Synonym |
Ac-Cys-D-2-Nal-Cys-MSH(11-22) |
Species |
Human |
Protein Accession |
P41159 |
Purity |
≥ 95% |
Endotoxin Level |
< 1.0 EU per μg protein |
Biological Activity |
N/A |
Expression System |
Chemical Synthesis |
Fusion Tag |
None |
Predicted Molecular Mass |
2613.0 Da |
Formulation |
Lyophilized from a 0.1 μm filtered solution of 20% acetonitrile and 0.1% TFA |
Reconstitution |
Centrifuge vial before opening. Reconstitute in 20 mM Tris, 150 mM NaCl, pH 7.5 to a
concentration of 0.1-1.0 mg/ml |
Storage & Stability |
Store at -20°C upon receipt. Recommend to aliquot the reconstituted protein for optimal storage.
|
FAQ
What is Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami and how does it work?
Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami is a modified peptide sequence derived from the
natural β-Melanocyte Stimulating Hormone (β-MSH). It is designed to mimic certain effects of the native
peptide by binding to melanocortin receptors, particularly the MC1R and MC4R receptors. These receptors
are part of the G protein-coupled receptor superfamily, which play crucial roles in numerous
physiological processes including pigmentation, energy homeostasis, inflammation, and neural functions.
The modifications in its structure, such as the acetylation and the presence of D-amino acids,
contribute to an increased biological stability and resistance to enzymatic degradation. This allows the
peptide to maintain its activity over a prolonged period compared to its natural counterpart. By
focusing on specific receptors, it can elicit powerful effects potentially useful in therapeutic
applications like weight management, anti-inflammatory responses, or neurological health.
Can
Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami be used for weight management or metabolic conditions?
Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami holds a promising aspect for use in weight
management or metabolic conditions, primarily because of its interaction with the melanocortin system.
The MC4R receptor, in particular, is central to the regulation of energy balance and appetite.
Activation of this receptor can suppress food intake and increase energy expenditure, making it a target
for anti-obesity therapies. Experimental studies indicate that modulating this pathway by using agonists
like Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami could help restore the balance in individuals with
obesity and metabolic syndrome. However, it's important to recognize that while these findings are
promising, most have been conducted in preclinical models, and comprehensive human studies are
essential. Understanding the precise dosing, long-term effects, and safety profile remains crucial
before this peptide can be considered a viable treatment option for metabolic issues.
What
potential therapeutic benefits could Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami provide beyond
pigmentation and metabolism?
The potential therapeutic benefits of
Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami extend beyond pigmentation and metabolic regulation,
owing to the widespread presence and multifaceted roles of melanocortin receptors throughout the body.
In immune response and inflammatory processes, melanocortin peptides are known to exhibit
anti-inflammatory properties. Therefore, Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami, by targeting
these receptors, may help modulate immune responses, potentially offering therapeutic benefits in
conditions marked by chronic inflammation, such as autoimmune diseases or allergies. Moreover, this
peptide could hold neuroprotective potential. The nervous system expresses melanocortin receptors, where
their activation is linked to neuronal health, influencing processes such as neurogenesis, synaptic
plasticity, and neural repair mechanisms. This suggests a possibility of utilizing such peptides in
treating neurodegenerative disorders or brain injuries. It's crucial to continue research to delineate
these potential benefits, focusing on the peptide's action mechanisms, efficacy, and safety in such
therapeutic contexts.
Are there any known side effects or risks associated with using
Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami?
As with any bioactive compound, assessing the
safety profile of Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami is critical. Current scientific
investigations aim at thoroughly understanding both its therapeutic potential and any potential adverse
effects. In general, the known risks linked to peptides interacting with the melanocortin system can
range from mild to significant, contingent on the dosage, individual metabolic responses, and the
duration of administration. Some peptides in this class have been noted to cause changes in blood
pressure, alterations in appetite or mood, and potential pigmentation changes, given their action on
melanocortin receptors. Therefore, while Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami might present
some similar risks, precise side effects and safety margin specifics would require robust clinical
trials to establish. Researchers emphasize a cautious approach, ensuring that comprehensive risk
assessments and monitoring accompany any therapeutic application.
How is
Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami synthesized, and how does this process ensure its
efficacy and safety?
The synthesis of Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami involves
complex processes typical of peptide synthesis, specifically leveraging solid-phase peptide synthesis
(SPPS). This method allows for the precise assembly of peptide chains by sequentially adding activated
amino acids to a growing chain anchored to a solid resin. The incorporation of specific modified amino
acids like D-2-Nal (2-naphthylalanine) and acetylation at defined positions tailors the peptide’s
bioactivities, granting it enhanced stability and targeted receptor binding. During synthesis, rigorous
purification techniques such as high-performance liquid chromatography (HPLC) are employed to isolate
the desired peptide with high purity, reducing the likelihood of impurities that may affect efficacy or
safety. Post-synthesis, detailed analytical verification follows, including mass spectrometry and amino
acid analysis, ensuring the peptide's integrity and correct molecular configuration. This meticulous
process is fundamental to producing a peptide that is not only effective in eliciting the desired
biological response but also safe for potential future therapeutic application.
Where is the
research currently heading with Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami in clinical therapies?
The trajectory of research concerning Acetyl-(Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) ami is steering
towards detailed clinical exploration and validation. Researchers are currently focused on delineating
its precise biological mechanisms of action and therapeutic windows in various conditions, including
metabolic disorders, inflammatory conditions, and potentially neurodegenerative diseases. These studies
are pivotal in providing a comprehensive understanding of its effect on specific melanocortin receptors,
which could translate into groundbreaking therapeutic approaches. Additionally, significant attention is
being placed on optimizing doses that maximize efficacy while minimizing any adverse effects. As
research advances, clinical trials will likely emerge as the next step, assessing its safety,
tolerability, and therapeutic outcomes in human subjects. Collaborative efforts across scientific
disciplines, including pharmacology, molecular biology, and clinical medicine, are crucial in driving
this promising peptide from the laboratory bench towards real-world medical applications. The success of
such endeavors could potentially revolutionize the treatment landscapes for several challenging health
conditions.