首页> 外文会议>8th International Conference on Isotopes 2014 >Synthesis of ~(123)Iiodoanthraquinones as a Radiotracer of Breast Cancer
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Synthesis of ~(123)Iiodoanthraquinones as a Radiotracer of Breast Cancer

机译:合成〜(123)I碘蒽醌作为乳腺癌的放射性示踪剂

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摘要

We have synthesized and evaluated [~(123)I]anthraquinones as inhibitors of HER-2eu receptor. [~(123)I]anthraquinones is more effective blocking of SK-BR-3 than MCF-7. It has proven that [~(123)I]anthraquinones have a specific activity on HER-2eu overexpressed cell. This preliminary study suggests [~(123)I]anthraquinones are potent breast cancer imaging reagent. The more biological experiments are is on going.
机译:我们已经合成并评估了[〜(123)I]蒽醌作为HER-2 / neu受体的抑制剂。 [〜(123)I]蒽醌比MCF-7更有效地阻断SK-BR-3。已经证明[〜(123)I]蒽醌对HER-2 / neu过表达的细胞具有特定的活性。这项初步研究表明[〜(123)I]蒽醌是有效的乳腺癌显像剂。正在进行更多的生物学实验。

著录项

  • 来源
  • 会议地点 Chicago IL(US)
  • 作者单位

    Radiation Instrumentation Research Division, Korea Atomic Energy Research Institute, Jeongeup, Republic of Korea;

    Radiation Instrumentation Research Division, Korea Atomic Energy Research Institute, Jeongeup, Republic of Korea,Department of Advanced Material Chemistry Dongguk University-Gyeongju, Gyeongju, Republic of Korea;

    Radiation Instrumentation Research Division, Korea Atomic Energy Research Institute, Jeongeup, Republic of Korea;

    Radiation Instrumentation Research Division, Korea Atomic Energy Research Institute, Jeongeup, Republic of Korea;

    Department of Advanced Material Chemistry Dongguk University-Gyeongju, Gyeongju, Republic of Korea;

    Department of Chemistry, Dongguk University-Seoul, Seoul, Republic of Korea;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Anthraquinone; HER-2eu; ~(123)I; breast cancer;

    机译:蒽醌; HER-2 / neu; 〜(123)我;乳腺癌;

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