Melanoten-2

Product Name:

Melanoten-2

Chemical Information:

• Molecular Formula: C₅₀H₆₉N₁₅O₉
• Molecular Weight: 1024.18 g/mol
• Sequence: Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH2
• Molecular Structure:

↺ + − ⛶

Product Description:

Melanoten-2 is a synthetic peptide provided exclusively for in vitro laboratory research to study cellular pathways and receptor interactions under controlled experimental conditions. This compound is intended solely for use in qualified research settings to investigate molecular mechanisms and structural characteristics.

Research Applications:

Melanoten-2 is utilized in controlled research environments to support investigation of:

• Melanocortin receptor binding and signaling pathway analysis
• Peptide–receptor interaction dynamics in melanocortin system models
• Intracellular signaling cascade evaluation associated with peptide ligands
• Structure-function analysis of cyclic peptide analogs
• Stability, degradation, and analytical profiling in assay-based systems

All research applications are conducted in non-human, non-clinical experimental settings.

Storage and Handling:

• Store lyophilized material at −20°C (−4°F)
• After reconstitution, store at 2–8°C (36–46°F) and use promptly
• Avoid repeated freeze-thaw cycles
• Maintain aseptic techniques during laboratory handling

Product Specifications:

• Purity: ≥99% (HPLC Certified)
• Appearance: Lyophilized white powder
• Solubility: Soluble in suitable laboratory agents

Compliance Notice:

Melanoten-2 is FOR RESEARCH USE ONLY. It is not intended for human or veterinary use. This product has not been evaluated by the FDA. Buyers are solely responsible for determining the legality of this compound in their jurisdiction, including compliance with the Federal Analog Act (21 U.S.C. § 813) and any applicable state analog statutes. Misuse of this product is strictly prohibited and may violate federal, state, or local laws. By purchasing this product, buyer represents and warrants that it will be used only for in vitro research purposes.