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潜在的放射增敏剂。5. 2-取代苯并咪唑衍生物。

Potential radiosensitizing agents. 5. 2-Substituted benzimidazole derivatives.

作者信息

Gupta R P, Larroquette C A, Agrawal K C

出版信息

J Med Chem. 1982 Nov;25(11):1342-6. doi: 10.1021/jm00353a014.

Abstract

A series of 2-substituted benzimidazoles and their derivatives have been synthesized and tested for their ability to selectively sensitize hypoxic Chinese hamster cells (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-methylfonyl analogue 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 Chinese hamster cells (V-79) in culture indicated that the 2-nitro-substituted analogues were the most effective sensitizers in this series.

摘要

已合成了一系列2-取代苯并咪唑及其衍生物,并测试了它们选择性地使缺氧的中国仓鼠细胞(V-79)对电离辐射的致死效应敏感的能力。这些化合物是通过在碳酸钾存在下使2-取代苯并咪唑与1,2-环氧-3-甲氧基丙烷反应制备的。2-硝基和2-甲磺酰基类似物与环氧化物的反应也产生了一种环化物质,经证实为苯并咪唑并[2,1-b]恶唑。为了提高电子亲和力,还合成了5-或6-硝基-2-取代苯并咪唑,然后使其与环氧化物反应以生成相应的1-取代衍生物。这些试剂对培养中的中国仓鼠细胞(V-79)的放射增敏活性的生物学测试结果表明,2-硝基取代类似物是该系列中最有效的增敏剂。

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