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3-Fumarylpyruvic acid

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This is an old revision of this page, as edited by WildCation (talk | contribs) at 15:39, 18 April 2017 (Chembox edits: Added CSID, InChIs, KEGG). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

3-Fumarylpyruvic acid
Names
IUPAC name
(E)-4,6-Dioxohept-2-enedioic acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
  • 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).

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]

References

  1. ^ Lack L (1961). "Enzymic cis-trans isomerization of maleylpyruvic acid". J. Biol. Chem. 236: 2835–2840. 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: 3057–3063. doi:10.1128/JB.01188-10. PMC 3133195. PMID 21498645. {{cite journal}}: Unknown parameter |last-author-amp= ignored (|name-list-style= suggested) (help)