代谢
异硫代氰酸酯不会通过隔离的大鼠肝微粒体转化为吡咯代谢物。然而,它在大鼠肠道中被还原为 retrorsine,可能是通过肠道菌群的作用,这就解释了为什么异硫代氰酸酯口服给药比静脉注射毒性大幅增加的原因。
Isatidine is not converted into pyrrolic metabolites by isolated rat liver microsomes. It is, However, reduced to retrorsine in the intestinal tract of rats, possibly by the gut flora, thus accounting for the large increase in toxicity when isatidine is administered by mouth rather than parenterally.
来源:Hazardous Substances Data Bank (HSDB)