3-Fumarylpyruvic acid

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]

3-Fumarylpyruvic acid
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
UNII
  • InChI=1S/C7H6O6/c8-4(1-2-6(10)11)3-5(9)7(12)13/h1-2H,3H2,(H,10,11)(H,12,13)/b2-1+
    Key: AZCFLHZUFANAOR-OWOJBTEDSA-N
  • OC(=O)\C=C\C(=O)CC(=O)C(O)=O
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

References
  1. Lack L (1961). "Enzymic cis-trans isomerization of maleylpyruvic acid". J. Biol. Chem. 236 (11): 2835–2840. doi:10.1016/S0021-9258(19)76386-8. PMID 14461395.
  2. Qu, Y. & Spain, J.C. (2011). "Molecular and biochemical characterization of the 5-nitroanthranilic acid degradation pathway in Bradyrhizobium sp. strain JS329". J. Bacteriol. 193 (12): 3057–3063. doi:10.1128/JB.01188-10. PMC 3133195. PMID 21498645.


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