首页> 外文期刊>Journal of Labelled Compounds and Radiopharmaceuticals >Design and synthesis of enantiopure 18 18 F‐labelled [ 18 18 F]trifluoromethyltryptophan from 2‐halotryptophan derivatives via copper(I)‐mediated [ 18 18 F]trifluoromethylation and evaluation of its in vitro characterization for the serotonergic system imaging
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Design and synthesis of enantiopure 18 18 F‐labelled [ 18 18 F]trifluoromethyltryptophan from 2‐halotryptophan derivatives via copper(I)‐mediated [ 18 18 F]trifluoromethylation and evaluation of its in vitro characterization for the serotonergic system imaging

机译:通过铜(I)介导的2-卤蛋白衍生物(I)介导的对映号[18 18f]三氟甲基三抗体的设计和合成[18 18°F]三氟甲基化及其对Serotonergic系统成像的体外表征的评价

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We synthesized [ 18 F]trifluoromethyl‐ l ‐tryptophan ([ 18 F]CF 3 ‐ l ‐Trp) using Cu(I)‐mediated [ 18 F]trifluoromethylation to image serotonergic system. Radiochemical yield was 6 ± 1.5% (n = 9), and radiochemical purity was over 99%. The molar activity was 0.44 to 0.76 GBq/μmol. [ 18 F]CF 3 ‐ l ‐Trp was stable for up to 6 hours in mouse and human sera at 37°C. Protein‐binding was 0.26 ± 0.03% and 0.34 ± 0.02% in human and mouse serum at 60 minutes, respectively. In conclusion, enantiopure [ 18 F]CF 3 ‐ l ‐Trp was synthesized as a feasible imaging agent for the serotonergic system.
机译:使用Cu(I)介导的[18 f]三氟甲基化与图像血清烯化学系统合成[18 f]三氟甲基-1-基霉([18f] cf 3 - l -trp)。 放射化学产率为6±1.5%(n = 9),放射化学纯度超过99%。 摩尔活性为0.44至0.76gBQ /μmol。 [18 f] CF 3 - L -TRP在小鼠和37℃下稳定在小鼠和人血清中长达6小时。 60分钟分别在人和小鼠血清中蛋白质结合为0.26±0.03%和0.34±0.02%。 总之,映射[18f] CF 3 - L -TRP作为Serotonergic系统的可行成像剂合成。

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