Produktinformation
- (2S,3R)-2-[(Benzyloxycarbonyl)amino]-3-hydroxybutanoic acid
- (2S,3R)-2-{[(benzyloxy)carbonyl]amino}-3-hydroxybutanoate
- <span class="text-smallcaps">L</span>-Threonine, N-[(phenylmethoxy)carbonyl]-
- Cbz-L-threonine
- Cbz-Thr-OH
- N-Benzyloxycarbonyl-<span class="text-smallcaps">L</span>-threonine
- N-Carbobenzoxy-<span class="text-smallcaps">L</span>-threonine
- N-Cbz-<span class="text-smallcaps">L</span>-threonine
- N-Cbz-L-Threonine
- N-[(Phenylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-threonine
- Mehr Synonyme anzeigen
- N-[(benzyloxy)carbonyl]threonine
- N-benzyloxycarbonyl-l-threonine
- NSC 333749
- Threonine, N-carboxy-, N-benzyl ester, <span class="text-smallcaps">L</span>-
- Z-Thr-OH
- benzyl [(1S,2R)-1-carbamoyl-2-hydroxypropyl]carbamate
- N-Carbobenzoxy-L-threonine
- Threonine, N-carboxy-, N-benzyl ester, L-
- N-[(Phenylmethoxy)carbonyl]-L-threonine
- L-Threonine, N-[(phenylmethoxy)carbonyl]-
Z-L-Thr-OH is a synthetic peptide that contains the amino acid sequence of l-threonine. It is an amide with a carbamic acid and chloride functional group. The monomers are linked by ring-opening reactions, which are sequences of reactions in which the bond between two adjacent carbon atoms is broken and then immediately formed again with the addition of another molecule. Z-L-Thr-OH has been shown to hydrolyze leukocytes and inhibit bacterial growth in vitro. In vivo studies have also shown that Z-L-Thr-OH inhibits neutrophil recruitment, degranulation, and oxidative burst in response to chemoattractants or bacteria. This peptide has also been shown to be effective against methicillin resistant Staphylococcus aureus (MRSA) and other clinically significant pathogens.
Chemische Eigenschaften
Technische Anfrage zu: 3D-FT39052 Z-L-Thr-OH
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