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1-甲基-3-(3-吡啶基)-5-(2-羟甲基苯基)-1H-1,2,4-三唑(一种潜在的镇静催眠化合物)在处置和代谢方面的种属差异。

Species differences in the disposition and metabolism of 1-methyl-3-(3-pyridyl)-5-(2-hydroxy-methylphenyl)-1H-1,2,4-triazole, a potential sedative-hypnotic compound.

作者信息

Assandri A, Omodei-Salè A, Ferrari P, Tuan G, Perazzi A, Ripamonti A, Martinelli E

出版信息

Xenobiotica. 1982 Jan;12(1):19-30. doi: 10.3109/00498258209052451.

Abstract
  1. Disposition and metabolism of 1-methyl-3-(3-pyridyl)-5-(2-hydroxy-methylphenyl)-1H-1,2,4-triazole, a new sedative-hypnotic, were studied in rats (i.v. and p.o.), cats (i.v.) and human volunteers (p.o.) with 14C-labelled drug. 2. In rat and man, the compound is well absorbed, extensively metabolized, and excreted mostly through the kidney; it has short plasma half-lives, 0.6 h in rat, 0.9 h in man, and 1.9 h in cat. 3. In rat and man metabolism involves N-oxidation of the pyridine ring (Metabolite I), and in cat oxidation of the hydroxymethyl group (Metabolite II). Four other conjugated metabolites (III-VI) isolated from rat urine and bile, and from urine of cats and man, have been characterized. 4. The unchanged compound, but not its metabolites, crosses the blood-brain barrier in rat and cat. 5. The species differences in the disposition and metabolism of the compound are consistent with previous pharmacological data indicating a greater and more prolonged effect in cat.
摘要
  1. 用14C标记的新型镇静催眠药1-甲基-3-(3-吡啶基)-5-(2-羟甲基苯基)-1H-1,2,4-三唑在大鼠(静脉注射和口服)、猫(静脉注射)和人类志愿者(口服)中进行了处置和代谢研究。2. 在大鼠和人类中,该化合物吸收良好,广泛代谢,主要通过肾脏排泄;其血浆半衰期较短,大鼠为0.6小时,人类为0.9小时,猫为1.9小时。3. 在大鼠和人类中,代谢涉及吡啶环的N-氧化(代谢物I),在猫中涉及羟甲基的氧化(代谢物II)。从大鼠尿液和胆汁以及猫和人类尿液中分离出的其他四种共轭代谢物(III-VI)已得到表征。4. 未变化的化合物而非其代谢物在大鼠和猫中可穿过血脑屏障。5. 该化合物在处置和代谢方面的种属差异与先前的药理学数据一致,表明在猫中作用更强且持续时间更长。

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