models, with effects noted to persist for hours. For researchers investigating dermal models, this forced muscle relaxation has been correlated with observable reductions in wrinkle depth and skin surface roughness. One clinical study noted visible smoothing and immediate skin tightening in experimental models, with wrinkle reduction observed in approximately 50% of a test cohort after 28 days of controlled, twice-daily application.

Key Points for Your Research:

• Mechanism: Non-depolarizing neuromuscular blocker. Acts as an antagonist at peripheral nicotinic acetylcholine receptors (N-AChR).
• Primary Research Interest: Studying localized, temporary muscle relaxation and its effects on dermal models, specifically regarding wrinkle formation and skin texture.
• Sequence: Gly-Pro-Arg-Pro-Ala
• Molecular Formula: C21H37N9O5
• Molecular Weight: 495.58 g/mol
• Purity: >99% (HPLC verified). Each vial contains 200mg of lyophilized powder.

Important Laboratory Protocol: This material requires reconstitution with sterile bacteriostatic water or saline for in-vitro research. Proper laboratory safety protocols must be followed at all times.

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