5-Hidroksi-izourinat

5-Hidroksi-izourinat
Nazivi
	IUPAC naziv 5-hidroksi-3,7-dihidropurin-2,6,8-trion
Identifikacija
CAS broj	6960-30-1;
3D model (Jmol)	interaktivna slika; interaktivna slika;
ChEBI	CHEBI:18072 ;
ChemSpider	219288 ;
KEGG	C11821 ;
MeSH	5-Hydroxyisourate
PubChem C ID	250388;
	SMILES C12=NC(=O)NC1(C(=O)NC(=O)N2)O; O=C1NC(=O)N/C2=N/C(=O)NC12O; ; ; ; ;
Svojstva
Hemijska formula	C5H4N4O4
Molarna masa	184,11 g/mol
	Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa).
	verifikuj (šta je ?)
	Reference infokutije

5-Hidroksi-izourinat je molekul sa formulom C₅H₄N₄O₄ i molekulskom težinom od 184,110 g/mol. On je product oksidacije urinske kiseline posredstvom enzima urat oksidaza.^[4]^[5]

Reference

^ Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
^ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
^ Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
^ Perry A. Frey,Dexter B. Northrop (1999). Enzymatic mechanisms. IOS Press. ISBN 978-90-5199-432-2.
^ Silverman, Richard B. (2002). The organic chemistry of enzyme-catalyzed reactions. Academic Press. ISBN 978-0-12-643731-7.

Perry A. Frey,Dexter B. Northrop (1999). Enzymatic mechanisms. IOS Press. ISBN 978-90-5199-432-2.