Exact Mass: 131.025

Exact Mass Matches: 131.025

Found 50 metabolites which its exact mass value is equals to given mass value 131.025, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

2-Oxosuccinamate

3-(C-hydroxycarbonimidoyl)-2-oxopropanoic acid

C4H5NO4 (131.0219)


This compound belongs to the family of Short-chain Keto Acids and Derivatives. These are keto acids with an alkyl chain the contains less than 6 carbon atoms

   

Iminoaspartic acid

alpha-Iminosuccinic acid

C4H5NO4 (131.0219)


D018377 - Neurotransmitter Agents > D018846 - Excitatory Amino Acids Iminoaspartic acid is a substrate for D-aspartate oxidase. [HMDB] Iminoaspartic acid is a substrate for D-aspartate oxidase.

   

2,3-Aziridinedicarboxylic acid

aziridine-2,3-dicarboxylic acid

C4H5NO4 (131.0219)


   

Iminoaspartic acid

2-imino-butanedioic acid

C4H5NO4 (131.0219)


D018377 - Neurotransmitter Agents > D018846 - Excitatory Amino Acids A succinic acid derivative having an imino group at the 2-position.

   

4-AMINO-2,6-DIFLUOROPYRIMIDINE

4-AMINO-2,6-DIFLUOROPYRIMIDINE

C4H3F2N3 (131.0295)


   

5-(chloromethyl)-1-methyl-1,2,4-triazole

5-(chloromethyl)-1-methyl-1,2,4-triazole

C4H6ClN3 (131.025)


   

3-(Chloromethyl)-1-methyl-1H-1,2,4-triazole

3-(Chloromethyl)-1-methyl-1H-1,2,4-triazole

C4H6ClN3 (131.025)


   

5-Methoxy-1,3,4-thiadiazol-2-amine

5-Methoxy-1,3,4-thiadiazol-2-amine

C3H5N3OS (131.0153)


   

trimethylsilyl isothiocyanate

trimethylsilyl isothiocyanate

C4H9NSSi (131.0225)


   

2,2-difluoropropylamine hydrochloride

2,2-difluoropropylamine hydrochloride

C3H8ClF2N (131.0313)


   

3-Methoxy-1,2,4-Thiadiazol-5-Amine

3-Methoxy-1,2,4-Thiadiazol-5-Amine

C3H5N3OS (131.0153)


   

2,2-difluoro-N-methylethanamine hydrochloride

2,2-difluoro-N-methylethanamine hydrochloride

C3H8ClF2N (131.0313)


   

2,3-DIFLUOROPYRIDIN-4-OL

2,3-DIFLUOROPYRIDIN-4-OL

C5H3F2NO (131.0183)


   

3-Aminopyridazine hydrochloride

3-Aminopyridazine hydrochloride

C4H6ClN3 (131.025)


   

3,5-difluoro-1H-pyridin-2-one

3,5-difluoro-1H-pyridin-2-one

C5H3F2NO (131.0183)


   

3,5-DIFLUOROPYRIDINE 1-OXIDE

3,5-DIFLUOROPYRIDINE 1-OXIDE

C5H3F2NO (131.0183)


   

3-(CHLOROMETHYL)-4-METHYL-4H-1,2,4-TRIAZOLE

3-(CHLOROMETHYL)-4-METHYL-4H-1,2,4-TRIAZOLE

C4H6ClN3 (131.025)


   

4,6-Difluoro-2-pyrimidinamine

4,6-Difluoro-2-pyrimidinamine

C4H3F2N3 (131.0295)


   

3-Pyridinol,2,6-difluoro-(9CI)

3-Pyridinol,2,6-difluoro-(9CI)

C5H3F2NO (131.0183)


   

4-Chloro-5-methyl-1H-pyrazol-3-amine

4-Chloro-5-methyl-1H-pyrazol-3-amine

C4H6ClN3 (131.025)


   

3-AMINO-5-METHOXY-1,2,4-THIADIAZOLE

3-AMINO-5-METHOXY-1,2,4-THIADIAZOLE

C3H5N3OS (131.0153)


   

ammonium trifluoroacetate

ammonium trifluoroacetate

C2H4F3NO2 (131.0194)


   

1,2,4-Oxadiazol-5-amine,3-(methylthio)-

1,2,4-Oxadiazol-5-amine,3-(methylthio)-

C3H5N3OS (131.0153)


   

4-Pyridinol,2,6-difluoro-(9CI)

