Chemical Formula: C3H5NO3

Chemical Formula C3H5NO3

Found 24 metabolite its formula value is C3H5NO3

Pyruvatoxime

(2E)-2-(hydroxyimino)propanoic acid

C3H5NO3 (103.026942)


Synthetic dimer was found to react rapidly with pyruvate to form the expected oxime. 1H NMR spectrum of the purified oxime is superimposable with that arising when the dimer and pyruvate are mixed and the spectrum taken immediately thereafter. Then the mass spectrum of the reaction product of cycloserine dimer and methylpyruvate is totally consistent with the formation of a stable oxime derivative. Furthermore, when cycloserine is incubated with pyruvate the oxime derived from the dimer is found.(PMID: 2495795) [HMDB] Synthetic dimer was found to react rapidly with pyruvate to form the expected oxime. 1H NMR spectrum of the purified oxime is superimposable with that arising when the dimer and pyruvate are mixed and the spectrum taken immediately thereafter. Then the mass spectrum of the reaction product of cycloserine dimer and methylpyruvate is totally consistent with the formation of a stable oxime derivative. Furthermore, when cycloserine is incubated with pyruvate the oxime derived from the dimer is found.(PMID: 2495795).

   

3-Oxoalanine

amino-(8CI)malonaldehydic acid

C3H5NO3 (103.026942)


Human lysosomal arylsulfate A (ASA) is a member of the sulfatase family which requires the posttranslational oxidation of thiol group of a cysteine that is conserved among all eukaryotic sulfatases, yielding 2-formylglycine. (PMID: 9521684) [HMDB] Human lysosomal arylsulfate A (ASA) is a member of the sulfatase family which requires the posttranslational oxidation of thiol group of a cysteine that is conserved among all eukaryotic sulfatases, yielding 2-formylglycine. (PMID: 9521684).

   

(Z)-3-aminoperacrylic acid

(Z)-3-aminoperacrylic acid

C3H5NO3 (103.026942)


   

3-Amino-3-oxopropanoic acid

Propanoic acid,3-amino-3-oxo-

C3H5NO3 (103.026942)


   

Ammonia pyruvate

amino 2-oxopropanoate

C3H5NO3 (103.026942)


   

N-Formylglycine

2-Formamidoacetic acid

C3H5NO3 (103.026942)


   

N-Formylglycine

N-Formylglycine

C3H5NO3 (103.026942)


N-Formylglycine is an endogenous metabolite.

   

methyl 2-hydroxyiminoacetate

methyl 2-hydroxyiminoacetate

C3H5NO3 (103.026942)


   

2-(methylamino)-2-oxoacetic acid

2-(methylamino)-2-oxoacetic acid

C3H5NO3 (103.026942)


   

3-oxoalanine

amino-(8CI)malonaldehydic acid

C3H5NO3 (103.026942)


A non-proteinogenic alpha-amino acid that is alanine in which a keto group is incorporated at C-3.

   

METHYL FORMYLCARBAMATE

METHYL FORMYLCARBAMATE

C3H5NO3 (103.026942)


   

3-nitropropanal

3-nitropropanal

C3H5NO3 (103.026942)


   

3-Nitrooxetane

3-Nitrooxetane

C3H5NO3 (103.026942)


   

Acetic acid, aminooxo-, methyl ester

Acetic acid, aminooxo-, methyl ester

C3H5NO3 (103.026942)


   

1-Nitroacetone

1-Nitroacetone

C3H5NO3 (103.026942)


   

3-(2,3-dihydrobenzofuran-5-yl)propanoic acid

3-(2,3-dihydrobenzofuran-5-yl)propanoic acid

C3H5NO3 (103.026942)


   

L-alpha-Formylglycine

L-alpha-Formylglycine

C3H5NO3 (103.026942)


   

Methyl glyoxylate oxime

Methyl glyoxylate oxime

C3H5NO3 (103.026942)


   

2-Aminomalonate semialdehyde

2-Ammoniomalonate semialdehyde

C3H5NO3 (103.026942)


   

(Z)-3-aminoperacrylic acid

(Z)-3-aminoperacrylic acid

C3H5NO3 (103.026942)


   

Pyruvate oxime

Pyruvate oxime

C3H5NO3 (103.026942)


   

L-3-oxoalanine

L-3-oxoalanine

C3H5NO3 (103.026942)


The L-enantiomer of 3-oxoalanine.

   

L-3-oxoalanine zwitterion

L-3-oxoalanine zwitterion

C3H5NO3 (103.026942)


An amino acid zwitterion obtained by transfer of a proton from the amino to the carboxy group of L-3-oxoalanine; major microspecies at pH 7.3 (according to Marvin v 6.2.0.).