Exact Mass: 167.9744

Exact Mass Matches: 167.9744

Found 59 metabolites which its exact mass value is equals to given mass value 167.9744, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Phosphoenolpyruvic acid

Phosphoenolpyruvic Acid Trisodium Salt monohydrate

C3H5O6P (167.9824)


Phosphoenolpyruvate, also known as pep or 2-(phosphonooxy)-2-propenoic acid, is a member of the class of compounds known as phosphate esters. Phosphate esters are organic compounds containing phosphoric acid ester functional group, with the general structure R1P(=O)(R2)OR3. R1,R2 = O,N, or halogen atom; R3 = organyl group. Phosphoenolpyruvate is soluble (in water) and an extremely strong acidic compound (based on its pKa). Phosphoenolpyruvate can be found in a number of food items such as okra, endive, chestnut, and dandelion, which makes phosphoenolpyruvate a potential biomarker for the consumption of these food products. Phosphoenolpyruvate can be found primarily in blood, cellular cytoplasm, and saliva, as well as in human prostate tissue. Phosphoenolpyruvate exists in all living species, ranging from bacteria to humans. In humans, phosphoenolpyruvate is involved in several metabolic pathways, some of which include glycolysis, amino sugar metabolism, gluconeogenesis, and glycogenosis, type IC. Phosphoenolpyruvate is also involved in several metabolic disorders, some of which include glycogen storage disease type 1A (GSD1A) or von gierke disease, salla disease/infantile sialic acid storage disease, phosphoenolpyruvate carboxykinase deficiency 1 (PEPCK1), and pyruvate dehydrogenase complex deficiency. Phosphoenolpyruvate (2-phosphoenolpyruvate, PEP) as the ester derived from the enol of pyruvate and phosphate. It exists as an anion; the parent acid, which is only of theoretical interest, is phosphoenolpyruvic acid. PEP is an important intermediate in biochemistry. It has the highest-energy phosphate bond found (−61.9 kJ/mol) in living organisms, and is involved in glycolysis and gluconeogenesis. In plants, it is also involved in the biosynthesis of various aromatic compounds, and in carbon fixation; in bacteria, it is also used as the source of energy for the phosphotransferase system . Phosphoenolpyruvate (PEP) is an important chemical compound in biochemistry. It has a high energy phosphate bond, and is involved in glycolysis and gluconeogenesis. In glycolysis, PEP is formed by the action of the enzyme enolase on 2-phosphoglycerate. Metabolism of PEP to pyruvate by pyruvate kinase (PK) generates 1 molecule of adenosine triphosphate (ATP) via substrate-level phosphorylation. ATP is one of the major currencies of chemical energy within cells. In gluconeogenesis, PEP is formed from the decarboxylation of oxaloacetate and hydrolysis of 1 guanosine triphosphate molecule. This reaction is catalyzed by the enzyme phosphoenolpyruvate carboxykinase (PEPCK). This reaction is a rate-limiting step in gluconeogenesis. (wikipedia). [Spectral] Phosphoenolpyruvate (exact mass = 167.98237) and 6-Phospho-D-gluconate (exact mass = 276.02463) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. Acquisition and generation of the data is financially supported in part by CREST/JST. KEIO_ID P007

   

PHOSPHONOPYRUVATE

3-Phosphonopyruvate

C3H5O6P (167.9824)


   

3-Sulfopyruvic acid

2-Carboxy-2-oxoethanesulphonic acid

C3H4O6S (167.9729)


Sulfopyruvate, also known as 2-carboxy-2-oxoethanesulfonic acid or beta-sulfopyruvic acid, belongs to alpha-keto acids and derivatives class of compounds. Those are organic compounds containing an aldehyde substituted with a keto group on the adjacent carbon. Sulfopyruvate is soluble (in water) and an extremely strong acidic compound (based on its pKa). Sulfopyruvate can be found in a number of food items such as french plantain, sago palm, sweet cherry, and ostrich fern, which makes sulfopyruvate a potential biomarker for the consumption of these food products. Sulfopyruvate exists in all living organisms, ranging from bacteria to humans. 3-Sulfopyruvic acid is the product of the transamination of cysteinesulfonate in a reaction catalyzed by aspartate aminotransferase. 3-sulfopyruvic acid is stable and is reduced by malate dehydrogenase to beta-sulfolactate, which is excreted in the urine. Cysteinesulfonate, 3-sulfopyruvic acid, and beta-sulfolactate are reversibly interconverted in vivo. (PMID: 3346220).

