5-Hydroxyisourate

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5-Hydroxyisourate

IUPAC name 5-hydroxy-3,7-dihydropurine-2,6,8-trione
Identifiers
CAS number	6960-30-1
PubChem	250388
ChemSpider	219288^Y
KEGG	C11821^Y
MeSH	5-Hydroxyisourate
ChEBI	CHEBI:18072^Y
Jmol-3D images	Image 1 Image 2
SMILES C12=NC(=O)NC1(C(=O)NC(=O)N2)O O=C1NC(=O)N/C2=N/C(=O)NC12O
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
Properties
Molecular formula	C₅H₄N₄O₄
Molar mass	184.11 g/mol
Y (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
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

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)

Biochemical families: carbohydrates
- alcohols
- glycoproteins
- glycosides
lipids
- eicosanoids
- fatty acids / intermediates
- phospholipids
- sphingolipids
- steroids
nucleic acids
- constituents / intermediates
proteins
- Amino acids / intermediates
tetrapyrroles / intermediates

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