5-Hidroksi-izourinat
| 5-Hidroksi-izourinat | |||
|---|---|---|---|
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| IUPAC ime |
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| Identifikacija | |||
| CAS registarski broj | 6960-30-1 | ||
| PubChem[1][2] | 250388 | ||
| ChemSpider[3] | 219288  Y | ||
| KEGG[4] | C11821 | ||
| MeSH | 5-Hydroxyisourate | ||
| ChEBI | 18072 | ||
| Jmol-3D slike | Slika 1 Slika 2 | ||
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| Svojstva | |||
| Molekulska formula | C5H4N4O4 | ||
| Molarna masa | 184,11 g/mol | ||
| Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala | |||
| Infobox references | |||
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.[5][6]
Reference
- ↑ 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. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
- ↑ 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.
- ↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
- ↑ 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.
- ↑ Perry A. Frey,Dexter B. Northrop (1999). Enzymatic mechanisms. IOS Press. ISBN 978-9051994322.
- ↑ Silverman, Richard B. (2002). The organic chemistry of enzyme-catalyzed reactions. Academic Press. ISBN 978-0-12-643731-7.
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