CAS 19728-63-3
:Z-Trois-OH
- (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
- 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
- Voir plus de synonymes
N-Benzyloxycarbonyl-L-threonine
CAS :Formule :C12H15NO5Degré de pureté :>98.0%(T)(HPLC)Couleur et forme :White to Almost white powder to crystalMasse moléculaire :253.25N-Benzyloxycarbonyl-L-threonine, 99%
CAS :This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formule :C12H15NO5Degré de pureté :99%Couleur et forme :Powder, WhiteMasse moléculaire :253.25L-Threonine, N-[(phenylmethoxy)carbonyl]-
CAS :Formule :C12H15NO5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :253.2512Z-L-Threonine extrapure, 99%
CAS :Formule :C12H15NO5Degré de pureté :min. 99 %Couleur et forme :White to off- white, Crystalline powderMasse moléculaire :253.3Z-Thr-OH
CAS :M03056 - Z-Thr-OH
Formule :C12H15NO5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :253.254Z-L-Thr-OH
CAS :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.
Formule :C12H15NO5Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :253.25 g/molZ-Thr-OH
CAS :Z-Thr-OH is a useful organic compound for research related to life sciences. The catalog number is T67545 and the CAS number is 19728-63-3.Formule :C12H15NO5Couleur et forme :SolidMasse moléculaire :253.254








