对乙酰氨基酚
药理学
化学
肝损伤
代谢物
止痛药
解热药
戒毒(替代医学)
氧化磷酸化
新陈代谢
药物代谢
酚中毒
葡萄糖醛酸
加药
重编程
活性代谢物
细胞色素P450
氧化应激
毒性
细胞凋亡
胆汁淤积
药代动力学
药品
肝毒性
作者
Shuanglong Chen,Jiaxin Chang,沙裕彬,Desheng Du,Qingqing Wang,Zhenzhou Jiang,Jianguo Sun,Weiwei Guo,Yueqin Zheng
标识
DOI:10.1021/acs.jmedchem.6c01005
摘要
Acetaminophen (APAP) overdose is a leading cause of acute liver failure, and N -acetylcysteine therapy is highly time dependent. APAP hepatotoxicity results from cytochrome P450–mediated oxidative bioactivation to N -acetyl- p -benzoquinone imine (NAPQI). Here, we report an electron effect–guided metabolic reprogramming strategy based on amide-to-thioamide modification to suppress APAP bioactivation while preserving efficacy. We synthesized a thioamide-modified APAP analogue, SAPAP, and evaluated its metabolism, hepatic safety, and pharmacological activity. SAPAP redirected metabolic flux toward glucuronide and sulfate conjugation while minimizing oxidative metabolite formation. In acute overdose and 28-day subchronic dosing models, SAPAP caused markedly less liver injury than equimolar APAP, with improved histopathology, reduced serum transaminases, and attenuated inflammatory responses. SAPAP also retained analgesic and antipyretic efficacy in established models. These findings demonstrate that thiocarbonyl-driven electronic effects can decouple therapeutic efficacy from hepatotoxic liability, offering a preventive strategy against APAP-induced liver injury.
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