CAS 2646-64-2

Glycine, N-[N-[1-[N-[(phenylmethoxy)carbonyl]glycyl]-L-prolyl]-L-leucyl]-

Description:

The chemical substance known as Glycine, N-[N-[1-[N-[(phenylmethoxy)carbonyl]glycyl]-L-prolyl]-L-leucyl]- is a peptide derivative characterized by its complex structure, which includes multiple amino acid residues and a phenylmethoxycarbonyl (Pmc) protecting group. This compound is a synthetic peptide that incorporates glycine, proline, and leucine, which are essential amino acids contributing to its biological activity. The presence of the Pmc group suggests that this compound may be used in peptide synthesis, particularly for protecting the amino group during chemical reactions. Glycine, being the simplest amino acid, imparts flexibility to the peptide chain, while proline introduces a unique cyclic structure that can influence the peptide's conformation. The phenylmethoxy group enhances the compound's hydrophobic characteristics, potentially affecting its solubility and interaction with biological targets. Overall, this compound is of interest in biochemical research and pharmaceutical applications, particularly in the development of peptide-based therapeutics.

Formula: C₂₃H₃₂N₄O₇

Glycine, N-[(phenylmethoxy)carbonyl]glycyl-L-prolyl-L-leucyl-

CAS: 2646-64-2

Formula: C₂₃H₃₂N₄O₇

Molecular weight: 476.5228

Ref: IN-DA002TBV

Z-Gly-Pro-Leu-Gly

CAS: 2646-64-2

Z-Gly-Pro-Leu-Gly is a synthetic peptide with a kinetic and biochemical profile that is similar to that of the bacterial enzyme monoiodotyrosine hydroxylase. Z-Gly-Pro-Leu-Gly has been shown to react with the substrate, monoiodotyrosine, by forming hydrogen bonds. The enzyme activities of Z-Gly-Pro-Leu-Gly are inhibited by neutral pH and increased at acidic pH. The optimum pH for this reaction is 4.5. When injected subcutaneously, Z-Gly-Pro-Leu-Gly can penetrate the skin and hydrolyze monoiodotyrosine in ascidians.

Formula: C₂₃H₃₂N₄O₇

Purity: Min. 95%

Molecular weight: 476.52 g/mol

Ref: 3D-SGG-3040