CAS 7540-67-2
:O-Acetyl-L-homoserine
Description:
O-Acetyl-L-homoserine is an organic compound characterized by its acetylated amino acid structure. It is a derivative of L-homoserine, which is an important intermediate in the biosynthesis of amino acids and other biomolecules. The compound features an acetyl group attached to the hydroxyl group of the homoserine backbone, enhancing its reactivity and solubility in various solvents. O-Acetyl-L-homoserine is typically a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols. It plays a significant role in metabolic pathways, particularly in the synthesis of methionine and cysteine, and is utilized in biochemical research and applications. The compound is also of interest in the study of plant and microbial metabolism, as it can influence various physiological processes. Safety data indicates that, like many chemical substances, it should be handled with care, following appropriate safety protocols to avoid exposure.
Formula:C6H11NO4
InChI:InChI=1S/C6H11NO4/c1-4(8)11-3-2-5(7)6(9)10/h5H,2-3,7H2,1H3,(H,9,10)/t5-/m0/s1
InChI key:InChIKey=FCXZBWSIAGGPCB-YFKPBYRVSA-N
SMILES:C([C@@H](C(O)=O)N)COC(C)=O
Synonyms:- O-Acetyl-L-homoserine
- O-Acetylhomoserine
- L-Homoserine, acetate (ester)
- Butyric acid, 2-amino-4-hydroxy-, acetate (ester), L-
- L-Homoserine, O-acetyl-
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Found 4 products.
(2s)-4-(Acetyloxy)-2-aminobutanoic acid
CAS:(2s)-4-(Acetyloxy)-2-aminobutanoic acidPurity:98%Molecular weight:161.16g/molO-Acetylhomoserine
CAS:Controlled ProductFormula:C6H11NO4Color and Shape:Off-WhiteMolecular weight:161.16(2S)-4-(Acetyloxy)-2-aminobutanoic acid
CAS:<p>(2S)-4-(Acetyloxy)-2-aminobutanoic acid is a sulfhydrylase inhibitor that has been shown to have in vitro antifungal activity against group P2 bacteria. This compound binds to sulfhydrylases, which are enzymes that catalyze the conversion of sulfides to thiols, and prevents the formation of disulfide bonds. (2S)-4-(Acetyloxy)-2-aminobutanoic acid has also been shown to inhibit bacterial growth by binding to the surface of cells and inhibiting enzymatic reactions on the cell surface. The enzyme activities of this compound are not inhibited by water vapor or sephadex g-100. Structural analysis revealed that (2S)-4-(acetyloxy)-2-aminobutanoic acid contains a disulfide bond.</p>Formula:C6H11NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:161.16 g/mol
