Taiy Chemical
H-β-Ala-β-Ala-OH
Synonym H-β-Ala-β-Ala-OH
Species N/A
Protein Accession N/A
Purity ≥ 95%
Endotoxin Level <0.1 EU per 1 μg of protein
Biological Activity N/A
Expression System N/A
Fusion Tag N/A
Predicted Molecular Mass N/A
Formulation Supplied as a lyophilized powder
Reconstitution Reconstitute in water to a concentration of 0.1-1.0 mg/ml
Storage & Stability Store at -20°C. For long-term storage, store at -80°C. Once reconstituted, stable for up to one week at 2-8°C.
FAQ
What is H-β-Ala-β-Ala-OH, and how is it relevant in modern scientific applications?
H-β-Ala-β-Ala-OH, commonly referred to as beta-alanine-beta-alanine, is a dipeptide compound formed by the linkage of two beta-alanine molecules. Beta-alanine, a naturally occurring beta-amino acid, is noted for its role in the biosynthesis of dipeptides like carnosine and anserine, which are significantly important in muscle performance and endurance. This dipeptide structure is interesting for researchers and industry professionals because it serves as a model compound to study peptide bonds and their biochemical properties. In modern scientific applications, H-β-Ala-β-Ala-OH is invaluable for its diverse roles, ranging from pharmaceutical development to biochemical research.

Biochemically, understanding the properties of H-β-Ala-β-Ala-OH can yield insights into how peptides function at a molecular level, offering a scaffold to explore other more complex compounds. Researchers may use this dipeptide for determining how similar peptides can be synthesized, helping to elucidate the pathway of peptide synthesis both in synthetic environments and within biological systems. Its simplicity compared to larger biomolecules allows it to be a suitable candidate for computational studies to predict peptide behavior and interactions with other molecules, which is crucial in designing bioactive compounds or drugs.

In pharmaceutical science, H-β-Ala-β-Ala-OH's role is particularly noted in the development of delivery systems for peptides and the potential modification of peptide-drug conjugates. With the understanding gained from studying such compounds, it becomes possible to better design peptides as therapeutic agents that maintain stability and efficacy, making it a subject of great interest for drug delivery applications. Furthermore, understanding the stability, solubility, and reactivity of simple dipeptides like H-β-Ala-β-Ala-OH provides foundational knowledge that can be adapted to more intricate pharmaceutical compounds.

Moreover, H-β-Ala-β-Ala-OH helps in the study of enzyme activity and the role peptides play in enzymatic processes, which are pivotal in the pharmaceutical industry's search for novel enzyme inhibitors or activators. Notably, beta-alanine residues in peptides are researched for their potential antioxidative and antiaging properties, enhancing their appeal in health-related applications. Thus, H-β-Ala-β-Ala-OH encapsulates a small yet highly potent area of study that contributes significantly to advancing biochemistry and pharmacology.

What are the primary research areas benefiting from studies on H-β-Ala-β-Ala-OH?
Research on H-β-Ala-β-Ala-OH primarily benefits several key areas: peptide synthesis, pharmaceutical development, enzymology, and molecular biology. In peptide synthesis, this dipeptide is a critical component in understanding peptide bond formation, an essential aspect of both chemical and enzymatic peptide synthesis. Researchers leverage H-β-Ala-β-Ala-OH as a model to study various synthesis techniques, including solid-phase synthesis methods and enzymatic approaches, which are pivotal in manufacturing peptides and proteins for a variety of applications.

In pharmaceutical developments, H-β-Ala-β-Ala-OH is instrumental in studying the creation of peptide-based drugs. These studies explore the potential for peptides to act as drugs themselves or to be used in drug-delivery systems. Peptides offer numerous advantages as therapeutic agents due to their biochemical characteristics, including high specificity and low toxicity. Studying simple peptides like H-β-Ala-β-Ala-OH helps researchers understand how to improve peptide stability and efficacy in vivo, leading to the development of more robust peptide therapeutics.

