Exact Mass: 148.016

Exact Mass Matches: 148.016

Found 48 metabolites which its exact mass value is equals to given mass value 148.016, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

2-Oxo-4-methylthiobutanoic acid

2-Keto-4-methylthiobutyric acid, monosodium salt

C5H8O3S (148.0194)


2-oxo-4-methylthiobutanoate, also known as 2-keto-4-methylthiobutyric acid, 2-keto-4-methylthiobutyrate or 4-(methylsulfanyl)-2-oxobutanoic acid, is a member of the class of compounds known as thia- fatty acids. Thia-fatty acids are fatty acid derivatives obtained by insertion of a sulfur atom at specific positions in the chain. Thus, 2-oxo-4-methylthiobutanoate is a fatty acid lipid molecule. 2-oxo-4-methylthiobutanoate is slightly soluble (in water) and a weakly acidic compound (based on its pKa). 2-oxo-4-methylthiobutanoate can be synthesized from L-methionine and butyric acid. 2-oxo-4-methylthiobutanoate can also be synthesized into S-adenosyl-4-methylthio-2-oxobutanoic acid. 2-oxo-4-methylthiobutanoate can be found in a number of food items such as cloves, highbush blueberries, common beets, and cashew nuts. 2-oxo-4-methylthiobutanoate can be found in urine. Within the cell, 2-oxo-4-methylthiobutanoate is primarily located in the cytoplasm and in the membrane. 2-oxo-4-methylthiobutanoate has been found in all living species, from bacteria to humans. In humans, 2-oxo-4-methylthiobutanoate is found to be involved in several metabolic disorders, some of those are S-adenosylhomocysteine (SAH) hydrolase deficiency, methylenetetrahydrofolate reductase deficiency (MTHFRD), methionine adenosyltransferase deficiency, and glycine N-methyltransferase deficiency. 4-Methylthio-2-oxobutanoic acid is the direct precursor of methional, which is a potent inducer of apoptosis in a BAF3 murine lymphoid cell line which is interleukin-3 (IL3)-dependent (PMID: 7848263). 2-oxo-4-methylthiobutanoic acid, also known as 2-keto-4-methylthiobutyrate or 4-methylthio-2-oxobutanoate, is a member of the class of compounds known as thia fatty acids. Thia fatty acids are fatty acid derivatives obtained by insertion of a sulfur atom at specific positions in the chain. Thus, 2-oxo-4-methylthiobutanoic acid is considered to be a fatty acid lipid molecule. 2-oxo-4-methylthiobutanoic acid is slightly soluble (in water) and a weakly acidic compound (based on its pKa). 2-oxo-4-methylthiobutanoic acid can be synthesized from L-methionine and butyric acid. 2-oxo-4-methylthiobutanoic acid can also be synthesized into S-adenosyl-4-methylthio-2-oxobutanoic acid. 2-oxo-4-methylthiobutanoic acid can be found in a number of food items such as leek, hickory nut, brussel sprouts, and giant butterbur, which makes 2-oxo-4-methylthiobutanoic acid a potential biomarker for the consumption of these food products. 2-oxo-4-methylthiobutanoic acid can be found primarily in urine. 2-oxo-4-methylthiobutanoic acid exists in all living species, ranging from bacteria to humans. In humans, 2-oxo-4-methylthiobutanoic acid is involved in the methionine metabolism. 2-oxo-4-methylthiobutanoic acid is also involved in several metabolic disorders, some of which include s-adenosylhomocysteine (SAH) hydrolase deficiency, homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblg complementation type, glycine n-methyltransferase deficiency, and cystathionine beta-synthase deficiency.

   

2,4-Diimidotricarbonic acid

2,4-Diimidotricarbonic acid

C3H4N2O5 (148.012)


   

Phthalic anhydride

1,2-Benzenedicarboxylic acid anhydride

C8H4O3 (148.016)


Phthalic anhydride is the organic compound with the formula C6H4(CO)2O. It is the anhydride of phthalic acid. Phthalic anhydride is a principal commercial form of phthalic acid. It was the first anhydride of a dicarboxylic acid to be used commercially. This white solid is an important industrial chemical, especially for the large-scale production of plasticizers for plastics. In 2000, the worldwide production volume was estimated to be about 3 million tonnes per year.

