Taiy Chemical
(Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3
Synonym (Des-Cys3,Nle4,D-Arg5,D-2-Nal7,Cys11)-α-MSH (3
Species Human
Protein Accession P01193
Purity ≥ 95%
Endotoxin Level < 1.0 EU per µg
Biological Activity N/A
Expression System Chemical Synthesis
Fusion Tag None
Predicted Molecular Mass 2897.4 Da
Formulation Lyophilized from a 0.2 µm filtered solution in Acetonitrile and TFA
Reconstitution Reconstitute in water to a concentration of 0.1-1.0 mg/ml.
Storage & Stability Store at -20°C. Use within 12 months.
FAQ
What is (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) and what are its primary uses?

(Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) is a synthetic analog of the alpha-melanocyte-stimulating hormone, commonly abbreviated as α-MSH. This compound is specifically designed to mimic the effects of the natural α-MSH peptide, which is a key player in the regulation of skin pigmentation among other physiological roles. The primary use of this analog is in research settings where scientists are interested in exploring its potential beyond its natural functions. For example, in the context of skin research, it is utilized to understand the mechanisms behind pigmentation, such as how the melanin production pathways are activated in skin cells. This type of research can lead to the development of therapies for conditions like vitiligo or hyperpigmentation disorders.

Additionally, there are investigations into its potential in influencing energy homeostasis and appetite regulation, as α-MSH is known to be involved in these processes as well. Studies are aimed at understanding how manipulating this pathway could contribute to novel treatments for obesity and metabolic disorders. Another promising area of research is its anti-inflammatory properties. α-MSH and its analogs have been shown to exhibit immunomodulatory effects which could be harnessed in treating inflammatory diseases or autoimmune conditions. However, it is important to note that while these research pathways are promising, the compound is currently not approved for therapeutic use in humans and is still undergoing extensive study to better understand its full range of biological activities and potential benefits.

How does (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) interact with melanocortin receptors?

The mechanism of action of (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) largely centers around its interaction with melanocortin receptors, specifically the melanocortin-1 receptor (MC1R) which is predominantly expressed in melanocytes—the cells responsible for producing the pigment melanin. Binding of this synthetic analog to MC1R mimics the effect of natural α-MSH and stimulates a signaling cascade involving the activation of adenylate cyclase, increasing levels of cyclic AMP (cAMP), and ultimately leading to the enhanced synthesis of melanin. This signaling pathway is crucial for the process of melanogenesis and the resulting skin pigmentation, providing insights into how pigmentation can be modulated at a cellular level.

In addition to MC1R, (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) may also interact with other melanocortin receptors such as MC3R and MC4R, which are involved in regulating energy balance and appetite. Researchers are actively exploring how these interactions can influence body weight regulation and energy homeostasis. The binding affinity and selectivity of the analog for different melanocortin receptors are critical parameters that determine its potential applications and effectiveness in various research contexts. Understanding these properties helps in enhancing its specificity for desired receptors while minimizing potential off-target effects.

Furthermore, the compound's interaction with melanocortin receptors extends to its anti-inflammatory effects. By engaging these receptors, (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) can exert an anti-inflammatory response through the inhibition of pro-inflammatory cytokines, a feature that is particularly intriguing for the potential treatment of inflammatory conditions. Clinical research is ongoing to fully elucidate these interactions and develop therapeutic strategies that can target specific pathways with minimal side effects.

Are there any safety concerns or side effects associated with the use of (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3)?

While (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) is primarily used in research studies and not for direct clinical applications, understanding its safety profile is essential for both research purposes and potential future therapeutic use. Generally, the safety concerns associated with this compound are often deduced from the known effects of its natural counterpart, α-MSH, and the broader family of melanocortin analogs.

The most notable side effect related to melanocortin analogs, including α-MSH, is the potential for skin pigmentation changes. This is because one of the primary actions of α-MSH is the increased production of melanin, leading to a darker skin tone. For individuals using this compound, particularly in research settings that involve topical or systemic application, such pigmentation changes can be prominent and should be closely monitored. Participants in such studies may also experience local erythema or redness at the site of application or injection, which generally subsides without intervention.

