Chemical Formula: C6H12N2O4S
Chemical Formula C6H12N2O4S
Found 18 metabolite its formula value is C6H12N2O4S
Cysteinyl-Serine
C6H12N2O4S (208.05177519999998)
Cysteinyl-Serine is a dipeptide composed of cysteine and serine. It is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis. This dipeptide has not yet been identified in human tissues or biofluids and so it is classified as an Expected metabolite.
Serylcysteine
C6H12N2O4S (208.05177519999998)
Serylcysteine is a dipeptide composed of serine and cysteine. It is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis.
Lanthionine
C6H12N2O4S (208.05177519999998)
Lanthionine is a nonproteinogenic amino acid with the chemical formula (HOOC-CH(NH2)-CH2-S-CH2-CH(NH2)-COOH). It is typically formed by a cysteine residue and a dehydrated serine residue. Despite its name, lanthionine does not contain the element lanthanum. Lanthionine belongs to the class of organic compounds known as L-cysteine-S-conjugates. These are compounds containing L-cysteine where the thio-group is conjugated. Lanthionine is a uremic toxin (PMID: 30087103). In 1941, lanthionine was first isolated by treating wool with sodium carbonate. It was found to be a sulfur-containing amino acid; accordingly it was given the name lanthionine [wool (Latin: Lana), sulfur (Greek: theîon)].[1] Lanthionine was first synthesized by alkylation of cysteine with β-chloroalanine.[2] Lanthionines are found widely in nature. They have been isolated from human hair, lactalbumin, and feathers. Lanthionines have also been found in bacterial cell walls and are the components of a group of gene-encoded peptide antibiotics called lantibiotics, which includes nisin (a food preservative), subtilin, epidermin (effective against Staphylococcus and Streptococcus), and ancovenin (an enzyme inhibitor).[3][4] L-Lanthionine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=922-55-4 (retrieved 2024-06-29) (CAS RN: 922-55-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
DL-Lanthionine
C6H12N2O4S (208.05177519999998)
Lanthionine
C6H12N2O4S (208.05177519999998)
An alanine derivative in which two alanine residues are linked on their beta-carbons by a thioether linkage.
Cys-ser
C6H12N2O4S (208.05177519999998)
A dipeptide composed of L-cysteine and L-serine joined by a peptide linkage.
2-oxo-N-propan-2-yl-1,3-oxazolidine-3-sulfonamide
C6H12N2O4S (208.05177519999998)
1-Ethyl-3-methylimidazolium hydrogen sulfate
C6H12N2O4S (208.05177519999998)
1,3-DiMethyliMidazoliuM Methylsulfate
C6H12N2O4S (208.05177519999998)
Meso-lanthionine
C6H12N2O4S (208.05177519999998)
The meso-isomer of lanthionine. It is a key constituent of bacterial peptidoglycan type A51 and A3delta.
(2S)-2-azaniumyl-3-[(2R)-2-azaniumyl-2-carboxylatoethyl]sulfanylpropanoate
C6H12N2O4S (208.05177519999998)
L-lanthionine dizwitterion
C6H12N2O4S (208.05177519999998)
An L-alpha-amino acid zwitterion that is the dizwitterionic form of L-lanthionine obtained by migration of protons from both carboxy groups to the amino groups; major species at pH 7.3.