CAS 30411-84-8

N-(Aminocarbonyl)methionine

Description:

N-(Aminocarbonyl)methionine, also known by its CAS number 30411-84-8, is an amino acid derivative that features a methionine backbone with an aminocarbonyl group attached. This compound is characterized by its polar nature due to the presence of both amino and carbonyl functional groups, which can engage in hydrogen bonding. It is typically soluble in water, making it suitable for various biochemical applications. The structure of N-(Aminocarbonyl)methionine allows it to participate in peptide synthesis and may play a role in metabolic processes involving sulfur-containing amino acids. Additionally, it can serve as a building block in the synthesis of peptides and proteins, contributing to the study of protein structure and function. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in laboratory settings. Overall, N-(Aminocarbonyl)methionine is a valuable compound in biochemical research and applications related to amino acid chemistry.

Formula: C₆H₁₂N₂O₃S

InChI: InChI=1S/C6H12N2O3S/c1-12-3-2-4(5(9)10)8-6(7)11/h4H,2-3H2,1H3,(H,9,10)(H3,7,8,11)

InChI key: InChIKey=DEWDMTSMCKXBNP-UHFFFAOYSA-N

SMILES: C(NC(N)=O)(C(O)=O)CCSC

Synonyms:

• N-(Aminocarbonyl)methionine
• Methionine, N-(aminocarbonyl)-
• N-Carbamyl-DL-methionine
• DL-Methionine, N-(aminocarbonyl)-
• Methionine, N-carbamoyl-, DL-

Methionine, N-(aminocarbonyl)-

CAS: 30411-84-8

Formula: C₆H₁₂N₂O₃S

Purity: %

Molecular weight: 192.2361

Ref: IN-DA003010

4-(Methylthio)-2-ureidobutanoic acid

CAS: 30411-84-8

4-(Methylthio)-2-ureidobutanoic acid

Purity: 95%

Molecular weight: 192.24g/mol

Ref: 54-OR1064975

2-(Carbamoylamino)-4-(methylsulfanyl)butanoic acid

CAS: 30411-84-8

2-(Carbamoylamino)-4-(methylsulfanyl)butanoic acid is the substrate for the enzyme l-amino acid oxidase, which catalyses the oxidation of L-amino acids to α-keto acids and ammonia. This activity is dependent on sodium carbonate as a cofactor, pH, and metal ion (e.g., zinc). The optimum temperature for this reaction is 60°C. The kinetic constant for this reaction was determined by measuring the rate at different concentrations of 2-(carbamoylamino)-4-(methylsulfanyl)butanoic acid.
2-(Carbamoylamino)-4-(methylsulfanyl)butanoic acid has been shown to inhibit the production of malondialdehyde in rat liver mitochondria.

Formula: C₆H₁₂N₂O₃S

Purity: Min. 95%

Molecular weight: 192.24 g/mol

Ref: 3D-FBA41184