Taiy Chemical
Acetyl-α-MSH (11-13)
Synonym Ac-α-MSH (11-13)
Species Human
Protein Accession N/A
Purity ≥ 95%
Endotoxin Level < 1.0 EU/µg
Biological Activity N/A
Expression System Chemical synthesis
Fusion Tag Acetyl
Predicted Molecular Mass 619.66 Da
Formulation Lyophilized from a 0.1% TFA in H2O
Reconstitution Centrifuge vial before opening. Reconstitute in sterile, non-adhesive polypropylene vial
Storage & Stability Lyophilized product is stable at room temperature for up to 3 weeks. Store reconstituted product at -20°C
FAQ
What is Acetyl-α-MSH (11-13), and how does it work?

Acetyl-α-MSH (11-13) is a synthetic peptide segment derived from the naturally occurring melanocyte-stimulating hormones (MSH), particularly the short sequence from positions 11 to 13. These hormones are part of the larger class of melanocortins, peptides involved in a variety of physiological functions such as pigmentation, energy homeostasis, and appetite regulation. The specific sequence 11-13 refers to a subset of amino acids within the larger alpha-MSH peptide, and the acetylation of this sequence is believed to enhance certain biological activities, such as binding affinity and stability.

The way Acetyl-α-MSH (11-13) works is largely through its interaction with melanocortin receptors, especially MC1R and MC4R, which are distributed in different tissues throughout the body. Upon binding to these receptors, Acetyl-α-MSH (11-13) can trigger a cascade of intracellular events that lead to diverse outcomes based on the type of receptor and tissue involved. For instance, at MC1R located primarily in the skin, this peptide can stimulate melanogenesis, leading to increased melanin production and thus affecting pigmentation processes. Meanwhile, interaction with MC4R, which is also expressed in the brain, can influence energy balance and food intake. The peptide’s precise mechanisms can vary, invoking secondary messengers like cAMP and activating different signaling pathways depending on the targeted receptor.

The peptide's ability to predominantly function through these receptor-mediated interactions makes it an interesting focus for research, with potential applications not only in dermatology but also in areas such as metabolic functions and even immunomodulation. Scientists are exploring how modifications, such as acetylation, can be optimized to develop more effective therapeutic agents with minimized side effects. Given these diverse capabilities, Acetyl-α-MSH (11-13) is a promising candidate for a wide range of biotechnological and therapeutic applications, although precise outcomes depend significantly on dosage, method of delivery, and receptor selectivity.

What are the potential benefits of using Acetyl-α-MSH (11-13)?

Acetyl-α-MSH (11-13) offers a range of potential benefits largely due to its activity at melanocortin receptors, which play variegated roles in the human body. One of the primary benefits is its role in skin pigmentation. By interacting with MC1R on melanocytes, it can stimulate melanin production, thus enhancing pigmentation. This feature not only offers cosmetic benefits, potentially providing a sunless tanning effect but also serves a protective role, as melanin can absorb harmful UV radiation. The use of this peptide could be beneficial as a protective agent against UV-induced damage or in conditions where increased pigmentation is desired, such as in vitiligo treatment or depigmentation issues.

Beyond skin applications, Acetyl-α-MSH (11-13) could provide benefits in energy metabolism and weight management. Its action at the MC4R in particular is associated with the regulation of food intake and energy homeostasis. Studies suggest that stimulation of this receptor can lead to decreased appetite and increased energy expenditure, which might be leveraged in developing treatments for obesity or metabolic disorders.

Moreover, there is emerging interest in its potential anti-inflammatory and immunomodulatory effects. Melanocortins, in general, have been associated with exerting anti-inflammatory actions, and while the specific effects of the (11-13) sequence are still under research, there's potential for this peptide to influence inflammatory pathways. This opens avenues for its possible use in managing inflammatory or autoimmune conditions.

Furthermore, because melanocortins can affect neurological functions, Acetyl-α-MSH (11-13) might also impart cognitive or neuroprotective benefits. While preliminary, some research does focus on the role of melanocortin peptides in neurodegenerative diseases or brain injuries, exploring their capacity to potentially support neuronal health.

These conceptual benefits mean that Acetyl-α-MSH (11-13) is under considerable scientific investigation. While promising, it's essential that these potential applications are backed by rigorous clinical studies to establish safety and efficacy; thus, it’s mostly being explored in controlled research settings rather than widespread clinical practice currently.

Are there any risks or side effects associated with Acetyl-α-MSH (11-13)?

While Acetyl-α-MSH (11-13) holds promise for various therapeutic applications, as with any bioactive peptide, its use could present certain risks and side effects. Understanding these potential adversities is crucial for safely harnessing its benefits. The primary area of concern arises from its interaction with melanocortin receptors, which are involved in multiple physiological systems.

One immediate concern is the peptide’s effect on pigmentation. While increased melanin production can be beneficial and desirable in some contexts, it may not be suitable for everyone. Enhanced pigmentation can lead to hyperpigmentation issues, especially in individuals prone to such conditions. Additionally, uneven distribution of pigmentation effects could result, depending on where and how the peptide is administered.

From a systemic standpoint, potential issues could also arise from its impacts on the central nervous system. Since melanocortin receptors like MC4R are involved in regulating appetite and energy expenditure, there’s a possibility for unintended effects on eating behaviors. In theory, overstimulation of these receptors could lead to anorexia or other appetite-related disorders, although such outcomes would typically depend on dosage and individual susceptibility.

