5-Hydroxyisourate: Difference between revisions

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Revision as of 16:08, 18 March 2023 editSmokefoot (talk \| contribs)Autopatrolled, Extended confirmed users, Pending changes reviewers, Rollbackers74,602 edits thumb\|sequence of oxidation of ureate ← Previous edit		Revision as of 16:10, 18 March 2023 edit undoSmokefoot (talk \| contribs)Autopatrolled, Extended confirmed users, Pending changes reviewers, Rollbackers74,602 edits AllantoinNext edit →
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	'''5-Hydroxyisourate''' is an ] that is produced by the ] of ]. The conversion is a major pathway in the antioxidant properties of ~~ureate~~. The conversion is catalysed by ].<ref>{{cite book \|author =Perry A. Frey,Dexter B. Northrop \| title =Enzymatic ~~mechanisms~~ \| date =1999 \| publisher = IOS Press \| isbn = 978-9051994322 }}</ref><ref>{{cite book \| author =Richard B. Silverman \| title =The organic chemistry of enzyme-catalyzed reactions \| date =2002 \| publisher = Academic Press \| isbn = 978-0-12-643731-7}}</ref><ref>{{cite journal \|doi=10.1007/s00253-010-2455-0\|title=Cofactor-independent oxidases and oxygenases \|year=2010 \|last1=Fetzner \|first1=Susanne \|last2=Steiner \|first2=Roberto A. \|journal=Applied Microbiology and Biotechnology \|volume=86 \|issue=3 \|pages=791–804 \|pmid=20157809 \|s2cid=25377247 }}</ref>		'''5-Hydroxyisourate''' is an ] that is produced by the ] of ]. The conversion is a major pathway in the antioxidant properties of urate. The conversion is catalysed by ].<ref>{{cite book \|author =Perry A. Frey,Dexter B. Northrop \| title =Enzymatic Mechanisms \| date =1999 \| publisher = IOS Press \| isbn = 978-9051994322 }}</ref><ref>{{cite book \| author =Richard B. Silverman \| title =The organic chemistry of enzyme-catalyzed reactions \| date =2002 \| publisher = Academic Press \| isbn = 978-0-12-643731-7}}</ref><ref>{{cite journal \|doi=10.1007/s00253-010-2455-0\|title=Cofactor-independent oxidases and oxygenases \|year=2010 \|last1=Fetzner \|first1=Susanne \|last2=Steiner \|first2=Roberto A. \|journal=Applied Microbiology and Biotechnology \|volume=86 \|issue=3 \|pages=791–804 \|pmid=20157809 \|s2cid=25377247 }}</ref>
	]~~{{clear}}~~		]
			5-Hydroxyisourate rearranges to ].

			{{clear}}
	==References==		==References==
	{{reflist}}		{{reflist}}

Revision as of 16:10, 18 March 2023

5-Hydroxyisourate
Names

IUPAC name 5-hydroxy-3,7-dihydropurine-2,6,8-trione
Identifiers
CAS Number	6960-30-1
3D model (JSmol)	Interactive image Interactive image
ChEBI	CHEBI:18072
ChemSpider	219288
KEGG	C11821
MeSH	5-Hydroxyisourate
PubChem CID	250388
UNII	DU6PJ7L9BX
CompTox Dashboard (EPA)	DTXSID10290591
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)Key: LTQYPAVLAYVKTK-UHFFFAOYSA-N 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 , 100 kPa). N verify (what is ?) Infobox references

Chemical compound

5-Hydroxyisourate is an organic compound that is produced by the oxidation of uric acid. The conversion is a major pathway in the antioxidant properties of urate. The conversion is catalysed by urate oxidase.

5-Hydroxyisourate rearranges to allantoin.

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.
Fetzner, Susanne; Steiner, Roberto A. (2010). "Cofactor-independent oxidases and oxygenases". Applied Microbiology and Biotechnology. 86 (3): 791–804. doi:10.1007/s00253-010-2455-0. PMID 20157809. S2CID 25377247.

Misplaced Pages

5-Hydroxyisourate: Difference between revisions

Revision as of 16:10, 18 March 2023

References

See also