1. Academic Validation
  2. Design, Synthesis, and Biological Evaluation of Boron-Containing Macrocyclic Polyamines and Their Zinc(II) Complexes for Boron Neutron Capture Therapy

Design, Synthesis, and Biological Evaluation of Boron-Containing Macrocyclic Polyamines and Their Zinc(II) Complexes for Boron Neutron Capture Therapy

  • J Med Chem. 2021 Jun 24;64(12):8523-8544. doi: 10.1021/acs.jmedchem.1c00445.
Hiroki Ueda 1 Minoru Suzuki 2 Reiko Kuroda 3 Tomohiro Tanaka 1 Shin Aoki 1 3 4
Affiliations

Affiliations

  • 1 Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.
  • 2 Institute for Integrated Radiation and Nuclear Science, Kyoto University, 2-Asashiro-nishi, Kumatori, Osaka 590-0494, Japan.
  • 3 Research Institute for Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.
  • 4 Research Institute for Biomedical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.
Abstract

Boron neutron capture therapy (BNCT) is a binary therapeutic method for Cancer treatment based on the use of a combination of a cancer-specific drug containing boron-10 (10B) and thermal neutron irradiation. For successful BNCT, 10B-containing molecules need to accumulate specifically in Cancer cells, because destructive effect of the generated heavy particles is limited basically to boron-containing cells. Herein, we report on the design and synthesis of boron compounds that are functionalized with 9-, 12-, and 15-membered macrocyclic polyamines and their Zn2+ complexes. Their cytotoxicity, intracellular uptake activity into Cancer cells and normal cells, and BNCT effect are also reported. The experimental data suggest that mono- and/or diprotonated forms of metal-free [12]aneN4- and [15]aneN5-type ligands are uptaken into Cancer cells, and their complexes with intracellular metals such as Zn2+ would induce cell death upon thermal neutron irradiation, possibly via interactions with DNA.

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