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具有抗肿瘤活性的亚氨基硒代氨基甲酸酯的新型结构见解与其生成甲基硒醇的能力有关。

Novel structural insights for imidoselenocarbamates with antitumoral activity related to their ability to generate methylselenol.

机构信息

Sección de Modelización Molecular, Departamento de Química Orgánica y Farmacéutica, University of Navarra, Irunlarrea 1, E-31008 Pamplona, Spain.

出版信息

Bioorg Med Chem. 2012 Sep 1;20(17):5110-6. doi: 10.1016/j.bmc.2012.07.013. Epub 2012 Jul 15.

Abstract

In the search for molecules with potential antiangiogenic activity we found that several imidoselenocarbamate derivatives, which have pro-apoptotic and antiproliferative activities, under hypoxic conditions release methylselenol, a volatile and highly reactive gas that was considered to be responsible for the observed biological activity. The kinetic for the liberation of methylselenol is highly dependent on the nature of the overall structure and correlate with their proven pro-apoptotic activity in lung cancer cell line H157. The preliminary structure-activity relationships allow us to select as the basic structural element a scaffold constructed with an imidoselenocarbamate fragment decorated with a methyl residue on the Se central atom and two heteroaromatic lateral rings. These imidoselenocarbamate derivatives may be of interest both for their antitumoral activities and because they have a structure that can be considered as a template for the design of new derivatives with apoptotic activity. This activity is related to the controlled delivery of methylselenol and makes this an interesting approach to develop new antitumoral agents.

摘要

在寻找具有潜在抗血管生成活性的分子的过程中,我们发现几种亚氨基硒代氨基甲酸酯衍生物在缺氧条件下释放甲基硒醇,这是一种挥发性和高反应性气体,被认为是导致观察到的生物活性的原因。甲基硒醇释放的动力学高度依赖于整体结构的性质,并与它们在肺癌细胞系 H157 中已证明的促凋亡活性相关。初步的结构-活性关系使我们能够选择一个由亚氨基硒代氨基甲酸酯片段构建的基本结构单元,该片段用 Se 中心原子上的一个甲基残基和两个杂芳环进行修饰。这些亚氨基硒代氨基甲酸酯衍生物可能因其抗肿瘤活性而引起关注,并且因为它们的结构可以被认为是设计具有凋亡活性的新衍生物的模板。这种活性与甲基硒醇的控制释放有关,这是开发新的抗肿瘤药物的一个有趣方法。

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