Z-Ala-Ala-OH

CAS: 16012-70-7

Ref. 3D-FA47260

Produktinformation

• Name: Z-Ala-Ala-OH
• Synonyme: Z-L-alanyl-L-alanine, <span class="text-smallcaps">L</smallcap>-Alanine, N-[(phenylmethoxy)carbonyl]-<smallcap>L</span>-alanyl-, <span class="text-smallcaps">L</smallcap>-Alanine, N-[N-[(phenylmethoxy)carbonyl]-<smallcap>L</span>-alanyl]-, Alanine, N-(N-carboxy-<span class="text-smallcaps">L</smallcap>-alanyl)-, N-benzyl ester, <smallcap>L</span>-, Alanine, N-(N-carboxyalanyl)-, N-benzyl ester, Benzyloxycarbonyl-<span class="text-smallcaps">L</smallcap>-alanyl-<smallcap>L</span>-alanine, N-(Benzyloxycarbonyl)-<span class="text-smallcaps">L</smallcap>-alanyl-<smallcap>L</span>-alanine, N-(Benzyloxycarbonyl)alanylalanine, N-[(Phenylmethoxy)carbonyl]-<span class="text-smallcaps">L</smallcap>-alanyl-<smallcap>L</span>-alanine, N-[(benzyloxy)carbonyl]alanylalanine
• CAS: 16012-70-7

Beschreibung

Z-Ala-Ala-OH is an amide that has been shown to inhibit the activity of serine proteases, such as elastase and cathepsin G. It has been used to study the biological function of these enzymes in mammalian tissue. Z-Ala-Ala-OH has been shown to inhibit the activity of a number of other proteases, including trypsin, chymotrypsin, and plasmin. The phosphate group on this molecule may be hydrolyzed by phosphatases, which are found in many cells. This hydrolysis may result in the release of acetic acid, acetaldehyde, and ammonia. Z-Ala-Ala-OH is synthesized from cyclobutanone by an acylation reaction with a carboxylic acid or an amine.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 294.3 g/mol
• Formel: C₁₄H₁₈N₂O₅
• Reinheit: Min. 95%