CAS 123984-00-9
:Z-Pro-Leu-Ala-NHOH
Description:
Z-Pro-Leu-Ala-NHOH, also known as a peptide derivative, is characterized by its structure, which includes a Z (benzyloxycarbonyl) protecting group on the proline (Pro) residue, followed by leucine (Leu) and alanine (Ala) amino acids, and an hydroxylamine (NHOH) functional group. This compound is typically utilized in biochemical research and pharmaceutical applications, particularly in the study of peptide synthesis and modifications. The presence of the Z group enhances the stability and solubility of the peptide, while the hydroxylamine moiety can participate in various chemical reactions, including those involving nucleophilic attack. The compound's properties, such as solubility, reactivity, and stability, can be influenced by the specific amino acid sequence and the protecting groups used. Overall, Z-Pro-Leu-Ala-NHOH serves as a valuable tool in peptide chemistry, enabling researchers to explore peptide interactions and modifications in biological systems.
Formula:C22H32N4O6
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Found 2 products.
Collagenase Inhibitor (MMP1)
CAS:<p>Collagenase Inhibitor (MMP1)</p>Color and Shape:PowderMolecular weight:448.51g/molZ-Pro-Leu-Ala-NHOH
CAS:<p>Z-Pro-Leu-Ala-NHOH is a potent inhibitor of stromal cells. It is a hydroxamic acid molecule that acts as an inhibitor of protein synthesis in the ribosome. Z-Pro-Leu-Ala-NHOH has been shown to have potent inhibitory activity against ethyl palmitate and lipiodol, which are used for therapeutic purposes. The molecule also inhibits viscosity in pharmaceutical preparations and pluripotent stem cells. This compound has shown inhibitory activities against stromal cells, which are responsible for growth, differentiation, and tissue repair. It also prevents the formation of embryoid bodies or pluripotent stem cells by suppressing the expression of proteins needed for early development.</p>Formula:C22H32N4O6Purity:Min. 95%Molecular weight:448.51 g/mol

