Exact Mass: 149.0147

Exact Mass Matches: 149.0147

Found 52 metabolites which its exact mass value is equals to given mass value 149.0147, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

L-2-Amino-4-chloropent-4-enoate

(2S)-2-amino-4-chloropent-4-enoic acid

C5H8ClNO2 (149.0244)


   

3-(2-Chloroethyl)oxazolidin-2-one

3-(2-chloroethyl)-1,3-oxazolidin-2-one

C5H8ClNO2 (149.0244)


D000890 - Anti-Infective Agents > D023303 - Oxazolidinones

   

3-Chloro-4,4-dimethyl-2-oxazolidinone

3-chloro-4,4-dimethyl-1,3-oxazolidin-2-one

C5H8ClNO2 (149.0244)


D000890 - Anti-Infective Agents > D023303 - Oxazolidinones

   

N-(Mercaptoacetyl)glycine

2-[(1-Hydroxy-2-sulphanylethylidene)amino]acetic acid

C4H7NO3S (149.0147)


   

Aluminum nicotinate

λ¹-alumanylium pyridine-3-carboxylate

C6H4AlNO2 (149.0057)


It is used as a food additive .

   

(Z)-2-Amino-5-chloro-4-pentenoic acid

(S)-cis-Amino-5-chloro-4-pentenoic acid

C5H8ClNO2 (149.0244)


   

2,3-Pyridinedicarboxylic anhydride

2,3-Pyridinedicarboxylic anhydride

C7H3NO3 (149.0113)


   

2-amino-5-chloro-4-pentenoic acid

2-amino-5-chloro-4-pentenoic acid

C5H8ClNO2 (149.0244)


   

5-cyanopyrazine-2-carboxylic acid

5-cyanopyrazine-2-carboxylic acid

C6H3N3O2 (149.0225)


   

Furo[3,4-c]pyridine-1,3-dione

Furo[3,4-c]pyridine-1,3-dione

C7H3NO3 (149.0113)


   

2-Cyano-4-nitropyridine

2-Cyano-4-nitropyridine

C6H3N3O2 (149.0225)


   

5-Nitropicolinonitrile

5-Nitropicolinonitrile

C6H3N3O2 (149.0225)


   

3,3,3-Trifluoropropan-1-amine hydrochloride

3,3,3-Trifluoropropan-1-amine hydrochloride

C3H7ClF3N (149.0219)


   

DL-Propargylglycine

DL-Propargylglycine

C5H8ClNO2 (149.0244)


   

2-chloro-n-methylacetoacetamide

2-chloro-n-methylacetoacetamide

C5H8ClNO2 (149.0244)


   

1,1,1-Trifluoro-2-propanamine hydrochloride (1:1)

1,1,1-Trifluoro-2-propanamine hydrochloride (1:1)

C3H7ClF3N (149.0219)


   

Piperidine-3,5-dione hydrochloride

Piperidine-3,5-dione hydrochloride

C5H8ClNO2 (149.0244)


   

3-Chloro-4-hydroxy-2-piperidinone

3-Chloro-4-hydroxy-2-piperidinone

C5H8ClNO2 (149.0244)


   

5-METHYLTHIOPHEN-2-AMINE HYDROCHLORIDE

5-METHYLTHIOPHEN-2-AMINE HYDROCHLORIDE

C5H8ClNS (149.0066)


   

3-CYANO-4-NITROPYRIDINE

3-CYANO-4-NITROPYRIDINE

C6H3N3O2 (149.0225)


   

1,1-dioxothiazinan-3-one

1,1-dioxothiazinan-3-one

C4H7NO3S (149.0147)


   

4-(Chloroformyl)morpholine

4-(Chloroformyl)morpholine

C5H8ClNO2 (149.0244)


   
   

3,4-Dehydro-L-proline hydrochloride

3,4-Dehydro-L-proline hydrochloride

C5H8ClNO2 (149.0244)


   

3,5,6-Trifluoro-2-pyridinol

3,5,6-Trifluoro-2-pyridinol

C5H2F3NO (149.0088)


   

4-Pyridinecarbonitrile,3-nitro-(9CI)

4-Pyridinecarbonitrile,3-nitro-(9CI)

C6H3N3O2 (149.0225)


   

2-Thienylmethylamine hydrochloride

2-Thienylmethylamine hydrochloride

C5H8ClNS (149.0066)


   