Enzymology also benefits significantly, as H-β-Ala-β-Ala-OH allows scientists to model the substrates and mechanisms of action for a variety of enzymes. By examining how this dipeptide interacts with specific enzymes, researchers can gain insights into enzyme specificity and catalytic processes. This knowledge is fundamental in the design of enzyme inhibitors or activators, which can serve as therapeutic agents themselves or as tools for further biochemical research.

Moreover, molecular biology research utilizes H-β-Ala-β-Ala-OH as a model compound to elucidate how peptides interact at the cellular level, which can inform studies on cell signaling, protein folding, and gene expression regulation. By understanding these interactions, scientists can better comprehend how cells use peptides in everyday functions, contributing to innovations in synthetic biology and medicine.

Finally, H-β-Ala-β-Ala-OH is used in studies focused on understanding peptide degradation and stability. These insights help in the design of peptides with enhanced longevity and activity, crucial for their use in drug development and nutritional supplements. Collectively, research on H-β-Ala-β-Ala-OH impacts a variety of scientific domains by improving our understanding of peptide chemistry, broadening the potential for therapeutic innovations, and enhancing biochemical research methodologies.

How is the stability of H-β-Ala-β-Ala-OH evaluated, and why is this important?
Evaluating the stability of H-β-Ala-β-Ala-OH is a crucial aspect of its research and application. Stability studies typically involve examining how this compound reacts under various environmental conditions, such as changes in temperature, pH, light exposure, and in the presence of enzymes or other reactive compounds. These studies are vital because they provide information about the dipeptide's shelf-life, reactivity potential, and suitability for various industrial and research applications.

One common method to evaluate stability is through accelerated aging tests, where H-β-Ala-β-Ala-OH is subjected to elevated temperatures and humidity levels for an extended period. The compound is then analyzed using techniques like high-performance liquid chromatography (HPLC) to detect any degradation products that may have formed. This allows researchers to predict the compound's shelf-life and to understand how storage conditions could affect its integrity. Additionally, assessing stability in different pH environments can reveal how H-β-Ala-β-Ala-OH might behave in the stomach or bloodstream, informing its potential as a drug or a dietary supplement.

Thermal analysis, such as differential scanning calorimetry (DSC), can be used to identify the temperature at which the compound degrades. This is particularly important in manufacturing processes where temperature control is necessary to maintain the integrity of H-β-Ala-β-Ala-OH. Light exposure tests can determine the compound's photo-stability, which is essential for understanding if special packaging is required to protect it from light-induced degradation.

Moreover, enzyme stability tests are imperative when evaluating potential uses of H-β-Ala-β-Ala-OH in biological settings. These tests can determine how enzymes present in the human body or in other living organisms might interact with the compound, further influencing its effectiveness and longevity when used in therapeutic applications.

Understanding the stability of H-β-Ala-β-Ala-OH is important for several reasons. First, it aids in the formulation of pharmaceuticals, ensuring efficacy and safety throughout a drug's shelf-life. Second, it helps in the design of peptide-based products, such as nutritional supplements, where stability can affect product quality and consumer safety. Lastly, stability information is essential in research and development settings, where reproducibility of results is dependent on the consistent quality of the compounds used.

What are the challenges in synthesizing H-β-Ala-β-Ala-OH, and how are they addressed?
Synthesizing H-β-Ala-β-Ala-OH presents several challenges typical of dipeptide synthesis, primarily centered around achieving high purity, efficiency, and yield. One of the main difficulties lies in ensuring the selective formation of the peptide bond between two beta-alanine molecules, as improper conditions can lead to unwanted byproducts or incomplete reactions. This necessitates the use of precise synthetic techniques and conditions, which can sometimes be resource-intensive and require stringent control.