   

PHTHALIC ANHYDRIDE

PHTHALIC ANHYDRIDE

C8H4O3 (148.016)


[Raw Data] CB132_Phthalic-anhydride_pos_30eV_CB000046.txt [Raw Data] CB132_Phthalic-anhydride_pos_20eV_CB000046.txt [Raw Data] CB132_Phthalic-anhydride_pos_10eV_CB000046.txt

   

alpha-Keto-gamma-(methylthio)butyric acid

alpha-Keto-gamma-(methylthio)butyric acid

C5H8O3S (148.0194)


   

4-Methylthio-2-oxobutanoic acid

2-oxo-4-methylthio-butanoic acid

C5H8O3S (148.0194)


A 2-oxo monocarboxylic acid derived from L-methionine via the action of methionine transaminase.

   

3-(Acetylthio)propionic acid

3-(Acetylthio)propionic acid

C5H8O3S (148.0194)


   

2-FLUORO-PYRIDIN-3-YL-AMINE HCL

2-FLUORO-PYRIDIN-3-YL-AMINE HCL

C5H6ClFN2 (148.0204)


   

Potassium cyclopropyl-1-trifluoroborate

Potassium cyclopropyl-1-trifluoroborate

C3H5BF3K (148.0073)


   

Potassium allyl(trifluoro)borate(1-)

Potassium allyl(trifluoro)borate(1-)

C3H5BF3K (148.0073)


   

(1H-PYRAZOL-4-YL)BORONIC ACID HYDROCHLORIDE

(1H-PYRAZOL-4-YL)BORONIC ACID HYDROCHLORIDE

C3H6BClN2O2 (148.0211)


   

4-(trifluoromethyl)pyrimidine

4-(trifluoromethyl)pyrimidine

C5H3F3N2 (148.0248)


   

2-(trifluoromethyl)pyrimidine

2-(trifluoromethyl)pyrimidine

C5H3F3N2 (148.0248)


   

2-(Trifluoromethyl)pyrazine

2-(Trifluoromethyl)pyrazine

C5H3F3N2 (148.0248)


   

3,5,6-Trifluoro-2-pyridinamine

3,5,6-Trifluoro-2-pyridinamine

C5H3F3N2 (148.0248)


   

2,3,5-TRIFLUORO-PYRIDIN-4-YLAMINE

2,3,5-TRIFLUORO-PYRIDIN-4-YLAMINE

C5H3F3N2 (148.0248)


   

Coumarandione

Coumarandione

C8H4O3 (148.016)


   

3,4,5-Trifluorophenol

3,4,5-Trifluorophenol

C6H3F3O (148.0136)


   

2,3,4-Trifluorophenol

2,3,4-Trifluorophenol

C6H3F3O (148.0136)


   

2,4,6-Trifluorophenol

2,4,6-Trifluorophenol

C6H3F3O (148.0136)


   

1H-Imidazole-4-carboxylicacid,2,5-difluoro-(9CI)

1H-Imidazole-4-carboxylicacid,2,5-difluoro-(9CI)

C4H2F2N2O2 (148.0084)


   

Tetrahydrothiopyran-4-one 1,1-dioxide

Tetrahydrothiopyran-4-one 1,1-dioxide

C5H8O3S (148.0194)


   

5,7-Dioxa-6-thia-spiro[2,5]octane-6-oxide

5,7-Dioxa-6-thia-spiro[2,5]octane-6-oxide

C5H8O3S (148.0194)


   
   

2-(Aminooxy)ethanamine dihydrochloride

2-(Aminooxy)ethanamine dihydrochloride

C2H10Cl2N2O (148.017)


   

