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Mass spectrometric analyses of urinary clomiphene and toremifene metabolites in doping control by liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QTOF)

机译:液相色谱四极杆飞行时间质谱(LC-QTOF)对掺杂控制中的尿克罗米芬和托瑞米芬代谢产物进行质谱分析

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Clomiphene and toremifene, two chlorine-containing selective estrogen receptor modulators (SERMs) with a common triphenylethylene structure, are prohibited by World Anti-Doping Agency (WADA) out-of-competition and in-competition. In this paper, we investigated the metabolic pathway and different drug metabolites in human urine collected from healthy volunteers by liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QTOF) with accurate mass measurement. Four unreported metabolites of toremifene at m/z 418.2015 and 456.1937 and three clomiphene metabolites at m/z 482.2094 and 468.1936 were detected in positive full scan mode using an electrospray ionization source, and further structural elucidation was carried out in targeted MS/MS mode. Based on the fragmentation pattern observed for those metabolites available as reference standards, the chemical structures of these unreported metabolites were identified. Of all these new metabolites, an unordinary dimethoxylated metabolite of clomiphene was first reported.
机译:世界反兴奋剂机构(WADA)在比赛期间和比赛期间禁止使用克罗米芬和托瑞米芬这两种具有共同三苯乙烯结构的含氯选择性雌激素受体调节剂(SERM)。在本文中,我们通过液相色谱四极杆飞行时间质谱(LC-QTOF)和准确的质量测量,研究了从健康志愿者那里收集的人体尿液中的代谢途径和不同的药物代谢物。使用电喷雾电离源在正全扫描模式下检测到m / z 418.2015和456.1937处的托瑞米芬4种未报告的代谢物以及m / z 482.2094和468.1936处的3种克罗米芬代谢物,并在目标MS / MS模式下进行了进一步的结构解析。基于观察到的那些作为参考标准品的代谢物的碎片图谱,鉴定了这些未报告代谢物的化学结构。在所有这些新的代谢产物中,首次报道了克罗米酚的非常规二甲氧基化代谢产物。

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