SNAP-8 Peptide (200mg)
$175.00
SNAP-8 peptide provides 200 mg of high-purity, laboratory-verified octapeptide in a sterile research vial. An elongation of the Argireline sequence, SNAP-8 (Acetyl Octapeptide-3) is extensively evaluated in cosmetic biochemistry and cell biology for its capacity to mimic the N-terminal end of SNAP-25, thereby competing for a position in the SNARE complex. Standardized to a purity exceeding 99%, this compound serves as a reliable model for studying neuromuscular signaling modulation, catecholamine release inhibition, and topical wrinkle depth reduction dynamics. Strictly for research use only.
Description
SNAP-8 Peptide
Synaptosomal-associated protein 8, or the SNAP-8 peptide, is a synthetic octapeptide analog of the N-terminal end of the SNAP-25 peptide. The peptide is made of eight amino acids. It is acetylated at the N-terminus and amidated at the C-terminus, which leads to the following structure: Ac-Glu-Glu-Met-Gln-Arg-Arg-Ala-Asp-NH2.
Overview
This peptide was developed to compete with the SNAP-25 protein to bind with the vehicle-associated membrane proteins. The SNAP-25 protein, which stands for Synaptosomal-Associated Protein of 25 kDa, is considered a key component in neurotransmitter release. It normally interacts with vehicle-associated membrane proteins to facilitate the fusion of vesicles with the cell membrane, releasing their contents into the synaptic gap. Such a vesicle-associated membrane protein is thought to be synaptic vesicle protein Synaptotagmin 1 (Syt1). Synaptotagmin 1 (Syt1) serves as a calcium sensor and is deemed crucial for regulating neurotransmitter release in response to changes in calcium ion concentrations inside nerve cells.
Molecular docking experiments posited that SNAP-8 and other peptides might bind to the C2AāC2B interface, primarily driven by hydrophobic contacts, suggesting a plausible site for inhibitory action on Syt1. The C2A and C2B regions are parts of the protein structure of Synaptotagmin 1 involved in calcium binding and membrane interaction. The binding at this interface by SNAP-8 suggests that the peptide might interfere with Synaptotagmin 1ās ability to respond to calcium signals, potentially disrupting normal neurotransmission. Once the SNAP-8 peptide binds with these proteins, it appears to destabilize the formation of the Soluble N-ethylmaleimide-sensitive factor Attachment Protein Receptor (SNARE) complex.
The SNARE complex is instrumental in the docking and fusion of vesicles at the cell membrane. Destabilization of this complex may prevent the release of acetylcholine, reducing localized muscle contractions. Acetylcholine is a neurotransmitter involved in stimulating muscle contractions. Its reduced release may therefore lead to decreased muscle activity and reduced wrinkle depth. Ultimately, all these biological activities induced by SNAP-8 peptide may cause a reduction in lines and wrinkles.(1) Thus, the potential of SNAP-8 to interact at the molecular level with components of the neurotransmitter release mechanism showcases it may act as a modulator of neural and muscular function, specifically in experimental models of skin cell aging.
Chemical Makeup(2)
Molecular Formula: C41H70N16O6S
Molecular Weight: 1075.16 g/mol
Other Known Titles: SNAP-8 (Acetyl Glutamyl Heptapeptide-3), Synaptosomal-associated protein 8, Acetyl octapeptide-3
Research and Clinical Studies
SNAP-8 Peptide and Skin Wrinkling
A study(3) was conducted in 2021 to study the potential of the peptide on expression lines and wrinkles. In this double-blind, randomized clinical trial, 55 research models were observed. The entire cohort exhibited Fitzpatrick skin type I to VI, and were exposed either the peptide serum or a control compound twice a day for 12 weeks. Short-term peptide impact was measured 15 minutes after exposure, and long-term impact was measured at weeks 4, 8, and 12. After completing this study, it was observed that the peptide appeared to cause a notable reduction in the lines within 15 minutes after introduction. For long-term impact, it was suggested by the researchers that the peptide had the potential to induce significant skin improvement after 12 weeks.
In another clinical trial conducted in 2013,(4) scientists focused on the Argireline peptide, a synthetic analog of the N-terminal end of the SNAP-25 peptide, which was developed for anti-aging action within the cell by inhibiting the catecholamine release (as opposed to acetylcholine release). Since both peptides are similar in structure, this study’s results may reflect parallel actions of the SNAP-8 peptide. For this trial, 60 models were examined, of which 45 were presented with the peptide, and 15 were presented with a control compound. The peptide or the control was introduced every day for four weeks. After the completion of the study, it was reported that the peptide group appeared to have improved skin, with almost a 49% reduction in lines and decreased skin roughness. As per Yuan Wang et al.:
“In the subjective evaluation, the total anti-wrinkle efficacy in the argireline group was 48.9%, compared with 0% in the placebo group. In the objective evaluation, the parameters of roughness were all decreased in the argireline group (p < 0.01), while no decrease was obvious in the placebo group (p > 0.05).ā
SNAP-8 Peptide and Skin Topography
A study(5) aimed to evaluate whether the SNAP-8 peptide might be incorporated into an oil and water emulsion form to understand the peptideās stability. When the 10% peptide oil-in-water emulsion was evaluated over a month-long routine exposure, there appeared to be a ~30% reduction in the depth and appearance of wrinkles. Researchers suggest that the peptide potentially mimics the action of botulinum neurotoxins.(6)
SNAP-8 Peptide and SNARE Protein Complex
SNAP-8 peptide has shown the potential to reduce muscle contractions by modulating the SNARE protein complex. One study reported that the peptide appeared to reduce the release of glutamate amino acid by almost 43%. Researchers reportedly claimed that the SNAP-8 peptide might reduce wrinkles by an average of 35%, up to a maximum of 62%,(7) a notable improvement in skin texture.
