止痛药
羟吗啡酮
药理学
羟考酮
代谢物
药代动力学
类阿片
CYP2D6型
药品
活性代谢物
化学
医学
受体
细胞色素P450
内科学
新陈代谢
作者
R. Klimas,Diana Witticke,Sarah El Fallah,Gerd Mikus
标识
DOI:10.1517/17425255.2013.779669
摘要
This article's calculations demonstrate that OC itself is responsible for the analgesic effect. Although OM and noroxymorphone have much higher µ-receptor affinity than the parent drug, the metabolite concentrations at the site of action are very low. This suggests that there is a minimal analgesic effect from these metabolites.
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