A common method for synthesizing H-β-Ala-β-Ala-OH utilizes solution-phase peptide synthesis or solid-phase peptide synthesis (SPPS). In these methods, protecting groups are often employed to prevent undesirable reactions at functional sites. Choosing the appropriate protecting groups and deprotecting conditions is critical to the success of the synthetic procedure. These methods address the synthesis challenge by allowing chemists to build up the peptide in a controlled sequence of reactions, minimizing side-reactions and increasing yield.

Coupling reagents are also essential in facilitating the formation of peptide bonds. Selecting the right coupling reagent can address solubility issues and improve reaction efficiency, ultimately enhancing the overall yield of the desired dipeptide. The choice of solvents and purification methods, such as recrystallization or chromatographic techniques, further refines the purity of the final product. Advances in molecular techniques and equipment, including automated synthesizers, have significantly mitigated these challenges by enhancing the precision and reproducibility of peptide synthesis.

However, scale-up can still pose challenges when transitioning from laboratory-scale synthesis to industrial production. This often involves optimizing reaction conditions and purification processes to accommodate larger quantities without sacrificing quality. Addressing these issues may involve iterative cycles of chemical engineering and process optimization.

Overcoming these challenges has also been facilitated by advancements in computational chemistry, where predictive models assist in identifying optimal reaction pathways and conditions. This enables researchers to anticipate potential synthetic hurdles and adjust their strategies accordingly before commencing the actual lab work. Moreover, understanding the compound's stability and degradation pathways further informs synthesis and post-synthesis handling, ensuring that the compound retains its desired properties throughout its lifecycle.

Synthesis challenges are addressed by a combination of methodological innovations, precise control over reaction conditions, and iterative optimization strategies. Through the continual development of synthetic techniques and computational tools, the efficient and high-purity production of H-β-Ala-β-Ala-OH is becoming increasingly achievable.

What role does H-β-Ala-β-Ala-OH play in healthcare, and what are its potential benefits?
In healthcare, H-β-Ala-β-Ala-OH serves as a promising compound due to its potential applications in pharmaceuticals and nutraceuticals. Beta-alanine, the precursor of H-β-Ala-β-Ala-OH, is already recognized for its importance in muscle performance enhancement and endurance. When studied further for healthcare applications, H-β-Ala-β-Ala-OH offers a window into novel therapeutic avenues and health benefits.

H-β-Ala-β-Ala-OH might be investigated for its potential as an ingredient in supplements that aim to enhance athletic performance. By understanding its interaction within biological systems, researchers explore how such dipeptides can be metabolized into active forms like carnosine, which buffers acid in muscles, reducing fatigue and improving exercise performance. With precise insights from studies involving H-β-Ala-β-Ala-OH, supplements could be tailored more effectively to harness these benefits.

Furthermore, this compound's potential antioxidative properties can be explored for applications in combating oxidative stress-related diseases. Researchers are interested in how peptides like H-β-Ala-β-Ala-OH could inhibit oxidative processes at a cellular level, potentially contributing to the prevention or mitigation of conditions such as neurodegenerative diseases, cardiovascular disorders, and other age-related ailments.

Pharmaceutical applications may also benefit from H-β-Ala-β-Ala-OH when considering the development of peptide-based drugs. Its stability and potential solubility properties can inform the design of new therapeutic peptides that require longevity and bioavailability in the human body. This becomes increasingly valuable for chronic conditions where long-term drug exposure is necessary, and enhancing drug properties could significantly improve patient outcomes.

The study of H-β-Ala-β-Ala-OH extends into the realm of enzyme activity modulation. Researchers investigate how peptides can influence enzymes responsible for vital biological functions, which is critical in creating treatments that either impede or enhance specific enzymatic actions. This can include the development of enzyme inhibitors, which are used in various pharmacological treatments ranging from cancer to viral infections.

In healthcare, the potential benefits of H-β-Ala-β-Ala-OH are increasingly recognized through its contributions to athletic performance, its antioxidative properties, and its potential in drug development. As research advances, this compound may play a significant role in shaping future nutraceuticals and pharmaceuticals by offering enhanced efficacy, stability, and safety, ultimately leading to improved health outcomes.
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