Names | |
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Preferred IUPAC name
2-(Phosphonooxy)prop-2-enoic acid | |
Other names
Phosphoenolpyruvic acid, PEP
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
DrugBank | |
ECHA InfoCard | 100.004.830 |
KEGG | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C3H5O6P | |
Molar mass | 168.042 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Phosphoenolpyruvate (2-phosphoenolpyruvate, PEP) is the carboxylic acid derived from the enol of pyruvate and phosphate. It exists as an anion. PEP is an important intermediate in biochemistry. It has the highest-energy phosphate bond found (−61.9 kJ/mol) in 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.[1][2]