羧酸酯酶
药效学
药代动力学
药理学
哌醋甲酯
医学
生物
酶
生物化学
精神科
注意缺陷多动障碍
作者
Yaping Liu,Jiapeng Li,Hao‐Jie Zhu
标识
DOI:10.1080/17425255.2024.2348491
摘要
Current research revealed modest associations of CES genetic polymorphisms with drug exposure and response. Beyond genomic polymorphisms, transcriptional and posttranslational regulations can also significantly affect CES expression and activity and consequently alter PK and PD. Recent advances in plasma biomarkers of drug-metabolizing enzymes encourage the research of plasma protein and metabolite biomarkers for CES1 and CES2, which could lead to the establishment of precision pharmacotherapy regimens for drugs metabolized by CESs. Moreover, our understanding of tissue-specific expression and substrate selectivity of CES1 and CES2 has shed light on improving the design of CES1- and CES2-activated prodrugs.
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