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5-Hydroxyisourate
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Names
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IUPAC name
5-hydroxy-3,7-dihydropurine-2,6,8-trione
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Identifiers
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3D model (JSmol)
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ChEBI
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ChemSpider
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KEGG
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MeSH
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5-Hydroxyisourate
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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) YKey: LTQYPAVLAYVKTK-UHFFFAOYSA-N YInChI=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
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C12=NC(=O)NC1(C(=O)NC(=O)N2)O O=C1NC(=O)N/C2=N/C(=O)NC12O
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Properties
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C5H4N4O4
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Molar mass
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184.11 g/mol
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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N (what is YN ?)
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Infobox references
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Chemical compound
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[]
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