3-Maleylpyruvic acid
| Names | |
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| Preferred IUPAC name
(2Z)-4,6-Dioxohept-2-enedioic acid | |
| Identifiers | |
3D model (JSmol)
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| 1725756 | |
| ChEBI | |
| ChemSpider | |
| KEGG | |
PubChem CID
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| Properties | |
| C7H6O6 | |
| Molar mass | 186.119 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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3-Maleylpyruvic acid, or 3-maleylpyruvate, is a dicarboxylic acid formed by the oxidative ring opening of gentisic acid by gentisate 1,2-dioxygenase during the metabolism of tyrosine. It is converted into 3-fumarylpyruvate by maleylpyruvate isomerase.