Names | |
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Preferred IUPAC name
(2E)-4,6-Dioxohept-2-enedioic acid | |
Other names
(E)-4,6-Dioxohept-2-enedioic acid
| |
Identifiers | |
| |
3D model (
JSmol)
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|
ChEBI | |
ChemSpider | |
KEGG | |
PubChem
CID
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UNII | |
CompTox Dashboard (
EPA)
|
|
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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).
|
3-Fumarylpyruvic acid, or 3-fumarylpyruvate, is a dicarboxylic acid formed from the isomerisation of 3-maleylpyruvate by maleylpyruvate isomerase. [1] It is converted into fumarate and pyruvate by 3-fumarylpyruvate hydrolase. [2]
Names | |
---|---|
Preferred IUPAC name
(2E)-4,6-Dioxohept-2-enedioic acid | |
Other names
(E)-4,6-Dioxohept-2-enedioic acid
| |
Identifiers | |
| |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
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).
|
3-Fumarylpyruvic acid, or 3-fumarylpyruvate, is a dicarboxylic acid formed from the isomerisation of 3-maleylpyruvate by maleylpyruvate isomerase. [1] It is converted into fumarate and pyruvate by 3-fumarylpyruvate hydrolase. [2]