5-Hydroxyisourate

5-Hydroxyisourate
Names

IUPAC name 5-hydroxy-3,7-dihydropurine-2,6,8-trione
Identifiers
CAS Number	6960-30-1^N
3D model (JSmol)	Interactive image Interactive image
ChEBI	CHEBI:18072^Y
ChemSpider	219288^Y
KEGG	C11821^Y
MeSH	5-Hydroxyisourate
PubChem CID	250388
InChI 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)^Y Key: LTQYPAVLAYVKTK-UHFFFAOYSA-N^Y 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
SMILES C12=NC(=O)NC1(C(=O)NC(=O)N2)O O=C1NC(=O)N/C2=N/C(=O)NC12O
Properties
Chemical formula	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 verify (what is ^YN ?)
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

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

See also

Nucleotide metabolic intermediates

Purine metabolism

Anabolism

R5P→IMP:	R5P PRPP PRA GAR FGAR FGAM AIR CAIR SAICAR AICAR FAICAR
IMP→AMP:	Adenylosuccinate
IMP→GMP:	Xanthosine monophosphate

Catabolism

Pyrimidine metabolism

Anabolism

Catabolism

uracil:	Dihydrouracil 3-Ureidopropionic acid β-Alanine
thymine:	Dihydrothymine β-Ureidoisobutyric acid 3-Aminoisobutyric acid

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