Melanotan II (MT-2) peptide 10 mg – Research Overview
Melanotan II peptide (MT-2) is a synthetic research-grade peptide derived from alpha-melanocyte-stimulating hormone (α-MSH). Researchers study Melanotan II peptide in experimental models focused on melanocortin signaling, skin biology, and neuroendocrine regulation. Therefore, Melanotan II peptide has attracted sustained interest within dermatological, metabolic, and neurobiological research fields.
Scientists use Melanotan II peptide to investigate mechanisms related to melanin production, pigmentation signaling, and adaptive responses to environmental stimuli. In this context, experimental models allow researchers to analyze how melanocortin pathways influence cellular signaling, energy balance, and systemic regulation. At the same time, these studies explore how melanocortin receptors participate in broader neuroendocrine communication networks.
Unlike compounds designed to target a single biological outcome, Melanotan II peptide provides a multifunctional research model. As a result, researchers can observe how melanocortin signaling coordinates responses across skin, metabolic, and central nervous system–related pathways under controlled laboratory conditions.
Melanotan II peptide in skin and pigmentation research
In skin-focused research, scientists frequently reference Melanotan II peptide in experimental models examining pigment regulation and cellular responses to UV-related stress factors. Additionally, these models support investigation of how melanocortin signaling influences melanocyte activity and adaptive pigmentation processes.
Researchers also evaluate Melanotan II peptide in laboratory studies focused on skin protection mechanisms and environmental stress adaptation. Through these studies, research teams analyze how signaling pathways regulate cellular defense responses and structural stability within skin tissues.
Moreover, Melanotan II peptide often appears in comparative research alongside Melanotan I peptide, allowing scientists to examine differences between selective and broader melanocortin signaling profiles. These comparisons support deeper understanding of pathway specificity and receptor interaction dynamics.
Melanotan II peptide in metabolic and neuroendocrine research
Beyond skin biology, researchers include Melanotan II peptide in experimental models focused on energy regulation and systemic adaptation. Consequently, these models help scientists study how melanocortin signaling participates in metabolic coordination and adaptive physiological regulation.
Researchers also explore Melanotan II peptide in neurobiological settings that examine central nervous system signaling and behavioral regulation pathways. In these contexts, experimental research investigates how melanocortin-related signals integrate with neuroendocrine communication networks.
Public scientific databases, including PubChem, provide biochemical and molecular reference data for Melanotan II peptide. Accordingly, researchers rely on these standardized resources when designing experimental protocols and validating laboratory research data.
Research handling and laboratory use
Laboratories handle Melanotan II peptide exclusively in controlled research environments. Additionally, proper storage conditions and standardized handling procedures help maintain peptide stability and integrity. In turn, consistent laboratory protocols support reliable and reproducible research outcomes.
Therefore, all research involving Melanotan II peptide remains limited to laboratory and experimental research models. Accordingly, these activities do not include clinical, cosmetic, therapeutic, or diagnostic use.
Important Notice
This product is intended exclusively for laboratory and scientific research purposes.
Not intended for human or veterinary use.
Not intended for diagnostic, therapeutic, cosmetic, or clinical applications.
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Compound
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Melanotan II
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Chemical name
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[Cys⁴, D-Phe⁷]-α-melanocyte-stimulating hormone (α-MSH) analog
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Quantity
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10mg
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Form
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Lyophilized peptide powder
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Purity
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High-purity research grade
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Packaging
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Glass vial with sterile closure
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Storage conditions
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Store lyophilized at 2–8 °C. Keep desiccated and protected from light.
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Molecular formula
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C₅₀H₆₉N₁₅O₉S₂
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Molecular weight
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≈ 1024.2 g/mol
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Sequence
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Ac-Nle-Asp-His-D-Phe-Arg-Trp-Lys-Cys-Pro-Asp-Gly-Ala-NH₂
(cyclic α-MSH analog)
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CAS Number
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121062-08-6
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