Chemistry:3-Maleylpyruvic acid
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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 | |
Tracking categories (test):
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.[1] It is converted into 3-fumarylpyruvate by maleylpyruvate isomerase.[2]
References
Original source: https://en.wikipedia.org/wiki/3-Maleylpyruvic acid.
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