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

Look, here’s the straight talk on Vialox. It’s a synthetic pentapeptide (Gly-Pro-Arg-Pro-Ala) modeled after a compound found in snake venom. Its primary research focus is its observed mechanism: it appears to act as a non-depolarizing neuromuscular blocker at the peripheral nicotinic acetylcholine receptors (N-AChR). In simpler lab terms, it may temporarily disrupt the signal from nerve to muscle, leading to a reduction in muscular contraction.

This isn’t guesswork. The research is modeled on established compounds like tubocurarine (curare). Studies suggest Vialox may bind to the receptor sites on muscle cells, potentially inhibiting acetylcholine from attaching. No binding, no sodium ion influx, no depolarization, no contraction. The muscle relaxes. Published data indicates this action may lead to a significant reduction in muscle contraction frequency and intensity in experimental models.

Key Research Points & Specifications

• Sequence: Gly-Pro-Arg-Pro-Ala
• Molecular Formula: C21H37N9O5
• Molecular Weight: 495.58 g/mol
• PubChem CID: 67073230
• Appears to target peripheral N-AChRs with minimal central impact.
• In vitro studies cite potential for softened wrinkles and reduced skin roughness due to forced muscle relaxation.
• One clinical study noted visible skin smoothing and immediate tightening in experimental models.

Bottom line for researchers: If your work involves studying neuromuscular junction blockade, muscle contraction mechanisms, or the dermal effects of targeted muscle relaxation, Vialox is a precise tool. The data is compelling and points to a specific, repeatable action.

We ship this 200mg vial same-day if your order is in by 12 PM PST. It’s sealed, pure, and ready for your controlled laboratory environment.

Price: $231.00