In the expansive field of peptide chemistry, the ser phe dipeptide (L-Seryl-L-phenylalanine) stands out as a significant subject of study for researchers focused on molecular building blocks. As a enthusiast of biochemical research tools, I have found that understanding the nuances of these short-chain sequences is essential for anyone interested in the structural complexity of proteins.
Structural Characteristics and Chemical Identity
The ser phe dipeptide is defined by its molecular formula, C12H16N2O4, and is commonly referenced in databases like PubChem under CID 7009598. It is the N-(L-seryl) derivative of L-phenylalanine. When comparing it to its isomer, Phe-Ser (which is the N-(L-phenylalanyl) derivative of L-serine), we see distinct functional roles in metabolic pathways. Both represent essential dipeptides that serve as critical components in laboratory-grade peptide research.
From a structural perspective, these molecules are elegant in their simplicity. The SER (Serine) residue provides a polar, uncharged side chain, while the PHE (Phenylalanine) residue contributes a Fmoc-Phe-Ser(ψ Me,Me pro)-OH [878797-01-4] hydrophobic side chain. This combination allows for unique interactions. In my experience reviewing technical documentation, the molecular formula: C12H16N2O4 is a standard identifier used to ensure purity and consistency during procurement.
Technical Applications and Synthesis
My interest in this area often leads me to explore how these sequences are utilized in laboratory settings. For instance, H-Ser-Phe-OH is a polypeptide that can be found by peptide screening, and it is frequently used to understand how specific sequences interact with various receptors.
One specialized tool I have encountered is the pseudoproline dipeptide, specifically Fmoc-Phe-Ser(ψMe,Me pro)-OH. This compound is a sophisticated Fmoc-Phe-Ser(psi(Me,Me)pro)-OH is a dipeptide that researchers use to overcome aggregation challenges during solid H-Phe-Ser-OH is adipeptide. Para uso exclusivo en investigación. No vendemos a pacientes. Síntesis de péptidos personalizados. -phase synthesis. By utilizing this modified building block, chemists can significantly enhance the quality of the final peptide product. It is fasci Fmoc-Phe-Ser(psi(Me,Me)pro)-OH is a dipeptide. For research use only. We do not sell to patients. Custom Peptide Synthesis. Fmoc-Phe-Ser(psi(Me,Me)pro)-OH. nating to note how the self-assembly of short peptides into nanostructures is often driven by motifs like the Phenylalanylph Ser-Phe-OH | 化学物質情報 | J-GLOBAL 科学技術総合リンク enylalanine (Phe-Phe), which underscores why studying sequences like Ser-Phe is so vital for material science.
Comparative Insights
When evaluating these compounds, it is important to Synonym: Fmoc-Phe-Ser(ψ Me,Me pro)-OH CAS Number: [878797-01-4] Molecular Weight: 514.6 Molecular Formula: C 3 0 H 3 0 N 2 O 6 distinguish between various configurations. For example:
* Ser-Phe (H-Ser-Phe-OH) is distinct from H-Phe-Ser-OH is a dipeptide, which carries different biochemical properties.
* In some enzymatic studies, it is noted that both dipeptides have a C-terminal basic amino acid when they are part of longer chains, w The polar, uncharged amino acids serine (Ser, S), threonine (Thr, T), asparagine (Asn, N) and glutamine (Gln, Q) readily form hydrogen bonds with water and hich dictates how they are cleaved by enzymes like trypsin.
* Larger sequences, such as Arg-Ser-Phe, provide even deeper insights into how the addition of a basic amino acid residue alters the overall peptide conformation.
Practical Considerations for Research Use
When sourcing these materials, it is standard practice to rely on professional synthesis services. Many providers now offer comprehensive dipeptides and tripeptides synthesis services, allowing for the creation of specific sequences ranging from milligram to kilogram scales.
Whether you are investigating the Phe Ser motif or analyzing the linear formula: C6H5CH2CH(NH2)CONHCH(CH2C6H5)COOH · H2O associated with related phenylalanine sequences, the precision of the synthesis is paramount. It is vital to remember that these materials are strictly for research purposes—H-Phe-Ser-OH is a dipeptide intended for laboratory investigation, not for personal or human use.
Understanding the Phe and Ser interaction remains a cornerstone of my interest in peptide chemistry. By focusing on the structural integrity and the controlled synthesis of these dipeptides, researchers can continue to pu Ser-Phe is a dipeptide that is the N-(L-seryl) derivative of L-phenylalanine. It has a role as a metabolite. It is functionally related to a L-serine and a sh the boundaries of what is possible in the world of molecular science. Whether it is the Val Phe interactio by B Yan · 2014 · Cited by 46 — In this paper, the conformational preferences of the capped dipeptides Ac-Phe-Ser-NH 2 (FS) and Ac-Phe-Cys-NH 2 (FC) are resolved under laser-desorbed jet n or the specific Ser-Phe-OH configuration, each discovery adds a new layer to our understanding of the fundamental building blocks of biology.