Chemical Formula: C7H14N2O3S

Chemical Formula C7H14N2O3S

Found 18 metabolite its formula value is C7H14N2O3S

Glycyl-Methionine

2-[(2-Amino-1-hydroxyethylidene)amino]-4-(methylsulphanyl)butanoic acid

C7H14N2O3S (206.0725094)


Glycyl-Methionine is a dipeptide composed of glycine and methionine. 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.

   

Methionyl-Glycine

2-{[2-amino-1-hydroxy-4-(methylsulphanyl)butylidene]amino}acetic acid

C7H14N2O3S (206.0725094)


Methionyl-Glycine is a dipeptide composed of methionine and glycine. 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.

   

Aldicarb sulfoxide

(2-Methanesulphinyl-2-methylpropylidene)[(methyl-C-hydroxycarbonimidoyl)oxy]amine

C7H14N2O3S (206.0725094)


   
   

UNII:5X736K018B

Pesticide2_Aldicarb sulfoxide_C7H14N2O3S_Propanal, 2-methyl-2-(methylsulfinyl)-, O-[(methylamino)carbonyl]oxime, (1E)-

C7H14N2O3S (206.0725094)


   

Gly-met

2-[2-amino-4-(methylsulfanyl)butanamido]acetic acid

C7H14N2O3S (206.0725094)


A dipeptide formed from glycine and L-methionine residues.

   

Met-gly

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

C7H14N2O3S (206.0725094)


A dipeptide formed from L-methionine and glycine residues.

   
   
   

butocarboxim sulfoxide

butocarboxim sulfoxide

C7H14N2O3S (206.0725094)


   

1-Ethyl-3-methylimidazolium Methanesulfonate

1-Ethyl-3-methylimidazolium Methanesulfonate

C7H14N2O3S (206.0725094)


   
   

2-[[(2S)-2-amino-4-methylsulfanylbutanoyl]amino]acetic acid

2-[[(2S)-2-amino-4-methylsulfanylbutanoyl]amino]acetic acid

C7H14N2O3S (206.0725094)


   

(2R)-3-(2-acetamidoethylsulfanyl)-2-aminopropanoic acid

(2R)-3-(2-acetamidoethylsulfanyl)-2-aminopropanoic acid

C7H14N2O3S (206.0725094)


   

(2S)-2-[(azaniumylacetyl)amino]-4-(methylsulfanyl)butanoate

(2S)-2-[(azaniumylacetyl)amino]-4-(methylsulfanyl)butanoate

C7H14N2O3S (206.0725094)


   

N-acetyl-L-thialysine zwitterion

N-acetyl-L-thialysine zwitterion

C7H14N2O3S (206.0725094)


A S-alkyl-L-cysteine zwitterion resulting from the transfer of a proton from the carboxy group to the amino group of N-acetyl-L-thialysine. Major microspecies at pH 7.3.

   

Gly-Met zwitterion

Gly-Met zwitterion

C7H14N2O3S (206.0725094)


A peptide zwitterion obtained by transfer of a proton from the carboxy to the amino terminus of Gly-Met.

   

N-acetyl-L-thialysine

N-acetyl-L-thialysine

C7H14N2O3S (206.0725094)


An L-cysteine thioether resulting from the formal condensation of the carboxy group of acetic acid with the amino group of L-thialysine.