CAS 2488-11-1
:L-Methionine, L-histidyl-
Description:
L-Methionine, L-histidyl- is a dipeptide composed of the amino acids L-methionine and L-histidine. It is characterized by its role in protein synthesis and its involvement in various metabolic processes. This compound features a peptide bond linking the carboxyl group of L-methionine to the amino group of L-histidine. L-methionine is a sulfur-containing amino acid essential for human health, playing a critical role in methylation reactions and serving as a precursor for other important biomolecules, including cysteine and taurine. L-histidine, on the other hand, is an essential amino acid that contributes to the synthesis of histamine and is vital for various physiological functions, including the regulation of pH and the maintenance of myelin sheaths in nerve cells. The dipeptide form may exhibit unique properties, such as enhanced solubility and stability compared to its constituent amino acids. Its potential applications span nutritional supplements, pharmaceuticals, and research in biochemistry, particularly in studies related to protein structure and function.
Formula:C11H18N4O3S
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Found 2 products.
H-His-Met-OH
CAS:<p>Bachem ID: 4003456.</p>Formula:C11H18N4O3SPurity:> 98%Color and Shape:White PowderMolecular weight:286.36H-His-Met-OH
CAS:<p>H-His-Met-OH is a histidine derivative that has been shown to have antioxidant properties. It is classified as an amide, and also acts as a chelating agent. The molecule can bind to metal ions and thereby scavenge free radicals. H-His-Met-OH has been shown to have anti-cancer activity in vitro and in vivo against kidney cancer cells. This compound also has the ability to inhibit the growth of Pseudomonas aeruginosa, which is an activated form of this bacterium, by preventing its respiration. H-His-Met-OH inhibits energy metabolism in cancer cells, which may be due to its ability to inhibit glucose uptake by inhibiting the glycolytic pathway.</p>Formula:C11H18N4O3SPurity:Min. 95%Molecular weight:286.35 g/mol

