5-Hydroxyisourate

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5-Hydroxyisourate
5-Hydroxyisourate.svg
Names
IUPAC name
5-hydroxy-3,7-dihydropurine-2,6,8-trione
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
MeSH 5-Hydroxyisourate
  • InChI=1S/C5H4N4O4/c10-2-5(13)1(6-3(11)8-2)7-4(12)9-5/h13H,(H3,6,7,8,9,10,11,12) checkY
    Key: LTQYPAVLAYVKTK-UHFFFAOYSA-N checkY
  • InChI=1/C5H4N4O4/c10-2-5(13)1(6-3(11)8-2)7-4(12)9-5/h13H,(H3,6,7,8,9,10,11,12)
    Key: LTQYPAVLAYVKTK-UHFFFAOYAS
  • C12=NC(=O)NC1(C(=O)NC(=O)N2)O
  • O=C1NC(=O)N/C2=N/C(=O)NC12O
Properties
C5H4N4O4
Molar mass 184.11 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N  (what is checkY☒N ?)
Infobox references

5-Hydroxyisourate is a molecule with a formula of C5H4N4O4 and molecular weight of 184.110 g/mol. It is the product of the oxidation of uric acid by urate oxidase.[1][2]

References[]

  1. ^ Perry A. Frey,Dexter B. Northrop (1999). Enzymatic mechanisms. IOS Press. ISBN 978-9051994322.
  2. ^ Richard B. Silverman (2002). The organic chemistry of enzyme-catalyzed reactions. Academic Press. ISBN 978-0-12-643731-7.

See also[]



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