Furthermore, the peptide’s potential anti-inflammatory effects also need careful management. While reducing inflammation is often desired, improper or excessive modulation of the immune response could render a person more susceptible to infections or negatively affect wound healing processes.

Another aspect to consider is the risk of allergic reactions or hypersensitivity, which is inherent in any biologically active peptide therapy. The possibility of developing antibodies against the peptide could also diminish its efficacy over time or lead to adverse immunological responses.

Importantly, these risks highlight the necessity for controlled use within research settings where dosages are carefully calibrated. Researchers aim to tailor acetylation and other modifications to enhance the peptide’s profile for therapeutic use while minimizing its side effects. As with any investigational compound, extensive clinical trials are essential to evaluate safety comprehensively. It's worth noting that comprehensive safety data and guidelines should be followed if Acetyl-α-MSH (11-13) transitions into broader clinical applications from the research-focused interest it currently garners.

How does Acetyl-α-MSH (11-13) compare to other melanocyte-stimulating hormones?

Acetyl-α-MSH (11-13) is a distinct yet related derivative within the family of melanocyte-stimulating hormones, known as melanocortins. Understanding how it compares with other members of this family involves examining its biochemical uniqueness and functional specificity. Melanocyte-stimulating hormones such as alpha-MSH, beta-MSH, and gamma-MSH are naturally occurring peptides that play crucial roles in regulating pigmentation, energy homeostasis, and immune responses by binding to melanocortin receptors located throughout the body.

The key difference between Acetyl-α-MSH (11-13) and its larger counterparts lies in its peptide structure and the effect of acetylation. While alpha-MSH is itself a segment of the larger proopiomelanocortin (POMC) polypeptide chain, Acetyl-α-MSH (11-13) is a shortened, acetylated form. Acetylation can enhance peptide stability and receptor binding affinity, potentially offering more potent or prolonged effects compared to non-acetylated forms.

Functionally, while alpha-MSH (the full-length version) acts broadly across several melanocortin receptors and has a well-characterized role in skin pigmentation and anti-inflammatory activity, Acetyl-α-MSH (11-13) might offer a more targeted approach with distinct biochemical properties. The precise impacts of such peptides can vary based on their receptor selectivity. For example, some derivatives might show higher affinity for certain receptor subtypes, influencing pigmentation more than metabolism or vice versa.

In terms of therapeutic exploration, the specific characteristics of Acetyl-α-MSH (11-13) might offer advantages in areas like receptor selectivity or bioavailability that could make it preferable in certain settings, such as dermatological applications where targeted action and minimized systemic activity are desirable. Comparatively, full-length MSH might be more broadly effective but also more likely to cause systemic effects.

Overall, while all melanocyte-stimulating hormones share common biological terrains—such as affecting pigmentation and metabolism—the nuances in their molecular structures mean that Acetyl-α-MSH (11-13) could potentially be optimized for specific therapeutic functions with distinct safety and efficacy profiles. The ongoing research seeks to establish these comparisons more robustly, aiming to tap into benefits that might not be as achievable with the naturally occurring full-length peptides.

What current research exists on Acetyl-α-MSH (11-13), and what does it focus on?

Current research on Acetyl-α-MSH (11-13) explores its potential across various biomedical domains, driven by its activity at melanocortin receptors and the promise of acetylation-enhanced efficacy. This peptide’s unique ability to modulate pigmentation, energy metabolism, and immune responses positions it as a subject of interest for several therapeutic applications.

One prominent focus of research is the dermatological application of Acetyl-α-MSH (11-13), particularly its potential as a tanning agent or for treating pigmentary disorders like vitiligo. Scientists are examining how this peptide can effectively increase melanin production with the intent to provide safe and controlled pigmentation in clinical scenarios. Such studies are significant because they help establish parameters, such as dosage and delivery methods, optimizing the peptide for desirable cosmetic outcomes without adverse side effects.

Another active area of research is on its metabolic effects, especially concerning weight management and appetite regulation. Given its action on MC4R, studies aim to evaluate the peptide’s influence on energy balance and food intake, which could translate to novel treatments for obesity or metabolic syndromes. Animal and early phase human trials might assess changes in metabolic rate, energy expenditure, and appetite following treatment with Acetyl-α-MSH (11-13), providing insights into its potential clinical utility in metabolic disorders.

Additionally, research is exploring its immunomodulatory properties. There is interest in understanding how Acetyl-α-MSH (11-13) can modulate inflammatory processes, with animal models often employed to assess its effectiveness in conditions characterized by excessive inflammation or immune dysregulation.

The exploration into neurological impacts—potential cognitive or neuroprotective benefits related to its interaction with brain-expressed melanocortin receptors—is another intriguing angle. Such studies might investigate the peptide’s effects in neurodegenerative diseases or cognitive disorders, assessing neuroprotection, synaptic plasticity, or overall brain health impacts.

Overall, current research is heterogeneous, spanning preclinical trials and some early-stage clinical investigations. Researchers strive to translate the promising biological mechanisms observed in vitro and animal models into tangible clinical therapies. However, each application requires careful evaluation through comprehensive studies to ascertain safety, efficacy, and long-term outcomes. This expanding body of research aims to unlock therapeutic avenues and refine the application landscape for Acetyl-α-MSH (11-13) through rigorous scientific inquiry.
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