   

Hydroxypyruvaldehyde phosphate

Hydroxypyruvaldehyde phosphate

C3H5O6P (167.9824)


   

L-glyceraldehyde 3-phosphate

Glyceraldehyde 3-phosphoric acid dianion

C3H5O6P (167.9824)


L-glyceraldehyde 3-phosphate, also known as 3 phosphoglyceraldehyde, is a member of the class of compounds known as glyceraldehyde-3-phosphates. Glyceraldehyde-3-phosphates are compounds containing a glyceraldehyde substituted at position O3 by a phosphate group. L-glyceraldehyde 3-phosphate is soluble (in water) and a moderately acidic compound (based on its pKa). L-glyceraldehyde 3-phosphate can be found in a number of food items such as fruits, cowpea, common sage, and brussel sprouts, which makes L-glyceraldehyde 3-phosphate a potential biomarker for the consumption of these food products.

   

Phosphonopyruvic acid

Phosphonopyruvic acid

C3H5O6P (167.9824)


   

3,3-dichloro-acrylic acid ethyl ester

3,3-dichloro-acrylic acid ethyl ester

C5H6Cl2O2 (167.9745)


   

PHOSPHO(ENOL)PYRUVIC ACID

PHOSPHO(ENOL)PYRUVIC ACID

C3H5O6P (167.9824)


   

2-dihydroxyphosphinoyloxyacrylic acid

Phosphoenolpyruvic Acid Trisodium Salt monohydrate

C3H5O6P (167.9824)


   

Phosphoenolpyruvic acid

2-dihydroxyphosphinoyloxyacrylic acid

C3H5O6P (167.9824)


A monocarboxylic acid that is acrylic acid substituted by a phosphonooxy group at position 2. It is a metabolic intermediate in pathways like glycolysis and gluconeogenesis.

   

phosphoenolpyruvate

2-dihydroxyphosphinoyloxyacrylic acid

C3H5O6P (167.9824)


   

5-Chloro-2,4,6-trifluoropyrimidine

5-Chloro-2,4,6-trifluoropyrimidine

C4ClF3N2 (167.9702)


   

ethyl bromoacetate-2,2-d2

ethyl bromoacetate-2,2-d2

C4H5BrD2O2 (167.9755)


   

4-Chloro-1-benzothiophene

4-Chloro-1-benzothiophene

C8H5ClS (167.98)


   

1-Bromo-2-(methoxymethoxy)ethane

1-Bromo-2-(methoxymethoxy)ethane

C4H9BrO2 (167.9786)


   

flupropanate-sodium

flupropanate-sodium

C3HF4NaO2 (167.981)


   

Bromo-PEG2-alcohol

Bromo-PEG2-alcohol

C4H9BrO2 (167.9786)


   

2,2-DICHLORO-1-METHYLCYCLOPROPANECARBOXYLIC ACID

2,2-DICHLORO-1-METHYLCYCLOPROPANECARBOXYLIC ACID

C5H6Cl2O2 (167.9745)


   

1-Chloro-1,1,3,3,3-pentafluoropropane

1-Chloro-1,1,3,3,3-pentafluoropropane

C3H2ClF5 (167.9765)


   

Cyclohexanehexone

Cyclohexanehexone

C6O6 (167.9695)


   

7-Chlorobenzo[b]thiophene

7-Chlorobenzo[b]thiophene

C8H5ClS (167.98)


   

CALCIUM ITACONATE

CALCIUM ITACONATE

C5H4CaO4 (167.9735)


   

3H-1,2-BENZODITHIOL-3-ONE

3H-1,2-BENZODITHIOL-3-ONE

C7H4OS2 (167.9704)


   

1-bromo-3-methoxypropan-1-ol

1-bromo-3-methoxypropan-1-ol

C4H9BrO2 (167.9786)


   

dimethylmalonyl chloride

dimethylmalonyl chloride

C5H6Cl2O2 (167.9745)


   

Thiazolo[4,5-c]pyridine-2-thiol

Thiazolo[4,5-c]pyridine-2-thiol

C6H4N2S2 (167.9816)


   

1,2-Butanediol, 4-bromo-

1,2-Butanediol, 4-bromo-

C4H9BrO2 (167.9786)


   

6-Chloro-1-benzothiophene

6-Chloro-1-benzothiophene

C8H5ClS (167.98)


   

1,3-benzodithiol-2-one

1,3-benzodithiol-2-one

C7H4OS2 (167.9704)


   

pyrido[3,2-d][1,3]thiazole-2-thiol

pyrido[3,2-d][1,3]thiazole-2-thiol

C6H4N2S2 (167.9816)


   

Arsonic acid,As-propyl-

Arsonic acid,As-propyl-

C3H9AsO3 (167.9768)


