Rendić S, Ruf H H
Xenobiotica. 1985 May;15(5):399-405. doi: 10.3109/00498258509045010.
Pirenzepine interacts with the haem iron of cytochrome P-450 from rat-and pig-liver microsomes, to give absorption spectra with max. at 424-429 nm, and min. at 391-399 nm. Binding to cytochrome P-450 was not detected with human-liver microsomes. Inhibition of 7-ethoxycoumarin dealkylation by pirenzepine using rat-liver microsomes gave values of I50 = 5 mM and Kis = 0.53 mM. E.p.r. spectra showed that pirenzepine probably interacts with the haem iron through the pirenzepine N-4(1) tertiary amine group.
哌仑西平与大鼠和猪肝微粒体中的细胞色素P-450的血红素铁相互作用,产生最大吸收光谱在424 - 429nm,最小吸收光谱在391 - 399nm。未检测到哌仑西平与人肝微粒体结合。使用大鼠肝微粒体时,哌仑西平对7-乙氧基香豆素脱烷基作用的抑制给出I50 = 5 mM和Kis = 0.53 mM的值。电子顺磁共振光谱表明,哌仑西平可能通过哌仑西平的N-4(1)叔胺基团与血红素铁相互作用。