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On the metabolism of allopurinol. Formation of allopurinol-1-riboside in purine nucleoside phosphorylase deficiency.

作者信息

Reiter S, Simmonds H A, Webster D R, Watson A R

出版信息

Biochem Pharmacol. 1983 Jul 15;32(14):2167-74. doi: 10.1016/0006-2952(83)90222-8.

DOI:10.1016/0006-2952(83)90222-8
PMID:6409116
Abstract

Allopurinol-1-riboside, a major metabolite of allopurinol, is commonly thought to be directly synthesized by purine nucleoside phosphorylase (PNP) in vivo. As this enzyme is otherwise believed to function in vivo primarily in the direction of nucleoside breakdown, we have determined by high performance liquid chromatography and a conventional chromatographic method the urinary metabolites of allopurinol in a child deficient of PNP. In this patient approximately 40% of urinary allopurinol metabolites consisted of allopurinol-1-riboside, thus proving the possibility of indirect formation of allopurinol-1-riboside via allopurinol-1-ribotide in vivo, catalysed by hypoxanthine guanine phosphoribosyltransferase (HGPRT) and a phosphatase.

摘要

相似文献

1
On the metabolism of allopurinol. Formation of allopurinol-1-riboside in purine nucleoside phosphorylase deficiency.
Biochem Pharmacol. 1983 Jul 15;32(14):2167-74. doi: 10.1016/0006-2952(83)90222-8.
2
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4
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Altered purine and pyrimidine metabolism in erythrocytes with purine nucleoside phosphorylase deficiency.嘌呤核苷磷酸化酶缺乏的红细胞中嘌呤和嘧啶代谢的改变。
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