Exact Mass: 177.9452

Exact Mass Matches: 177.9452

Found 19 metabolites which its exact mass value is equals to given mass value 177.9452, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Pyrophosphate

phosphono dihydrogen phosphate

H4O7P2 (177.9432)


The anion, the salts, and the esters of pyrophosphoric acid are called pyrophosphates. The pyrophosphate anion is abbreviated PPi and is formed by the hydrolysis of ATP into AMP in cells. This hydrolysis is called pyrophosphorolysis. The pyrophosphate anion has the structure P2O74-, and is an acid anhydride of phosphate. It is unstable in aqueous solution and rapidly hydrolyzes into inorganic phosphate. Pyrophosphate is an osteotoxin (arrests bone development) and an arthritogen (promotes arthritis). It is also a metabotoxin (an endogenously produced metabolite that causes adverse health affects at chronically high levels). Chronically high levels of pyrophosphate are associated with hypophosphatasia. Hypophosphatasia (also called deficiency of alkaline phosphatase or phosphoethanolaminuria) is a rare, and sometimes fatal, metabolic bone disease. Hypophosphatasia is associated with a molecular defect in the gene encoding tissue non-specific alkaline phosphatase (TNSALP). TNSALP is an enzyme that is tethered to the outer surface of osteoblasts and chondrocytes. TNSALP hydrolyzes several substances, including inorganic pyrophosphate (PPi) and pyridoxal 5-phosphate (PLP), a major form of vitamin B6. When TSNALP is low, inorganic pyrophosphate (PPi) accumulates outside of cells and inhibits the formation of hydroxyapatite, one of the main components of bone, causing rickets in infants and children and osteomalacia (soft bones) in adults. Vitamin B6 must be dephosphorylated by TNSALP before it can cross the cell membrane. Vitamin B6 deficiency in the brain impairs synthesis of neurotransmitters which can cause seizures. In some cases, a build-up of calcium pyrophosphate dihydrate crystals in the joints can cause pseudogout. COVID info from WikiPathways Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

2,2,2-Trichloro-1-methoxyethanol

2,2,2-Trichloro-1-methoxyethanol

C3H5Cl3O2 (177.9355)


   

Pyrophosphate

Pyrophosphate

H4O7P2 (177.9432)


   

2,4-Dichlorobenzenethiol

2,4-Dichlorobenzenethiol

C6H4Cl2S (177.9411)


   

3,4-Dichlorobenzenethiol

3,4-Dichlorobenzenethiol

C6H4Cl2S (177.9411)


   

5-BROMOHYDANTOIN

5-BROMOHYDANTOIN

C3H3BrN2O2 (177.9378)


   

Dichlorophenylphosphine

Dichlorophenylphosphine

C6H5Cl2P (177.9506)


   

2-Methyl-1-oxo-1-phenylpropan-2-yl methanesulfonate

2-Methyl-1-oxo-1-phenylpropan-2-yl methanesulfonate

C6H4Cl2S (177.9411)


   

Propanoic acid,2-hydroxy-, strontium salt (2:1)

Propanoic acid,2-hydroxy-, strontium salt (2:1)

C3H6O3Sr++ (177.9373)


   

4-bromo-3,6-dihydro-2H-thiopyran

4-bromo-3,6-dihydro-2H-thiopyran

C5H7BrS (177.9452)


   

2,6-Dichlorobenzenethiol

2,6-Dichlorobenzenethiol

C6H4Cl2S (177.9411)


   

2,3-Dichlorobenzenethiol

2,3-Dichlorobenzenethiol

C6H4Cl2S (177.9411)


   

3,5-Dichlorobenzenethiol

3,5-Dichlorobenzenethiol

C6H4Cl2S (177.9411)


   

2-(Fluorosulfonyl)difluoroacetic acid

2-(Fluorosulfonyl)difluoroacetic acid

C2HF3O4S (177.9548)


   

2,5-Dichlorobenzenethiol

2,5-Dichlorobenzenethiol

C6H4Cl2S (177.9411)


   

4,5-dichloro-1H-pyrrole-2-carboxylate

4,5-dichloro-1H-pyrrole-2-carboxylate

C5H2Cl2NO2- (177.9463)


   

2,5-Dichloro-6-hydroxypyridin-3-olate

2,5-Dichloro-6-hydroxypyridin-3-olate

C5H2Cl2NO2- (177.9463)


   

Diphosphoric acid

Pyrophosphoric acid

H4O7P2 (177.9432)


An acyclic phosphorus acid anhydride obtained by condensation of two molecules of phosphoric acid. COVID info from WikiPathways Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

3,6-dichloropyridine-2,5-diol(1-)

3,6-dichloropyridine-2,5-diol(1-)

C5H2Cl2NO2 (177.9463)


A organic anion that is the conjugate base of 3,6-dichloropyridine-2,5-diol, resulting from the deprotonation of the 5-hydroxy group.