Spontaneous hydroxylation of a cyclization intermediate of allopurinol
- 1 May 1985
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 50 (11) , 1847-1852
- https://doi.org/10.1021/jo00211a012
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Methylated 7‐Deazahypoxanthines as Regiochemical Probes of Xanthine OxidaseEuropean Journal of Biochemistry, 1983
- Nucleosides, 381) The Ribonucleosides of AllopurinolEuropean Journal of Inorganic Chemistry, 1981
- Allopurinol ribonucleoside as an antileishmanial agent. Biological effects, metabolism, and enzymatic phosphorylation.Journal of Biological Chemistry, 1979
- Synthesis of fused [1,2,6]thiadiazine 1,1-dioxides as potential transition-state analog inhibitors of xanthine oxidase and guanaseJournal of Medicinal Chemistry, 1979
- The mechanism of action of xanthine oxidase. The relationship between the rapid and very rapid molybdenum electron-paramagnetic-resonance signalsBiochemical Journal, 1979
- Studies on the chemical reactivity and the physical properties of allopurinol (pyrazolo[3,4-d]pyrimidin-4-one) and related compoundsJournal of the Chemical Society, Perkin Transactions 1, 1979
- Oxidation of N-methyl substituted hypoxanthines, xanthines, purine-6,8-diones and the corresponding 6-thioxo derivatives by bovine milk xanthine oxidaseBiochimica et Biophysica Acta (BBA) - Enzymology, 1976
- Potentiation by inhibition of drug degradation : 6-substituted purines and xanthine oxidaseBiochemical Pharmacology, 1963