化学
代谢稳定性
氟
药品
药物代谢
药物发现
组合化学
有机化学
透视图(图形)
计算化学
生化工程
药代动力学
新陈代谢
机制(生物学)
代谢途径
有机合成
工作(物理)
生物转化
化学稳定性
作者
Pankaj Bhattarai,Trevor A. Trombley,Ryan A. Altman
标识
DOI:10.1021/acs.jmedchem.5c02359
摘要
The incorporation of fluorine and fluorinated motifs into medicinally relevant scaffolds can improve the metabolic and pharmacokinetic properties (DMPK) of drug molecules. Typically, this phenomenon is attributed to differences in C-H vs C-F bond strengths, though such an explanation ignores accepted mechanisms of drug metabolism and how fluorine and fluorinated substituents perturb the physicochemical properties of small molecules. Instead of relying on bond strengths, this perspective will review established mechanisms of drug metabolism and provide a mechanistic rationale for the improved metabolic profiles achieved by fluorinating drug candidates. This discussion will connect observed trends in structure-metabolism relationships with known mechanistic features of relevant drug-metabolizing enzymes, with the ultimate goal of improving medicinal chemistry decision-making.
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