4-Pyridinol,2,6-difluoro-(9CI)

C5H3F2NO (131.0183)


   

1H-1,2,4-Triazole,3-chloro-1-ethyl-(9CI)

1H-1,2,4-Triazole,3-chloro-1-ethyl-(9CI)

C4H6ClN3 (131.025)


   

3,6-Difluorpyridazin

3,6-Difluorpyridazin

C5H3F2NO (131.0183)


   

1-(2-Chloroethyl)-1H-1,2,4-triazole

1-(2-Chloroethyl)-1H-1,2,4-triazole

C4H6ClN3 (131.025)


   

1,2,4-Triazolidin-3-one,4-methyl-5-thioxo-

1,2,4-Triazolidin-3-one,4-methyl-5-thioxo-

C3H5N3OS (131.0153)


   

4-Methoxy-4-oxobutanoate

4-Methoxy-4-oxobutanoate

C5H7O4- (131.0344)


   

(S)-4-hydroxy-2-oxopentanoate

(S)-4-hydroxy-2-oxopentanoate

C5H7O4- (131.0344)


An optically active form of 4-hydroxy-2-oxopentanoate having 4S-configuration.

   

4-Hydroxy-2-oxopentanoate

4-Hydroxy-2-oxopentanoate

C5H7O4- (131.0344)


A 2-oxo monocarboxylic acid corresponding to the conjugate base of 4-hydroxy-2-oxopentanoic acid; major species at pH 7.3.

   

(2S)-2-Hydroxy-2-methyl-3-oxobutanoate

(2S)-2-Hydroxy-2-methyl-3-oxobutanoate

C5H7O4- (131.0344)


conjugate base of (2S)-2-hydroxy-2-methyl-3-oxobutanoic acid.

   

3-Hydroxy-3-methyl-2-oxobutanoate

3-Hydroxy-3-methyl-2-oxobutanoate

C5H7O4- (131.0344)


   

2-(Hydroxymethyl)-4-oxobutanoate

2-(Hydroxymethyl)-4-oxobutanoate

C5H7O4- (131.0344)


   

5-Hydroxy-2-oxopentanoate

5-Hydroxy-2-oxopentanoate

C5H7O4- (131.0344)


   

5-Hydroxy-4-oxopentanoate

5-Hydroxy-4-oxopentanoate

C5H7O4- (131.0344)


   

(2Z)-2,4-dihydroxypent-2-enoate

(2Z)-2,4-dihydroxypent-2-enoate

C5H7O4- (131.0344)


   

Aspartate

Aspartate

C4H5NO4-2 (131.0219)


D018377 - Neurotransmitter Agents > D018846 - Excitatory Amino Acids

   

Iminodiacetate

Iminodiacetate

C4H5NO4-2 (131.0219)


   

2-Acetyllactate

2-Acetyllactate

C5H7O4- (131.0344)


The conjugate base of 2-acetyllactic acid; major species at pH 7.3.

   

Glutarate(1-)

Glutarate(1-)

C5H7O4- (131.0344)


A dicarboxylic acid monoanion that is the conjugate base of glutaric acid.

   

Didehydroaspartate

Didehydroaspartate

C4H5NO4 (131.0219)


   

2-Aminobutanedioate

2-Aminobutanedioate

C4H5NO4-2 (131.0219)


   

(2R)-2-Aminobutanedioate

(2R)-2-Aminobutanedioate

C4H5NO4-2 (131.0219)


   

2-Oxosuccinamic acid

2-Oxosuccinamic acid

C4H5NO4 (131.0219)


   

aspartate(2-)

aspartate(2-)

C4H5NO4 (131.0219)


A C4-dicarboxylate that is the dianion obtained by the deprotonation of both the carboxy groups of aspartic acid.

   

L-aspartate(2-)

L-aspartate(2-)

C4H5NO4 (131.0219)


An aspartate(2-) that is the conjugate base of L-aspartate(1-).

   

D-aspartate(2-)

D-aspartate(2-)

C4H5NO4 (131.0219)


An aspartate(2-) that is the conjugate base of D-aspartate(1-).

   

Iminodiacetate

Iminodiacetate

C4H5NO4 (131.0219)


A dicarboxylic acid dianion resulting from the removal of a proton from both of the carboxy groups of iminodiacetic acid.

   

Oxosuccinamic acid

Oxosuccinamic acid

C4H5NO4 (131.0219)