After absorption, prulifloxacin is metabolised by esterases to ulifloxacin, which inhibits the formation of superhelix, cell division and reproduction by interfering the DNA toposomerase.
为前体药,其活性代谢产物通过阻碍DNA拓扑异构酶使细菌DNA无法形
超螺旋,
致细菌细胞无法分裂繁殖。
After absorption, prulifloxacin is metabolised by esterases to ulifloxacin, which inhibits the formation of superhelix, cell division and reproduction by interfering the DNA toposomerase.
为前体药,其活性代谢产物通过阻碍DNA拓扑异构酶使细菌DNA无法形超螺旋,致细菌细胞无法分裂繁殖。
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