帕罗西汀
细胞色素P450
血红素
活动站点
化学
酶
立体化学
效力
生物化学
体外
受体
血清素
作者
Emadeldin M. Kamel,Al Mokhtar Lamsabhi
摘要
The potency of paroxetine as a P450 inhibitor is mainly attributed to the availability of two active sites on its structure, its compatibility with P450's active site and the ease of its tight coordination to heme iron.
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