CAS 128822-32-2

L-Phenylalaninamide,N-(3-carboxy-1-oxopropyl)-L-alanyl-L-tryptophyl-L-prolyl-N-(4-nitrophenyl)-

Description:

L-Phenylalaninamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-L-tryptophyl-L-prolyl-N-(4-nitrophenyl)-, identified by CAS number 128822-32-2, is a complex organic compound characterized by its multi-peptide structure. This substance features a combination of amino acids, including phenylalanine, alanine, tryptophan, and proline, which contribute to its potential biological activity. The presence of a nitrophenyl group suggests that it may exhibit unique electronic properties, possibly influencing its reactivity and interaction with biological targets. Additionally, the carboxylic acid functional group indicates potential for solubility in polar solvents and may play a role in its biological interactions. The compound's structure implies that it could be of interest in pharmaceutical research, particularly in the development of peptide-based therapeutics. However, specific characteristics such as solubility, stability, and biological activity would require empirical investigation to fully understand its potential applications and behavior in various environments.

Formula: C₃₈H₄₁N₇O₉

Suc-Ala-Trp-Pro-Phe-pNA

CAS: 128822-32-2

Suc-Ala-Trp-Pro-Phe-pNA is a cyclosporine analog that inhibits the activity of protein isomerases. It has been shown to inhibit the phosphatase activity of casein and stabilize peptide bonds in bovine serum albumin. Suc-Ala-Trp-Pro-Phe-pNA can also be used as a substrate for tyrosine kinase and amide bond formation. Suc-Ala-Trp-Pro-Phe-pNA is an inhibitor of FK506 binding to its receptor, which may be due to its ability to compete with tyrosine residues for binding sites. This compound also exhibits stabilization effects on protein structures by inhibiting the degradation of proteins by proteolytic enzymes or other chemical agents.

Formula: C₃₈H₄₁N₇O₉

Purity: Min. 95%

Molecular weight: 739.77 g/mol

Ref: 3D-FS110771