2,2,2-TRIFLUORO-N-METHYLETHANAMINE HYDROCHLORIDE

2,2,2-TRIFLUORO-N-METHYLETHANAMINE HYDROCHLORIDE

C3H7ClF3N (149.0219)


   

FURO(3,4-B)PYRIDINE-5,7-DIONE

FURO(3,4-B)PYRIDINE-5,7-DIONE

C7H3NO3 (149.0113)


   

2,3-Pyrazine dicarboxamide

2,3-Pyrazine dicarboxamide

C6H3N3O2 (149.0225)


   

3-Nitro-2-pyridinecarbonitrile

3-Nitro-2-pyridinecarbonitrile

C6H3N3O2 (149.0225)


   

2-Formylbenzoate

2-Formylbenzoate

C8H5O3- (149.0239)


A benzoate anion arising from deprotonation of the carboxy group of 2-formylbenzoic acid; major species at pH 7.3.

   

N-(Mercaptoacetyl)glycine

N-(Mercaptoacetyl)glycine

C4H7NO3S (149.0147)


   

Phenylglyoxylate

Phenylglyoxylate

C8H5O3- (149.0239)


A member of the class of glyoxylates, that is obtained by removal of a proton from the carboxylic acid group of phenylglyoxylic acid. D000890 - Anti-Infective Agents > D000892 - Anti-Infective Agents, Urinary > D008333 - Mandelic Acids

   

4-FORMYLBENZOate

4-FORMYLBENZOate

C8H5O3- (149.0239)


A benzoate that is the conjugate base of 4-formylbenzoic acid arising from the deprotonation of the carboxy group; Major microspecies at pH 7.3.

   

3-Formylbenzoate

3-Formylbenzoate

C8H5O3- (149.0239)


   

Nitrocarbamoylcarbamic acid

Nitrocarbamoylcarbamic acid

C2H3N3O5 (149.0073)


   

Bitartrate

Bitartrate

C4H5O6- (149.0086)


   

D-tartrate(1-)

D-tartrate(1-)

C4H5O6- (149.0086)


   

L-tartrate(1-)

L-tartrate(1-)

C4H5O6- (149.0086)


   

(2R,3S)-3-carboxy-2,3-dihydroxypropanoate

(2R,3S)-3-carboxy-2,3-dihydroxypropanoate

C4H5O6- (149.0086)


   

(2S,3R)-3-carboxy-2,3-dihydroxypropanoate

(2S,3R)-3-carboxy-2,3-dihydroxypropanoate

C4H5O6- (149.0086)


   

rel-(2R,3S)-3-carboxy-2,3-dihydroxypropanoate

rel-(2R,3S)-3-carboxy-2,3-dihydroxypropanoate

C4H5O6- (149.0086)


   

Methyl 2-cyanoethanesulfonate

Methyl 2-cyanoethanesulfonate

C4H7NO3S (149.0147)


   

L-2-amino-4-chloropent-4-enoic acid

(2S)-2-amino-4-chloropent-4-enoic acid

C5H8ClNO2 (149.0244)


An alpha-amino acid having a 2-chloro-2-propenyl group at the alpha-position and L-configuration.

   

L-2-amino-4-chloropent-4-enoic acid zwitterion

L-2-amino-4-chloropent-4-enoic acid zwitterion

C5H8ClNO2 (149.0244)


An L-alpha-amino acid zwitterion obtained from L-2-amino-4-chloropent-4-enoic acid by transfer of a proton from the carboxy group to the amino group. It is the major species at pH 7.3.

   

meso-tartrate(1-)

meso-tartrate(1-)

C4H5O6 (149.0086)


   

3-carboxy-2,3-dihydroxypropanoate

3-carboxy-2,3-dihydroxypropanoate

C4H5O6 (149.0086)


A tartaric acid anion that is the conjugate base of 2,3-dihydroxybutanedioic acid.

   

4-chloro-3-hydroxypent-4-enimidic acid

4-chloro-3-hydroxypent-4-enimidic acid

C5H8ClNO2 (149.0244)


   

(3r)-4-chloro-3-hydroxypent-4-enimidic acid

(3r)-4-chloro-3-hydroxypent-4-enimidic acid

C5H8ClNO2 (149.0244)


   

2-amino-5-chloropent-4-enoic acid

2-amino-5-chloropent-4-enoic acid

C5H8ClNO2 (149.0244)


   

(2s,4z)-2-amino-5-chloropent-4-enoic acid

(2s,4z)-2-amino-5-chloropent-4-enoic acid

C5H8ClNO2 (149.0244)