Reviews (0)
Be the first to review “SNAP-8 Peptide (200mg)” Cancel reply
Shipping and Delivery
MAECENAS IACULIS
Vestibulum curae torquent diam diam commodo parturient penatibus nunc dui adipiscing convallis bulum parturient suspendisse parturient a.Parturient in parturient scelerisque nibh lectus quam a natoque adipiscing a vestibulum hendrerit et pharetra fames nunc natoqueĀ dui.
ADIPISCING CONVALLIS BULUM
- Vestibulum penatibus nunc dui adipiscing convallis bulum parturient suspendisse.
- Abitur parturient praesent lectus quam a natoque adipiscing a vestibulum hendre.
- Diam parturient dictumst parturient scelerisque nibh lectus.
Scelerisque adipiscing bibendum sem vestibulum et in a a a purus lectus faucibus lobortis tincidunt purus lectus nisl class eros.Condimentum a et ullamcorper dictumst mus et tristique elementum nam inceptos hac parturient scelerisqueĀ vestibulum amet elit ut volutpat.
Related products
AICAR Peptide (50mg)
$62.00
AICAR 50 mg provides a high-purity, laboratory-verified lyophilized compound manufactured under strict quality control standards in the USA. Formulated with 50 mg of pure AICAR (5-Aminoimidazole-4-carboxamide ribonucleotide) per vial, this synthetic adenosine analog is widely utilized in cellular, metabolic, and exercise physiology research investigating AMP-activated protein kinase (AMPK) activation, cellular energy homeostasis, and mitochondrial biogenesis pathways.
Key Specifications
Ā Active Compound: AICAR (Acadesine / AICA Riboside)
Ā Chemical Formula: \text{C}_{9}\text{H}_{15}\text{N}_{4}\text{O}_{8}\text{P}
Ā Concentration: 50 mg per vial
Ā Purity Standard: Exceeds 99% (Third-Party HPLC Verified)
Ā Formulation: Sterile Lyophilized Powder
Ā Origin: Manufactured in USA
Ā Classification: Research Use Only
Primary Research Applications
Ā AMP-Activated Protein Kinase (AMPK) Activation: AICAR is intracellularly phosphorylated into ZMP, an AMP mimic that directly activates AMPK without altering cellular ATP/ADP ratios, facilitating targeted metabolic research.
Ā Mitochondrial Biogenesis & Endurance Pathways: Applied in cell cultures to analyze upregulated PGC-1$\alpha$ signaling, glucose uptake enhancement, and lipid oxidation mechanisms.
Ā Ischemic & Cellular Energy Homeostasis Studies: Extensively investigated in cardiac and skeletal muscle models measuring metabolic adaptation, cellular stress response, and insulin sensitivity.
AOD 9604 (5mg)
$41.00
AOD 9604 5mg is a premium, high-purity (\ge99% HPLC-verified) synthetic analog of the C-terminal region of human growth hormone (hGH 177-191). Engineered specifically to isolate lipolytic receptor activity without elevating IGF-1 levels or altering glucose metabolism, AOD 9604 is an essential tool for laboratory studies targeting lipid metabolism, adipocyte signaling, and cartilage matrix regeneration. Supplied as a sterile lyophilized powder strictly for scientific research use.
B7-33 (6mg)
$60.00
B7-33 6 mg provides a high-purity, laboratory-verified lyophilized peptide manufactured under strict quality control standards in the USA. Formulated with 6 mg of pure B7-33āa single-chain synthetic peptide functional analog of human gene-2 relaxin (H2 relaxin)āthis compound is widely utilized in cardiovascular, nephrology, and matrix biology research examining selective RXFP1 receptor signaling, extracellular matrix (ECM) remodeling, and anti-fibrotic signaling pathways without inducing tumor growth pathways.
Key Specifications
Active Compound: B7-33 (Relaxin-2 Receptor Agonist)
Chemical Formula: \text{C}_{136}\text{H}_{210}\text{N}_{40}\text{O}_{41}
Concentration: 6 mg per vial
Purity Standard: Exceeds 99% (Third-Party HPLC Verified)
Formulation: Sterile Lyophilized Powder
Origin: Manufactured in USA
Classification: Research Use Only
Primary Research Applications
Targeted Anti-Fibrotic Activity: B7-33 acts through the RXFP1 receptor to upregulate matrix metalloproteinases (MMPs) and suppress excessive collagen deposition, providing a targeted model for reversal of organ fibrosis.
