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[Elimination of triamterene, an antikaliuretic, and its phenolic metabolite, 2,4,7-triamino-6-p-hydroxyphenylpteridine, in the urine of subjects with normal liver function and in subjects suffering from liver cirrhosis].

作者信息

Andrasch H, Fink T, Schmid E

出版信息

Z Gastroenterol. 1971;9(4):240-5.

PMID:5164739
Abstract
摘要

相似文献

1
[Elimination of triamterene, an antikaliuretic, and its phenolic metabolite, 2,4,7-triamino-6-p-hydroxyphenylpteridine, in the urine of subjects with normal liver function and in subjects suffering from liver cirrhosis].
Z Gastroenterol. 1971;9(4):240-5.
2
Altered hydroxylation rate of triamterene in patients with liver cirrhosis.
Int J Clin Pharmacol Ther Toxicol. 1982 Aug;20(8):353-7.
3
Triamterene kinetics and dynamics in cirrhosis.氨苯蝶啶在肝硬化中的动力学和动态变化
Clin Pharmacol Ther. 1984 Jun;35(6):831-7. doi: 10.1038/clpt.1984.121.
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[Pharmacokinetics of xipamide and triamterene in healthy probands].
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Delayed elimination of triamterene and its active metabolite in chronic renal failure.
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9
[Studies of the metabolism of 7-chlor-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepin-2-on].[7-氯-1,3-二氢-3-羟基-5-苯基-2H-1,4-苯并二氮杂卓-2-酮的代谢研究]
Arzneimittelforschung. 1970 Sep;20(9):1232-5.
10
[Age dependence of the pharmacokinetics of triamterene].[氨苯蝶啶药代动力学的年龄依赖性]
Acta Biol Med Ger. 1973;30(1):121-32.

引用本文的文献

1
[Pharmacokinetics of triamterene in healthy subjects and patients with liver and kidney function disorders].氨苯蝶啶在健康受试者及肝肾功能障碍患者中的药代动力学
Klin Wochenschr. 1983 Sep 15;61(18):883-91. doi: 10.1007/BF01537528.
2
Pharmacokinetics of triamterene after i.v. administration to man: determination of bioavailability.氨苯蝶啶静脉注射给人体后的药代动力学:生物利用度的测定。
Eur J Clin Pharmacol. 1983;25(2):237-41. doi: 10.1007/BF00543797.
3
Sulphate conjugation of p-hydroxytriamterene by platelet phenol sulphotransferase: assay conditions and correlation with metabolism in man.
血小板酚磺基转移酶对对羟基氨苯蝶啶的硫酸结合作用:测定条件及其与人体代谢的相关性
Br J Clin Pharmacol. 1983 Feb;15(2):211-20. doi: 10.1111/j.1365-2125.1983.tb01488.x.
4
Plasma and urinary levels of triamterene and certain metabolites after oral administration to man.
Eur J Clin Pharmacol. 1979 Aug;16(1):39-44. doi: 10.1007/BF00644964.