氯丙嗪
化学
代谢物
镇静剂
吩噻嗪
聚合
药理学
体内
生物化学
生物
有机化学
聚合物
生物技术
作者
Elwyn Elias,James L. Boyer
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1979-12-21
卷期号:206 (4425): 1404-1406
被引量:68
标识
DOI:10.1126/science.574316
摘要
Hepatic hydroxylated metabolites of chlorpromazine (10(-5)M to 10(-4)M), a frequently used phenothiazine tranquilizer, produce solid gel formation with filamentous actin, but the less toxic chlorpromazine sulfoxide metabolite does not. At higher concentrations (5 x 10(-4)M) chlorpromazine inhibits actin polymerization. These dose-response relationships parallel the drug's hepatic toxicity in vivo and suggest that interactions between chloropromazine or chlorpromazine metabolites and actin could be an underlying mechanism of cell injury.
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