2,3,6-trifluoropyridin-4-amine

2,3,6-trifluoropyridin-4-amine

C5H3F3N2 (148.0248)


   

2,4,6-trifluoro-5-methylpyrimidine

2,4,6-trifluoro-5-methylpyrimidine

C5H3F3N2 (148.0248)


   

5-(Trifluoromethyl)pyrimidine

5-(Trifluoromethyl)pyrimidine

C5H3F3N2 (148.0248)


   

2,3,6-trifluorophenol

2,3,6-trifluorophenol

C6H3F3O (148.0136)


   

2,4,5-TRIFLUOROPHENOL

2,4,5-TRIFLUOROPHENOL

C6H3F3O (148.0136)


   

2,3,5-trifluorophenol

2,3,5-trifluorophenol

C6H3F3O (148.0136)


   

Diethyldithiocarbamate

Diethyldithiocarbamate

C5H10NS2- (148.0255)


D000890 - Anti-Infective Agents > D000998 - Antiviral Agents D064449 - Sequestering Agents > D002614 - Chelating Agents D007155 - Immunologic Factors

   

Nitrobiuret

Nitrobiuret

C2H4N4O4 (148.0233)


   

Wiltrol P

Phthalic anhydride with >0.05\\% maleic anhydride [UN2214] [Corrosive]

C8H4O3 (148.016)


   

(3R)-3-hydroxy-L-aspartate

(3R)-3-hydroxy-L-aspartate

C4H6NO5- (148.0246)


D018377 - Neurotransmitter Agents > D018846 - Excitatory Amino Acids

   

(3S)-3-hydroxy-L-aspartate(1-)

(3S)-3-hydroxy-L-aspartate(1-)

C4H6NO5- (148.0246)


Conjugate base of (3S)-3-hydroxy-L-aspartic acid.

   

D-threo-3-hydroxyaspartate

D-threo-3-hydroxyaspartate

C4H6NO5- (148.0246)


   

D-erythro-3-Hydroxyaspartate

D-erythro-3-Hydroxyaspartate

C4H6NO5- (148.0246)


   

3-Hydroxyaspartate

3-Hydroxyaspartate

C4H6NO5- (148.0246)


   

3-Hydroxy-L-aspartate

3-Hydroxy-L-aspartate

C4H6NO5- (148.0246)


   

3-hydroxy-D-aspartate

3-hydroxy-D-aspartate

C4H6NO5- (148.0246)


   

(2S)-2-amino-4-chloropent-4-enoate

(2S)-2-amino-4-chloropent-4-enoate

C5H7ClNO2- (148.0165)


   

4-(METHYLsulfanyl)-2-oxobutanoIC ACID

4-(METHYLsulfanyl)-2-oxobutanoIC ACID

C5H8O3S (148.0194)


   

(3R)-3-hydroxy-L-aspartate(1-)

(3R)-3-hydroxy-L-aspartate(1-)

C4H6NO5 (148.0246)


Conjugate base of (3R)-3-hydroxy-L-aspartic acid arising from deprotonation of the two carboxy groups and protonation of the amino group; major species at pH 7.3.

   

(3S)-3-hydroxy-D-aspartate(1-)

(3S)-3-hydroxy-D-aspartate(1-)

C4H6NO5 (148.0246)


A D-alpha-amino acid anion which is obtained from (3S)-3-hydroxy-D-aspartic acid by formal deprotonation of both carboxyl groups and protonation of the amino group.

   

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

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

C5H7ClNO2 (148.0165)


   

(3R)-3-hydroxy-D-aspartate(1-)

(3R)-3-hydroxy-D-aspartate(1-)

C4H6NO5 (148.0246)


A D-alpha-amino acid anion which is obtained from (3R)-3-hydroxy-D-aspartic acid by formal deprotonation of both carboxyl groups and protonation of the amino group.

   

Oxomethylthiobutanoic acid

Oxomethylthiobutanoic acid

C5H8O3S (148.0194)