CAS 128802-77-7

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

Description:

L-Phenylalaninamide, N-(3-carboxy-1-oxopropyl)-L-alanylglycyl-L-prolyl-N-(4-nitrophenyl)-, with the CAS number 128802-77-7, is a synthetic compound that belongs to the class of peptides and amides. This substance features a complex structure characterized by the presence of multiple amino acid residues, including phenylalanine, alanine, glycine, and proline, which contribute to its biological activity. The compound contains a nitrophenyl group, which may impart specific electronic properties and enhance its reactivity. Its carboxylic acid functional group suggests potential for interactions in biochemical pathways, possibly influencing enzyme activity or protein synthesis. The presence of the amide bond indicates stability against hydrolysis compared to free amino acids. This compound may be of interest in pharmaceutical research, particularly in the development of peptide-based therapeutics or as a biochemical probe. However, detailed studies on its pharmacokinetics, toxicity, and specific biological functions would be necessary to fully understand its potential applications.

Formula: C₂₉H₃₄N₆O₉

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

CAS: 128802-77-7

Formula: C₂₉H₃₄N₆O₉

Molecular weight: 610.6151

Ref: IN-DA000YEC

Suc-Ala-Gly-Pro-Phe-pNA

CAS: 128802-77-7

Suc-Ala-Gly-Pro-Phe-pNA is an amide that has been synthesized for the stabilization of proteins, peptides and nucleic acids. It has shown to be effective in preventing isomerization of casein and phosphatase (casein kinase II) by stabilizing the alpha helix structure. Suc-Ala-Gly-Pro-Phe-pNA also prevents fk506 binding to endoplasmic reticulum protein tyrosine kinases and isomerizes tyrosine to phenylalanine. The tetrapeptide sequence has been shown to be similar to sequences found in cellular proteins. This compound is a synthetic analog of the natural amino acid proline and can be used as a substitute in peptides or nucleotide sequences, due to its ability to stabilize these molecules against proteolysis or hydrolysis.

Formula: C₂₉H₃₄N₆O₉

Purity: Min. 95%

Molecular weight: 610.62 g/mol

Ref: 3D-FS110761