Science for Life Laboratory, Department of Medicinal Chemistry, Uppsala University, Box 574, SE-75123, Uppsala, Sweden.
Org Biomol Chem. 2018 Jan 31;16(5):698-702. doi: 10.1039/c7ob03030d.
Selective androgen receptor modulators (SARMs) are a class of androgen receptor drugs, which have a high potential to be performance enhancers in human and animal sports. Arylpropionamides are one of the major SARM classes and get rapidly metabolized significantly complicating simple detection of misconduct in blood or urine sample analysis. Specific drug-derived metabolites are required as references due to a short half-life of the parent compound but are generally lacking. The difficulty in metabolism studies is the determination of the correct regio and stereoselectivity during metabolic conversion processes. In this study, we have elucidated and verified the chemical structure of two major equine arylpropionamide-based SARM metabolites using a combination of chemical synthesis and liquid chromatography-mass spectrometry (LC-MS) analysis. These synthesized SARM-derived metabolites can readily be utilized as reference standards for routine mass spectrometry-based doping control analysis of at least three commonly used performance-enhancing drugs to unambigously identify misconduct.
选择性雄激素受体调节剂 (SARMs) 是一类雄激素受体药物,在人类和动物运动中具有成为性能增强剂的巨大潜力。芳基丙酰胺类是主要的 SARM 类别之一,代谢迅速,大大增加了血液或尿液样本分析中不当行为的简单检测的难度。由于母体化合物的半衰期短,通常缺乏特异性药物衍生代谢物,因此需要作为参考。代谢研究的难点在于确定代谢转化过程中正确的区域和立体选择性。在这项研究中,我们使用化学合成和液相色谱-质谱 (LC-MS) 分析相结合的方法,阐明并验证了两种主要的基于芳基丙酰胺的马用 SARM 代谢物的化学结构。这些合成的 SARM 衍生代谢物可以很容易地用作常规基于质谱的兴奋剂控制分析的参考标准,用于至少三种常用的性能增强药物,以明确识别不当行为。