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硫利达嗪及其代谢产物与血清蛋白的结合:一项体外研究。

Binding of thioridazine and thioridazine metabolites to serum proteins. An in vitro study.

作者信息

Nyberg G, Mårtensson E

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1982 Jun;319(3):189-96. doi: 10.1007/BF00495864.

Abstract

The binding constants of the binding between thioridazine and its metabolites, side-chain sulfoxide, side-chain sulfone and ring sulfoxide, on the one hand, and the plasma proteins, alpha 1-acid glycoprotein, albumin and total serum proteins, on the other, were determined. The binding constants between the drug substances and alpha 1-acid glycoprotein were found to be about a thousand times higher than the binding constants between the drug substances and albumin. The binding constants of whole serum were close to those of alpha 1-acid glycoprotein. Analysis of the binding data indicated competition between thioridazine and its metabolites. A number of drug substances were screened for possible binding interaction with thioridazine and its metabolites. Tricyclic antidepressants and propranolol significantly increased the free concentration of thioridazine. Also salicyclic acid and the plasticizing agent, TBEP, had this effect.

摘要

测定了硫利达嗪与其代谢产物(侧链亚砜、侧链砜和环亚砜)与血浆蛋白(α1-酸性糖蛋白、白蛋白和总血清蛋白)之间的结合常数。发现药物与α1-酸性糖蛋白之间的结合常数比药物与白蛋白之间的结合常数高约一千倍。全血清的结合常数与α1-酸性糖蛋白的接近。结合数据的分析表明硫利达嗪与其代谢产物之间存在竞争。筛选了多种药物与硫利达嗪及其代谢产物可能的结合相互作用。三环类抗抑郁药和普萘洛尔显著增加了硫利达嗪的游离浓度。水杨酸和增塑剂TBEP也有这种作用。

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