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匹那西泮:N-去甲基地西泮的前体。

Pinazepam: a precursor of N-desmethyldiazepam.

作者信息

Pacifici G M, Placidi G F, Fornaro P, Gomeni R

出版信息

Eur J Clin Pharmacol. 1982;22(3):225-8. doi: 10.1007/BF00545219.

Abstract

The plasma profile of a single oral dose of pinazepam 10 mg was studied in 6 healthy male volunteers, aged 26 to 31 years. The concentrations of the parent compound and of its metabolite in plasma were measured by gas-chromatography. The peak plasma levels of pinazepam was 36.8 +/- 5.1 ng/ml and of N-desmethyldiazepam 150 +/- 13.3 ng/ml. The plasma concentration of the metabolite become higher than that of the parent compound shortly after administration, suggesting that pinazepam acts as a prodrug.

摘要

对6名年龄在26至31岁的健康男性志愿者进行了研究,测定他们单次口服10毫克匹那西泮后的血浆情况。采用气相色谱法测定血浆中母体化合物及其代谢物的浓度。匹那西泮的血浆峰值水平为36.8±5.1纳克/毫升,N-去甲基地西泮为150±13.3纳克/毫升。给药后不久,代谢物的血浆浓度就高于母体化合物,这表明匹那西泮起前体药物的作用。

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