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Vialox

C21H37N9O5
Research Use Only. Vialox is a research compound intended strictly for laboratory and scientific research purposes. It is not approved for human consumption, therapeutic use, or veterinary use. Information on this page is provided for educational and research reference purposes only.

Overview

Vialox, also known by its INCI name Pentapeptide-3 and assigned CAS number 135679-88-8, is a synthetic pentapeptide composed of five amino acids — glycine, proline, arginine, proline, and alanine — arranged in a specific sequence that has drawn attention in cosmetic and biochemical research. It is classified as a neurotransmitter-inhibiting peptide, designed to mimic the mechanism of certain compounds that modulate acetylcholine receptor activity at the neuromuscular junction, a process that has made it of interest in skin biology research. Vialox is sometimes grouped alongside other cosmeceutical peptides studied for their potential interactions with the extracellular matrix and skin aging processes, including effects on collagen and elastin structure. Published research has begun exploring its antiaging properties through both computational modeling and laboratory-based methods, with early studies comparing its activity to related peptides such as Leuphasyl. As with all compounds featured on this site, Vialox is intended strictly for research and scientific study purposes and is not approved for human use or consumption.

Compound Data

CAS Number 135679-88-8
Molecular Formula C21H37N9O5
Molecular Weight 495.60 g/mol
IUPAC Name (2S)-1-(2-aminoacetyl)-N-[(2S)-1-[(2S)-2-[[(2S)-1-amino-1-oxopropan-2-yl]carbamoyl]pyrrolidin-1-yl]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]pyrrolidine-2-carboxamide
PubChem CID 11605666

Research & Bioactivity

Vialox is a synthetic pentapeptide that researchers have studied primarily in the context of skin biology, with particular attention to its potential role in processes related to extracellular matrix maintenance and the molecular mechanisms underlying skin aging. Studies have examined how this peptide interacts with components involved in the structural integrity of the skin, including collagen and elastin pathways, which are known to be affected by both intrinsic aging and environmental stressors. Research has employed computational approaches such as molecular docking and molecular dynamics simulations to investigate how Vialox may interact with relevant biological targets at a structural level. In vitro methodologies have also been incorporated into this research to complement the in silico findings, providing a more integrative picture of the peptide's potential bioactivity. This type of combined computational and laboratory-based investigation represents a growing area of interest in cosmeceutical peptide research, where scientists seek to better understand the mechanisms through which small peptides may influence cellular and molecular processes in skin tissue models.

Also Known As

Published Research

Integrative In Silico and In Vitro Evaluation of Vialox and Leuphasyl Pentapeptides for Antiaging Applications.

Akhan D, Bicak B, Kurtur OB, Budama-Kilinc Y, Gunduz SK — 2026
Skin aging arises from intrinsic and extrinsic factors that drive extracellular matrix degradation, particularly of collagen and elastin, leading to wrinkles, pigmentation, and loss of skin elasticity. This is the first integrative study to evaluate the antiaging potential of the cosmeceutical pentapeptides Vialox and Leuphasyl using a combined approach of molecular docking, molecular dynamics simulations, and in vitro cytotoxicity assays. Targeting matrix metalloproteinases (MMP-1, MMP-8, and MMP-13), which contribute to collagen breakdown, and Sirtuin-1 (SIRT-1), a regulator of cellular longevity, the peptides were evaluated for binding affinity, stability, and structural dynamics. Docking and molecular dynamics studies revealed that Leuphasyl showed stronger interactions with MMP-13, while Vialox preferentially targeted SIRT-1, underscoring their potential to modulate aging-related pathways. In silico ADME and toxicity predictions suggested favorable pharmacokinetic and safety profiles. Furthermore, both peptides showed no cytotoxicity on HaCaT cell line at concentrations up to 1 mg/mL. This is the first integrative study to evaluate both peptides using combined computational and experimental approaches. Overall, these findings provide mechanistic insight into the anti-aging activity of Vialox and Leuphasyl and support their promise as effective, noninvasive dermocosmetic  agents-offering a new avenue for healthier, youthful skin.