CAS 7801-38-9

Z-Pro-Leu-Gly-OH

Description:

Z-Pro-Leu-Gly-OH, also known as Z-Proline-Leucine-Glycine, is a peptide with a specific sequence of amino acids. The "Z" indicates that the proline is protected by a benzyloxycarbonyl (Z) group, which is commonly used in peptide synthesis to prevent unwanted reactions during the formation of peptide bonds. This compound features proline, leucine, and glycine, which are all naturally occurring amino acids. Proline is known for its unique cyclic structure, which contributes to the stability of peptide chains, while leucine is a branched-chain amino acid important for protein synthesis and metabolic functions. Glycine, the simplest amino acid, plays a crucial role in various biochemical processes. Z-Pro-Leu-Gly-OH is often utilized in research and pharmaceutical applications, particularly in studies related to peptide synthesis and the development of bioactive compounds. Its properties, such as solubility and stability, can be influenced by the presence of the Z group and the specific amino acid sequence, making it a valuable compound in biochemical research.

Formula: C₂₁H₂N₃O₆

Z-Pro-Leu-Gly-OH

CAS: 7801-38-9

Z-MIF I (free acid).

Formula: C₂₁H₂₉N₃O₆

Purity: > 99%

Color and Shape: White Powder

Molecular weight: 419.48

Ref: 01-4012145

Z-Pro-Leu-Gly-OH

Controlled Product

CAS: 7801-38-9

Applications Z-Pro-Leu-Gly-OH (CAS# 7801-38-9) is a useful research chemical compound.

Formula: C₂₁H₂₉N₃O₆

Color and Shape: Neat

Molecular weight: 419.471

Ref: TR-Z227515

Z-Pro-Leu-Gly-OH

CAS: 7801-38-9

Z-Pro-Leu-Gly-OH is a peptide that belongs to the class of amides, oxalate salts, and grignard reagents. It can be synthesized from the reaction between an oxalate salt and a grignard reagent. The synthesis of Z-Pro-Leu-Gly-OH is usually done by reacting an oxalate salt with a grignard reagent in presence of a ketone or ketomethylene.

Formula: C₂₁H₂₉N₃O₆

Purity: Min. 95%

Molecular weight: 419.47 g/mol

Ref: 3D-FP111510