   

glutaryl dichloride

glutaryl dichloride

C5H6Cl2O2 (167.9745)


   

5-Chloro-1-benzothiophene

5-Chloro-1-benzothiophene

C8H5ClS (167.98)


   

3,3-Dichlorocyclobutanecarboxylic acid

3,3-Dichlorocyclobutanecarboxylic acid

C5H6Cl2O2 (167.9745)


   

Thieno[2,3-d]pyrimidine-4-thiol

Thieno[2,3-d]pyrimidine-4-thiol

C6H4N2S2 (167.9816)


   

nickel(ii) fluoride tetrahydrate

nickel(ii) fluoride tetrahydrate

F2H8NiO4 (167.9744)


   

Bromoacetaldehyde dimethyl acetal

Bromoacetaldehyde dimethyl acetal

C4H9BrO2 (167.9786)


   

2,4-Pentanedione,1,5-dichloro-

2,4-Pentanedione,1,5-dichloro-

C5H6Cl2O2 (167.9745)


   

THIAZOLO[4,5-B]PYRIDINE-2(3H)-THIONE

THIAZOLO[4,5-B]PYRIDINE-2(3H)-THIONE

C6H4N2S2 (167.9816)


   

THIENO[3,2-B]THIOPHENE-2-CARBALDEHYDE

THIENO[3,2-B]THIOPHENE-2-CARBALDEHYDE

C7H4OS2 (167.9704)


   

DIHYDROXYACETONE PHOSPHATE

DIHYDROXYACETONE PHOSPHATE

C3H5O6P-- (167.9824)


   

(2-Hydroxy-3-oxopropyl) phosphate

(2-Hydroxy-3-oxopropyl) phosphate

C3H5O6P-2 (167.9824)


   

Glycerone phosphate(2-)

Glycerone phosphate(2-)

C3H5O6P-2 (167.9824)


COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

D-glyceraldehyde 3-phosphate(2-)

D-glyceraldehyde 3-phosphate(2-)

C3H5O6P-2 (167.9824)


COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

(R)-3-Sulfolactate

(R)-3-Sulfolactate

C3H4O6S-2 (167.9729)


   

(2S)-3-Sulfolactate

(2S)-3-Sulfolactate

C3H4O6S-2 (167.9729)


   

2-Hydroxy-3-sulfonatopropanoate

2-Hydroxy-3-sulfonatopropanoate

C3H4O6S-2 (167.9729)


   

(2R)-2-(sulfonatooxy)propanoate

(2R)-2-(sulfonatooxy)propanoate

C3H4O6S-2 (167.9729)


   

L-Glyceraldehyde-3-phosphate

L-Glyceraldehyde-3-phosphate

C3H5O6P-2 (167.9824)


   

(S)-2-(sulfonatooxy)propanoate

(S)-2-(sulfonatooxy)propanoate

C3H4O6S-2 (167.9729)


   

2-(Sulfooxy)propanoic acid

2-(Sulfooxy)propanoic acid

C3H4O6S-2 (167.9729)


   

2-phospho-L-lactate

2-phospho-L-lactate

C3H5O6P-2 (167.9824)


   

pentafluoridooxidochromate(V)

pentafluoridooxidochromate(V)

CrF5H5O (167.9666)


   

sulfopyruvate

sulfopyruvate

C3H4O6S (167.9729)


   

Glycerone phosphate(2-)

Glycerone phosphate(2-)

C3H5O6P (167.9824)


A dianionic form of glycerone phosphate arising from deprotonation of the phosphate OH groups; major species at pH 7.3.

   

D-glyceraldehyde 3-phosphate(2-)

D-glyceraldehyde 3-phosphate(2-)

C3H5O6P (167.9824)


Dianion of D-glyceraldehyde 3-phosphate arising from deprotonation of both OH groups of the phosphate.

   

(S)-3-sulfonatolactate(2-)

(S)-3-sulfonatolactate(2-)

C3H4O6S (167.9729)


An optically active form of (S)-3-sulfonatolactate having (S)-configuration.

   

glyceraldehyde 3-phosphate(2-)

glyceraldehyde 3-phosphate(2-)

C3H5O6P (167.9824)


An organophosphate oxoanion taht is the dianion of glyceraldehyde 3-phosphate arising from deprotonation of the phosphate OH groups; major species at pH 7.3.

   

3-Sulfopyruvic acid

3-Sulfopyruvic acid

C3H4O6S (167.9729)


A carboxyalkanesulfonic acid comprising pyruvic acid with a sulfo group attached at the C-3 position.