Cardiovascular & Renal Remodeling: Extensively evaluated in preclinical models of heart failure, renal scarring, and vascular stiffness to assess hemodynamic regulation and arterial compliance enhancement.
Biasing RXFP1 Receptor Signaling: Investigated for its ability to preferentially stimulate pERK signaling over cAMP accumulation, preventing unwanted inotropic or proliferative side effects associated with full-length native relaxin.
BPC-157 (10 mg)
$95.00
BPC-157 (10mg) is a high-purity (ā„98%) research-grade pentadecapeptide extensively studied for its powerful tissue regeneration, tendon healing, and gut mucosa protective properties. Supplied as a stable lyophilized powder, every batch undergoes strict HPLC and Mass Spectrometry testing to guarantee maximum purity and reliable research results.
For research and laboratory use only. Not for human consumption.
P21 Peptide (5mg)
$115.00
P21 5 mg provides a high-purity, laboratory-verified lyophilized peptide manufactured under strict quality control standards in the USA. Formulated with 5 mg of pure P21āa synthetic peptide mimetic derived from ciliary neurotrophic factor (CNTF)āthis compound is widely utilized in neurobiology, cognitive science, and neurodegenerative disease research examining neurogenesis, synaptic plasticity, BDNF signaling, and cognitive enhancement mechanisms.
Key Specifications
Ā Active Compound: P21 Peptide (CNTF-derived synthetic peptide)
Ā Chemical Formula: \text{C}_{30}\text{H}_{55}\text{N}_{9}\text{O}_{9}
Ā Concentration: 5 mg per vial
Ā Purity Standard: Exceeds 99% (Third-Party HPLC Verified)
Ā Formulation: Sterile Lyophilized Powder
Ā Origin: Manufactured in USA
Ā Classification: Research Use Only
Primary Research Applications
Ā Neurogenesis & Synaptogenesis: P21 is evaluated for its ability to promote neural progenitor cell proliferation and maturation in the dentate gyrus of the hippocampus, supporting research into structural brain plasticity.
Ā Neurotrophic Factor Expression: Extensively studied for enhancing endogenous brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) signaling pathways without inducing CNTF-receptor autoantibodies.
Ā Cognitive Enhancement & Neuroprotection: Investigated in animal models of cognitive impairment, Alzheimer's disease, and traumatic brain injury to analyze memory retention recovery and synaptic density preservation.
Semaglutide 5 mg
$70.00
Semaglutide 5 mg is a research-grade lyophilized peptide engineered for high-purity laboratory applications. Each vial contains 5 mg of HPLC-verified Semaglutide, third-party tested to guarantee over 99% purity and manufactured in the USA under strict quality standards. Formulated specifically for research investigating GLP-1 receptor activation, glucose-dependent insulin secretion, gastric emptying regulation, and metabolic homeostasis pathways, this product is strictly intended for research use only.
Thymalin Peptide (25mg)
$135.00
Thymalin peptide 25 mg provides a high-purity, laboratory-verified lyophilized peptide manufactured under strict quality control standards in the USA. Formulated with 25 mg of pure Thymalināa synthetic bioregulator peptide complex derived from thymic polypeptide fraction researchāthis compound is widely utilized in immunology, endocrinology, and biogerontology research examining T-lymphocyte differentiation, immune system homeostasis, and neuroendocrine-immune interactions.
Key Specifications
Active Compound: Thymalin (Thymic Peptide Bioregulator)
Chemical Structure: Synthetic Thymic Dipeptide Complex (Lys-Glu / Glu-Trp analogs)
Concentration: 25 mg per vial
Purity Standard: Exceeds 99% (Third-Party HPLC Verified)
Formulation: Sterile Lyophilized Powder
Origin: Manufactured in USA
Classification: Research Use Only
Primary Research Applications
Immunomodulation & T-Cell Maturation: Thymalin is studied for its ability to regulate T-lymphocyte differentiation, restore helper/suppressor T-cell ratios (CD4^+/CD8^+), and stimulate cellular immunity markers.
Thymic Involution & Immune Restoration: Evaluated in age-related immune dysfunction and immunosenescence models to measure restored thymic secretory capacity and cytokine balance.
Neuroendocrine-Immune Axis Regulation: Extensively investigated in peptide bioregulator research for its role in normalizing neuroendocrine response, pineal-thymus interaction, and gene expression pathways during chronic stress or pathology.
Tirzepatide (5mg)
$90.00
Tirzepatide (5mg) is a dual GIP and GLP-1 receptor agonist designed to study advanced weight loss, lipid metabolism, and glycemic control. Engineered for high potency, this peptide targets dual incretin pathways to optimize metabolic research outcomes. Supplied as a high-purity lyophilized powder for laboratory use.

Reviews
There are no reviews yet.