Fumarylacetoacetic acid
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| Preferred IUPAC name
(2E)-4,6-Dioxooct-2-enedioic acid | |
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3D model (JSmol)
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| ChemSpider | |
| MeSH | Fumarylacetoacetate |
PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C8H8O6 | |
| Molar mass | 200.146 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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Fumarylacetoacetic acid (fumarylacetoacetate) is an intermediate in the metabolism of tyrosine. It is formed through the conversion of 4-maleylacetoacetic acid into fumarylacetoacetic acid by the enzyme maleylacetoacetate isomerase. Fumarylacetoacetic acid is hydrolyzed by the enzyme fumarylacetoacetate hydrolase (FAH), producing acetoacetate and fumarate. These compounds may then enter various other metabolic pathways.