首页> 外文期刊>Journal of Labelled Compounds and Radiopharmaceuticals >New radiolabelling chemistry: synthesis of phosphorus-[~(~(18))F]fluorine compounds
【24h】

New radiolabelling chemistry: synthesis of phosphorus-[~(~(18))F]fluorine compounds

机译:新的放射性标记化学:磷-[〜(〜(18))F]氟化合物的合成

获取原文
获取原文并翻译 | 示例
           

摘要

The feasibility of synthesizing compounds containing the P-~(18)F bond has been demonstrated by labelling the pesticide, cholinesterase inhibitor Dimefox (N,N,N',N'-tetramethylphosphorodiamidic fluoride) with F-~(18). Radiolabelling was achieved in high radiochemical yield (96%) by nucleophilic substitution of the chloro group attached to phosphorus, in the oxidation state P(V), by ~(18)F (activated with tetrabutylammonium carbonate in acetonitrile). Given the large number of important biological molecules possessing phosphorus such as oligonucleotides, phospholipids as well as phosphorylated proteins, sugars and steroids, this new labelling chemistry may provide an additional route to radiolabelling these biologically important compounds for use in PET.
机译:通过用F-〜(18)标记农药胆碱酯酶抑制剂Dimefox(N,N,N',N'-四甲基磷酰二酰胺氟化物)证明了合成含P-〜(18)F键的化合物的可行性。放射性标记是通过〜(18)F(在乙腈中用碳酸四丁铵活化),以氧化态P(V),用磷取代连接的磷的氯基团,以高放射化学收率(96%)实现的。考虑到许多重要的具有磷的重要生物分子,例如寡核苷酸,磷脂以及磷酸化的蛋白质,糖和类固醇,这种新的标记化学方法可能为放射性标记这些对PET有用的重要生物化合物提供一条额外的途径。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号