CAS 7561-51-5
:L-Proline, L-prolylglycyl-
Description:
L-Proline, L-prolylglycyl- is a dipeptide composed of the amino acids L-proline and glycine. It is characterized by its unique structure, where L-proline, a cyclic amino acid, contributes to the stability and rigidity of the peptide chain. This dipeptide is known for its role in protein synthesis and its potential influence on various biological processes, including collagen formation and cellular signaling. L-Proline itself is non-polar and hydrophobic, which can affect the solubility and interaction of the dipeptide in aqueous environments. The CAS number 7561-51-5 identifies this specific compound, facilitating its recognition in chemical databases. L-Proline, L-prolylglycyl- may exhibit biological activity, making it of interest in pharmaceutical and nutritional research. Its properties, such as melting point, solubility, and reactivity, can vary based on environmental conditions and the presence of other compounds. Overall, this dipeptide serves as a valuable subject for studies in biochemistry and molecular biology.
Formula:C12H19N3O4
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Found 4 products.
H-Pro-Gly-Pro-OH
CAS:H-Pro-Gly-Pro-OH (PGP) is a tripeptide generated from the breakdown of extracellular matrix collagen and is specifically chemotactic for neutrophils in vitro and in vivo. Ac-PGP generated by N-terminal acetylation of PGP can enhance this chemotactic potential. PGP was identified as physiological substrate for the aminopeptidase activity of leukotriene A4 hydrolase. PGP is a biomarker for chronic obstructive pulmonary disease (COPD).Formula:C12H19N3O4Purity:95.7%Molecular weight:269.3H-Pro-Gly-Pro-OH
CAS:<p>H-Pro-Gly-Pro-OH is a peptide that is derived from the sequence of human proline-glycine-proline (HGP). It has been shown to have a number of physiological activities, including anti-inflammatory effects. This peptide can be used as a model compound for inflammatory genes and proteins. H-Pro-Gly-Pro-OH has been shown to inhibit the synthesis of inflammatory cytokines in mouse splenocytes and neutrophil recruitment in wild type mice. HGP also suppresses chemotactic activity and inhibits neutrophil migration in an experimental model. HGP has also been shown to reduce intracellular calcium concentration in cerebellar granule cells, which may be due to its ability to inhibit protein synthesis.</p>Formula:C12H19N3O4Purity:Min. 95%Molecular weight:269.3 g/mol