Systemic administration of melanocortin analogs can also lead to other effects, given the involvement of melanocortin receptors in various physiological processes. For instance, activation of melanocortin-4 receptors is known to influence appetite and energy expenditure, so users might encounter changes in appetite or weight. Additionally, there may be cardiovascular effects given the role of these peptides in modulating blood pressure and heart rate through central nervous system pathways.

It is essential for researchers to adhere to stringent ethical and safety guidelines when using (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) in studies, ensuring that subjects are fully informed of potential risks and side effects and that appropriate monitoring is in place. Any adverse events or unexpected responses need thorough investigation and documentation, contributing to a better understanding of the compound’s safety profile and guiding responsible utilization in subsequent research phases.

What are the research implications of (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) on metabolic disorders?

(Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) has significant implications in the research of metabolic disorders due to its interaction with the melanocortin system, which plays a critical role in energy balance regulation and body weight homeostasis. In particular, this synthetic analog is an important tool in exploring the pathways mediated by the melanocortin-4 receptor (MC4R), which is extensively studied for its influence on appetite control and metabolism. Dysregulation of the MC4R pathway is implicated in various metabolic conditions, including obesity, which is a growing global health concern.

Research utilizing (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) in animal models can help elucidate these pathways and identify how modulation of MC4R activity might contribute to preventing or managing obesity. By identifying the specific receptor interactions and downstream signaling events triggered by this analog, researchers can gain insights into the appetite-suppressing effects of melanocortin activation and how these might be harnessed therapeutically. Additionally, understanding the precise mechanisms of action can lead to the development of more potent and selective compounds with improved efficacy and reduced side effects for addressing obesity and related disorders.

Beyond obesity, the research on this analog is also crucial in understanding conditions like cachexia, a wasting syndrome often observed in chronic illnesses such as cancer, where maintaining a healthy body weight becomes challenging due to dysregulated metabolic processes. Here, the modulatory effects of melanocortin analogs on energy homeostasis present an opportunity to develop supportive treatments that help manage weight and overall patient well-being.

Overall, the implications for research on metabolic disorders using (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) are expansive, providing vital information that could lead to novel interventions in metabolic disease management. Ongoing and future studies are expected to continue unraveling the complex interplay between melanocortin receptors and metabolic regulation, ultimately informing the development of new therapies aimed at tackling these prevalent health challenges.

In what ways could (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) contribute to skin health advancements?

(Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) could play a transformative role in advancing skin health by providing insights into the regulation of skin pigmentation and its broader implications. As this analog significantly influences melanogenesis through its action on melanocortin receptors, it becomes an essential tool for understanding and potentially manipulating pigmentation processes for therapeutic purposes. For example, skin disorders such as vitiligo, which result in the depigmentation of skin, could benefit from therapies derived from research involving this compound by promoting repigmentation through targeted stimulation of melanocytes.

Moreover, this analog's potential in dermatology extends beyond pigmentation. It could offer protective effects against ultraviolet (UV) radiation damage due to its role in enhancing melanin production; melanin is a natural protector against UV-induced damage, reducing the risk of skin cancers and the premature aging effects of photooxidative stress. Researchers working with this compound in experimental models can explore its efficacy in inducing a protective tan without the harmful effects associated with UV exposure, a concept that might translate into preventative dermatological therapies.

Another promising research avenue is its potential anti-inflammatory properties. (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) mimics the natural α-MSH’s ability to modulate inflammatory responses, which is hugely beneficial in treating inflammatory skin conditions such as eczema and psoriasis. By attenuating inflammation, this analog could aid in reducing the symptoms and improving the quality of life for individuals affected by such chronic skin disorders.

Lastly, since skin health is closely connected to overall health, the understanding and application of knowledge gained from studies using this peptide could unravel broader physiological impacts related to immune function and systemic inflammation. While a lot of this potential remains to be fully understood, ongoing research continues to broaden our understanding of how synthetic analogs like (Deamino-Cys3,Nle4,Arg5,D-2-Nal7,Cys11)-α-MSH (3) can be integrated into comprehensive skincare strategies that promote both dermatological and general health.
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