Potential radiosensitizing agents. 5. 2-Substituted benzimidazole derivatives
- 1 November 1982
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 25 (11) , 1342-1346
- https://doi.org/10.1021/jm00353a014
Abstract
A series of 2-substituted benzimidazoles and their derivatives were synthesized and tested for their ability to selectively sensitize hypoxic Chinese hamster cells [lung fibroblast] (V-79) toward the lethal effect of ionizing radiation. These compounds were prepared by reacting the 2-substituted benzimidazoles with 1,2-epoxy-3-methoxypropane in the presence of potassium carbonate. Reaction of the 2-nitro and 2-methylsulfonyl analog with the epoxide also yielded a cyclized material, which was confirmed to be a benzimidazo[2,1-b]oxazole. In an attempt to increase the electron affinity, 5- or 6-nitro-2-substituted-benzimidazoles were also synthesized and then reacted with the epoxide to yield the corresponding 1-substituted derivatives. The results of the biological tests for the radiosensitizing activity of these agents against V-79 cells in culture indicated that the 2-nitro-substituted analogs were the most effective sensitizers in this series.This publication has 1 reference indexed in Scilit:
- Potential radiosensitizing agents. DinitroimidazolesJournal of Medicinal Chemistry, 1979