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WANG Wu-shang, ZHANG Jin-ming, LIU Bo-li. Preparation of [125I]TZDM[J]. Journal of Nuclear and Radiochemistry, 2010, 32(1): 57-60.
Citation: WANG Wu-shang, ZHANG Jin-ming, LIU Bo-li. Preparation of [125I]TZDM[J]. Journal of Nuclear and Radiochemistry, 2010, 32(1): 57-60.

Preparation of [125I]TZDM

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  • Received Date: December 31, 1899
  • Revised Date: December 31, 1899
  • An excellent Aβ imaging agent must have high affinity for Aβ plaques. The in vitro competition binding assay is an effective method for determining the affinity of unlabelled imaging agents for Aβ plaques. [125I]TZDM was often used as a radioactive ligand in the assay. In this paper, Bu3Sn-TZDM, a precursor compound of [125I]TZDM, was synthesized by four steps from 4-bromo-aniline. After the precursor compound was labeled with 125I, crude [125I]TZDM was obtained. The labelling yield is 62.5%. [125I]TZDM is separated with HPLC and has more than 97% radiochemical purity. The actual yield is 25%.
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