Synthesis and radiolabeling of a polar [125 I]I-1,2,4,5-tetrazine

J Labelled Comp Radiopharm. 2023 Jan;66(1):22-30. doi: 10.1002/jlcr.4009. Epub 2022 Dec 30.

Abstract

Pretargeting imaging has gained a lot of prominence, due to its excellent bioorthogonality and improved imaging contrast compared to conventional imaging. A new iodo tetrazine (Tz) derivative has been synthesized and further developed into the corresponding iodine-125 (125 I) analog (12), via the trimethylstannane precursor. Radiolabeling with either N-chlorosuccinimide or chloramine-T, in either MeCN or MeOH proceeded with a radiochemical conversion (RCC) of >80%. Subsequent deprotection only proved successful, among the tested conditions, when the radiolabeled Tz was stirred in 6-M HCl(aq.) at 60°C for 2.5 h. To the best of our knowledge, this is the first H-tetrazine labeled with iodine. In vivo investigations on the pretargeting ability of 12 are currently under way.

Keywords: bioorthogonal; click chemistry; idodine-125; pretargeting; tetrazine.

MeSH terms

  • Cell Line, Tumor
  • Click Chemistry / methods
  • Heterocyclic Compounds*
  • Iodine Radioisotopes
  • Radiopharmaceuticals*

Substances

  • Iodine-125
  • 1,2,4,5-tetrazine
  • Radiopharmaceuticals
  • Heterocyclic Compounds
  • Iodine Radioisotopes