The chemical substance you mentioned, with the name "Glycine, glycyl-L-cysteinyl-L-lysyl-L-lysyl-L-tyrosyl-L-arginyl-L-arginyl-L-phenylalanyl-L-arginyl-L-tryptophyl-L-lysyl-L-phenylalanyl-L-lysylglycyl-L-lysyl-L-phenylalanyl-L-tryptophyl-L-phenylalanyl-L-tryptophyl-" and CAS number 1322711-38-5, is a complex peptide composed of various amino acids. It features a sequence that includes glycine, cysteine, lysine, tyrosine, arginine, phenylalanine, and tryptophan, indicating a diverse range of functional groups and properties. This peptide is likely to exhibit characteristics typical of proteins, such as the ability to form secondary structures (like alpha-helices and beta-sheets) due to hydrogen bonding between amino acids. Its hydrophilicity or hydrophobicity will depend on the specific arrangement and proportion of the amino acids present. Additionally, the presence of sulfur from cysteine may allow for disulfide bond formation, influencing the peptide's stability and conformation. Overall, this substance may have potential applications in biochemistry and pharmaceuticals, particularly in areas related to protein synthesis and function.

Glycine, glycyl-L-cysteinyl-L-lysyl-L-lysyl-L-tyrosyl-L-arginyl-L-arginyl-L-phenylalanyl-L-arginyl-L-tryptophyl-L-lysyl-L-phenylalanyl-L-lysylglycyl-L-lysyl-L-phenylalanyl-L-tryptophyl-L-phenylalanyl-L-tryptophyl-

1322711-38-5: The chemical substance you mentioned, with the name "Glycine, glycyl-L-cysteinyl-L-lysyl-L-lysyl-L-tyrosyl-L-arginyl-L-arginyl-L-phenylalanyl-L-arginyl-L-tryptophyl-L-lysyl-L-phenylalanyl-L-lysylglycyl-L-lysyl-L-phenylalanyl-L-tryptophyl-L-phenylalanyl-L-tryptophyl-" and CAS number 1322711-38-5, is a complex peptide composed of various amino acids. It features a sequence that includes glycine, cysteine, lysine, tyrosine, arginine, phenylalanine, and tryptophan, indicating a diverse range of functional groups and properties. This peptide is likely to exhibit characteristics typical of proteins, such as the ability to form secondary structures (like alpha-helices and beta-sheets) due to hydrogen bonding between amino acids. Its hydrophilicity or hydrophobicity will depend on the specific arrangement and proportion of the amino acids present. Additionally, the presence of sulfur from cysteine may allow for disulfide bond formation, influencing the peptide's stability and conformation. Overall, this substance may have potential applications in biochemistry and pharmaceuticals, particularly in areas related to protein synthesis and function.

<p>Pep19-2.5: Synthetic antitoxin peptide inhibits LP/LPS signals via PRRs, preventing inflammation and pyroptosis.</p>

CAS 1322711-38-5

Glycine, glycyl-L-cysteinyl-L-lysyl-L-lysyl-L-tyrosyl-L-arginyl-L-arginyl-L-phenylalanyl-L-arginyl-L-tryptophyl-L-lysyl-L-phenylalanyl-L-lysylglycyl-L-lysyl-L-phenylalanyl-L-tryptophyl-L-phenylalanyl-L-tryptophyl-

Pep19-2.5

Ref: TM-T76273