Chemistry:Oxipurinol
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Revision as of 06:41, 23 June 2022 by imported>Steve Marsio (add)
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| Names | |
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| Preferred IUPAC name
1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dione | |
| Other names
2,5-Dihydro-1H-pyrazolo[3,4-d]pyrimidine-4,6-dione
Alloxanthine | |
| Identifiers | |
3D model (JSmol)
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| 139956 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| EC Number |
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| KEGG | |
| MeSH | Oxypurinol |
PubChem CID
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| UNII | |
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| Properties | |
| C5H4N4O2 | |
| Molar mass | 152.11086 |
| Appearance | white crystals |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Oxipurinol (INN, or oxypurinol USAN) is an inhibitor of xanthine oxidase.[1] It is an active metabolite of allopurinol and it is cleared renally.[2] In cases of renal disease, this metabolite will accumulate to toxic levels. By inhibiting xanthine oxidase, it reduces uric acid production. High serum uric acid levels may result in gout, kidney stones, and other medical conditions.
References
- ↑ Stocker, Sophie L; McLachlan, Andrew J; Savic, Radojka M; Kirkpatrick, Carl M; Graham, Garry G; Williams, Kenneth M; Day, Richard O (2012). "The pharmacokinetics of oxypurinol in people with gout". British Journal of Clinical Pharmacology 74 (3): 477–489. doi:10.1111/j.1365-2125.2012.04207.x. PMID 22300439.
- ↑ Elion, Gertrude B; Yü, Ts'ai-Fan; Gutman, Alexander B; Hitchings, George H (1968). "Renal clearance of oxipurinol, the chief metabolite of allopurinol". The American Journal of Medicine 45 (1): 69–77. doi:10.1016/0002-9343(68)90008-9. PMID 5658870.
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